苯酚
光催化
污染物
矿化(土壤科学)
过氧化氢
光降解
降级(电信)
光化学
双金属片
催化作用
密度泛函理论
氧化还原
化学
化学工程
氮化碳
材料科学
石墨氮化碳
氮气
无机化学
有机化学
计算化学
电信
计算机科学
工程类
作者
Zichao Lian,Fangfang Gao,Han Xiao,Di Luo,Mengyuan Li,Duoduo Fang,Yupeng Yang,Jiangzhi Zi,Hexing Li
标识
DOI:10.1002/anie.202318927
摘要
Abstract Achieving the complete mineralization of persistent pollutants in wastewater is still a big challenge. Here, we propose an efficient photo‐self‐Fenton reaction for the degradation of different pollutants using the high‐density (Ag: 22 wt %) of atomically dispersed AgCo dual sites embedded in graphic carbon nitride (AgCo−CN). Comprehensive experimental measurements and density functional theory (DFT) calculations demonstrate that the Ag and Co dual sites in AgCo−CN play a critical role in accelerating the photoinduced charge separation and forming the self‐Fenton redox centers, respectively. The bimetallic AgCo−CN exhibited excellent photocatalytic performance toward the phenol even under extreme conditions due to an efficient degradation pathway and in situ generation of the hydrogen peroxide producing the main active oxygen species (⋅OH and 1 O 2 ) and showed long‐term activity in a self‐design photo‐Filter reactor for the purification of the phenol. Our discoveries pave the way for the design of efficient single‐atoms photocatalysts‐based photo‐self‐Fenton reaction for recalcitrant pollutant treatment.
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