异质结
光催化
材料科学
催化作用
共价键
硫化物
化学工程
纳米技术
化学
有机化学
光电子学
冶金
工程类
作者
Li Zhang,Qiang Shi,Sai Jin Xiao,Zhenwen Zhang,Yuting Luo,Chen Sun,Xiaolin Liu,Ru‐Ping Liang,Jian‐Ding Qiu
标识
DOI:10.1021/acsami.4c22218
摘要
In this study, a core-shell heterostructure of cuprous sulfide (Cu2S) nanoplates and covalent organic polymers (COPs) (Cu2S@COP) was constructed in situ by a Cu2S-catalyzed azide-alkyne reaction for efficient reduction and rapid removal of U(VI) from uranium mine wastewater. The simple in situ synthesis of heterojunctions through click chemistry reactions can create a tight bond at the interface and evade the laborious process of conventional composites. The different Fermi energy levels of Cu2S and COP induce the formation of a built-in electric field within the core-shell heterojunction, and the photogenerated charge transfer from the COP to Cu2S nanoplate results in a substantial boost in the efficiency of the photocatalytic reduction of U(VI). The Cu2S@COP heterojunction demonstrates a high U(VI) removal capacity of 1164.6 mg g-1 without the need of a sacrificial agent, which is 2.08 times higher than Cu2S nanoplates, 3.02 times higher than COP, and better than most other previous heterostructures. The present photocatalytic method involves good specificity and achieves a high U(VI) removal efficiency of 85.9% from uranium mine wastewater. The in situ preparation of the Cu2S@COP core-shell heterojunction via click chemistry provides a new design concept for composite construction and presents a novel strategy to modulate the photocatalytic activity for contaminant management.
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