光催化
双酚A
电子转移
光电流
材料科学
降级(电信)
光化学
化学工程
催化作用
化学
光电子学
复合材料
有机化学
计算机科学
环氧树脂
工程类
电信
作者
Heng Fei,Junxia Shao,Hua Li,Najun Li,Dongyun Chen,Qingfeng Xu,Jinghui He,Jianmei Lu
标识
DOI:10.1016/j.apcatb.2021.120623
摘要
g-C3N4 (CN), which shows enormous potential for photocatalysis, has long been studied, but still exhibits an unsatisfactory degradation rate. Herein, dual cocatalysts, Br and ultrafine RhOx nanoparticles, were constructed on ultrathin CN for synergetic photocatalysis. Ultrathin CN increased the exciton separation efficiency, while cocatalysts Br and RhOx can accelerated electron and hole transfer simultaneously, maximizing the photocatalytic degradation performance of CN. This CN-Br0.12/2%RhOx degraded 10 ppm bisphenol A (BPA) in 9 min, which represents the fastest degradation rate reported to date. This excellent performance was also demonstrated by a larger photocurrent response, higher separation efficiency, and faster transfer rate for electron–hole pairs than CN. This work obtained an enhanced electron–hole separation efficiency and migration rate by combing ultrathin CN with dual-channel cocatalysts, leading to the best photocatalytic degradation performance reported for CN.
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