过电位
双功能
析氧
氢氧化物
分解水
催化作用
电解质
掺杂剂
电解水
电解
碱性水电解
材料科学
吸附
金属
氢
化学工程
化学
无机化学
物理化学
电极
冶金
电化学
兴奋剂
光催化
有机化学
光电子学
工程类
作者
Bowei Zhang,Chongqin Zhu,Zishan Wu,Eli Stavitski,Yu Hui Lui,Tae‐Hoon Kim,Huan Liu,Ling Huang,Xuechen Luan,Lin Zhou,Kun Jiang,Wenyu Huang,Shan Hu,Hailiang Wang,Joseph S. Francisco
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-11-27
卷期号:20 (1): 136-144
被引量:146
标识
DOI:10.1021/acs.nanolett.9b03460
摘要
NiFe-layered double hydroxide (LDH) is thought of as a promising bifunctional water-splitting catalyst, owing to its excellent performances for alkaline oxygen evolution reactions (OERs). However, it shows extremely poor activity toward hydrogen evolution reactions (HERs) due to the weak hydrogen adsorption. We demonstrated that the integration of Rh species and NiFe-LDH can dramatically improve its HER kinetics without sacrificing the OER performance. The Rh species were initially integrated into NiFe-LDH as oxidized dopants and metallic clusters (< 1 nm). In 1 M KOH electrolyte, an overpotential of 58 mV is needed to catalyze 10 mA cm–2 HER current density. Furthermore, this catalyst only requires 1.46 V to drive an electrolyzer at 10 mA cm–2. A strong interaction between metallic Rh clusters and NiFe hydroxide during the HER process is revealed. The theoretical calculation shows the Rh ions replace Fe ions as the major active sites that are responsible for OERs.
科研通智能强力驱动
Strongly Powered by AbleSci AI