亚稳态
石墨
基面
钻石
机制(生物学)
材料科学
六方晶系
休克(循环)
石墨烯
碳纤维
相变
凝聚态物理
化学物理
纳米技术
结晶学
复合数
复合材料
化学
物理
医学
内科学
量子力学
有机化学
作者
Gu-Wen Chen,Shengcai Zhu,Liang Xu,Yaomin Li,Zhi‐Pan Liu,Yanglong Hou,Ho‐kwang Mao
出处
期刊:JACS Au
[American Chemical Society]
日期:2024-08-25
卷期号:4 (9): 3413-3420
被引量:20
标识
DOI:10.1021/jacsau.4c00523
摘要
High Resolution Image Download MS PowerPoint Slide The formation of a hexagonal diamond represents one of the most intriguing questions in materials science. Under shock conditions, the graphite basal plane tends to slide and pucker to form diamond. However, how the shock strength determines the phase selectivity remains unclear. In this work, using a DFT-trained carbon global neural network model, we studied the shock-induced graphite transition. The poor sliding caused by scarce sliding time under high-strength shock leads to metastable hexagonal diamond with an orientation relationship of (001) G //(100) HD +[010] G //[010] HD, while under low-strength shock due to long sliding distance cubic diamond forms with the orientation (001) G //(111) CD +[100] G //[110] CD, unveiling the strength-dependent graphite transition mechanism. We for the first time provide computational evidence of the strength-dependent graphite transition from first-principles, clarifying the long-term unresolved shock-induced hexagonal diamond formation mechanism and the structural source of the strength-dependent trend, which facilitates the hexagonal diamond synthesis via controlled experiment.
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