Liu Yang, Liu Sen, Zhao Guoqiang, Shen Maoqiang, Gao Xinyue, Zhao Yanhao, Liu Xuesen, Hou Linrui, Yuan Changzhou
School of Materials Science & Engineering, University of Jinan, 250022, Jinan, P. R. China.
Angew Chem Int Ed Engl. 2025 Feb 17;64(8):e202420287. doi: 10.1002/anie.202420287. Epub 2024 Dec 11.
The rising of MXenes not only enriches the two-dimensional material family but also brings more opportunities for diverse functional applications. However, the controllable synthesis of MXenes is still unsatisfied via the common liquid-solid etching route, considering the unsolved problems like safety risk, time cost and easy oxidation. Herein, a facile yet efficient gas-solid (G-S) reaction methodology is devised by using hydrogen fluoride gas derived from fluorinated organics as the MAX etchant toward high-efficiency fabrication of multiple MXenes and their derivatives. The innovative G-S reaction strategy exhibits superb versatility to achieve different gram-level MXenes (VC, TiC, NbC, TiN, TiCN, (MoY)C) in a very short time, and even realizes in situ heteroatom doping or synchronous phase conversion of MXenes directly from MAX phases. The obtained MXenes and their derivatives exhibit excellent structure stability and high electron/ion conductivity, making them promising materials for electrochemical applications. In particular, the N-doped VC MXene shows superior adsorption and catalytic activity toward lithium polysulfides for advanced lithium sulfur batteries.
MXenes的兴起不仅丰富了二维材料家族,也为多样化的功能应用带来了更多机遇。然而,考虑到安全风险、时间成本和易氧化等未解决问题,通过常见的液固蚀刻路线对MXenes进行可控合成仍不尽人意。在此,我们设计了一种简便而高效的气固(G-S)反应方法,使用源自氟化有机物的氟化氢气体作为MAX相的蚀刻剂,以高效制备多种MXenes及其衍生物。这种创新的G-S反应策略具有卓越的通用性,能够在极短时间内制备出不同克级的MXenes(VC、TiC、NbC、TiN、TiCN、(MoY)C),甚至能直接从MAX相实现MXenes的原位杂原子掺杂或同步相转换。所获得的MXenes及其衍生物表现出优异的结构稳定性和高电子/离子导电性,使其成为电化学应用的有前景材料。特别是,N掺杂的VC MXene对先进锂硫电池的多硫化锂表现出优异的吸附和催化活性。