22nd International Symposium on Plasma Chemistry July 5-10, 2015; Antwerp, Belgium Reactive plasmas in multi-ICP system: spatial characterization by threedimensional simulation J. Brcka1 1 Tokyo Electron US Holdings Inc., Technology Development Center, Austin, TX, U.S.A. Abstract: A multi-ICP system can be used to increase plasma uniformity, which makes it possible to increase the processing area and provide additional variables for controlling the plasma. The 3D model of an asymmetric multi-coil ICP using COMSOL multiphysics software is explored to characterize reactive plasma parameters of different gases (Ar, H 2 , CH 4 , CO) and their mixtures. Keywords: inductively coupled plasma, multi-coil, 3D simulation, COMSOL 1. Introduction Beginning from the first generations of the tools designated for plasma processing of the planar silicon in ICs fabrication, there was always development trend to match tool capabilities with increased wafer size. Scaling plasma sources to larger substrate size was always complicated due to many technical issues that were needed to be resolved. The most important aspect was to provide uniform performance of reactive plasma source over the full size silicon wafer. Current uniformity requirements are very stringent; typically nonuniformity should be below 3 % across the wafer. A multi-ICP source is suggested to enhance the plasma uniformity for large-area, low pressure plasma processing [1]. A parallel configuration of the ICP sources will decrease the total impedance of the system and enable a higher electron density. Additionally, it offers additional variables for controlling the plasma. Scaling plasma sources is also challenged by the plasma chemistry. Recently, Okada [2] reported preparation of nano-structured carbon materials (such as nanocrystalline diamond, carbon nanotubes, and carbon nanocapsules) from a CH 4 /CO/H 2 mixture in an ICP plasma and speculated on the role of CO in nanocarbon generation. For industrial applications this process would need to be scaled to large area semiconductor manufacturing technology with a minimized design and development cost. A plasma discharge model with reasonable accuracy is needed to support the prediction of the scaled up plasma tool and processing procedure. The model can further be used to design the optimal configuration and operational parameters of the final plasma tool design to be used for semiconductor manufacturing. Models of ICP plasmas were described elsewhere [3-7]. The numerical simulation techniques commonly used for simulating low-temperature plasma discharge mainly include fluid dynamic, kinetic and hybrid models. These models are significantly different in principles, strengths, applications and limitations. The fluid models are used widely for simulation of plasma tools because of its efficient computational cost. This option makes special P-II-5-3 significance when the technical solution brings additional factors into consideration such are asymmetry, dimensional scale, transient performance, etc. Content and approach in this work is challenging technological, computational, dimensional scaling and plasma chemistry aspects under one framework. 2. Model Plasma simulation is becoming an essential technology used to develop new semiconductor manufacturing equipment and develop improved process control schemes. In ICP systems the inductive antenna is coupled to the excited plasma inside the low pressure gas reactor. Using multiple antennae the mutual inductance between them and to the plasma can influence plasma distribution inside the chamber and impact the overall performance of the source. Assembling the source from individual sources changes the symmetry of the system. Operation of the multi-source configuration is sensitive either to return RF currents in the hardware or inside the plasma. To perform our feasibility investigation we formulated a 3D plasma model using COMSOL Multiphysics [8] suite which is time-efficient for computation for most of the two-dimensional models and flexible in setting the geometry of the actual chamber. As mentioned previously, the proposed plasma tool configuration involves a certain degree of asymmetry due to the multicoil ICP source configuration (Fig. 1). Each coil is represented by a spiral tube (∅3 mm copper tube) with five turns (R max =85 mm, R min =50 mm and 7 mm radial pitch). Formally, for modelling purpose the power from the RF generator (13.56 MHz) is delivered to a small section of each coil to establish identical conditions in power distribution between the coils. The actual power distribution requires additional equipment which is not described within the scope of this work. The coils are separated from the plasma by a dielectric window. Electrostatic coupling between the coils and plasma is inevitable and may cause an electrical asymmetry in the plasma. We accounted for this within the geometrical model with a domain under the dielectric window to be 1 assigned features to serve as a grounded shield with embedded slots. In this work we used a cross section set obtained from IST-LISBON data at LXCat open-access database [10-13] and limited the reaction scheme (Fig. 3) to primary electron collisions with hydrogen molecules. Fig. 2. Primary electron collisions with argon atoms. a) Fig. 3. Primary electron reactions assumed in simple plasma model of hydrogen. b) Fig. 1. Chamber cross-section (a) and top view on multiICP source with four spirals. The goal was to investigate the plasma characteristics in a chamber scaled towards large area (450 mm and above) silicon wafer processing and coupled to CH 4 /CO/H 2 chemistry. Baseline plasma characterization of the multiICP system was initially performed in pure argon gas and further investigations were done under increased complexity of the reaction scheme, either in CH 4 , CO, H 2 or their mixtures. We used limited cross sections for the reaction scheme (Fig. 2) of electron-argon collisions that were obtained from MORGAN data at LXCat openaccess database [9]. Electron collisions drive the entire processing plasma chemistry and are among the most important and critical processes that we need consider. Hydrogen (H 2 ) is considered a carrier gas (typically, 90 % of the mixture). 2 Methane (CH 4 ) has been the subject of investigation for many years and its cross sections were easily the most studied ones when comparing to other gases heavily used in semiconductor manufacturing, such are CF 4 or SiH 4 . Mantzaris et al. [14] developed a self-consistent, 1D simulator for the physics and chemistry of radio frequency (RF) plasmas. The model for CH 4 chemistry considers four species, CH 4 CH 3 CH 2 , and H. The authors determined that CH 4 plasmas are electropositive with negative ion densities one order of magnitude less than those of electrons. The high-energy tail of the electron energy distribution function (EEDF) in CH 4 , lies below both the Druyvensteyn and Maxwell distributions. In our model we used a limited reaction scheme (Fig. 4) for CH 4 cross sections and recommendations from work by Morgan [15] and references therein. Species and rates for neutral gas reactions in CH 4 and H 2 (see details in work by Petrov and Giuliani [16]) either unimolecular or bimolecular were not included in the model at this stage and will be considered later together when coupling the plasma model to a heat transfer model. The following species due to primary collisions with electrons were considered for CH 4 molecules: the ions CH 4 +, CH 3 +, CH 3 , CH 4 * vibrational excitations into σ v (2,4) and P-II-5-3 σ v (1,3), and total electronic excitations into CH 4 ** leading to dissociation [15]. Fig. 4. Electron reactions in plasma model for methane. Fig. 5. Electron reactions used in plasma model of CO gas. Carbon monoxide (CO) cross section data downloaded from the website jila.colorado.edu contained compilation of Phelps data, and according to the author’s note is very similar to the original cross sections by Land [17]. We accounted for individual cross sections for published vibrational excitations but a single excited molecule CO* was considered as resultant product. Similarly, the electronic excitation state CO** represents 5 different excitation levels. Considered plasma species in the case of CO molecules, were CO, CO+, CO* (all vibrational excitations) and CO** (all electronic excitations). Suggested reaction scheme for CO plasma is shown in Fig. 5. Oxygen (O) cross sections [18,19] were considered as the second order collisions in plasma of H 2 +CH 4 +CO mixture. Molecular gases tend to be readily dissociated by electron collisions (Maxwell EEDF was used in the model). Rate coefficients for dissociative recombination (e.g., AB++e-→A+B) of molecular ions CO+, O 2 +, CH 4 +, CH 3 +, CH 2 + and CH+ were obtained from Mitchell [20], where gas temperature was substituted by electron temperature. Volumetric electron loss process (collisional radiative recombination) was approximated by net recombination rate [21]. Consideration of the species and cross sections mentioned does not mean we included all possible P-II-5-3 collision processes that will occur in the plasma. The proposed scheme is a formal approach to match the actual reaction set but with a limited set of participating species, thus our model is rather limited on chemistry aspects. 3. Multi-ICP source operation and simulation results Operation of the multi-ICP source can be performed in several modes. The system can run with all coils in parallel connection to the RF generator or controlled individually by a controller. In this work a spatial plasma distribution was investigated with respect to the phase applied at each coil. Three configurations were proposed for simulation (Fig. 6). The baseline case assumed an identical phase on each coil. The antiphase case consisted of π phase difference between the coils. The last configuration refers to π phase difference between two sets of coils. Fig. 6. Simulation cases in spatial characterization of the reactive plasma. Work on computation is ongoing, robust cases are converging within several days up to week. Discussion of ongoing simulations and obtained results extends the limited space within the abstract. The results will be reported during conference event. 4. Conclusions Computational framework in 3D geometry allowed successful prediction of the spatial distributions of plasma and reactants in large area multi-ICP system. Global uniformity of the plasma at diverse process conditions can be controlled by the RF phase on individual coils. MultiICP configuration provides dynamic control of plasma composition. 5. References [1] Y. S. Lee, J. W. Lee, G.J. Park, and H. Y Chang, Proc. of SPIE, 9054, (2014). [2] K. Okada, Int. Symp. On Plasma Chemistry, Cairns, Australia (2013). [3] M. J. Kushner, W. Z. Collison, M. J. Grapperhaus, J. P. Holland and M. S. Barnes, J. Appl. Phys. 80, 3 (1996). [4] J. L. Giuliani et al., IEEE Trans. Plas. Sci., 27, 5 (1999). [5] S. Tinck and A. Bogaerts, Plasma Sources Sci. Technol., 20 (2011). [6] M. Shigeta, Plasma Sources Sci. Technol., 21 (2012). 3 [7] J. Cheng, L. Ji, K. Wang, Ch. Han, and Y.Shi, Journal of Semiconductors, 34, 6 (2013). [8] www.comsol.com [9] MORGAN database, www.lxcat.laplace.univ -tlse.fr [10] IST-LISBON database, www.lxcat.laplace.univ tlse.fr [11] L. L. Alves, Journal of Physics: Conference Series 565 (2014) [12] S. J. Buckman and A. V. Phelps, J. Chem. Phys., 82, 4999; JILA information Center Report No. 27, University of Colorado, (1985). [13] H. Tawara, Y. Itikawa, H. Nishimura, M. Yoshino, J. Phys. Chem. Ref. Data, 19, 617 (1990). [14] N. V. Mantzaris, E. Gogolides, A. G. Boudouvis, Plasm. Chem. and Plasm. Processing, 16, 3, 301-327 (1996). 4 [15] W. L. Morgan, Plasma Chemistry and Plasma Processing, 12, 4 (1992). [16] G. M. Petrov and J. L. Giuliani, J. Appl. Phys., 90, 2 (2001). [17] J. Land, J. Appl. Phys. 49, 5716 (1978). [18] R. R. Laher and F. R. Gilmore, J. Phys. Chem. Ref. Data, 19, 277 (1990). [19] Y. Itikawa and A Ichimura, J. Phys. Chem. Ref. Data, 19, 637 (1990). [20] J. B. A. Mitchell, Physics Reports, 186, 215 (1998) cited in: W. L. Morgan, Advances in Atomic, Molecular, and Optical Physics, 43, Academic Press, 102 (2000). [21] M. R. Flannery, in G. W. Drake (Ed.), Atomic, molecular and optical physics handbook. American Institute of Physics, Woodburry, NY (1996). P-II-5-3
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