过电位
析氧
塔菲尔方程
双功能
分解水
催化作用
电催化剂
金属有机骨架
材料科学
无机化学
化学工程
等结构
钼
金属
化学
电化学
晶体结构
物理化学
电极
结晶学
有机化学
冶金
光催化
吸附
工程类
作者
Lifan Yang,Li Zhang,Guan‐Cheng Xu,Xin Ma,Weiwei Wang,Huijun Song,Dianzeng Jia
标识
DOI:10.1021/acssuschemeng.8b02428
摘要
Electrocatalytic water-splitting catalysts play important roles in clean energy conversion systems. Herein, metal–organic framework-derived (MOF-derived) hollow CoSx@MoS2 microcubes were successfully synthesized by a novel method. Co-MOF [(CH3)2NH2][Co(HCOO)3] prepared by a simple liquid precipitation method at room temperature reacted with S2– released from thioacetamide (TAA) to generate Co9S8 under solvothermal conditions. Through hydrothermal treatment, numerous MoS2 nanosheets grew on the surface of CoSx vertically and uniformly after introduction of sulfur and molybdenum sources, finally generating CoSx@MoS2 heterostructures. As bifunctional electrocatalysts, the heterostructures exhibited remarkable performance for the hydrogen evolution reaction with a low overpotential of 239 mV when the current density increased up to 10 mA cm–2 and a small Tafel slope of 103 mV dec–1 in 0.5 M H2SO4. They also worked effectively for the oxygen evolution reaction with a low overpotential of 347 mV at 10 mA cm–2 in 1 M KOH. The enhanced electrocatalytic activities of CoSx@MoS2 can be ascribed to their unique heterostructures and the synergism between CoSx and MoS2.
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