过电位
分解水
析氧
电子转移
纳米线
脱质子化
质子耦合电子转移
催化作用
质子
光化学
配体(生物化学)
密度泛函理论
化学
材料科学
化学物理
纳米技术
光催化
物理化学
计算化学
离子
物理
电化学
有机化学
生物化学
受体
电极
量子力学
作者
Xiaoyan Wang,Zhikun Wang,Ben Jia,Chunling Li,Shuangqing Sun,Songqing Hu
标识
DOI:10.1016/j.cej.2023.147450
摘要
Inspired by the oxygen-evolving complex (OEC) in photosystem II (PS-II), self-supported Fe-doped NiCoP nanowire arrays modified with carboxylate (NCFCP@NF) is constructed to boost industrial-level overall water splitting by the concerted proton-coupled electron transfer (c-PET) mechanism. NCFCP@NF exhibits 283 mV at the current density of 3000 mA cm−2 for HER, which is attributed to the H2O adsorption sites provided by Fe and Ni, as well as the electrons provided by carboxyl ligand. Also, NCFCP@NF shows remarkable OER catalytic activity with overpotential of 329 mV to afford 3000 mA cm−2. Herein, the introduction of Fe promotes the formation of *OOH, and carboxyl ligand accelerate the deprotonation process of OER. Furthermore, NCFCP@NF displays the ultralong durability (200 h) at 1000 mA cm−2 for overall water splitting. This study offers a new perspective on designing efficient overall water splitting catalyst at the industrial-level current density by the concerted proton-coupled electron transfer mechanism.
科研通智能强力驱动
Strongly Powered by AbleSci AI