Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 G581 0013-4651/2001/148共10兲/G581/6/$7.00 © The Electrochemical Society, Inc. Modeling and Experimental Analysis of the Material Removal Rate in the Chemical Mechanical Planarization of Dielectric Films and Bare Silicon Wafers H. Hocheng,a,z H. Y. Tsai,a and Y. T. Sub a Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu, Taiwan Department of Mechanical Engineering, National Chung Shan University, Kaoshiung, Taiwan b An analytic model of the material removal rate is proposed for chemical mechanical planarization 共CMP兲. The effects of the applied pressure and the polishing velocity between the wafer surface and the pad surface are derived considering the chemical reaction as well as the mechanical bear-and-shear process. The mechanism of microscopic material removal is presented. The material removal rate is found less linearly correlated to the pressure and relative velocity between the pad and the wafer, which was predicted by the frequently cited empirical Preston equation obtained from glass polishing. 关I. F. W. Preston, J. Soc. Glass. Technol., 11, 214 共1927兲兴. It provides the analytical modification of the Preston equation in the dielectrics CMP. The experimental results of authors and independent researchers are discussed. © 2001 The Electrochemical Society. 关DOI: 10.1149/1.1401087兴 All rights reserved. Manuscript submitted January 2, 2001; revised manuscript received June 1, 2001. Available electronically September 4, 2001. Historically chemical mechanical planarization 共CMP兲 has been used to polish optically flat surfaces. As the wiring density in highperformance chips increases and the device size scales down to submicrometers 共as shown in Table I兲, planarization technology becomes indispensable during both device fabrication and formation of multilevel interconnects. CMP has emerged recently as a processing technique for a higher degree of planarization in submicrometer very large scale integration 共VLSI兲, and is widely accepted for planarizing interlevel dielectrics and selective removal of aluminum, tungsten, copper, and titanium overburden following metal filling of studs and interconnects. A schematic diagram of a CMP is shown in Fig. 1 共view from top and side兲. The wafer is held face down by a rotating carrier pressed against the polishing pad, which is rotating as well. A down force is applied onto the wafer. The polishing colloidal slurry, which consists of chemical reagents, is dispensed onto the pad surface. The slurry is distributed across the pad by the centrifugal force of the rotating pad to wet the polishing pad and the wafer. The chemical reaction in CMP softens the dielectric or hardens the metal surface material of the wafer. The treated material is then removed mechanically by fine abrasives. In balance between the chemical and mechanical actions, the process removes material continuously. Although quite a few papers discuss the experimental results and the effects of the process parameters, the material removal mechanism is addressed less. Some authors consider the material removal mechanism at the direct contact between the wafer and the pad, while others consider that there is a thin fluid film between the wafer and the pad. Warnock presented the dependence of the polish rate on the wafer shape, though it is completely a phenomenological model.1 Yu et al. presented a physical CMP model that includes the effects of polishing pad roughness and dynamic interaction between pad and wafer. Two new feature-scale-polishing mechanisms based on asperity theory are proposed and investigated experimentally. However, it is not clear whether or how the asperity affects the global quality of planarization.2 Warnock and Yu et al. both derive the reduction rate of the step height assuming direct contact between pad and wafer without considering the role of abrasive flow in between. Liu assumes that the abrasive cuts the wafer under the loaded pressure and the relative velocity between the wafer and the pad. The model is capable of delineating the role of the mechanical properties of the slurry particles and the surface film to be polished. Liu assumes that the deformed volume to be composed of three regions, namely, the regions of elastic deformation, plastic deformation, and microcutting. He also assumes the deformation volume during con- z E-mail: [email protected] tact to be approximately equal to the volume of microcutting and calculates the removal rate by the Hertzian elastic equation. The results were also compared with the wear model of Cook,3 which is derived from the glass polishing process.4 Cook and Liu both believe that the removal of wafer is primarily due to the direct contact between abrasives and wafer, and the Hertzian contact is adopted. Cook’s results did not reveal the detail of material removal rate, and Liu did not characterize the role of flow. Runnels presented two CMP models in 1994. One is the tribology analysis of CMP, and the other is the feature-scale fluid-based erosion model for CMP. Runnels considers that the knowledge of the stress distribution on the wafer surface is required in order to explain the variation of material removal rate on a wafer during CMP. This study analyzes the fluid film between the wafer and pad, and demonstrates that hydroplaning is possible for standard CMP processes. The importance of wafer curvature, slurry viscosity, and rotation speed on the thickness of the fluid film is also demonstrated. Although the analysis is novel, the model can only estimate the thickness of the film between pad and wafer, and Runnels admitted that the assumption of the spherical wafer needs modification.5 The other physical-based feature-scale erosion model is critical to the understanding of CMP, because it establishes the link between the chemical effects at the particle scale and the process conditions at the wafer scale utilizing a hydrodynamic slurry layer. Given some assumptions, the fluid flow is modeled by the steady-state twodimensional Navier-Stokes equations for incompressible Newtonian flow.6 Runnels later implemented Warnock’s phenomenological erosion model. The improved development allows for closer fits to the experimental data and uniform discretization of the wafer feature.7 Although Runnels takes into account that it is the slurry flow that erodes the pattern of wafer, his model does not account for the effects of the abrasives in the slurry. Tseng and Wang combined Runnels’ and Cook’s work without physical interpretation. A model of removal rate was obtained to account for the dependence of the removal rate on the down pressure and the rotation speed during the CMP process based on the theory of elasticity.8 Although CMP has been widely practiced in semiconductor manufacturing for a few years, the mechanism of material removal remains to be explored. The macroscopic empirical Preston equation obtained from glass polishing is often considered the major reference. The current paper presents a model based on individual abrasive material removal in a flow field. It considers that the abrasives remove the material by a bear-and-shear process, while the slurry flow between the wafer and the pad plays a role in transporting the chemical means. Preston’s equation can be properly interpreted and used with modification. The analysis and the independent experimental results are discussed in the following. Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 G582 Table I. Roadmap of semiconductor industry. Year Minimum feature size 共m兲 Maximum substrate diameter 共mm兲 DRAM Numbers of metal levels Contacts 共nm兲 MPU Numbers of metal levels Contacts 共nm兲 Depth of focus 共m兲 1999 2000 2001 2002 2003 2004 2005 0.18 200 0.18 200 0.15 300 0.13 300 0.13 300 0.13 300 0.1 300 3 200 3 185 3 170 3-4 150 4 145 4 140 4 130 6-7 230 0.7 6-7 210 0.7 7 180 0.7 7-8 160 0.6 8 145 0.6 8 130 0.6 8-9 115 0.5 Bear-and-Shear Process Model Chemical and mechanical action.—First consider the chemical reaction of silicon dioxide SiO2 ⫹ 2H2O → Si共OH兲4 关1兴 There exists a rate constant in a chemical reaction. The rate constant often increases rapidly with the increasing temperature. A rough rule valid for typical reactions in solution is that it doubles or triples for each increase of 10°C in temperature. Arrhenius pointed out that the constant k fits the expression9 k ⫽ Ce⫺Ea /RT 关2兴 where R is the gas constant, E a is the Arrhenius activation energy, and C is the pre-exponential factor 共or frequency factor兲. The unit of C is the same as k. The unit of E a is the same as RT, namely, energy per mole 共kcal/mol or kJ/mol兲. C and E a characterize the reaction. As mentioned above, the reaction rate is proportional to the rate constant at the constant molecular concentration of water in CMP. Therefore, the material removal rate in view of the chemical action is proportional to the rate constant. Once the top surface is removed mechanically, the silicon dioxide film exposed to the slurry will keep on reacting chemically. These reactions are in sequence, that is, the chemical reaction first and then the mechanical removal repeatedly. Besides, the following facts exist. The dissolution rate of glass into water increases with compressive stress;10 therefore the hydrate reaction rate of silica is accelerated by the pressure of the slurry particle against the surface layer of the wafer. The compressive stress decreases the activation energy and thus increases the rate constant and the chemical reaction rate. If the chemical reaction were the limiting step, the material removal rate would not increase with the solid content in the slurry.11 Hence the mechanical removal is considered to be the bottle neck in the material removal process chain and is worthy of analysis. In other words, the material removal is proportional to the mechanical removal rate. Once the products 关 Si共OH兲4 兴 are produced by the chemical reaction, the slurry particles carried by the slurry flow remove the products. The polishing by mechanical means in CMP is further considered as follows. 1. The slurry film between pad and wafer supports the down pressure, and the carrier 共i.e., the wafer兲 holds a nonparallel but slightly inclined configuration relative to pad. 2. The slurry particles carrying kinetic energy approach and remove the molecules of the wafer surface material. The major aspects in the process are described in the following. Thrust bearing analogy.—The thrust load of rotary machinery is often counterbalanced by self-acting or hydrodynamic bearings shown in Fig. 2.12 A thrust plate attached to, or forming part of, the rotating shaft is separated from the sector-shaped bearing pads by a Figure 1. Schematic diagram of CMP. Figure 2. Thrust bearing.12 Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 G583 Figure 3. Simple pivoted pad bearing.12 Figure 4. Schematic of couette flow between two plates.13 lubricant film. The load-carrying capacity of the bearing arises entirely from the pressures generated by the geometry of the thrust plate over the bearing pads. The simplest form of the pivoted pad bearing provides straightline motion only and consists of a flat surface sliding over a pivoted pad as shown in Fig. 3. If the pad is in equilibrium under a given set of operating conditions, any change in these conditions 共such as load, speed, or viscosity兲 will alter the pressure distribution and thus momentarily shift the center of pressure. This event will create a moment that causes the pad to change its inclination and shoulder height (S h). A pivoted pad slider bearing is thus supported at a single point so that the angle of the inclination becomes a variable and has much better stability than a fixed inclined slider under varying conditions of operation. This behavior is similar to the relationship between the gimbal mechanism of the carrier and the pad during CMP, except that the positions of the gimbal mechanism of the carrier and the pad are reversed. The location of the shoe pivot can be found from the equilibrium of moments acting on the shoe about the point. For all practical purposes, the force due to friction in the pivot is ignored. The minimum fluid film thickness in designing a pivoted pad thrust bearing is found as h0 ⬀ 冉 冊 V F 1/2 关3兴 Coutte flows in turbulence.—In Fig. 4, two infinite plates are 2h apart, and the upper plate moves at speed V relative to the lower. The fluid pressure p is assumed constant. The upper plate is held at temperature T 1 and the lower plate at T 0 . These boundary conditions are independent of coordinates x or z 共called infinite plate兲; hence it follows that u ⫽ u(y) and T ⫽ T(y). The reduced basic equations are Momentum equation Energy equation k u ⫽ C1y ⫹ C2 u ⫽0 x 关4兴 d 2u ⫽0 dy 2 关5兴 冉 冊 du d 2T 2 ⫹ dy dy 2 ⫽0 关6兴 关7兴 Using the no-slip boundary conditions, i.e., u(⫺h) ⫽ 0 and u(⫹h) ⫽ V one obtains C 1 ⫽ V/2h and C 2 ⫽ V/2. Thus the velocity distribution is u⫽ 冉 V y 1⫹ 2 h 冊 关8兴 This is the exact steady-flow solution of the Navier-Stokes equation, called laminar flow, and has a smooth-streamline character. It is well known that all laminar flows become unstable beyond a finite value of a critical parameter 共Reynolds number兲. A different type of flow then ensues on an entirely new fluctuating flow regime, called turbulent. The pattern changes into a randomly fluctuating flow, sketched by Reichardt in 1956 as shown in Fig. 3, varies slightly with Reynolds number, and increases the wall shear by two orders of magnitude.13 Therefore, the relationship between velocity and the position from the middle of the gap to the upper wall is expressed as u ⫽ ay n where is the viscosity of the film, V is the velocity, and F is the applied normal load. Although the exponential values other than 1/2 have been proposed for various applications, Bhushan and Runnels, etc., considered it to be 1/2 in the CMP process.5,11 Continuity equation where the continuity merely verifies the assumption that u ⫽ u(y). Equation 5 can be integrated twice to obtain 关9兴 where n is a number larger than 100. The no-slip condition is u ⫽ V/2 at y ⫽ h, or a ⫽ Vh ⫺n /2, hence the wall shear can be determined ⫽ u nV ⫽ nah n⫺1 ⫽ y 2h 关10兴 Equation 10 tells us that the wall shear becomes two orders of magnitude larger. The wall shear stress produced by Couette flows is applied to the derivation of the relative polishing velocity in CMP. Energy balance.—When a slurry particle binds to the molecule Si共OH兲4 of the wafer surface and removes the molecule, the shear force must be larger than the binding force of the molecule, larger energy than the surface energy of the generated new surface must be transmitted. Consider a slurry particle pulling the molecules off the wafer surface, as shown in Fig. 5; the shear stress of slurry flow is assumed to be uniformly distributed around the particle. In order to remove one molecule from surface, the following condition must be satisfied14 Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 G584 ⬀ n 共 V PA 兲 1/2 关15兴 where A is the area of the wafer. Combining Eq. 13 and 15, one obtains the volumetric material removal rate Ṁ ⬀ f • 冉 2 nD 2p D m 12␥ 冊 共 A 兲 1/2共 PV 兲 1/2 关16兴 The removal rate in thickness per unit time is obtained by Ḣ ⫽ Ṁ A 关17兴 It shows the removal rate increases with the increasing polishing speed and pressure to the power of 1/2. The experimental results are discussed in the following. Results and Discussion Figure 5. Schematic of the chemical products carried by the slurry particle. 冉 冊 D 2p 4 D m ⭓ 2␥A mN 关11兴 where ␥ is the surface energy between the surface and sublayer molecule, D p is the diameter of the slurry particle, D m and A m are the diameter and the cross-sectional area of the Si共OH兲4 molecule, respectively, and N is the number of molecules to be removed. In this case, N is considered quite large because the ratio of the diameter of the molecule to the diameter of the abrasive is about 1/100. The left side of Eq. 11 is an approximation of the energy transmitted to the wafer surface to move the particle for a distance D m , which is defined as the molecule that will be sheared off once the moving distance is larger than D m . The right side of Eq. 11 is the surface energy of the newly generated surface, when one molecule is moved. Equation 11 can be rearranged as N⫽ D 2p The experiments are carried out on both the silicon dielectric film and the bare silicon wafer by two polishers, IPEC372M and PeterWaltersAC1400, respectively. IPEC 372M polisher.—The parameters of the material removal experiments are listed in Table II. The experimental results of polishing silicon dioxide are shown in Fig. 6. The material removal rate increases with the increasing velocity by the power of 0.65, slightly larger than the predicted 0.5. The reason lies in that a small portion of the wafer is polished in the direct contact mode as a result of a not ideally conformed pad 共particularly at the wafer edge兲, where the material removal rate is linearly proportional to the polishing velocity.15 The empirical Preston equation based on glass polishing also applies to this part of the process. In fact, the total material removal rate consists of the contribution from the direct contact mode as well as the noncontact mode, i.e. Table II. Parameters of experiment of silicon dioxide. Polisher Pad type Slurry type 关12兴 2␥D m Slurry flow rate 共mL/min兲 Down pressure 共psi兲 Back pressure 共psi兲 Platen speed 共rpm兲a Polishing time 共min兲 Equation 12 indicates that the number 共N兲 of removed Si共OH兲4 is proportional to the wall shear stress. The role of the slurry particles in the film between the pad and the wafer is to shear off the chemical products, meanwhile Si共OH兲4 is continuously produced. Material Removal Rate a IPEC 372M polisher Rodel IC1400 Cabot SS25 共1:1 dilute by DI water兲 pH 10.8 150 5, 8, 10 3 10, 20, 30, 40, 50, 60, 70, 80 1 Carrier speed is equal to platen speed. The volumetric material removal rate 共Ṁ兲 is determined by the volume 共ⵜ兲 of removed molecules of the chemical products 共Eq. 12兲 and the encounter frequency 共f 兲 of the slurry particles on the removed surface Ṁ ⬀ N • ⵜ • f ⫽ 3 D 2p D m 2␥D m 6 f 关13兴 where f is a function of the solid content and the characteristics of the turbulent flow. One recalls that in Eq. 10 the wall shear is proportional to the reciprocal of the film thickness. Substituting Eq. 3 into Eq. 10, one obtains ⫽ 冉 冊 nV V ⬀ nV 2h F ⫺1/2 Since the force F is equal to PA, Eq. 14 can be reduced to 关14兴 Figure 6. Relationship between the removal rate of SiO2 and polishing velocity. Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 G585 Table III. Parameters of experiment of bare silicon. Polisher Pad type Slurry type Peter-Wolters ac1400-p polisher Rodel-Nitta Suba 600 Rodel-Nitta Nalco 2350 共1:20 dilute by DI water兲 pH 10.3 750 1.42 15 8, 4, 0.1, ⫺4, ⫺8 ⫺5.7/⫺20, ⫺5.7/⫺13, ⫺5.7/⫺5.7, ⫺5.7/1, ⫺5.7/8, ⫺16.7/⫺16.7, ⫺11.2/⫺11.2, ⫺22.2/⫺22.2, ⫺0.18/⫺0.18 10 Slurry flow rate 共mL/min兲 Down pressure 共psi兲 Sun gear speed 共rpm兲 Ring gear speed 共rpm兲 Upper/lower pad speed 共rpm兲 Polishing time 共min兲 Ḣ ⫽ ␣K 1 V 0.5 ⫹ K 2 V 1.0 ⫽ K 3 V 0.65 关18兴 where ␣ and  represent the fraction of the noncontact and the contact area between wafer and pad during CMP, respectively, and ␣ ⫹  ⫽ 1. K 1 , K 2 , and K 3 are the proportionality constants between the removal rate and velocity. As shown by Eq. 3, the minimum film thickness increases with the velocity, thus the fraction of the contact area 共兲 decreases with the increasing velocity. The effect of the polishing velocity in the current experiment is indicated by its exponent of 0.65, which is indeed between 0.5 and 1.0, close to 0.5. Peter-Wolters ac 1400-P polisher.—The parameters of the material removal experiments are listed in Table III. The experimental results of bare silicon wafer polishing are shown in Fig. 7. The material removal rate increases with the increasing relative velocity by the power of 0.45, slightly lower than the predicted 0.5. This is attributed to the fact that the wafer is purposefully not held tightly within the carrier of the polishing machine. Designed by the machine builder to avoid the danger of stress-induced cross-wafer cracking, there is a clearance between wafer and inner rim of the carrier. The wafer is thus allowed to rotate slightly within the carrier due to the fluid drag, therefore the wafer velocity is slightly lower than the carrier velocity. The actual relative velocity between wafer and pad is less than the calculated velocity assuming full engagement. As a result, the effect of the polishing velocity contributes less to the material removal rate than expected. The exponent of the velocity is slightly less than 0.5 in use of this type of machine for polishing a bare silicon wafer. by the power between 0.44 and 0.56 for different dielectric thin films. These results exactly fall into the prediction in the current model of removal rate. Case 2.—Tseng and Wang proposed a model to predict the removal rate increasing with the velocity by the power of 0.5 on thermal dioxide film.8,18 Their experimental results are redrawn in Fig. 9. One notices that the polishing speed is in fact proportional to the carrier speed.19 The power law of the velocity lies between 0.42 and 0.54, mostly 0.50. These experimental results agree well with the current model. Case 3.—Evans et al. published the experimental results of the removal rate of dielectrics as a function of the table speed in 1998.20 It is redrawn in Fig. 10. One also notices that the polishing speed is proportional to the table speed. The oxide removal rate increases with increasing velocity by the power of 0.52 and 0.55 for ceria slurry and interlevel dielectric 共ILD兲 1300 slurry, respectively. These results follow the prediction in the current study. Independent experimental results.—Case 1.—Sun et al. published the experimental results of the removal rate of dielectrics as a function of the platen rotation speed.16,17 These are redrawn in Fig. 8. The material removal rate increases with the increasing velocity Figure 8. Relationship between the removal rate and polishing velocity in Sun’s experiment.16 Figure 7. Relationship between the removal rate of bare silicon wafer and polishing velocity. Figure 9. Relationship between the removal rate and carrier speed in Tseng’s experiment.18 G586 Journal of The Electrochemical Society, 148 共10兲 G581-G586 共2001兲 ticles and the wafer surface being attracted to each other will increase the encounter frequency and the removal rate as a result. Conclusions Figure 10. Relationship between the removal rate and table speed in Evans’ experiment.20 The clearance between the wafer surface and the pad is defined by the minimum fluid film thickness determined by the parameters including the load, the velocity, and the viscosity, similar to the design of a thrust bearing. The abrasives in the slurry flow carry the energy to take the chemically treated products off the wafer surface. Based on the bear-and-shear process model, the material removal rate increases with the polishing velocity by the power of approximately 1/2. This is verified by the polishing experiments of the authors as well as independent researchers. The widely cited empirical Preston equation obtained from glass polishing can find an analytical ground for modification in the extended application of dielectrics CMP. The current model summarizes some representative existing works and serves as a guide for the practical prediction of material removal rate during CMP. Acknowledgments The paper was supported by the National Science Council under contract 87-2212-E007-008. National Tsung Hua University assisted in meeting the publication costs of this article. References Figure 11. Relationship between the removal rate and polishing velocity in Steigerwald’s experiment.17 Case 4.—In the case of metal CMP, Steigerwald et al. showed the experimental results of the copper polishing rate vs. the polishing velocity using Strassbaugh 6CU polisher, Suba500 pad, and Suba550 pad. The results are redrawn in Fig. 11.17 The removal rate increases with increasing polishing velocity by the power of 0.64 and 0.60 for Suba550 and Suba500, respectively. The results are considered a positive reference to the prediction of the current model. Extended support.—The proposed model also predicts that the removal rate increases with the encounter frequency, f, which is determined by the solid particle content in the slurry. Bhushan’s experimental results prove that the removal rate increases with the increasing solid content.11 Huang’s work concluded that, when the abrasives and the wafer surface are attracted to each other, the removal rate will be higher where the attraction is stronger.21 These effects can be well explained by the current model. The slurry par- 1. J. Warnock, J. Electrochem. Soc., 138, 2398 共1991兲. 2. T.-K. Yu, C. C. Yu, and M. Orlowski, Tech. Dig. Int. Electron Devices Meet., 1993, 865. 3. L. M. Cook, J. Non-Cryst. Solids, 120, 152 共1990兲. 4. C. W. Liu, B. T. Dai, and C. F. Yeh, J. Electrochem. Soc., 143, 716 共1996兲. 5. S. R. Runnels and L. M. Eyman, J. Electrochem. Soc., 141, 1698 共1994兲. 6. S. R. Runnels, J. Electrochem. Soc., 141, 1900 共1994兲. 7. S. R. Runnels and T. Olavson, J. Electrochem. Soc., 142, 2032 共1995兲. 8. W. T. Tseng and Y. L. Wang, J. Electrochem. Soc., 144, L15 共1997兲. 9. I. N. Levine, Physical Chemistry, p. 522, McGraw-Hill, New York 共1983兲. 10. M. Nogami and M. Tomozawa, J. Am. Ceram. Soc., 67, 151 共1984兲. 11. M. Bhushan, R. Rouse, and J. E. Lukens, J. Electrochem. Soc., 142, 3845 共1995兲. 12. B. J. Hamrock, Fundamentals of Fluid Film Lubrication, pp. 170, 210, McGrawHill, New York 共1994兲. 13. F. M. White, Viscous Fluid Flow, p. 113, McGraw-Hill, New York 共1991兲. 14. Y. T. Su, T. C. Hung, and Y. Y. Cheng, Wear, 188, 77 共1995兲. 15. H. Hocheng and H. Y. Tsai, in ASME International Mechanical Engineering Congress and Exposition, Vol. 8, p. 33, J. Lee, Editor, The American Society of Mechanical Engineering Proceedings Series, New York 共1998兲. 16. S. C. Sun, F. L. Yeh, and H. Z. Tien, Mater. Res. Soc. Symp. Proc., 337, 139 共1994兲. 17. J. M. Steigerwald, S. P. Murarka, and R. J. Gutmann, Chemical Mechanical Planarization of Microelectronic Materials, p. 154, John Wiley & Sons, New York 共1997兲. 18. D.-Z. Chen and B.-S. Lee, J. Electrochem. Soc., 146, 744 共1999兲. 19. H. Hocheng, H. Y. Tsai, and L.-J. Chen, in Chemical-Mechanical Planarization for ULSI Multilevel Interconnection, T. E. Wade, Editor, p. 277, VMIC Proceedings Series, Santa Clara, CA 共1997兲. 20. D. R. Evans, B. D. Ulrich, and M. R. Oliver, in Chemical-Mechanical Planarization for ULSI Multilevel Interconnection, T. E. Wade, Editor, p. 347, VMIC Proceedings Series, Santa Clara, CA 共1998兲. 21. C. W. Huang, Master Thesis, National Chiao Tung University, Taiwan 共1998兲.
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