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碳布基底上的花状1T-MoS₂/NiCoS₂作为析氢反应的高效电催化剂。

Flower-like 1T-MoS/NiCoS on a carbon cloth substrate as an efficient electrocatalyst for the hydrogen evolution reaction.

作者信息

Zheng Meng, Chen Qianqiao, Zhong Qin

机构信息

School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.

出版信息

Dalton Trans. 2021 Oct 5;50(38):13320-13328. doi: 10.1039/d1dt01948a.

Abstract

The 1T-MoS/NiCoS composite grown on carbon cloth (CC) was successfully prepared by a two-step hydrothermal method as an efficient electrode for the hydrogen evolution reaction. The morphology and composition characterization show that the composite has a flower-like structure with a large number of edges and surfaces exposed, and the content of the 1T phase in MoS is 63%. 1T-MoS/NiCoS/CC exhibits an overpotential of 107 mV at 10 mA cm, and a Tafel slope of 66.4 mV dec in an alkaline electrolyte. After continuous electrolysis for 24 h at an overpotential of 170 mV, 86% of the original current density was retained in an chronoamperometry measurement. The outstanding catalytic performance of the composite is ascribed to its unique structure, high 1T-MoS content and the synergistic catalysis between 1T-MoS and NiCoS. This work provides a facile and effective strategy for fabricating the 1T-MoS/NiCoS/CC composite and demonstrates that the composite is expected to be a competitive non-noble HER catalyst.

摘要

通过两步水热法成功制备了生长在碳布(CC)上的1T-MoS/NiCoS复合材料,作为析氢反应的高效电极。形貌和成分表征表明,该复合材料具有花状结构,大量边缘和表面暴露,MoS中1T相的含量为63%。在碱性电解质中,1T-MoS/NiCoS/CC在10 mA cm时的过电位为107 mV,塔菲尔斜率为66.4 mV dec。在170 mV过电位下连续电解24 h后,计时电流法测量中保留了86%的原始电流密度。该复合材料优异的催化性能归因于其独特的结构、高含量的1T-MoS以及1T-MoS与NiCoS之间的协同催化作用。这项工作为制备1T-MoS/NiCoS/CC复合材料提供了一种简便有效的策略,并证明该复合材料有望成为一种有竞争力的非贵金属析氢催化剂。

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