普鲁士蓝
铀
带隙
光催化
催化作用
异质结
纳米技术
化学
材料科学
化学工程
光化学
物理化学
冶金
光电子学
有机化学
工程类
电极
电化学
作者
Hao Ye,Rou-Ming Wen,Ming‐Bang Wu,Zi-Hao Yuan,Jun Cao,Chaorong Li,Juming Yao
标识
DOI:10.1016/j.cej.2024.149731
摘要
Photoreduction of soluble U(VI) to insoluble U(IV) by CdS-based catalysts shows great potential in remediating radioactive wastewater in terms of environmental friendliness and desirable bandgap as well as the availability of CdS, but is still limited by undesirable efficiency and stability from photogenerated carrier recombination and photocorrosion. Herein, we have elegantly designed tailor-made CdS@Prussian blue with homo/heterojunctions via one-pot kinetic regulation. The key to such a structure is to leverage the outstanding binding affinity between cyanogroups of Prussian blue and Cd2+ to create diversity of local precursor concentration differences. With such unique structure and rational energy band distribution, our photocatalysts demonstrate an unprecedented U(VI) removal efficiency as high as 2.5 times that of the pristine CdS. More importantly, the strong chelation between cyanogroups and Cd2+ endows our catalysts with extremely excellent stability compared with other state-of-the-art composite photocatalysts. This work provides a facile and universal inspiration for homo/heterojunction engineering of high-performance photocatalysts for photoreduction of uranium.
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