Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 11, Pages 6231-6241Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta09954j
Keywords
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Funding
- National Natural Science Foundation of China [92061109, 22033005]
- Natural Science Basic Research Program of Shaanxi [S2020-JC-WT-0001]
- Open Project Program of Fujian Key Laboratory of Functional Marine Sensing Materials [MJUKF-FMSM202002]
- Shenzhen Science and Technology Innovation Committee [RCBS20200714114919174]
- Guangdong Provincial Key Laboratory of Catalysis [2020B121201002]
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Cu-1-ZnO/GPET composite material with Cu atom dopants shows significantly enhanced photocatalytic activity. The Cu atoms capture photogenerated electrons and help separate them from holes, leading to the activation of O2 and the generation of hydroxyl radicals through reaction with water, resulting in efficient degradation of pollutants.
Defects can predominantly dictate the properties of oxide materials, in particular, photocatalytic and electrical properties. By implanting the defects of metallic element, Cu atom doped ZnO (Cu-1-ZnO) supported by graphene-coated polyethylene-terephthalate (GPET) transparent substrate has been successfully synthesized via hydrothermal method. Our Cu-ZnO/GPET presents a high enhancement of photocatalytic activity by ultraviolet (UV) light illumination, with the degradation efficiency of methylene blue (MB) as high as 83.6%, which is superior to pure ZnO/GPET photocatalyst. Cu can be observed in the form of single atoms through HAADF-STEM tomography. First-principles theoretical calculations show that the d-states of Cu atoms in Cu-1-ZnO/GPET become closer to the Fermi level than those of Zn atoms. Upon UV irradiation, doped Cu metal atoms could capture electrons in the conductive band of Cu-1-ZnO/GPET and help to separate photogenerated electrons and holes via monovalent Cu and O atoms. Then, electron-rich Cu atoms could activate O-2 to form superoxide radicals while the generated holes as oxygen-centered radicals could react with water to form highly active hydroxyl radicals, thus effectively degrading the MB solution.
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