摘要
In this paper, carbon supported Bi 2 O 3 -BiOCl-Bi heterostructures were successfully synthesized via a facile and simple hydrothermal method. A series of structure and morphology testing clearly showed that carbon and metallic Bi were deposited on the surface margin of Bi 2 O 3 -BiOCl, which benefited the rapid transfer of internal photogenerated electrons. Photophysical experiments including electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) indicated that the amount of surface oxygen vacancies (OVs) was significantly increased, which act as reactive active sites and therefore effectively enhance the photocatalytic performance. The photocatalytic N 2 reduction yield of C@Bi 2 O 3 -BiOCl-Bi was remarkably improved to 400 μg·L −1 , which was 3.63 times higher than that of BiOCl. This research demonstrated a feasible strategy to construct advanced photocatalyst by incorporating defect-rich structures and surface engineering.
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