Huan‐Huan Liu,Hongliang Guo,Daming Huang,L. P. Zhou,Jia Lei,Yan Liu,Wenkun Zhu
出处
期刊:ACS materials letters [American Chemical Society] 日期:2024-12-19卷期号:7 (1): 295-303
标识
DOI:10.1021/acsmaterialslett.4c02121
摘要
Photoassisted capture of uranium provides a promising strategy for the sustainable utilization of nuclear energy. Herein, we constructed Cu2O/CuO heterojunctions in situ by a wet-etching method, showing ultrafast reaction kinetics and photocatalytic activity for U(VI) reduction. In 8 ppm of uranium-containing wastewater, the Cu2O/CuO heterojunctions exhibited a remarkable uranium extraction efficiency of 94.6% within 10 min under irradiation, which exceeded most recently reported photocatalysts. The photocatalytic reaction rate constant of Cu2O/CuO heterojunctions was 5.8-time larger than that of pure Cu2O. A mechanism study indicated that the photogenerated electrons reduced CuO species in Cu2O/CuO heterojunctions and in situ created the oxygen vacancy during the photocatalysis process, which strengthened the binding of UO22+. The rapid electron transfer rate over the in situ heterojunction interfaces and the enhanced UO22+ binding strength by the in situ formed oxygen vacancy accounted for the ultrafast reaction kinetics.