Chemical mechanical planarization (CMP) of on-axis Si-face SiC wafer using catalyst nanoparticles in slurry

被引:105
作者
Zhou, Yan
Pan, Guoshun
Shi, Xiaolei
Gong, Hua
Luo, Guihai
Gu, Zhonghua
机构
[1] Tsinghua Univ, State Key Lab Tribol, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Res Inst, Shenzhen Key Lab Micro Nano Mfg, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金; 对外科技合作项目(国际科技项目);
关键词
Silicon carbide (SiC); Chemical mechanical planarization (CMP); Catalyst; Removal; Atomic step structure; DAMAGE; GAN;
D O I
10.1016/j.surfcoat.2014.03.044
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The application of catalyst nanoparticles in the slurry is developed for chemical mechanical planarization (CMP) of on-axis Si-face (0001) SiC wafer, so as to obtain higher material removal rate (MRR) and defect-free ultra-smooth surface. Fe nanoparticles, as well as Pt/C nanoparticles were used as a catalyst into the slurry, and the polishing experiment results indicate that an Fe catalyst is preferable to CMP of SiC. The removal behaviors of catalyst assisted CMP were studied and the removal mechanism was discussed. The detection results of *OH hydroxyl radicals reveal that the slurries with catalysts could produce *OH radicals so as to induce the oxidation of SiC. The relationship between the removal of SiC wafer by different catalysts and polishing time was investigated. The removal characteristics with different downward pressure and platen rotation speed and relative local temperature were presented. Optical microscope, optical interferometry profiler and atomic force microscope (AFM) were applied to observe the processed surface by the proposed method. Total planarization of the atomically flat defect-free surface with atomic step-terrace structure and extremely low Ra about 0.05 nm was achieved for SiC wafer by using an Fe catalyst slurry. The results affirm that the promising method is helpful to the surface preparation of super-hard and inert materials with high efficiency and high flatness. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 55
页数:8
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