Hierarchical spheres constructed by defect-rich MoS2/carbon nanosheets for efficient electrocatalytic hydrogen evolution

被引:270
作者
Yang, Linjing [1 ]
Zhou, Weijia [1 ]
Lu, Jia [1 ]
Hou, Dongman [2 ]
Ke, Yunting [1 ]
Li, Guoqiang [2 ]
Tang, Zhenghua [1 ]
Kang, Xiongwu [1 ]
Chen, Shaowei [1 ,3 ]
机构
[1] S China Univ Technol, Guangzhou Higher Educ Mega Ctr, Sch Environm & Energy, New Energy Res Inst, Guangzhou 510006, Guangdong, Peoples R China
[2] S China Univ Technol, State Key Lab Luminescent Mat & Devices, Engn Res Ctr Solid State Lighting & Its Informati, 381 Wushan Rd, Guangzhou 510641, Guangdong, Peoples R China
[3] Univ Calif Santa Cruz, Dept Chem & Biochem, 1156 High St, Santa Cruz, CA 95064 USA
基金
中国国家自然科学基金;
关键词
Micro-emulsion; MoS2/carbon; Hierarchical spheres; Active sites; Inverted molybdenum reaction; ELECTROCHEMICAL H-2 EVOLUTION; MOS2 ULTRATHIN NANOSHEETS; ACTIVE EDGE SITES; GRAPHENE OXIDE; CATALYST; NITROGEN; NANOPARTICLES; SURFACE; LAYER; FILMS;
D O I
10.1016/j.nanoen.2016.02.056
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
Highly active and stable MoS2/carbon hierarchical spheres with abundant active edge sites were fabricated by a simple micro-emulsion procedure where PVP was used as the carbon source, and carbon disulfide as the sulfur source and oil phase in micro-emulsion to control the morphology of MoS2. Hierarchical spheres of MoS2/carbon with a diameter of ca. 500 nm were obtained and characterized by scanning and transmission electron microscopic measurements. With a high electrochemically accessible surface area and defect-rich MoS2 nanosheets, the MoS2/carbon hierarchical spheres exhibited an excellent electrocatalytic activity for hydrogen evolution reaction with a low onset potential of -103 mV (vs. RHE), small Tafel of 56.1 mV dec(-1), as well as extraordinary catalytic stability. The results were accounted for by the "inverted molybdenum reaction" that served as a novel way of regulating Mo catalytic sites of MoS2 electrocatalysts. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:490 / 498
页数:9
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