过电位
分解水
催化作用
析氧
材料科学
钼
密度泛函理论
纳米线
钴
化学工程
氮化物
电解水
无机化学
电极
纳米技术
电解
化学
电化学
光催化
物理化学
计算化学
图层(电子)
工程类
电解质
生物化学
作者
Weixia Huang,Yun Tong,Dongmei Feng,Zhendong Guo,Runze Ye,Pengzuo Chen
出处
期刊:Chemsuschem
[Wiley]
日期:2023-02-08
卷期号:16 (10)
被引量:16
标识
DOI:10.1002/cssc.202202078
摘要
Rational design of efficient electrocatalysts is highly imperative but still a challenge for overall water splitting. Herein, we construct self-supported Co3 N nanowire arrays with different Mo doping contents by hydrothermal and nitridation processes that serve as robust electrocatalysts for overall water splitting. The optimal Co3 N-Mo0.2 /Ni foam (NF) electrode delivers a low overpotential of 97 mV at a current density of 50 mA cm-2 as well as a highly stable hydrogen evolution reaction (HER). Density functional theory (DFT) calculations prove that Mo doping can effectively modulate the electronic structure and surface adsorption energies of H2 O and hydrogen intermediates on Co3 N, leading to improved reaction kinetics with high catalytic activity. Further modification with FeOOH species on the surface of Co3 N-Mo0.2 /NF improves the oxygen evolution reaction (OER) performance benefiting from the synergistic effect of dual Co-Fe catalytic centers. As a result, the Co3 N-Mo0.2 @FeOOH/NF catalysts display outstanding OER catalytic performance with a low overpotential of 250 mV at 50 1 mA cm-2 . The constructed Co3 N-Mo0.2 /NF||Co3 N-Mo0.2 @FeOOH/NF water electrolyzer exhibits a small voltage of 1.48 V to achieve a high current density of 50 mA cm-2 at 80 °C, which is superior to most of the reported electrocatalysts. This work provides a new approach to developing robust electrode materials for electrocatalytic water splitting.
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