化学
过电位
电催化剂
塔菲尔方程
催化作用
阳极
分解水
析氧
化学工程
电解质
电化学
纳米技术
无机化学
物理化学
材料科学
电极
有机化学
工程类
光催化
作者
Dongmei Liu,Hui Xu,Cheng Wang,Hongyuan Shang,Rui Yu,Yuan Wang,Jie Li,Xingchi Li,Yukou Du
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-04-02
卷期号:60 (8): 5882-5889
被引量:106
标识
DOI:10.1021/acs.inorgchem.1c00295
摘要
Developing high-performance and cost-efficient catalysts toward oxygen evolution reaction (OER) is an important but daunting task due to the sluggish kinetics hindered by the four-electron transfer process. Herein, an advanced class of ultralow Ru-doped NiCo-MOF hollow porous nanospheres (denoted as Ru@NiCo-MOF HPNs) has been reported in this work. Benefiting from the high porosity and large surface area of the metal–organic frameworks (MOFs) and optimized electronic properties by Ru doping, the as-prepared Ru@NiCo-MOF HPNs exhibit superior performance for water oxidation with the overpotential of only 284 mV to reach a current density of 10 mA·cm–2 in alkaline electrolyte, as well as a small Tafel slope of 78.8 mV·dec–1, outperforming the NiCo-MOF HPNs (358 mV) and commercial RuO2 catalyst (326 mV). The incorporation of Ru in NiCo-MOF HPNs enables a stable OER activity for at least 39 h. Moreover, we have probed the interaction between the content of Ru and OER performance, impressively, Ru@NiCo-MOF HPNs with 13.5 atom % Ru doping (denoted as Ru@NiCo-MOF-4) exhibited the highest OER activity with the excellent mass activity of 310 mA·mg–1 at an overpotential of 284 mV. Besides, a two-electrode cell with Ru@NiCo-MOF-4 as the anode and commercial Pt/C catalyst as the cathode also demonstrated outstanding electrocatalytic overall water splitting performance with a cell potential of merely 1.57 V to deliver a current density of 10 mA·cm–2.
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