分解水
氢氧化物
电化学
对偶(语法数字)
材料科学
催化作用
无机化学
纳米技术
化学
电极
物理化学
光催化
生物化学
文学类
艺术
作者
Haibin Yao,Fuhe Le,Wei Jia,Yali Cao,Sheng Rui,Zhenjiang Lu,Xianhao Chen,Dianzeng Jia
出处
期刊:Small
[Wiley]
日期:2023-05-01
卷期号:19 (36)
被引量:7
标识
DOI:10.1002/smll.202301294
摘要
Nickel-iron based hydroxides have been proven to be excellent oxygen evolution reaction (OER) electrocatalysts, whereas they are inactive toward hydrogen evolution reaction (HER), which severely limits their large-scale applications in electrochemical water splitting. Herein, a heterostructure consisted of NiFeV hydroxide and iron oxide supported on iron foam (NiFeV@FeOx /IF) has been designed as a highly efficient bifunctional (OER and HER) electrocatalyst. The V doping and intimate contact between NiFeV hydroxide and FeOx not only improve the entire electrical conductivity of the catalyst but also afford more high-valence Ni which serves as active sites for OER. Meanwhile, the introduction of V and FeOx reduces the electron density on lattice oxygen, which greatly facilitates desorption of Hads . All of these endow the NiFeV@FeOx /IF with exceptionally low overpotentials of 218 and 105 mV to achieve a current density of 100 mA cm-2 for OER and HER, respectively. More impressively, the electrolyzer requires an ultra-low cell voltage of 1.57 V to achieve 100 mA cm-2 and displays superior electrochemical stability for 180 h, which outperforms commercial RuO2 ||Pt/C and most of the representative catalysts reported to date. This work provides a unique route for developing high-efficiency electrocatalyst for overall water splitting.
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