One-pot hydrothermal approach towards 2D/2D heterostructure based on 1 T MoS2 chemically bonding with GO for extremely high electrocatalytic performance

被引:35
作者
Lv, Ying [1 ]
Pan, Hui [1 ]
Lin, Jingyi [1 ]
Chen, Zhixin [2 ]
Li, Yao [1 ]
Li, Hua [1 ]
Shi, Mei [3 ]
Yin, Renjie [3 ]
Zhu, Shenmin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai, Peoples R China
[2] Univ Wollongong, Sch Mech Mat Mechatron & Biomed Engn, Wollongong 2522, Australia
[3] Shanghai Elect Digital Ecotech Co Ltd, Shanghai 200040, Peoples R China
基金
国家重点研发计划;
关键词
Hydrogen evolution reaction; Molybdenum disulfide; Metallic 1T phase; Electrocatalyst; Phase engineering; HYDROGEN EVOLUTION; ACTIVE CATALYST; DOPED GRAPHENE; HYBRID; NANOSHEETS; WATER; TRANSITION; EFFICIENT; COCATALYST; ELECTRODES;
D O I
10.1016/j.cej.2021.132072
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Molybdenum disulfide (MoS2) has become a promising low-cost alternative to Pt catalyst for electrochemical Hydrogen evolution reactions (HER). However, the poor conductivity and limited active sites of thermody-namically stable 2H-Phase MoS2 hinder its catalytic performance. Utilizing phase engineering to convert 2H MoS2 to metallic 1 T MoS2 is an effective strategy to improve the catalytic activity of MoS2. The commonly used synthetic and phase engineering methods such as electrochemical exfoliation involve using a complicated synthesis route or under strict experimental conditions or both. Herein, we develop a one-pot hydrothermal method to in-situ synthesize a 2D (1 T MoS2)/2D (GO) heterostructure with a face-to-face contact between the ultrathin MoS2 (few layers) and Graphene oxide (GO). The content of 1 T MoS2 in the prepared 1 T MoS2/GO reaches as high as 76.7%. When used as a catalyst, 1 T MoS2/GO exhibited an outstanding HER performance, with a small overpotential of 209 mV at a cathode current density of 10 mA cm(-2), and an extremely low Tafel slope of 45.5 mV Dec(-1), which is very close to that of Pt/C (40.0 mV Dec(-1)). Moreover, it demonstrated an excellent stability after a storage of 212 days in air. The high electrocatalytic performance could be attributed to the high 1 T-phase content in the MoS2, as the 1 T phase provides numerous active sites and improves the electronic conductivity of the catalyst. Strong interactions between 1 T MoS2 and GO substrate stabilizes the structure of the 1 T MoS2 and allows rapid charge transfer kinetics. This work proposes a facile and effective strategy for the design and synthesis of transition metal chalcogenides with high HER performance.
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页数:11
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