光降解
光催化
异质结
盐酸四环素
材料科学
降级(电信)
可见光谱
光化学
吸收(声学)
激进的
催化作用
化学工程
原位
盐酸盐
四环素
反应机理
吸收光谱法
核化学
反应中间体
动力学
碳化作用
光电子学
作者
Song Wang,Xi Tan,Liangjun Long,Xinyi Luo,Luxiang Tang,Gang Chen,Guizhi Zhang,Lintao Xu,Wenhao Xie
出处
期刊:NANO
[World Scientific]
日期:2026-03-13
标识
DOI:10.1142/s179329202650102x
摘要
Photocatalysis is an eco-friendly technology to remove tetracycline hydrochloride (TCH) and can completely mineralize it to CO 2 and H 2 O under light irradiation. Bi[Formula: see text]O[Formula: see text]Cl 2 is a typical photocatalyst, but the high recombination of electrons and holes restricts the photocatalytic performance of bare Bi[Formula: see text]O[Formula: see text]Cl 2 . Herein, we design and in situ synthesize a 2D/2D Bi[Formula: see text]O[Formula: see text]Cl 2 /Ti 3 C 2 heterojunction using a solvothermal method. The Bi[Formula: see text]O[Formula: see text]Cl 2 /Ti 3 C 2 heterojunction exhibits enhanced photodegradation performance for TCH under visible light irradiation. The mechanism study indicated that the improved light absorption capacity, efficient electron–hole separation and transport capability and superoxide free radicals with strong oxidation capacity facilitate photocatalytic degradation of TCH. Moreover, the TCH’s possible degradation routes were put forward based on intermediates detected by LC–MS. This work proposes a new tactic for constructing Bi[Formula: see text]O[Formula: see text]Cl 2 heterojunction to promote its photocatalytic performance.
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