PAGE 1 INFLUENCE OF GOLD PARTICLES ON GALLIUM ARSENIDE SUBSTRATE WHEN ETCHED IN CHLORINE PLASMA By ERIKA COURTNEY LENT A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2005 PAGE 2 Copyright 2004 By Erika Courtney Lent PAGE 3 ACKNOWLEDGEMENTS I would like to thank and acknowledge my advisor, Dr. Claudia Milz, and Dr. Mark Davidson for their guidance and support with this research. I would like to extend my sincerest thanks and gratitude towards my family and friends for their endless support and encouragement. I could not have done it without them. They gave me the courage to keep going when things looked dark and the inspiration to surpass my own expectations to achieve all that I have. iii PAGE 4 TABLE OF CONTENTS Page ACKNOWLEDGEMENTS................................................................................................iii LIST OF TABLES..............................................................................................................vi LIST OF FIGURES...........................................................................................................vii ABSTRACT......................................................................................................................xii CHAPTER 1 INTRODUCTION...................................................................................................1 2 EXPERIMENTATION..........................................................................................14 2.1 Sample Preparation....................................................................................14 2.2 Analysis Techniques..................................................................................20 3 RESULTS..............................................................................................................22 3.1 Atomic Force Microscopy.........................................................................22 3.1.1 Sample 1.........................................................................................22 3.1.2 Sample 2.........................................................................................23 3.1.3 Sample 3.........................................................................................23 3.1.4 Sample 6.........................................................................................25 3.1.5 Sample 5.........................................................................................26 3.2 Field Emission Scanning Electron Microscopy and Energy Dispersive Spectroscopy..........................................................................................28 3.2.1 Sample 1.........................................................................................28 3.2.2 Sample 2.........................................................................................33 3.2.3 Sample 3.........................................................................................36 3.2.4 Sample 6.........................................................................................40 3.2.5 Sample 5.........................................................................................43 4 DISCUSSION AND CONCLUSIONS.................................................................52 4.1 Atomic Force Microscopy.........................................................................52 4.2 Field Emission Scanning Electron Microscopy and Energy Dispersive Spectroscopy..........................................................................................54 iv PAGE 5 5 SUMMARY...........................................................................................................58 APPENDIX A ADDITIONAL AFM RESULTS...........................................................................60 B ADDITIONAL SEM/EDS RESULTS..................................................................62 REFERENCE LIST...........................................................................................................75 BIOGRAPHICAL SKETCH.............................................................................................77 v PAGE 6 LIST OF TABLES Table Page 1 General trends of etch conditions when a parameter is increased...9 2 Etch recipes for each sample..19 3 Average height and standard deviation for Samples 1, 2, 3, 5, and 6....28 vi PAGE 7 LIST OF FIGURES Figures Page 1 The two basic methods of pattern transfer ..........................................2 2 Anisotropic etching.......................... 3 A simple plasma reactor.......................................5 4 The plasma sheath........5 5 A schematic of the plasma reactor.......8 6 Sputtering versus chemical etching...10 7 Non-directional versus directional etching 8 Etch profiles due to increased chlorine flow..11 9 Increased Ar flow increases etch depth and anisotropy of GaAs..................12 10 Increased pressure decreases etch rate...13 11 Electron-beam Lithography apparatus... 12 The development of the pattern.....16 13 Metal evaporator 14 Optical microscope image of the gold star array on GaAs....18 15 AFM image and line scan plot of sample 1 unetched 16 AFM image and line scan plot of sample 2 etched in chlorine/argon plasma...24 17 AFM image and line scan plot of sample 3 etched in chlorine/argon plasma...25 18 AFM image and line scan plot of sample 6 unetched 19 AFM image and line scan plot of sample 5 etched in chlorine/argon plasma...27 vii PAGE 8 20 Secondary electron image of sample 1 unetched...28 21 Backscatter electron image of sample 1 unetched.29 22 Secondary electron image with map of EDS points......................................29 23 EDS spectrum for point 1 at the center of a star on sample 1 unetched....30 24 EDS spectrum for point 3 on the substrate of sample 1 unetched.....................31 25 EDS spectrum for point 5 on the particle on the tip of the star................. 26 EDS spectrum for point 6 on a dark dot on the substrate of sample 1...32 27 EDS gold line scan spectrum on sample 1 unetched.....32 28 Secondary electron image of sample 2 etched in chlorine/argon plasma......33 29 Backscatter electron image of sample 2 etched in chlorine/argon plasma....34 30 Backscatter electron image with map of EDS points.................................34 31 EDS spectrum for point 1 on the center of the star of sample 2 etched.............35 32 EDS spectrum for point 3 on the substrate of sample 2 etched.........35 33 EDS line scan spectrum for gold for sample 2 etched.......36 34 Secondary electron image of sample 3 etched in chlorine/argon plasma......37 35 Backscatter electron image of sample 3 etched in chlorine/argon plasma....37 36 Backscatter electron image with map of EDS points.................................38 37 EDS spectrum for point 1 on the star of sample 3 etched..............38 38 EDS spectrum for point 3 on the substrate of sample 3 etched.........39 39 EDS spectrum for point 5 on the dark area on the tip of the star...........................39 40 EDS line scan spectrum for gold on sample 3 etched........................40 41 Secondary electron image of sample 6 unetched...................................................41 42 Backscatter electron image of sample 6 unetched.................................................42 viii PAGE 9 43 Backscatter electron image of sample 6 unetched with map of EDS points.........42 44 EDS spectrum for point 1 on sample 6 unetched...................................................43 45 EDS spectrum for point 3 on the substrate of sample 6 unetched.........................43 46 Secondary electron image of star A on sample 5 etched in chlorine/argon plasma....................................................................................................................44 47 Backscatter electron image of star A on sample 5 etched in chlorine/argon plasma....................................................................................................................45 48 Secondary electron image of star A on sample 5, etched, with map of EDS points.........................................................................................................45 49 EDS spectrum for point 1 on star A on sample 5 etched.......................................46 50 EDS spectrum for point 3 on the substrate near star A on sample 5.....................46 51 EDS spectrum for point 5, a particle on star A of sample 5..................................47 52 EDS spectrum for point 6, a brighter area on the tip of star A on sample 5..........47 53 Secondary electron image of star B on sample 5 etched in chlorine/argon plasma....................................................................................................................48 54 Backscatter electron image of star B on sample 5 etched in chlorine/argon plasma....................................................................................................................48 55 Secondary electron image of star B on sample 5 etched, with map of EDS points.........................................................................................................49 56 EDS spectrum for point 1 at the center of star B on sample 5 etched...................49 57 EDS spectrum for point 3 on the substrate near star B on sample 5 etched..........50 58 EDS spectrum for point 7, star B...........................................................................50 59 EDS spectrum for point 8 on a particle on star B, sample 5, etched.....................51 60 This is a plot of the etched samples 2 and 3 line scans superimposed...................53 61 This is a plot of the etched sample 5 line scan superimposed...............................54 62 AFM image and line scan plot of sample 3 etched in chlorine/argon plasma.......60 ix PAGE 10 63 AFM image and line scan plot of sample 5 etched in chlorine/argon plasma.......61 64 EDS spectrum for point 2 on the star of sample 1 unetched..................................62 65 EDS spectrum for point 4 on the substrate of sample 1 unetched.........................63 66 EDS spectrum for point 2 on the star of sample 2 etched......................................63 67 EDS spectrum for point 4 on the substrate of sample 2 etched.............................64 68 EDS spectrum for point 2 on a star of sample 3 etched.........................................64 69 EDS spectrum for point 4 on the substrate of sample 3 etched.............................65 70 EDS spectrum for point 2 on a star of sample 6 unetched.....................................65 71 EDS spectrum for point 4 on the substrate of sample 6 unetched.........................66 72 EDS spectrum for point 2 on star A of sample 5 etched in chlorine/argon plasma....................................................................................................................66 73 EDS spectrum for point 4 on the substrate of sample 5 etched in chlorine/argon plasma....................................................................................................................67 74 EDS spectrum for point 2 on star B of sample 5 etched in chlorine/argon plasma....................................................................................................................67 75 EDS spectrum for point 4 on the substrate of sample 5 etched in chlorine/argon plasma....................................................................................................................68 76 Secondary electron image of star C on sample 5 etched in chlorine/argon plasma....................................................................................................................68 77 Backscatter electron image of star C on sample 5 etched in chlorine/argon plasma....................................................................................................................69 78 Secondary electron image of star C on sample 5, etched, with map of EDS points.........................................................................................................69 79 EDS spectrum of point 1 on star C of sample 5 etched.........................................70 80 EDS spectrum of point 2 on star C of sample 5 etched.........................................70 81 EDS spectrum of point 3 on the substrate near star C of sample 5........................71 82 EDS spectrum of point 4 on the substrate of sample 5..........................................71 x PAGE 11 83 Secondary electron image of star D on sample 5 etched in chlorine/argon plasma....................................................................................................................72 84 Backscatter electron image of star D on sample 5 etched in chlorine/argon plasma....................................................................................................................72 85 Secondary electron image of star D with a map of EDS points.............................73 86 EDS spectrum for point 1 on star D of sample 5 etched........................................73 87 EDS spectrum for point 2 on star D of sample 5 etched........................................74 xi PAGE 12 Abstract of Thesis Presented to the Graduate School of the University of Florida in Partial Fulfillment of the Requirements for the Degree of Master of Science INFLUENCE OF GOLD PARTICLES ON GALLIUM ARSENIDE SUBSTRATE WHEN ETCHED IN CHLORINE PLASMA By Erika Courtney Lent May 2005 Chair: Claudia Milz Major Department: Materials Science and Engineering Gallium arsenide is a valuable semiconductor material used in many applications including microelectronic devices, optoelectronics, and integrated circuits. The desire to continuously improve upon the current applications and generate new and innovative applications necessitates advancements in the processing techniques. One key step in the processing technique is the development of the features through plasma etching. As the feature sizes become smaller, precision in the formation of the features becomes more critical. Chlorine-based plasmas are the most commonly used to dry etch gallium arsenide wafers during device manufacturing primarily because of the volatility of the chlorides that are formed by the reaction. There has been some thought that gold may be used as a catalyst to enhance the etching process. A sample was prepared with gold stars on a gallium arsenide substrate and then etched in chlorine/argon plasma. Electron beam lithography was used to create the xii PAGE 13 template for the star array. Gold was then deposited onto the sample with a metal evaporator filling the voids created during electron beam lithography to form the gold stars. The samples were then analyzed for any changes in surface characteristics after being etched using atomic force microscopy, scanning electron microscopy and energy dispersive spectroscopy techniques. Scanning electron microscopy and energy dispersive results show that the gold stars remained intact on the substrate surface. There was no significant change in surface conditions between etched and unetched samples, indicating that the presence of gold did not enhance the etching of the gallium arsenide. Analysis with atomic force microscopy gave results that led to the same conclusion. The atomic force microscopy results did show that the surface was etched. Unetched samples had a relatively smooth surface while the etched samples exhibited a rough surface characteristic of etching. Through this research using these methods it was shown that gold does not influence the etching of gallium arsenide in chlorine plasma. xiii PAGE 14 CHAPTER 1 INTRODUCTION Background This research aims to describe and understand the corrosion mechanisms of a gallium arsenide substrate decorated with gold particles when etched in plasma with the intent of creating nanostructures. Gallium arsenide (GaAs) is a valuable semiconductor material used in many applications including microelectronic devices, optoelectronics, and integrated circuits. It is desirable for its superior electronic properties over Silicon, another material often used in the semiconductor industry. GaAs has a high electron mobility that allows for operation at high frequencies (>250GHz) with minimal noise [1, 2]. Another advantage of GaAs is that it has the ability to emit light due to its direct band gap. One major disadvantage of GaAs compared to silicon is cost; silicon is very inexpensive because it is the second most abundant element on Earth and has fewer processing limitations than GaAs [1, 2]. May and Sze point out that since the beginning of the microelectronics era, the minimum feature length of an integrated circuit has been reduced at a rate of about 13% per year. By the year 2010 the minimum feature length is estimated to be 50nm. Along with the shrinking sizes of devices come the advantages of reduced unit cost per circuit function, increased device speed, expanded functional throughput rates, and decreased power consumption [1, 3]. The consumer demand for such devices could drive the growth of the gallium industry even faster than the forecasted 290 metric tons by the year 2008 [4]. Thus, the desire to continuously 1 PAGE 15 2 improve upon the current applications and generate new and innovative applications necessitates advancements in the processing techniques. A key step in the processing technique is the development of the features. As the feature sizes become smaller, precision in the formation of the features becomes critical; any deviation could result in a failed device. Before the features are formed it is necessary to create a template on the material through either an additive or subtractive process to define where the features are to be located as shown in Figure 1. In the subtractive process, the feature material is deposited directly onto the substrate. To pattern this film, a mask is formed next, usually by photolithography [3]. The mask material, or resist, is a light-sensitive polymer that is spun onto the wafer and dried. It is exposed to light through a mask containing the desired pattern. The exposed areas of resist can then be removed. In the additive process, the mask is created first and is then followed by deposition of the feature material. Unexposed areas of resist are removed with a developer [3]. Figure 1. The two basic methods of pattern transfer are: subtractive, where the material is removed from areas not protected by the mask; and additive, where the material is deposited over the mask pattern and the mask with the undesired material deposits is later removed [3, 5]. PAGE 16 3 Now that a template has been established, the next step is etching. There are two main methods used in industry to create the features, wet etching or dry etching. Wet etching occurs when a material is dissolved when submersed in a chemical solution. A disadvantage of wet etching is the isotropic nature which increases the difficulty to control critical feature dimensions [3, 5]. Isotropic etching is when a material etches at the same rate in all directions; undercutting is often a problem as shown in Figure 2. Anisotropic etching, when a material etches at different rates in different directions can also be a problem. Certain crystallographic planes of some materials etch at different rates. However, if those planes are not vertical to the surface being etched, the hole being created will not have perfectly vertical sidewalls (Figure 2). Figure 2. Anisotropic etching, different etch rates in different directions, with off-vertical sidewalls. Isotropic etching, same etch rate in all directions, with undercutting of the mask. [5] These are extreme examples of each case; it is possible to have a combination of anisotropic and isotropic etching characteristics. Dry etching occurs when a material is sputtered off or dissolved using reactive ions or a vapor phase etchant. An advantage of dry etching is the ability to better control feature dimensions; there is greater resolution of the features. However, the cost of dry etching is significantly greater than for wet etching. Wet chemical etching is used extensively in PAGE 17 4 semiconductor processing [1]. However, it is best suitable for whole surface etching and not for patterning as a major disadvantage is the undercutting of the material below the mask, resulting in a loss of resolution of the final features [1]. Thus, regardless of the increased costs, industry has adopted the dry etch method to achieve the small features needed to keep up with the demands for smaller and smaller devices [1, 3, 5]. Plasma etching is a dry etching method and is of particular interest because of its efficiency in producing micron-sized features of specific dimensions and extensive use in the semiconductor industry. In general, a plasma can be described as an ionized gas that is charge neutral. This means that there are equal numbers of free positive and negative charges [1, 3]. The charges are generated when a voltage is applied between two electrodes inducing a current flow to form the plasma as shown in Figure 3. The positive charge is mostly in the form of singly ionized neutrals, including atoms, radicals, or molecules, that have been stripped of one electron [3]. The negative charges are usually free electrons [3]. As the diffusion of charge to the walls and recombination on the sample surface occurs, there is a depletion of charge in the adjacent gas. Because the electrons are light and have high energy, they diffuse the fastest, leaving a thin boundary layer of positive charge referred to as the sheath [3]. Positive ions are accelerated towards the surface of the substrate which has accumulated a negative charge from the electrons that have diffused to the substrate and strike at near-normal incidence. This causes directional etching and results in features with vertical sidewalls. Figure 4 illustrates the sheath and near-normal incidence of the ion striking to produce vertical sidewalls. PAGE 18 5 Figure 3. A simple plasma reactor consisting of opposed parallel plate electrodes in a vacuum chamber. There is a continuous gas feed in and a port for pumping out. A radio frequency power source is coupled to the electrodes to generate a plasma. [3] Plasma ++++++ ++ --------Sheath Substrate Electrode Figure 4. The plasma sheath. The diffusion of electrons from the gas adjacent to the sample to the walls or surfaces creates a positive layer called the sheath. The accumulated negative charge on the substrate attracts the positive charges of the sheath which accelerate towards and strike the the substrate a near-normal incidence. This produces vertical sidewalls. PAGE 19 6 The reactive neutral and charged species generated from the plasma react with the substrate to form volatile species. For example, in Cl 2 chemistry, Cl and Cl 2 neutrals and charged Cl radicals form AsCl x volatiles with a GaAs substrate. Chemical etching occurs when the volatile species evaporate, reducing the substrate thickness usually isotropically. In addition, the electrostatic fields created by the particles of the plasma may accelerate charged species so that substrate material is removed due to the ion bombardment, mechanical etching which tends to be anisotropic. Non-volatile, or less volatile, etch products (GaCl x ) may also be removed through ion bombardment. It is the relationship between the physical sputtering and the chemical reaction mechanisms that greatly influence the dimensions of the features, both of which can be influenced by etch parameters that will be discussed later in this paper. Selectivity, the ratio of etch rates between different materials when exposed to the same environment [6], also is an important factor in feature dimensions. Chemical etching is more selective than mechanical etching and is inherently sensitive to differences in bonds and the consistency of the substrate [3]. The degree of selective etching of one material relative to others can most easily be manipulated through changes in plasma chemistry [6]. Materials may also exhibit selectivity of one crystallographic plane over another as in GaAs. For GaAs in Cl 2 plasma, the relative etch rates of the crystal planes are As-rich [111]>[100]>[110]>Ga-rich [111] [3]. Gold Plasma Etching Gold has been determined to be relatively inert during plasma etching and therefore has been used as a mask material when creating nanostructures, IC circuits, and other microelectronic devices [7,8,9]. If gold is etched, it tends to be physically sputtered PAGE 20 7 off through ion-bombardment with an inert gas such as Argon. Efremov, Kim, and Kim have shown that physical etching of gold is more effective than chemical etching with an etch rate in pure Argon more than double that of the etch rate in pure chlorine [10]. They have also shown that there is an accumulation of the reaction products, AuCl x with the increase of chlorine content. The accumulation is due to the low volatility of AuCl x To encourage the gold chlorides to leave the sample surface, an inert gas is often introduced to the system which provides a physical motivation. There has been some thought that gold may be used as a catalyst to enhance the etching process. Though there is not much known about the details of this process, it is believed that when small clusters or particles of gold, approximately 3-5nm in size, are deposited onto the surface of a substrate the etch rate is enhanced [8, 9]. Some of the reactions catalyzed by gold include the oxidation of carbon monoxide and hydrocarbons, hydrogenation of carbon monoxide and carbon dioxide, and the removal of carbon monoxide from hydrogen streams [8, 9]. Thompson reports that the use of gold for heterogeneous catalysis, in which the catalyst and reactants are in different phases, could have considerable industrial significance. Hence, this is the reason for using gold as a potential catalyst for the system in this research. Plasma Etching A Plasmatherm 770 Electron Cyclotron Resonance/Reactive Ion Etching reactor was used to etch the substrate. A diagram of the apparatus is shown in Figure 5. In an electron cyclotron resonance (ECR) reactor, microwave power and a static magnetic field work together to force the electrons to circulate around the magnetic field lines with an angular frequency. When the frequency of the circulating electrons matches that of the PAGE 21 8 applied microwave frequency, a high degree of dissociation and ionization (10 -2 for ECR compared with 10 -6 for RIE) results due to the coupling between the electron energy and the applied electric field [9]. The ECR creates high density plasma in which the concentration of charged particles is approximately 10 11 cm -3 [1,3,11]. A high density plasma can potentially produce higher etch rates because of the increased concentration of charged particles and typically exhibits less damage than that produced from a reactive ion etching reactor [1, 11]. Figure 5. A schematic of the plasma reactor is pictured. Note the circulation of electrons in the plasma induced by the magnetic coil in the upper region of the etch chamber. The reactive ion etching (RIE) part of the reactor consists of a radio frequency applied to the sample platform acts as a grounded electrode with an area the size of the reactor chamber. As electrons attach to the sample surface a negative self-bias occurs which attracts the energetic ions of the plasma to the surface. There is a load lock chamber where the sample is inserted before being transferred into the etch chamber by PAGE 22 9 an automatic arm. An applied radio frequency (RF) substrate power influences the ion speed; a higher RF power increases the ion speed and the amount of sputtering, mechanical etching, which occurs. The microwave power influences the plasma density; an increase in microwave power results in a more dense plasma with more ionized particles that will enhance chemical etching. Table 1 summarizes these parameters. Table 1. General trends of etch conditions when a parameter is increased Parameters Sputter Etching Chemical Etching Etch Rate Vertical Sidewalls Pressure Temperature Cl 2 Flow Ar Flow Microwave Power RF Power Chlorine-based plasmas are the most commonly used to dry etch GaAs wafers during device manufacturing [12]. This is primarily because of the volatility of the chlorides that are formed by the reaction. Group III chlorides, GaCl 2 and InCl 2 are suitably volatile at practical processing temperatures where as Group III fluorides, GaF 3 and InF 3 are not, making Cl 2 chemistry the preferred choice [3]. It is for these reasons that chlorine has been selected as the etchant of choice for this research. Etch Mechanisms From previous research, it is understood that the chemical etching mechanism leads to a more isotropic etch characteristic, and undercutting, while physical sputtering leads to a more anisotropic etch (Figure 6). The chemical etch of a material depends on the reaction between the reactive neutral species (i.e., Cl, Cl 2 ) with the sample. PAGE 23 10 Mechanical etching or ion-assisted etching (bombarding ions remove non-volatile etch products) is driven by the acceleration of the charged species in the plasma towards the oppositely charged sample due to the applied RF power as illustrated in Figure 7. Thus chemical etching is more probable to occur than direct ion bombardment on the feature sidewalls. For example, an increased flow rate of Cl 2 increased the concentration of Cl that are able to form volatile species with the GaAs substrate resulting in sidewalls that are more rounded [13] (Figure 8a). It is also expected that as the concentration of Cl is increased, a layer of increasing thickness of GaCl 3 forms, limiting the etch rate [3, 14]. The GaCl 3 forms at the surface of the GaAs. Its low volatility prevents it from desorbing off of the GaAs substrate unless it is energetically removed by ion bombardment. The etch depth and sharpness of the feature dimensions decreased with increasing Cl 2 flow rate (Figure 8b). Similar results are expected for increasing Cl 2 flow rates from our experimentation. Future TEM analysis would show the crystallographic selectivity of GaAs planes with the As rich planes having a higher etch rate than the Ga rich planes due to the formation of more volatile As chloride species. Werbaneth et al, reported that an increased Cl 2 flow decreased the etch profile, more tapered sidewalls, and increased the Au etch rate. At a high enough Cl 2 flow, it is expected that some reduction in the gold layer will occur. Figure 6. Sputtering versus chemical etching. PAGE 24 11 Figure 7. Non-directional versus directional etching. Figure 8. Etch profiles due to increased chlorine flow. Adding Ar into the plasma chemistry enhanced anisotropic etching. It created ion bombardment by a non-reactive species that encouraged the volatilization of etchants such as the often rate limiting GaCl 3 species. Because of this, it is expected that as the Ar flow rate increases, the amount of ion bombardment increases, reducing the GaCl 3 layer Au Au Au Au GaCl 3 GaAs GaAs a) Rounded sidewalls due to increased chlorine flow. The concentration of chlorine reactants is increased. This increases the amount of chemical etching which tends to be isotropic. b) The accumulation of GaCl 3 a less volatile species, at the bottom and sides of the feature often result in a loss of etch depth and feature definition. With increased chlorine flow and the increase in chlorine reactant concentration, more GaCl 3 is formed. non-volatile (GaCl x ) Ar or Cl Cl 2 volatile (AsCl x ) sample (GaAs) sample (GaAs) a) Reactive neutral species combine with sample surface to form a volatile species that leaves the substrate; non-directional etching. b) Charged ions accelerated toward substrate at near-normal incidence. Removal of substrate material or non-volatile etch product may occur. Etching is directional. PAGE 25 12 thickness by encouraging volatilization and increasing the etch depth (Figure 9). Since ion bombardment occurs predominantly at the bottom of a feature, the overall etch rate in that direction becomes more rapid than the rate in all other directions resulting in anisotropic etching [11]. The Au etch rate also increased as the Ar flow increased and the sidewalls became more tapered [7, 8]. a) Low Ar flow c) High Ar flow b) Intermediate Ar flow Figure 9. Increased Ar flow increases etch depth and anisotropy of GaAs. For optimal etching, where the conditions are the most favorable for etching to occur, it is desirable to maximize the amount of species present at the substrate surface. This increases the likelihood of and the opportunity for the species to react with the surface to form a volatile product resulting in the etching of that surface. At pressures higher than 2 mTorr, the reactive species are more likely to collide and recombine before reaching the substrate surface resulting in a decreased etch rate and shallow etch depth. The shallow etch depth may also be attributed to the reduced sputtering due to energy losses suffered from the particle collisions. It seems likely that the resulting features will have low angle sidewalls. At pressures lower than 2 mTorr, there is sufficient species present at the substrate surface for etching. The etch profile at 2 mTorr is expected to have close to vertical sidewalls and greater etch depths than other pressures (Figure 10). However, at pressures below 1 mTorr, insufficient amounts of Cl 2 limit etching [3]. The PAGE 26 13 resulting etch profile is expected to be similar to that of pressures greater than 2 mTorr due to the lack of reactive species present to cause etching. < 2mTorr Samples 1 Figure 10. Increased pressure decreases etch rate. PAGE 27 CHAPTER 2 EXPERIMENTATION 2.1 Sample Preparation Using a Spincoater Model P6700 Series by Specialty Coating Systems, Inc., a 2 GaAs(001) wafer is spin-coated with 950 molecular weight polymethyl methacrylate (PMMA) to form a film approximately 400nm thick. The wafer is placed into the spincoater and is held in place by vacuum force from below on the sample holder. The sample holder then begins to spin the wafer. The wafer is cleaned before being coated with PMMA, first with acetone and then with methanol to prevent contamination from particulates and impurities in the acetone. Once dry, the spinning is stopped to deposit the PMMA onto the wafer. A pipette is used to draw the PMMA from the center of an unshaken bottle to avoid any particles that may have settled. The PMMA is deposited onto the center of the wafer until it covers as much of the wafer as possible without dripping over the edge also being careful to avoid air bubbles. Spinning is resumed and continues until the PMMA is evenly distributed over the wafer. When spinning is complete, the wafer is baked on a hot plate at 160C for 15 minutes to drive out any residual solvent. The wafer is then cleaved into quarters for ease of handling and processing. 14 PAGE 28 15 Figure 11. Electron-beam Lithography apparatus. The Computer Control instructs the patterning of the mask by both adjusting the beam blanking and table positioning to achieve the desired pattern as set by the operator with the CAD program [15]. Electron-beam lithography is used next to create an ordered pattern in the PMMA resist. Design CAD is the program that is used to create a pattern and then instructs the electron-beam apparatus of the FEI XL-40 field emission microscope how to create that pattern. An apparatus is shown in Figure 11. The computer controls the areas of the photoresist that are exposed to the electron beam through manipulation of beam blankers and the sample table to achieve the specified pattern. The pattern created was based on a single fractal star with an intricate perimeter and several points of strain to maximize the possible effects of the gold particles on GaAs. An array of 20 stars by 20 stars was repeated 100 times, 10 times in the x-direction and 10 times in the y-direction, onto the PAGE 29 16 wafer. The distance between stars is 100nm in this array. The pattern is shown on a smaller scale in Figure 12. Sampl e a) b) c) c) Figure 12. The development of the pattern is shown in smaller scale. a) This is the original star chosen from a menu in the Design CAD program. b) The program is commanded to create an array of these stars, 20 stars in the x-direction and 20 stars in the y-direction; shown is 2 stars in the x-direction and 2 stars in the y-direction. c) The program is commanded to repeat this array to create the final pattern, 10 arrays in the x-direction and 10 arrays in the y-direction; shown is 2 arrays in the x-direction and 2 arrays in the y-direction. Drawing not to scale of actual pattern. This takes approximately two hours to complete. The areas exposed to the electron beam must now be removed. The PMMA in the areas that are exposed to the electron beam breaks down and can be easily removed once developed. The areas not exposed to electron beam during patterning are not removed in the developing process. To remove the exposed areas, the wafer is submerged in a 1 to 3 ratio of MIBK to isopropyl alcohol developing solution for 70 seconds. Upon removal from the developing solution, the wafer is rinsed in deionized water and dried by helium gas to prevent contamination from particulates in the developing solution or deionized water. What is left is a layer of resist PAGE 30 17 with an array of holes, exposing the GaAs in the shape of fractal stars. Field emission microscope images showed that the lithography was successful in creating an array of fractal stars in the resist. It is important to be aware of the potential for overexposure or underexposure with electron-beam lithography as both situations influence the final pattern. If overexposed, the features become less defined around the edges. Underexposure results in incomplete features or possibly no features at all because the resist cannot be removed when developed. In both cases the dosage can be adjusted to alleviate the problem; decreased if overexposed, increased if underexposed. The typical appropriate dose for these patterns was around 190,000 C/cm 2 Gold is then deposited onto the wafer filling in the areas where the resist was removed to form gold stars. This was done using a metal evaporator to achieve a uniform layer thickness (Figure 13). The gold is heated by a current until it begins to evaporate and deposit onto the wafer held above. A layer thickness of 100 was deposited at a rate of 1/s at 8 -6 Torr. To remove the remaining resist, the wafer is soaked patterned side up, in an acetone bath for 30 minutes or until the PMMA resist has lifted off. It is then rinsed with isopropanol to prevent contamination from particulates in the acetone. Left behind is an array of gold fractal stars approximately 100 thick with 100m between each star on the GaAs wafer substrate. The array of gold stars on GaAs was observed with an optical microscope (Figure 14). During gold deposition, there is the potential for sample contamination. The contamination most likely comes from the other materials that have been evaporated in the chamber, deposited on the chamberwalls, and either flaked or re-evaporated off the walls onto the sample. To reduce this type of contamination, it may be desirable to do a PAGE 31 18 blank run in which nothing or something that will be non-reactive with the sample is heated in the chamber. Another way to reduce contamination would be to run the evaporator at the lowest pressure feasible within time constraints and instrument capability. Figure 13. Metal evaporator with electron beam heating source. The wafer is clamped onto the wafer holder. A shutter blocks the wafer from the metal source until ready for metal deposition. The electron beam heats the metal source such that the metal begins to evaporate. The shutter is then opened allowing the evaporated metal to redeposit onto the wafer. Figure 14. Optical microscope image of the gold star array on GaAs wafer. Each star is approximately 10 microns tip to tip with 100 microns between each star. PAGE 32 19 Lastly, the sample is etched in the Plasmatherm model 770 Electron cyclotron resonance (ECR) reactive ion etcher (RIE). Initially the reactor conditions are set according to a known GaAs etch recipe for the Plasmatherm 770 using Cl 2 gas and Ar gas as follows: Chamber Pressure: 2 mTorr Heat Exchanger Temperature: 20C Cl 2 Flow: 10 sccm Ar Flow: 20 sccm Microwave Power: 900 Watts RF Substrate Power: 30 Watts Etch Rate: ~3000 /min It was found that the above recipe was too harsh for the samples used, removing the gold entirely from the substrate surface. Since the interface between the GaAs substrate and gold is of critical interest, the recipe had to be adjusted. Conditions were then set to encourage plasma etching while minimizing the potential for excessive damage to the sample as had occurred with the initial recipe. Several new recipes were tested to ensure that the sample was being etched. Those recipes are listed below for each sample in Table 2. Table 2. Etch recipes for each sample Sample # Parameters 2 3 5 Original Recipe Pressure (mTorr) 10 5 5 2 Temperature (C) 25 25 25 25 Cl 2 Flow (sccm) 10 10 10 10 Ar Flow (sccm) 5 5 5 20 Microwave Power (W) 100 100 100 900 RF Power (W) 20 20 20 30 Time (seconds) 90 60 90 90 Note: Samples 1 and 6 were not etched. PAGE 33 20 The new parameters were selected based on the trends shown previously in Table 1 to create an environment that would etch the sample but not so much as to eliminate the surface features. Increasing the pressure and decreasing both the microwave and RF power sources decrease the energy and speed of reactants to reduce the amount of physical sputtering. The Argon flow was also decreased to a rate below that of the chlorine which was held constant. Argon is an inert gas introduced into the system to increase the amount of sputtering for more anisotropic etching. It is also introduced into the system to assist in etching by encouraging less volatile species to leave the sample surface. The original etch recipe, when compared to the new recipes, appears to be more focused on anisotropic etching and vertical sidewalls for high feature resolution as would be expected from a recipe used in industry. All of the new recipes etch the samples without etching away the gold stars, as shown in AFM analysis, and are more suitable for the purpose of this research. 2.2 Analysis Techniques Several techniques were applied for the analysis of the prepared samples including scanning electron microscopy, energy dispersive spectroscopy, and atomic force microscopy. The techniques selected are useful for imaging the samples, examining the topography, and element detection. Scanning electron microscopy was done using a JEOL JSM-6335F. Secondary electron images were taken to show the topography of the sample especially the gold stars. Backscatter electron images are desired to show the composition of the sample. Though this imaging does not specify which elements are present, it does show the distribution of elements of the sample through differences in brightness. Higher atomic number elements appear brighter than PAGE 34 21 lower atomic number elements. Because gold has a higher atomic number than gallium and arsenide, the gold stars should appear brighter than the rest of the sample. Energy dispersive spectroscopy is also done using the JEOL JSM-6335F. This technique is useful for identifying the elements that are present. The data is displayed as a spectrum with peaks at energies characteristic for the element detected. For example, if gold is detected in a sample, a peak at 2.2keV will be observed in the spectrum. Atomic force microscopy was done using a Digital Instruments Nanoscope III SPM to obtain information about the surface of the sample. It is useful for surface imaging and profiling. A tip mounted on a cantilever is applied to the sample. By detecting the bending of the cantilever, the atomic force microscope is able to image the topography of a sample. For example, the roughness can be compared between the etched and unetched samples to determine if etching did occur. Any other significant changes in the surface or of feature dimensions would be revealed through atomic force microscopy. If such changes are observed, this could be an indication that gold has an effect on the etching of GaAs. Atomic force microscopy will be used to help determine if the sample surface has been altered or if it has remained the same. PAGE 35 CHAPTER 3 RESULTS 3.1 Atomic Force Microscopy 3.1.1 Sample 1 Unetched Gallium Arsenide with Gold Stars Sample 1 is gallium arsenide with gold stars that has not been etched. It is representative of Samples 2 and 3 prior to etching and will be used as a basis for comparison. Line scans were taken through twenty points of the edge of the star to obtain an average star height. The average height is 12.55nm. Figure 15a shows an AFM image of Sample 1 unetched. There is a line drawn in where one of the twenty line scans was taken. In Figure 15b is the plot of the height from that line scan. a) Figure 15. AFM image and line scan plot of sample 1 unetched. a) This is an AFM image of sample 1 unetched. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height as the AFM tip scans the line drawn in on the AFM image in Figure 15a of sample 1 unetched. Note the relative smoothness of the scanned surface. 22 PAGE 36 23 b) Sample 1 Unetched-20246810121401234micronsnm 5 Figure 15. Continued 3.1.2 Sample 2 Gallium Arsenide with Gold Stars Etched in Chlorine/Argon Plasma Sample 2 is gallium arsenide with gold stars that was etched for 90 seconds at 10mTorr in chlorine/argon plasma. Line scans were taken through twenty points of the edge of the star to obtain an average star height. The average height is 11.65nm. Figure 16a includes an AFM image of sample 2 etched. There is a line drawn in where one of the twenty line scan were taken. Shown in Figure 16b is the plot of the height from that line scan. 3.1.3 Sample 3 Gallium Arsenide with Gold Stars Etched in Chlorine/Argon Plasma Sample 3 is gallium arsenide with gold stars that was etched for 60 seconds at 5mTorr in chlorine/argon plasma. Two stars were analyzed on sample 3, 3A and 3B. Results for 3A follow; results for 3B are located in Appendix A. Line scans were taken through twenty points of the edge of the star to obtain an average star height. The average height is 11.48nm. Figure 17a is an AFM image of star 3A from etched sample 3. There is a line drawn in where one of the twenty line scan were taken. Shown in Figure 17b is the plot of the height from that line scan. PAGE 37 24 a) b) Sample 2 Etched-2024681012141618012345micronsnm Figure 16. AFM image and line scan plot of sample 2 etched in chlorine/argon plasma. a) This is an AFM image of sample 2 etched in chlorine/argon plasma. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn on the AFM image in Figure 16a of sample 2 etched. Note the roughness of the surface, particularly that of the gold star which appears more rough than the gallium arsenide surface. PAGE 38 25 a) b) Sample 3 Etched-2024681012141618012345micronsnm Figure 17. AFM image and line scan plot of sample 3 etched in chlorine/argon plasma. a) This is an AFM image of star A on the etched sample 3. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn on the AFM image in Figure 17a of star 3A on etched sample 3. Note the roughness of the sample surface. 3.1.4 Sample 6 Unetched Gallium Arsenide with Gold Stars Sample 6 is unetched gallium arsenide with gold stars. It is representative of sample 5 prior to etching and will be used as a basis for comparison. It is important to note that the shape of the stars on samples 5 and 6 are different from that of samples 1, 2, and 3 due to underexposure during the electron-beam lithography process. Line scans were taken through twenty points of the edge of the star to obtain an average star height. PAGE 39 26 The average height is 12.45nm. Figure 18a includes an AFM image of sample 6 unetched. There is a line drawn in where one of the twenty line scan were taken. Shown in Figure 18b is the plot of the height from that line scan. a) b) Sample 6 Unetched-20246810121416012345micronsnm Figure 18. AFM image and line scan plot of sample 6 unetched. a) This is an AFM image of sample 6 unetched. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn in on the AFM image in Figure 18a of sample 6 unetched. Note the relative smoothness of the scanned surface. 3.1.5 Sample 5 Gallium Arsenide with Gold Stars Etched in Chlorine/Argon Plasma Sample 5 is gallium arsenide with gold stars that was etched for 90 seconds at 5mTorr in chlorine/argon plasma. Two stars on etched sample 5 were analyzed, 5A and PAGE 40 27 5B. Results for 5A follow; results for 5B are located in Appendix A. Line scans were taken through twenty points of the edge of the star to obtain an average star height. The average height is 12.20nm. Figure 19a shows an AFM image of star A on the etched sample 5. There is a line drawn in where one of the twenty line scan were taken. Shown in Figure 19b is the plot of the height from that line scan. a) b) Sample 5 Etched-20246810121416012345micronsnm Figure 19. AFM image and line scan plot of sample 5 etched in chlorine/argon plasma. a) This is an AFM image of sample 5 etched in chlorine/argon plasma. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn on the AFM image in Figure 19a of star A on etched sample 5. PAGE 41 28 Table 3. Average height and standard deviation for Samples 1, 2, 3, 5, and 6 Sample 1 2A 2B 3A 3B 6 5A 5B Average Height (nm) 12.55 11.65 11.50 12.00 10.95 12.45 12.20 13.30 Standard Deviation 1.00 2.01 2.04 1.75 2.26 1.64 2.50 1.13 3.2 Field Emission Scanning Electron Microscopy and Energy Dispersive Spectroscopy 3.2.1 Sample 1 Unetched Gallium Arsenide with Gold Stars Sample 1 is gallium arsenide with gold stars that has not been etched. It is representative of samples 2 and 3 prior to etching and will be used as a basis for comparison. Figure 20. Secondary electron image of sample 1 unetched showing surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. PAGE 42 29 Figure 21. Backscatter electron image of sample 1 unetched. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. Figure 22. Secondary electron image with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. Point 5 is on the particle on the tip of the star. Point 6 is on a surface dot. PAGE 43 30 Energy dispersive spectroscopy spectrums for both points 1 and 2 on sample 1 were similar and showed gold peaks indicating the presence of gold. Figure 23 is the spectrum for point 1. Note the gold peak at approximately 2.2keV. Points 3 and 4 are located off of the star. Both spectrums showed peaks for gallium and arsenic but no peak for gold. Figure 24 is the spectrum for point 3. The spectrum for point 2 and point 4 are located in Appendix B. Spectrums for point 5 and point 6 are shown in Figure 25 and Figure 26. Figure 27 is the spectrum from a line scan of sample 1 unetched. Figure 23. EDS spectrum for point 1 at the center of a star on sample 1 unetched. Gallium, arsenic, and gold peaks are present. PAGE 44 31 Figure 24. EDS spectrum for point 3 on the substrate of sample 1 unetched. Gallium and arsenic peaks are present. Figure 25. EDS spectrum for point 5 on the particle on the tip of the star of sample 1 unetched. Gallium, arsenic, and gold peaks are present. PAGE 45 32 Figure 26. EDS spectrum for point 6 on a dark dot on the substrate of sample 1 unetched. Gallium and arsenic peaks are present. Figure 27. EDS gold line scan spectrum on sample 1 unetched. PAGE 46 33 3.2.2 Sample 2 Gallium Arsenide with Gold Particles Etched in Chlorine/Argon Plasma Sample 2 is gallium arsenide with gold stars that was etched for 90 seconds at 10mTorr in chlorine/argon plasma. The following figures include secondary electron image, backscatter electron image, energy dispersive spectroscopy point map, and energy dispersive spectroscopy spectrum for those points. Points 1 and 2 on the star of etched sample 2 had similar spectrums, thus only the spectrum for point 1 is shown. Points 3 and 4 on the substrate of etched sample 2 had similar spectrums, thus only the spectrum for point 3 is shown. The spectrums for points 2 and 4 are located in Appendix B. Figure 28. Secondary electron image of sample 2 etched in chlorine/argon plasma showing the surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. PAGE 47 34 Figure 29. Backscatter electron image of sample 2 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. Figure 30. Backscatter electron image with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. PAGE 48 35 Figure 31. EDS spectrum for point 1 on the center of the star of sample 2 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. Figure 32. EDS spectrum for point 3 on the substrate of sample 2 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. PAGE 49 36 Figure 33. EDS line scan spectrum for gold for sample 2 etched in chlorine/argon plasma. The line drops down when off of the star. This indicates that gold is on the star but not on the substrate. 3.2.3 Sample 3 Gallium Arsenide with Gold Particles Etched in Chlorine/Argon Plasma Sample 3 is gallium arsenide with gold stars that was etched for 60 seconds at 5mTorr in chlorine/argon plasma. The following figures include secondary electron image, backscatter electron image, an energy dispersive spectroscopy point map, and energy dispersive spectroscopy spectrum for those points. Points 1 and 2 on the star of etched sample 3 had similar spectrums, thus only the spectrum for point 1 is shown. Points 3 and 4 on the substrate of etched sample 3 had similar spectrums, thus only the spectrum for point 3 is shown. The spectrums for points 2 and 4 are located in Appendix B. PAGE 50 37 Figure 34. Secondary electron image of sample 3 etched in chlorine/argon plasma showing the surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. Also present in this image is a particle on the tip of the star. Figure 35. Backscatter electron image of sample 3 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two predominant compositions are observed in this image distinguishing the star from the substrate. PAGE 51 38 Figure 36. Backscatter electron image with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. Point 5 is on the dark area on the tip of the star. Figure 37. EDS spectrum for point 1 on the star of sample 3 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 52 39 Figure 38. EDS spectrum for point 3 on the substrate of sample 3 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 39. EDS spectrum for point 5 on the dark area on the tip of the star in sample 3 etched in chlorine/argon plasma. Gallium, arsenic, and carbon peaks are present. PAGE 53 40 Figure 40. EDS line scan spectrum for gold on sample 3 etched in chlorine/argon plasma. 3.2.4 Sample 6 Unetched Gallium Arsenide with Gold Stars Sample 6 is gallium arsenide with gold stars that has not been etched. It is representative of Sample 5 prior to etching and will be used as a basis for comparison. It is important to note that the shape of the stars on samples 5 and 6 are different from that of samples 1, 2, and 3 due to underexposure during the electron-beam lithography process. Energy dispersive spectroscopy spectrums for both points 1 and 2 on the star of sample 6 were similar and showed gold peaks indicating the presence of gold. Figure 44 PAGE 54 41 is the spectrum for point 1. Note the gold peak at approximately 2.2keV. Points 3 and 4 are located off of the star on the substrate. Both spectrums showed peaks for gallium and arsenic but no peak for gold. Figure 45 is the spectrum for point 3. The spectrum for point 2 and point 4 are located in Appendix B. Figure 41. Secondary electron image of sample 6 unetched showing surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. PAGE 55 42 Figure 42. Backscatter electron image of sample 6 unetched. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. Figure 43. Backscatter electron image of sample 6 unetched with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. PAGE 56 43 Figure 44. EDS spectrum for point 1 on sample 6 unetched. Gallium, arsenic, and gold peaks are present. Figure 45. EDS spectrum for point 3 on the substrate of sample 6 unetched. Gallium and arsenic peaks are present. 3.2.5 Sample 5 Gallium Arsenide with Gold Stars Etched in Chlorine/Argon Plasma Sample 5 is gallium arsenide with gold stars that was etched for 90 seconds at 5mTorr in chlorine/argon plasma. The following figures include secondary electron image, backscatter electron image, an energy dispersive spectroscopy point map, and PAGE 57 44 energy dispersive spectroscopy spectrum for those points. Points 1 and 2 on star A of sample 5 had similar spectrums, thus only the spectrum for point 1 is shown. Points 3 and 4 on the substrate of sample 5 had similar spectrums, thus only the spectrum for point 3 is shown. The spectrums for points 2 and 4 are located in Appendix B. Four stars on sample 5, labeled A, B, C, and D, were analyzed. Due to similarities in the results, only results from stars A and B are presented as follows. Results for stars C and D are located in Appendix B. Figure 46. Secondary electron image of star A on sample 5 etched in chlorine/argon plasma showing surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. Also present are particles on the star identified as the brighter spots the image. PAGE 58 45 Figure 47. Backscatter electron image of star A on sample 5 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. Figure 48. Secondary electron image of star A on sample 5, etched, with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. Point 5 is on a particle on star. Point 6 is on the bright area on the tip of the star. PAGE 59 46 Figure 49. EDS spectrum for point 1 on star A of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. Figure 50. EDS spectrum for point 3 on the substrate near star A on sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. PAGE 60 47 Figure 51. EDS spectrum for point 5, a particle on star A of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. Figure 52. EDS spectrum for point 6, a brighter area on the tip of star A on sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 61 48 Figure 53. Secondary electron image of star B on sample 5 etched in chlorine/argon plasma showing surface features of the sample. The gold star is visible on the surface of the gallium arsenide. There also particles on the star which appear as brighter areas on the sample. Figure 54. Backscatter electron image of star B on sample 5 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. PAGE 62 49 Figure 55. Secondary electron image of star B, on sample 5 etched, with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. Points 7 and 8 are each on a particle on the star. Figure 56. EDS spectrum for point 1 at the center of star B on sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 63 50 Figure 57. EDS spectrum for point 3 on the substrate near star B on sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 58. EDS spectrum for point 7, star B, with gallium, arsenic, gold, and chlorine peaks PAGE 64 51 Figure 59. EDS spectrum for point 8 on a particle on star B, sample 5, etched in chlorine/argon plasma. Gallium, arsenic, gold, and chlorine peaks are present. PAGE 65 CHAPTER 4 DISCUSSION 4.1 Atomic Force Microscopy Results Atomic force microscopy was performed on each sample to determine the surface characteristics of the samples including roughness and height differences. Comparison of the unetched samples to the etched samples showed that there was no significant difference in surface characteristics between the samples. Sample 1 was the unetched sample; it exhibited a relatively smooth surface as shown in Figure 15b (pg 22). Samples 2 and 3 were etched in chlorine/argon plasma and exhibit a rougher surface especially over the tops of the gold stars; refer to Figures 16b (pg 24) and 17b (pg 26). The average height of a star on the unetched sample 1 was found to be 12.55nm, while the average height of stars on etched sample 2 and etched sample 3 were found to be 11.58nm and 11.48nm respectively. With instrument limitations considered, the difference in height between the samples is not significant. Initially it was unusual that the height of the star on an unetched sample is higher. However, this could be due to height differences from when the gold layer was deposited. It is possible to have slight variations in layer thickness from the deposition of gold in the metal evaporator. Another reason for the height difference could be attributed to the Argon flow rate. The flow may have been too high for this situation, causing ion bombardment that physically sputtered the entire surface to reduce the height of both the gold star and the gallium arsenide substrate. In addition, the standard deviation more than doubles for the etched Samples 2 and 3, which 52 PAGE 66 53 makes it more difficult to determine if there were any changes. Similar results were found for Samples 5 and 6. Sample 6 was the unetched sample and had an average star height of 12.45nm. Sample 5 was etched in chlorine/argon plasma and had an average star height of 12.25nm. The edge profile of the stars was also examined to determine if there was any change after etching. Again, comparison of the unetched sample to the etched samples showed no definitive difference in edge profiles between the samples. Figure 60 shows a plot of the etched Samples 2 and 3 line scans superimposed over the unetched Sample 1 line scan. There is an area where it appears that there has been a build up or deposition at the base of the star, possibly of gold chloride. There is also a loss of surface material on the gallium arsenide substrate as noted by the negative area of the curve. This is an indication that the gallium arsenide is being etched. Samples 1, 2, & 3 c) > 2mTorr Figure 60. This is a plot of the etched samples 2 and 3 line scans superimposed over the unetched sample 1 line scan. There is an area where it appears that there has been a build up or deposition at the base of the star, possibly of gold chloride. There is also a loss of surface material on the gallium arsenide substrate as noted by the negative area of the curve. -4 -2 0 2 4 6 8 10 12 14 16 18 Sample 1 nm Sample 2 0 1 2 3 4 5 microns Sample 3 PAGE 67 54 Sample 6 & 5-20246810121416012345micronsnm Sample 6 Sample 5 Figure 61. This is a plot of the etched sample 5 line scan superimposed over the unetched sample 6 line scan. There is a negative area where material has been removed close to the base of the gold star. Figure 61 shows a plot of the etched Sample 5 line scan superimposed over the unetched Sample 6 line scan. There is no sign of build up or deposition as was observed in Figure 60. Also in Figure 61, there is a negative area where material has been removed close to the base of the gold star. This is an indication that the gallium arsenide is being etched. Tilting the samples during AFM analysis allowed further investigation of the edge profile, specifically for possible undercutting of the gold. There appears to be no undercutting observed in the results as would be expected from a purely chemical etch mechanism. Thus, the AFM results show that the presence of gold during the etching of gallium arsenide has no visible influence using these methods. 4.2 Field Emission Scanning Electron Microscopy and Energy Dispersive Spectroscopy Sample 1 is unetched gallium arsenide with gold stars and is used as a guideline to determine if the etched samples, samples 2 and 3, exhibited any change in surface characteristics after being etched. A gold star on unetched sample 1 is clearly visible in PAGE 68 55 the secondary electron image (Figure 20, pg 28) indicating a change in topography between the star and the gallium arsenide substrate. Also seen in this image is one particle on the tip of the star, which is believed to be a contaminant. Backscatter electron imaging also suggests this particle may be a contaminant. In backscatter imaging elements with higher atomic number, such as gold, appear brighter than lower atomic elements, such as the gallium and arsenic. This is true in the backscatter image of the unetched sample 1 as shown in Figure 21 on page 29. The star is brighter than the surrounding gallium arsenide. The particle that appeared in the secondary electron image also appears in the backscatter electron image as a dark area. Since it is darker than the rest of the image, the particle is most likely a contaminant of a lighter element such as carbon. An energy dispersive spectroscopy spectrum of that area was taken to identify what the particle was, Figure 25 on page 31. The spectrum taken at that point was similar to other points taken on the star where there was no particle; only peaks for gallium, arsenic, and gold were observed. Thus, it is believed that this particle is most likely a particle of gallium arsenide that was broken off the sample. Other points on the sample were analyzed to determine where the gold was. As was expected, all points taken on the star displayed a gold peak in the spectrums, Figure 23 on page 30. All points taken off of the star on the substrate displayed only gallium and arsenic peaks, no gold peak, Figure 24 on page 31. Samples 2 and 3 are etched in chlorine/argon plasma. Images from both samples are similar to the images for sample 1. The secondary electron image indicates the topography difference between the star and the substrate. The gold star is brighter than the gallium arsenide substrate in the backscatter electron image. Energy dispersive PAGE 69 56 spectroscopy spectrums display gold peaks for points taken on the stars, but no gold peaks for those points taken off of the stars. Etched sample 3 exhibited a particle on its tip similar to that of unetched sample 1, Figure 34 on page 37. The spectrum from that point displayed a significant carbon peak as shown in Figure 39 on page 39. The lack of difference between unetched sample 1 and etched samples 2 and 3 indicate that the gold has had no significant or definitive influence on the etching of gallium arsenide. Samples 5 and 6, as mentioned previously, used a lower dosage when being patterned with the electron beam lithography resulting in underexposure of the resist and incomplete stars. This is evident when viewing the images of samples 5 and 6 with those of samples 1, 2, and 3. Sample 6 is unetched and is used as the basis for comparison for the etched sample 5. In the secondary electron image for sample 6 as shown in Figure 41 on page 41, the difference in topography between the star and substrate is observed. There are no unusual particles on the surface. The backscatter electron image is as expected with the gold star appearing brighter than the gallium arsenide substrate, Figure 42 on page 42. Energy dispersive spectroscopy spectrums are also as expected. The spectrums for points taken on the star displayed peaks of gold, while the spectrums for points taken off of the star did not. The secondary electron images of etched sample 5, unlike the clean image of unetched sample 6, showed many particles on the star but not on the substrate, Figure 46 on page 44. In the backscatter electron image the particles were not observed, indicating that they are most likely gold as is the star. Although both star A and star B on etched sample 5 exhibit these particles, only the energy dispersive spectroscopy spectrum for star B displayed chlorine peaks for those particles, Figures 58 and 59 on pages 50 and 51. PAGE 70 57 It is unclear exactly why only etched sample 5 has these chlorine particles while etched samples 2 and 3 do not even though all were exposed to similar chemistry. A possible explanation is that gold can form chlorides. However, these chlorides are more difficult to remove from the surface of the sample because of their low volatility as suggested by Efremov, Kim, and Kim. Several other stars on etched sample 5 were examined for comparison. The results for two of those stars star C and star D, are located in Appendix A-3. Star C had no particles on its surface, thus there were no chlorine peaks in the energy dispersive spectroscopy spectrums. Star D did have a few particles. However, the spectrums for star D do display chlorine peaks on the particles. As was the case for stars A and B, for stars C and D any particles that were observed in the secondary electron images are not observed in the backscatter electron image. There was no regular pattern as to where the particles were located (ie, the edges, the tips, or the center of the stars). The data was inconsistent to make any reasonable assumptions as to why there were or were not particles on the samples and why some of those particles exhibited chlorine peaks while others did not. PAGE 71 CHAPTER 5 SUMMARY Gallium arsenide is a valuable semiconductor material used in many applications including microelectronic devices, optoelectronics, and integrated circuits. The desire to continuously improve upon the current applications and generate new and innovative applications necessitates advancements in the processing techniques. One key step in the processing technique is the development of the features through plasma etching. As the feature sizes become smaller, precision in the formation of the features becomes more critical. Chlorine-based plasmas are the most commonly used to dry etch gallium arsenide wafers during device manufacturing primarily because of the volatility of the chlorides that are formed by the reaction [14]. Gold has been determined to be relatively inert during plasma etching and therefore has been used as a mask material when creating nanostructures, IC circuits, and other microelectronic devices [6,8,9]. There has been some thought that gold may be used as a catalyst to enhance the etching process. In oxidation and hydrogenation systems this has been proven true. However, does gold act as a catalyst in chlorine plasma to enhance the etching of gallium arsenide? A sample was prepared with gold stars on a gallium arsenide substrate and then etched in chlorine/argon plasma. Electron beam lithography was used to create the template for the star array. Gold was then deposited onto the sample with a metal evaporator filling the voids created during electron beam lithography to form the gold stars. The samples were then analyzed for any changes in surface characteristics after 58 PAGE 72 59 being etched using atomic force microscopy, scanning electron microscopy, and energy dispersive spectroscopy techniques. Scanning electron microscopy and energy dispersive results show that the gold stars remained intact on the substrate surface. There was no consistent or significant change in the profile at the edge of the star to indicate that the gold influenced the etching of the gallium arsenide. Analysis with atomic force microscopy gave results that lead to the same conclusion. The atomic force microscopy results did show that the surface of both the gallium arsenide and the gold was etched. Unetched samples had a relatively smooth surface while the etched samples exhibited a rough surface characteristic of etching. Through this research using these conditions it was shown that gold does not influence the etching of gallium arsenide in chlorine plasma. PAGE 73 APPENDIX A ADDITIONAL AFM RESULTS a) b) Sample 3 Etched, Star 3B-20246810121416012345micronsnm Figure 62. AFM image and line scan plot of sample 3 etched in chlorine/argon plasma. a) This is an AFM image of sample 3 etched in chlorine/argon plasma. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn on the AFM sample in Figure A1a of sample 3 etched. 60 PAGE 74 61 a) b) Sample 5 Etched, Star 5B-20246810121416012345micronsnm Figure 63. AFM image and line scan plot of sample 5 etched in chlorine/argon plasma. a) This is an AFM image of sample 5 etched in chlorine/argon plasma. The line drawn on the image represents the location of a line scan. b) The plot shown represents the change in height of the sample surface as the AFM tip scans the line drawn in Figure 63a of sample 5 etched in chlorine/argon plasma. PAGE 75 APPENDIX B ADDITIONAL SEM/EDS RESULTS Figure 64. EDS spectrum for point 2 on the star of sample 1 unetched. Gallium, arsenic, and gold peaks are present. 62 PAGE 76 63 Figure 65. EDS spectrum for point 4 on the substrate of sample 1 unetched. Gallium and arsenic peaks are present. Figure 66. EDS spectrum for point 2 on the star of sample 2 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 77 64 Figure 67. EDS spectrum for point 4 on the substrate of sample 2 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 68. EDS spectrum for point 2 on a star of sample 3 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 78 65 Figure 69. EDS spectrum for point 4 on the substrate of sample 3 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 70. EDS spectrum for point 2 on a star of sample 6 unetched. Gallium, arsenic, and gold peaks are present. PAGE 79 66 Figure 71. EDS spectrum for point 4 on the substrate of sample 6 unetched. Gallium and arsenic peaks are present. Figure 72. EDS spectrum for point 2 on star A of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 80 67 Figure 73. EDS spectrum for point 4 on the substrate of sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 74. EDS spectrum of point 2 on star B of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 81 68 Figure 75. EDS spectrum for point 4 on the substrate of sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 76. Secondary electron image of star C on sample 5 etched in chlorine/argon plasma showing surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. PAGE 82 69 Figure 77. Backscatter electron image of star C on sample 5 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. Figure 78. Secondary electron image of star C on sample 5, etched, with map of EDS points. Point 1 is at the center of the star. Point 2 is at the edge of the star. Point 3 is on the substrate close to the edge of the star. Point 4 is on the substrate. PAGE 83 70 Figure 79. EDS spectrum of point 1 on star C of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. Figure 80. EDS spectrum of point 2 on star C of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, and gold peaks are present. PAGE 84 71 Figure 81. EDS spectrum of point 3 on the substrate near star C of sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. Figure 82. EDS spectrum of point 4 on the substrate of sample 5 etched in chlorine/argon plasma. Gallium and arsenic peaks are present. PAGE 85 72 Figure 83. Secondary electron image of star D on sample 5 etched in chlorine/argon plasma showing surface features of the sample. There is little contrast in the image because the gold star is only 10nm thick. However, the gold star is visible on the surface of the gallium arsenide. There are also two particles on the star. Figure 84. Backscatter electron image of star D on sample 5 etched in chlorine/argon plasma. Areas of different composition are identified by differences in brightness. Two compositions are observed in this image distinguishing the star from the substrate. PAGE 86 73 Figure 85. Secondary electron image of star D with a map of EDS points. Point 1 is on a particle on star D. Point 2 is on a particle on the tip of star D. Figure 86. EDS spectrum for point 1 on star D of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, gold, and chlorine peaks are present. PAGE 87 74 Figure 87. EDS spectrum for point 2 on a particle on star D of sample 5 etched in chlorine/argon plasma. Gallium, arsenic, gold, and chlorine peaks are present. PAGE 88 REFERENCES [1] Gary S. May and Simon M. Sze, Fundamentals of Semiconductor Fabrication, Wiley, New York, 2004. [2] BrainyMedia, Gallium arsenide, Nov 2002, http://www.brainyencyclopedia.com/encyclopedia/g/ga/gallium_arsenide.html Nov 30, 2004. [3] D. Manos and D. Flamm (eds), Plasma Etching: An Introduction, Academic Press, Inc., Boston, 1989. [4] R.R. Moskalyk: Gallium: The backbone of the electronics industry Min. Eng. 16(10): 921-929, Oct 2003. [5] MEMS and Nanotechnology Clearinghouse, Etching processes, Nov 2004, http://www.memsnet.org/mems/beginner/etch.html Nov 30, 2004. [6] Subash Mahajan and K.S. Sree Harsha, Principles of Growth and Processing of Semiconductors, WCB/McGraw-Hill, Boston, 1999. [7] P. Werbaneth, Z. Hasan, P. Rajora, M. Rousey-Seidel, The reactive ion etching of Au on GaAs substrates in a high density plasma etch reactor, The International Conference on Compound Semiconductor Manufacturing Technology, GaAs Mantech, Inc, St. Louis, 1999. [8] R. Grisel, K.J. Weststrate, A. Gluhoi, B.E. Nieuwenhuys, Catalysis by gold nanoparticles, Gold Bulletin 35(2): 39-45, 2002. [9] D. Thompson, A golden future for catalysis, Nov 2001, http://www.chemsoc.org/chembytes/ezine/2001/thompson_nov01.htm Nov 30, 2004. [10] A.M. Efremov, Dong-Pyo Kim, and Chang-Il Kim, Etching characteristics and mechanism of Au thin films in inductively coupled Cl 2 /Ar plasma J. Vac. Sci. Technol. A 21(6): 1837-1842, Nov/Dec 2003. [11] R.J. Shul and S.J. Pearton (eds), Handbook of Advanced Plasma Processing Techniques, Springer, New York, 2000. 75 PAGE 89 76 [12] W.C. Simpson and J.A. Yarmoff: Fundamental studies of halogen reactions with III-V semiconductor surfaces, Annu. Rev. Phys. Chem. 47: 527-54, 1996. [13] M. Sugiyama, T. Yamaizumi, M. Nezuka, Y. Shimogaki, Y. Nakano, K. Tada, and H. Komiyama: Simple kinetic model of ECR reactive ion beam etching reactor for the optimization of GaAs etching process, Jpn. J. Appl. Phys. 35: 12351241, 1996. [14] W.N.G. Hitchon, Plasma Processes for Semiconductor Fabrication, Cambridge University Press, New York, 1999. [15] C.L. Henderson, Introduction to Electron Beam Lithography, http://dot.che.gatech.edu/henderson/intro%20to%20e-beam%20lithography2.htm Nov 30, 2004. PAGE 90 BIOGRAPHICAL SKETCH Erika Courtney Lent was born and raised in Cooper City, Florida. She lived with her parents Ken and Terry Lent and younger brothers Judd and Ross. After graduating from Cooper City High School in 1998, Erika enrolled as a freshman at the University of Florida to pursue her interest in engineering. Throughout college, she enjoyed involvement in the Society of Women Engineers, American Ceramics Society, and Alpha Xi Delta sorority. In August 2002, Erika graduated with a Bachelor of Science in Materials Science and Engineering degree from the University of Florida. Shortly thereafter, she was accepted into the graduate program in the Department of Materials Science and Engineering at the University of Florida. She will graduate with a Master of Science degree in May 2005. 77