电催化剂
氯
析氧
电化学
双功能
化学
电解质
无机化学
法拉第效率
吸附
氧气
钌
化学工程
金属
催化作用
自来水
次氯酸盐
反应机理
过渡金属
次氯酸钠
电极
双金属片
降级(电信)
作者
Long Chen,Xiaoge Peng,Zhenyang Dong,Jinglei Si,Wei Guo,Yichen Gu,Yang Ding,Yongyong Cao,Xing Zhong,Jianguo Wang,Long Chen,Xiaoge Peng,Zhenyang Dong,Jinglei Si,Wei Guo,Yichen Gu,Yang Ding,Yongyong Cao,Xing Zhong,Jianguo Wang
标识
DOI:10.1002/anie.202520036
摘要
Abstract The electrochemical production of sodium hypochlorite (NaClO) and reactive oxygen species (ROS) offers potential for water treatment. Although chlorine evolution reaction (CER) and ROS generation had been widely investigated in acidic media, further exploration was warranted under tap‐water conditions. In this study, a ruthenium single‐atom‐based electrocatalyst (Ru SAs/IrCeO x /Co 3 O 4 ) was developed, which achieved a Faradaic efficiency (FE) of 98.5% for CER in acidic electrolyte and demonstrated stable operation for 1750 h at 625 mA·cm −2 during an accelerated durability test. The electrocatalyst generated 1.4 ppm total oxidants within 2 min in simulated tap water, and showed stability for 1630 h in a medium‐salinity electrolyte. Theoretical analyses demonstrated that Ru SAs/Co 3 O 4 surface lowered the thermodynamic barrier for Cl 2 formation, the moderate chlorine adsorption energy of IrO 2 establishes an electrocatalytic interface for the reaction system, CeO 2 facilitated the spontaneous generation of *O species and promoted O‐O coupling, endowing the electrocatalyst with bifunctional activity toward both CER and ROS production under simulated tap water conditions. The electrocatalyst, coupled with a self‐designed continuous‐flow electrolyzer, achieves 95% pollutant degradation within 30 min. This study provides guidance for reducing the fabrication cost of commercial DSA electrodes and enabling their application in advanced electrochemical oxidation processes.
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