碳化物
材料科学
相(物质)
钼
纳米晶
焦耳加热
纳米技术
化学工程
冶金
复合材料
化学
工程类
有机化学
作者
Bing Deng,Zhe Wang,Weiyin Chen,John T. Li,Duy Xuan Luong,Robert A. Carter,Guanhui Gao,Boris I. Yakobson,Yufeng Zhao,James M. Tour
标识
DOI:10.1038/s41467-021-27878-1
摘要
Abstract Nanoscale carbides enhance ultra-strong ceramics and show activity as high-performance catalysts. Traditional lengthy carburization methods for carbide syntheses usually result in coked surface, large particle size, and uncontrolled phase. Here, a flash Joule heating process is developed for ultrafast synthesis of carbide nanocrystals within 1 s. Various interstitial transition metal carbides (TiC, ZrC, HfC, VC, NbC, TaC, Cr 2 C 3 , MoC, and W 2 C) and covalent carbides (B 4 C and SiC) are produced using low-cost precursors. By controlling pulse voltages, phase-pure molybdenum carbides including β-Mo 2 C and metastable α-MoC 1-x and η-MoC 1-x are selectively synthesized, demonstrating the excellent phase engineering ability of the flash Joule heating by broadly tunable energy input that can exceed 3000 K coupled with kinetically controlled ultrafast cooling (>10 4 K s −1 ). Theoretical calculation reveals carbon vacancies as the driving factor for topotactic transition of carbide phases. The phase-dependent hydrogen evolution capability of molybdenum carbides is investigated with β-Mo 2 C showing the best performance.
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