异质结
Boosting(机器学习)
光催化
材料科学
降级(电信)
化学工程
纳米技术
光电子学
化学
电子工程
催化作用
计算机科学
工程类
生物化学
机器学习
作者
Yurong Yang,Zhengxin Sun,Chang Liu,Jiahui Wang,Min Qiu,Guomin Yan,Kun Zhang
标识
DOI:10.1021/acsaem.2c03136
摘要
It is charming to develop direct Z-scheme heterostructure catalysts for efficiently boosting photocatalytic overall water splitting, but it is challenging for the interface to realize tight connection at the atomic level. Herein, a BiOBr/ZnIn2S4 direct Z-scheme heterostructure with a Bi–S bonded interface is designed and constructed by in situ growing ZnIn2S4 nanosheets on BiOBr nanosheets. The BiOBr subtrates extremely inhibit the aggregation of ZnIn2S4 nanosheets and enhance their stability. The designed BiOBr/ZnIn2S4 direct Z-scheme heterojunctions thermodynamically favor photocatalytic overall water splitting for simultaneous H2 and O2 production owing to their suitable band edge levels. Direct Z-scheme heterostructure and atomic-level interface connection synergistically promote the photogenerated carrier separation and transfer. As a result, the optimized BiOBr/ZnIn2S4 hybrid structure exhibits extraordinary photocalytic activity and superior cycling stability in the absence of any sacrificial agents. It achieves photocatalytic H2 and O2 production rates up to 628 and 304 μmol g–1 h–1 under sunlight irradiation, with 11.6-fold and 12.9-fold improvement compared to pristine ZnIn2S4 and BiOBr, respectively. Furthermore, the excellent photocalytic activity can remain unchanged for 24 h. This interfacial modulation will guide further developments to fabricating direct Z-scheme heterostructure.
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