High-Pressure Behaviors of Ag2S Nanosheets: An in Situ High-Pressure X-Ray Diffraction Research

被引:9
|
作者
Liu, Ran [1 ]
Liu, Bo [1 ]
Li, Quan-Jun [1 ]
Liu, Bing-Bing [1 ]
机构
[1] Jilin Univ, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
基金
国家重点研发计划;
关键词
Ag2S; nanosheets; high pressure; phase transitions; SILVER; NANOCRYSTALLINE; NANOTUBES; ROUTE;
D O I
10.3390/nano10091640
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An in situ high-pressure X-ray diffraction study was performed on Ag2S nanosheets, with an average lateral size of 29 nm and a relatively thin thickness. Based on the experimental data, we demonstrated that under high pressure, the samples experienced two different high-pressure structural phase transitions up to 29.4 GPa: from monoclinicP2(1)/nstructure (phase I,alpha-Ag2S) to orthorhombicP2(1)2(1)2(1)structure (phase II) at 8.9 GPa and then to monoclinicP2(1)/nstructure (phase III) at 12.4 GPa. The critical phase transition pressures for phase II and phase III are approximately 2-3 GPa higher than that of 30 nm Ag2S nanoparticles and bulk materials. Additionally, phase III was stable up to the highest pressure of 29.4 GPa. Bulk moduli of Ag2S nanosheets were obtained as 73(6) GPa for phase I and 141(4) GPa for phase III, which indicate that the samples are more difficult to compress than their bulk counterparts and some other reported Ag2S nanoparticles. Further analysis suggested that the nanosize effect arising from the smaller thickness of Ag2S nanosheets restricts the relative position slip of the interlayer atoms during the compression, which leads to the enhancing of phase stabilities and the elevating of bulk moduli.
引用
收藏
页码:1 / 9
页数:9
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