Defect-tailoring mediated electron–hole separation in single-unit-cell Bi₃O₄Br nanosheets for boosting photocatalytic hydrogen evolution and nitrogen fixation

• Main Authors: Di, Jun, Xia, Jiexiang, Chisholm, Matthew F., Zhong, Jun, Chen, Chao, Cao, Xingzhong, Dong, Fan, Chi, Zhen, Chen, Hailong, Weng, Yu-Xiang, Xiong, Jun, Yang, Shi-Ze, Li, Huaming, Liu, Zheng, Dai, Sheng
• 其他作者: School of Materials Science and Engineering
• 格式: Article
• 語言: English
• 出版: 2021
• 主題: Engineering::Materials; Charge Separation; Defect Engineering
• 在線閱讀: https://hdl.handle.net/10356/151602

Solar photocatalysis is a potential solution to satisfying energy demand and its resulting environmental impact. However, the low electron-hole separation efficiency in semiconductors has slowed the development of this technology. The effect of defects on electron-hole separation is not always clear. A model atomically thin structure of single-unit-cell Bi3 O4 Br nanosheets with surface defects is proposed to boost photocatalytic efficiency by simultaneously promoting bulk- and surface-charge separation. Defect-rich single-unit-cell Bi3 O4 Br displays 4.9 and 30.9 times enhanced photocatalytic hydrogen evolution and nitrogen fixation activity, respectively, than bulk Bi3 O4 Br. After the preparation of single-unit-cell structure, the bismuth defects are controlled to tune the oxygen defects. Benefiting from the unique single-unit-cell architecture and defects, the local atomic arrangement and electronic structure are tuned so as to greatly increase the charge separation efficiency and subsequently boost photocatalytic activity. This strategy provides an accessible pathway for next-generation photocatalysts.