Affiliation:
1. Beijing Key Laboratory for Chemical Power Source and Green Catalysis School of Chemistry and Chemical Engineering Beijing Institute of Technology Beijing 100081 P. R. China
2. School of Materials and Environment Beijing Institute of Technology Jinfeng Road No.6, Xiangzhou District Zhuhai 519085 P. R. China
Abstract
AbstractThe exploiting electrocatalysts for water/seawater electrolysis with remarkable activity and outstanding durability at industrial grade current density remains a huge challenge. Herein, CoMoNx and Fe‐doped CoMoNx nanosheet arrays are in‐situ grown on Ni foam, which possess plentiful holes, multilevel heterostructure, and lavish Co5.47N/MoN@NF and Fe‐Co5.47N/MoN@NF interfaces. They require low overpotentials of 213 and 296 mV for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) under alkaline media to achieve current density of 800 mA cm−2, respectively, and both possess low Tafel slopes (51.1 and 49.1 mV dec−1) and undiminished stability over 80 h. Moreover, the coupled Co5.47N/MoN@NF and Fe‐Co5.47N/MoN@NF electrolyzer requires low voltages of 1.735 V to yield 500 mA cm−2 in alkaline water. Notably, they also exhibit exceptional electrocatalytic properties in alkaline seawater (1.833 V@500 mA cm−2). The experimental studies and theoretical calculations verify that Fe doping does reduce the energy barrier from OH* to O* intermediates during OER process after catalyst reconstruction, and the non‐metallic N site from MoN exhibits the lowest theoretical overpotential. The splendid catalytic performance is attributed to the optimized local electron configuration and porous structure. This discovery provides a new design method toward low‐cost and excellent catalysts for water/seawater splitting to produce hydrogen.
Funder
National Natural Science Foundation of China
Cited by
7 articles.
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