Hierarchical ZnS@C@MoS2 core-shell nanostructures as efficient hydrogen evolution electrocatalyst for alkaline water electrolysis

被引:35
作者
Liu, Shanhu [1 ,2 ]
Li, Shengnan [1 ]
Sekar, Karthi [1 ]
Li, Rui [1 ]
Zhu, Yuanyuan [1 ]
Xing, Ruimin [1 ,2 ]
Nakata, Kazuya [2 ]
Fujishima, Akira [2 ]
机构
[1] Henan Univ, Coll Chem & Chem Engn, Henan Key Lab Polyoxometalate Chem, Henan Joint Int Res Lab Environm Pollut Control M, Kaifeng 475004, Peoples R China
[2] Tokyo Univ Sci, Res Inst Sci & Technol, Photocatalysis Int Res Ctr, 2641 Yamazaki, Noda, Chiba 2788510, Japan
基金
中国国家自然科学基金;
关键词
MOS2; NANOSHEETS; LITHIUM STORAGE; FOAM COMPOSITE; GRAPHENE; FABRICATION; NANOTUBES; CATALYSTS; HYBRID; GROWTH; OXIDE;
D O I
10.1016/j.ijhydene.2019.08.048
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Low-cost and highly efficient electrocatalysts are critical to advance the hydrogen production industry via water electrolysis in alkaline media. Molybdenum disulfide (MoS2) nanosheets as earth-abundant electrocatalyst became a star material due to its unique graphene-like layered structure favoring electron transfer for hydrogen evolution catalysis. However, its electrocatalytic activities greatly hindered by the poor conductivity and the fewer exposure of catalytically active edged sites. Herein, hierarchical ZnS@C@MoS2 coreshell nanostructures were designed by using a bottom-up strategy combined with a simple selective etching. The coexistence of semiconductor ZnS and defective porous carbonaceous shell as the core not only enhanced the electrical conductivity, but also separated and loaded the exfoliated MoS2 nanosheets which effectively proliferated the exposed catalytically active edge sites (Mo and S sites). Upon optimal conditions, hierarchical ZnS@C@MoS2 core-shell nanostructures gave an overpotential of 118 mV at 10 mA/cm(2) with a Tafel slope value of 55.4 mV/dec and better cycling stability after 500 cycles during the alkaline HER process, superior to pristine MoS2. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25310 / 25318
页数:9
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