电催化剂
双功能
析氧
催化作用
阳极
分解水
材料科学
化学工程
阴极
氢
交换电流密度
化学吸附
无机化学
可逆氢电极
电极
化学
电化学
物理化学
工作电极
有机化学
工程类
塔菲尔方程
光催化
作者
Shaowei Yang,Ying Guo,Yike Zhao,Ling Zhang,Haidong Shen,Jinhui Wang,Jinjin Li,Wu Chen,Wenbin Wang,Yueling Cao,Sifei Zhuo,Qiuyu Zhang,Hepeng Zhang
出处
期刊:Small
[Wiley]
日期:2022-05-16
卷期号:18 (24)
被引量:84
标识
DOI:10.1002/smll.202201306
摘要
Abstract The intrinsic sluggish kinetics of the oxygen evolution reaction (OER) limit the improvement of hydrogen evolution reaction (HER) performance, and substituting the anodic oxidation of biomass materials is an alternative approach, given its lower oxidation potential and higher added value compared to those of OER. In this study, a Ni 3 S 2 ‐MoS 2 nanoheterojunction catalyst with strong electronic interactions is prepared. It exhibits high efficiency for both the HER and the electrooxidation of 5‐hydroxymethylfurfural (HMF). In a two‐electrode cell with Ni 3 S 2 ‐MoS 2 serving as both the anode and cathode, the potential is only 1.44 V at a current density of 10 mA cm −2 , which is much lower than that of pure water splitting. Density functional theory calculations confirm that the strong chemisorption of H and HMF at the interface leads to outstanding electrocatalytic activity. The findings not only provide a strategy for developing efficient electrocatalysts, but also provide an approach for the continuous production of high value‐added products and H 2 .
科研通智能强力驱动
Strongly Powered by AbleSci AI