Colloidal preparation and electrocatalytic hydrogen production of MoS2 and WS2 nanosheets with controllable lateral sizes and layer numbers

被引:66
作者
Zhou, Miao [1 ]
Zhang, Zhuolei [1 ]
Huang, Keke [2 ]
Shi, Zhan [2 ]
Xie, Renguo [1 ]
Yang, Wensheng [1 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSITION-METAL DICHALCOGENIDES; ACTIVE EDGE SITES; SINGLE-LAYER; ULTRATHIN NANOSHEETS; LIQUID EXFOLIATION; CDSE NANOCRYSTALS; LARGE-AREA; ELECTRONIC-STRUCTURE; VAPOR-DEPOSITION; HIGH-PERFORMANCE;
D O I
10.1039/c6nr04775k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although layered transition metal dichalcogenide (TMD) nanosheets have attracted great attention due to their unique properties, it still remains challenge to develop a facile strategy for the precise control of the lateral sizes and layer numbers of TMD nanosheets. In this study, we demonstrate a solution-phase synthetic protocol to prepare colloidal MS2 (M = Mo, W) nanosheets which possess extremely small lateral dimensions from 15 to 40 nm and well-controlled odd numbers of layers, such as 1, 3, and 5 layers, as characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The size-and layer-dependence of the optical properties of colloidal MS2 (M = Mo, W) nanosheets are revealed by Raman and absorption spectra for the first time. These colloidal nanosheets, especially the single-layer ones, possess a large number of edge sites that serve as active sites for the hydrogen evolution reaction (HER). The catalysts exhibit a small HER overpotential and low Tafel slope of approximately 100 mV and 52 mV per decade for MoS2, and 80 mV and 46 mV per decade for WS2, respectively. Importantly, these products show enhanced stability after 500 potential cycles, and the current density remains almost unchanged during the test.
引用
收藏
页码:15262 / 15272
页数:11
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