生物炭
光催化
催化作用
锐钛矿
背景(考古学)
碳纤维
光降解
降级(电信)
化学
材料科学
化学工程
光化学
有机化学
复合数
工程类
生物
古生物学
复合材料
电信
计算机科学
热解
作者
Chen Wang,Zeqiang Zhan,Huanran Liu,Yaohui Li,Jianghua Wu,Peng Sun,Guoqing Shen
标识
DOI:10.1016/j.cej.2024.148906
摘要
The efficient and sustainable utilization of solar energy and biomass resources through photocatalysis is important for achieving a carbon–neutral energy cycle. Here, we report an efficient photocatalyst SA-Fe@TiO2, where single-atom Fe sites are anchored to nitrogen-doped biochar and coupled with anatase TiO2. This innovative biochar-supported single-atom catalyst serves as a novel cocatalyst that can facilitate charge carrier separation and transfer. SA-Fe@TiO2 achieves an increase of 4.3 times in apparent rate constant for the degradation of the antibiotic sulfamethoxazole (SMX) and exhibits superior capacity for inactivating antibiotic-resistant genes compared with pure TiO2. Experimental evidence reveals the remarkable resistance of SA-Fe@TiO2 against environmental interferences, unveiling the involvement of three primary reactive species (h+, •OH, and •O2−) in SMX photodegradation. In addition, we fabricate immobilized SA-Fe@TiO2 films that effectively degrade five distinct antibiotics within 20 min. This study presents a new method for developing single-atom photocatalysts for highly efficient environmental remediation in the context of carbon neutrality.
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