Ligand-Assistant Iced Photocatalytic Reduction to Synthesize Atomically Dispersed Cu Implanted Metal-Organic Frameworks for Photo-Enhanced Uranium Extraction from Seawater

被引:25
|
作者
Liu, Tao [1 ]
Gu, Anping [1 ]
Wei, Tao [1 ]
Chen, Mengwei [1 ]
Guo, Xi [1 ]
Tang, Shuai [1 ]
Yuan, Yihui [1 ]
Wang, Ning [1 ]
机构
[1] Hainan Univ, State Key Lab Marine Resource Utilizat South China, Haikou 570228, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 海南省自然科学基金;
关键词
Iced photocatalytic reduction reaction; metal-organic frameworks; photocatalytic activity; single-atoms; uranium extraction from seawater; SINGLE ATOMS; G-C3N4;
D O I
10.1002/smll.202208002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Uranium extraction from natural seawater is one of the most promising routes to address the shortage of uranium resources. By combination of ligand complexation and photocatalytic reduction, porous framework-based photocatalysts have been widely applied to uranium enrichment. However, their practical applicability is limited by poor photocatalytic activity and low adsorption capacity. Herein, atomically dispersed Cu implanted UiO-66-NH2 (Cu SA@UiO-66-NH2) photocatalysts are prepared via ligand-assistant iced photocatalytic reduction route. N-Cu-N moiety acts as an effective electron acceptor to potentially facilitate charge transfer kinetics. By contrast, there exist Cu sub-nanometer clusters by the typical liquid phase photoreduction, resulting in a relatively low photocatalytic activity. Cu SA@UiO-66-NH2 adsorbents exhibit superior antibacterial ability and improved photoreduction conversion of the adsorbed U(VI) to insoluble U(IV), leading to a high uranium sorption capacity of 9.16 mg-U/g-Ads from natural seawater. This study provides new insight for enhancing uranium uptake by designing SA-mediated MOF photocatalysts.
引用
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页数:9
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