石墨烯
材料科学
纳米团簇
无定形碳
碳纤维
氢
催化作用
碳氢化合物
无定形固体
化学工程
纳米颗粒
分解
纳米技术
复合材料
化学
有机化学
复合数
工程类
作者
Ruiyun Li,Xing Yang,Ming Ma,Junyan Zhang
出处
期刊:Small
[Wiley]
日期:2023-01-15
卷期号:19 (10)
被引量:3
标识
DOI:10.1002/smll.202206580
摘要
Abstract The solid‐state conversion of amorphous carbon into graphene is extremely difficult, but it can be achieved in the friction experiments that induce macroscale superlubricity. However, the underlying conversion mechanisms remain elusive. Here, the friction experiments with Cu nanoparticles and (non‐hydrogen (H) or H) a‐C in vacuum, show the H‐induced conversion of mechanical to chemical wear, resulting in the a‐C's tribosoftening and nanofragmentating that produce hydrocarbon nanoclusters or molecules. It is such exactly hydrocarbon species that yield graphene at hydrogen‐rich a‐C friction interface, through reaction of them with Cu nanoparticles. In comparison, graphene isn't formed at Cu/non‐H a‐C friction interface. Atomistic simulations reveal the hydrogen‐enhanced tribochemical decomposition of a‐C and demonstrate the energetically favorable graphitization transformation of hydrocarbons on Cu substrates. The findings are of importance to achieve solid‐state transformation between different carbon allotropes and provide a good strategy to synthesize other graphitic encapsulated catalysts with doped elements.
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