苯酚
光催化
吸附
化学
醌
激进的
纳米颗粒
材料科学
氧化还原
光化学
催化作用
电子转移
金属
无机化学
有机化学
纳米技术
作者
Jianqiu Gong,Weiwei Zhang,Tapas Sen,Yichen Yu,Yuchen Liu,Jinlong Zhang,Lingzhi Wang
标识
DOI:10.1021/acsanm.1c00119
摘要
Photocatalysis is a promising technology to treat dilute phenol–Cr(VI) mixture, where photoinduced electrons are commonly thought of as the main active species for Cr(VI) reduction. However, it generally depends on the surface adsorption to achieve efficient electron transfer. Meanwhile, the possible contribution of reductive quinone derivatives oxidized from phenol to Cr(VI) reduction has been rarely explored. The key is to explicitly understand the relation between the phenol oxidation pathway and Cr(VI) reduction. Herein, Ag/AgCl/MIL-101(Fe) prepared by directly loading Ag nanoparticles on MIL-101(Fe) was applied to the joint treatment of phenol and Cr(VI). The role of quinone derivatives in reducing Cr(VI) was revealed by excluding the surface adsorption. During the phenol oxidation, •OH radicals were more consumed in the initial stage for the ring opening of phenol. Meanwhile, 1O2 evolved from •O2– gradually caused the accumulation of reductive quinone intermediates, which dramatically accelerated the Cr(VI) reduction afterward. This study demonstrates the significance of controlling the evolution process of active oxygen species for the joint photocatalytic treatment of phenol–Cr(VI) mixture.
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