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Research Article

1T@2H-MoSe2 nanosheets directly arrayed on Ti plate: An efficient electrocatalytic electrode for hydrogen evolution reaction

Jingtong Zhang1Yalan Chen1Ming Liu1Kun Du1Yan Zhou1,2( )Yanpeng Li1Zhaojie Wang2Jun Zhang1( )
State Key Laboratory of Heavy Oil Processing China University of Petroleum (East China)Qingdao266580China
College of Science China University of Petroleum (East China)Qingdao266580China
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Abstract

Few-layered MoSe2 nanosheets with mixed 1T/2H phase were successfully arrayed on a Ti substrate (forming 1T@2H-MoSe2/Ti) through a facile one-step solvothermal process. After testing different synthesis conditions, it was found that the optimal process involves a temperature of 200 ℃ and a reaction time of 12 h. Structural characterizations reveal that the morphology of 1T@2H-MoSe2 consists of edge-terminated nanosheets with one to five layers, composed of a mixed 1T/2H phase dominated by the 1T one. The 1T@2H-MoSe2/Ti electrode shows excellent HER catalytic activity, with a small onset potential (-120 mV vs. reversible hydrogen electrode, RHE) and an electrode potential of only -133 mV (vs. RHE) to achieve a current density of 20 mA·cm-2. This excellent electrocatalytic activity is due to the synergistic effects of 1T metallic phase, few-layered nanosheet morphology, and direct growth of 1T@2H-MoSe2on the Ti substrate. In addition, the 1T@2H-MoSe2/Ti electrode shows excellent stability towards long-term electrolysis. This is due to the long-term stability of the valence states of Mo and Se, as shown by post-electrolysis X-ray photoelectron spectroscopy analysis.

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Nano Research
Pages 4587-4598

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Cite this article:
Zhang J, Chen Y, Liu M, et al. 1T@2H-MoSe2 nanosheets directly arrayed on Ti plate: An efficient electrocatalytic electrode for hydrogen evolution reaction. Nano Research, 2018, 11(9): 4587-4598. https://doi.org/10.1007/s12274-018-2040-x

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Received: 26 September 2017
Revised: 10 February 2018
Accepted: 02 March 2018
Published: 20 March 2018
© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2018