A novel photocatalytic platform based on the newly-constructed ternary composites with a double p-n heterojunction for contaminants degradation and bacteria inactivation

光催化 异质结 三元运算 材料科学 复合数 化学工程 降级(电信) 载流子 可见光谱 化学 光化学 复合材料 催化作用 光电子学 有机化学 计算机科学 电信 工程类 程序设计语言
作者
Shi‐Wen Lv,Jingmin Liu,Fei-Er Yang,Chunyang Li,Shuo Wang
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:409: 128269-128269 被引量:33
标识
DOI:10.1016/j.cej.2020.128269
摘要

Visible-light-induced photocatalytic technique is regarded as the most promising approach to tackle environmental pollution. Herein, a novel ternary [email protected]@10%PANI composite with a double p-n heterojunction was firstly synthesized through a step-by-step self-assembly strategy. Current results suggested that bimetallic Fe.Co-MIL-88B displayed excellent photocatalytic activity, and its combination with spherical COF-TPA/TPB effectively promoted separation and transfer of photoinduced carriers. Meanwhile, introducing PANI with π-π conjugated structure acted as a “bridge” of the charge transport could further boost carrier mobility and enhance absorption in visible light region. Benefiting from the formation of double p-n heterojunction, the recombination of photogenerated electron-hole pairs was inhibited effectively, thereby improving the photocatalytic activity. More significantly, in comparison with pristine COF-TPA/TPB, Fe.Co-MIL-88B and PANI, the [email protected]@10%PANI composite not only presented excellent degradation ability for various contaminants, but also exhibited superb sterilization effect for E. coli and S. aureus. The OH, O2−, h+ and e− were main active species in the photocatalytic reaction system, which were responsible for pollutant degradation and bacteria inactivation. Furthermore, it was proved by our experiment results that the separation and transfer routes of photogenerated charge carriers followed a traditional type-II heterojunction mechanism. All in all, this study could provide novel insights for preparation and application of highly efficient photocatalyst in future research.
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