Mechanochemical reactions of GaN-Al2O3 interface at the nanoasperity contact: Roles of crystallographic polarity and ambient humidity

被引:59
作者
Guo, Jian [1 ]
Gao, Jian [2 ]
Xiao, Chen [2 ,3 ]
Chen, Lei [2 ,4 ]
Qian, Linmao [2 ,4 ]
机构
[1] Univ South China, Sch Mech Engn, Hengyang 421001, Peoples R China
[2] Southwest Jiaotong Univ, Tribol Res Inst, State Key Lab Tract Power, Chengdu 610031, Peoples R China
[3] Adv Res Ctr Nanolithog ARCNL, Sci Pk 106, NL-1098XG Amsterdam, Netherlands
[4] Southwest Jiaotong Univ, Technol & Equipment Rail Transit Operat & Mainten, Chengdu 610031, Peoples R China
基金
中国国家自然科学基金;
关键词
crystallographic polarity; ambient humidity; mechanochemical removal; GaN-Al2O3; interface; SURFACE; GAN; DEFORMATION; ENERGY; LAYER; WEAR;
D O I
10.1007/s40544-021-0501-9
中图分类号
TH [机械、仪表工业];
学科分类号
0802 ;
摘要
Mechanochemical reactions of the GaN-Al2O3 interface offer a novel principle for scientific and technological merits in the micro-/nano-scale ultra-precision surface machining. In this work, the mechanochemical reactions on Ga- and N-faced GaN surfaces rubbed by the Al2O3 nanoasperity as a function of the environmental humidity were investigated. Experimental results indicate that the N-face exhibits much stronger mechanochemical removal over the relative humidity range of 20%-80% than the Ga-face. Increasing water molecules in environmental conditions significantly promotes the interfacial mechanochemical reactions and hence accelerates the atomic attrition on N-face. The hypothesized mechanism of the selective water-involved mechanochemical removal is associated with the dangling bond configuration, which affects the mechanically-stimulated chemical reactions via altering the activation energy barrier to form the bonding bridge across the sliding interface. These findings can enrich the understanding of the underlying mechanism of mechanochemical reactions at GaN-Al2O3 interface and a broad cognition for regulating the mechanochemical reactions widely existing in scientific and engineering applications.
引用
收藏
页码:1005 / 1018
页数:14
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