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Unprecedented differences in the diamond nucleation density between carbon-and silicon-faces of 4H-silicon carbides
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作者 Bo Wang Pitsiri Sukkaew +10 位作者 Guichen Song Andreas Rosenkranz Yunxiang Lu kazhihito nishimura Jia Wang Jilei Lyu Yang Cao Jian Yi Lars Ojamae He Li Nanjiang 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第7期2013-2018,共6页
4H-silicon carbides deposited by diamond films have wide applications in many fields such as semiconductor heterojunction,heat sink and mechanical sealing.Nucleation plays a critical role in the deposition of the diam... 4H-silicon carbides deposited by diamond films have wide applications in many fields such as semiconductor heterojunction,heat sink and mechanical sealing.Nucleation plays a critical role in the deposition of the diamond film on 4H-silicon carbides.Nevertheless,as a typical polar material,the fundamental mechanism of diamond nucleation on different faces of 4H-silicon carbides has not been fully understood yet.In this contribution,nucleation of diamond was performed on the carbon-and silicon-faces of 4H-silicon carbides in a direct current chemical vapor deposition device.The nucleation density on the carbon-face is higher by 2-3 orders of magnitude compared to the silicon-face.Transmission electron microscopy verifies that there are high density diamond nuclei on the interface between the carbon-face and the diamond film,which is different from columnar diamond growth structure on the silicon-face.Transition state theory calculation reveals that the unprecedented distinction of the nucleation density between the carbon-face and the silicon-face is attributed to different desorption rates of the absorbed hydrocarbon radicals.In addition,kinetic model simulations demonstrate that it is more difficult to form CH2(s)-CH2(s)dimers on silicon-faces than carbon-faces,resulting in much lower nucleation densities on silicon-faces. 展开更多
关键词 4H-silicon carbide Diamond nucleation mechanism Transmission electron microscopy Transition state theory Kinetic model simulation
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