过电位
析氧
分解水
双功能
催化作用
电解质
阳极
贵金属
材料科学
化学工程
金属有机骨架
化学
金属
电极
电化学
冶金
物理化学
工程类
吸附
光催化
生物化学
作者
Pinghua Chen,Xueqing Duan,Guifang Li,Xianhua Qiu,Shuai Wang,Yiping Huang,Anna Stavitskaya,Hualin Jiang
标识
DOI:10.1016/j.ijhydene.2022.11.080
摘要
Constructing bifunctional non-precious metal electrocatalysts is necessary for effective overall water splitting (OWS), but challenging. Herein, a novel hybrid nanostructure of ZIF-67/MIL-88(Fe, Ni), denoted as Co-M-Fe/Ni(x) (x represents the mass of ZIF-67), was successfully synthesized by hydrothermal and in-situ growth method, and showed a highly efficient and stable bifunctionality of both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline electrolyte. The Co-M-Fe/Ni(150) exhibited excellent OER performance with a low overpotential of 269 mV and 149 mV @ 10 mA cm−2 for OER and HER in 1 mol L−1 KOH, respectively. With Co-M-Fe/Ni(150) as cathode and anode, the integrated OWS device had achieved low potential of 1.52 V @ 10 mA cm−2, exhibiting its excellent performance of OWS. Based on the results of experiments, ZIF-67 and MIL-88(Fe, Ni), as metal-organic frameworks (MOFs), which have a large specific surface area, uniform distribution of porous structures facilitates charge transmission, promoting the penetration of electrolytes, and improves electron transfer rate. The mechanism of the superior electrocatalytic performance of Co-M-Fe/Ni(150) may be attributed to the synergy of ZIF-67 and MIL-88(Fe, Ni). This work provides guidance for the rational design or optimization of non-noble composites for energy conversion.
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