饮用水净化
污染物
催化作用
热的
降级(电信)
化学工程
材料科学
稳健性(进化)
氧化还原
活化能
电子转移
热能
水处理
化学
传热
反应速率常数
热氧化
多孔性
光化学
电子
羟基自由基
催化氧化
分解水
纳米技术
电子设备和系统的热管理
光催化
作者
Miao Fang,Zhiyuan Ning,He Guo,Xiaoteng Fan,Guodong Zhang,Qiuling Ma,Jian Zhou,Tiecheng Wang,Sihui Zhan
标识
DOI:10.1002/advs.202513730
摘要
Peroxyacetic acid (PAA) oxidation technology receives widespread concerns for water purification with minimal secondary pollution. Conventional heat-driven PAA activation generally wastes energy during solution heating. In this study, "light-gated thermal domains" concept is developed in a hollow porous carbon nanosphere (HPCS), and the confined heat hotspots lead to a higher temperature (80 °C) in the internal space than in the solution (40 °C). This endows the HPCS with exceptional redox capacity, optical response, and electron transfer capability. The degradation efficiency of sulfadiazine in the HPCS+PAA catalytic system reached more than 98% within 90 min of irradiation, with a reaction rate constant 11 times higher than that in the non-confined system. The "light-gated thermal domains" induces electron localization and decreases PAA activation energy barriers. In contrast to the non-confined system dominated by the radical oxidation pathway, heat-confinement exhibits synergies between the radical and non-radical pathways, enabling rapid pollutant degradation. Zebrafish embryo experiments validated the pollutant detoxification capabilities of this system. This "light-gated thermal domains" ensures long-lasting robustness of PAA activation and paves a novel way for the development of sustainable catalytic water purification technologies.
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