材料科学
电催化剂
催化作用
空位缺陷
氨硼烷
过电位
相(物质)
氢
化学工程
金属
过渡金属
物理化学
制氢
结晶学
化学
电化学
电极
工程类
冶金
生物化学
有机化学
作者
Jialin Cai,Jie Ding,Donghui Wei,Xin Xie,Baojun Li,Siyu Lu,Jianmin Zhang,Yushan Liu,Qiang Cai,Shuang‐Quan Zang
标识
DOI:10.1002/aenm.202100141
摘要
Abstract For most Mo‐based electrocatalysts, the hydrogen evolution reaction (HER) activity depends on their own active structural defects or extrinsic transition metal centers. In this work, in order to combine the advantages of these two different active centers, a solid‐phase interface reaction (SPIR) strategy is proposed, which simultaneously introduces oxygen vacancies (V O ) and metal centers (Ru) into the 2D Mo‐based catalyst. Briefly, this SPIR occurs at the interface between MoS 2 and RuO 2 nanoparticles of the RuO 2 /MoS 2 precursor when overcoming the kinetic barriers at a suitable temperature under an Ar atmosphere. Since the adjacent parts of RuO 2 and MoS 2 are converted to Ru and MoO 2 in situ, a composite system MiSC‐1 containing a large amount of active Ru and V O on MoO 2 plane is obtained. Furthermore, theoretical calculations confirm the proposed mechanism of SPIR. MiSC‐1 shows excellent stability and catalytic performance in the HER, with an overpotential value of 12 mV at 10 mA cm −2 in 1.0 M KOH. Additionally, MiSC‐1 exhibits excellent performance in the hydrolysis of ammonia borane. This report will provide a versatile platform for the preparation of a multi‐component catalyst with high total activity as well as the identification of the structural details of the catalysts.
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