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

塔菲尔方程 二硫化钼 过电位 剥脱关节 催化作用 材料科学 电化学 石墨烯 化学工程 基质(水族馆) 热液循环 相(物质) 异质结 电导率 氧化物 电催化剂 纳米技术 化学 光电子学 电极 复合材料 冶金 有机化学 物理化学 生物化学 工程类 地质学 海洋学
作者
Ying Lv,Hui Pan,Jingyi Lin,Zhixin Chen,Yao Li,Hua Li,Mei Shi,Renjie Yin,Shenmin Zhu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:428: 132072-132072 被引量:49
标识
DOI:10.1016/j.cej.2021.132072
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 thermodynamically 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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