塔菲尔方程
二硫化钼
电催化剂
吡啶
离子液体
相(物质)
溴化物
堆积
催化作用
位阻效应
离子键合
化学
材料科学
钼
化学工程
结晶学
无机化学
组合化学
电化学
立体化学
有机化学
电极
物理化学
离子
冶金
工程类
作者
Xin Zhang,Li He,Hui Yang,Fazhi Xie,Zhihao Yuan,Lenka Zajı́čková,Wenjiang Li
标识
DOI:10.1002/celc.202000745
摘要
Abstract Two‐dimensional (2D) molybdenum disulfide (MoS 2 ) has been regarded as an attractive non‐precious‐metal electrocatalyst for the hydrogen evolution reaction (HER). Engineering the crystal phase of MoS 2 to activate the basal planes/edges and simultaneously improve the electronic conductivity is currently an effective strategy for enhancing its HER activity. Herein, we report a facile and efficient hydrothermal route to prepare 1T/2H‐MoS 2 catalysts using ionic liquid (N‐butyl pyridinium bromide, [BPy]Br) as a structure‐directing agent, where the large steric hindrance of [BPy]Br and the mutual π‐stacking interaction induce the phase transition of MoS 2 from 2H to the 1T phase. By adding a suitable amount of [BPy]Br in the reaction system, the portion of the 1T phase in 1T/2H‐MoS 2 was increased, which can expose more active sites on its basal planes/edges as well as facilitate charge transfer for the HER. Consequently, 1T/2H‐MoS 2 with the 1T portion of 91.9 % exhibits a significantly enhanced HER activity compared to that of the MoS 2 synthesized without the aid of [BPy]Br, in terms of a lower Tafel slope of 59 mV dec −1 . This synthesis strategy provides valuable guidance for designing the phase structure of MoS 2 ‐based electrocatalysts to achieve high HER efficiency.
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