双功能
过电位
电催化剂
析氧
分解水
金属
材料科学
纳米花
复合数
水热合成
化学
无机化学
化学工程
热液循环
纳米技术
电化学
催化作用
电极
物理化学
冶金
纳米结构
有机化学
光催化
复合材料
工程类
作者
Zhiying Lin,Tao Feng,Xin Ma,Gang Liu
出处
期刊:Fuel
[Elsevier]
日期:2023-01-06
卷期号:339: 127395-127395
被引量:32
标识
DOI:10.1016/j.fuel.2023.127395
摘要
Due to the high electrical conductivity and abundant active sites, 1T MoS2 shows distinguished electrocatalytic activity in hydrogen evolution reaction (HER). However, 1T MoS2 is metastable and shows low activity toward oxygen evolution reaction (OER), preventing its wide application as bifunctional electrocatalyst. Herein, we demonstrate the preparation of 1T-rich MoS2 composite catalysts for enhanced HER and OER in alkaline condition. The preparation process includes hydrothermal synthesis of Fe/Ni bi-metallic organic framework (b-MOF) and subsequent in-situ fabrication of 1T/2H MoS2. The as-prepared composite MoS2@Fe/Ni-MOF600-x (x = 1, 2, 3) exhibits excellent electrocatalytic performance due to the specific nanoflower 3D structure, electron modulation effect of Fe/Ni, and high content of 1T MoS2. Typically, MoS2@Fe/Ni-MOF600-3 with a relatively high Fe/Ni-MOF600 feeding showed the best catalytic performance, including low overpotential of 140 and 340 mV (to achieve a current density of 10 mA·cm−2) and large electrochemically active surface area (ECSA) of 1312.5 and 912.5 cm2 for HER and OER, respectively. The study provides a novel strategy for the preparation of 1T-rich MoS2 composite catalyst for highly efficient hydrogen evolution and oxygen evolution.
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