Boosting charge transfer of BiOBr/AgBr S-scheme heterojunctions via interface Br atom co-sharing for enhanced visible-light photocatalytic activity

异质结 光催化 Boosting(机器学习) 材料科学 电荷(物理) 光化学 Atom(片上系统) 可见光谱 接口(物质) 光电子学 化学 物理 催化作用 计算机科学 有机化学 量子力学 毛细管数 机器学习 毛细管作用 复合材料 嵌入式系统
作者
Junhao Ma,Liang Xu,Zhaoyi Yin,Zhifeng Li,Zhiguo Song,Jianbei Qiu,Yongjin Li
出处
期刊:Green Energy & Environment [KeAi]
卷期号:10 (5): 1073-1084 被引量:17
标识
DOI:10.1016/j.gee.2024.11.003
摘要

Efficient interfacial charge transfer and robust interfacial interactions are crucial for achieving the superior spatial separation of carriers and developing efficient heterojunction photocatalysts. Herein, BiOBr/AgBr S-scheme heterojunctions are synthesized via the co-sharing of Br atoms using an ion-exchange approach, which involves the in-situ growth of AgBr nanoparticles on the surfaces of BiOBr nanosheets. It is revealed that successful construction of a high–quality interface with strong interactions via Br atom bridge between BiOBr and AgBr, which provided a rapid migration channel for charge carriers. In addition, in-situ XPS, Kelvin probe force microscopy, and electron spin resonance evaluations confirmed the establishment of an S-scheme charge-transfer pathway in this tightly contacted heterojunction, which could efficiently prevent the recombination of photogenerated carriers while retaining carriers with a high redox capacity. Finally, the photocatalytic test confirmed that the BiOBr/AgBr heterojunction showed excellent photocatalytic performance and wide applicability thanks to the construction of high quality heterojunction. Overall, this work highlights the importance of rational designing of heterogeneous interfaces at the atomic level in photocatalysis, and contributes to rationally design BiOBr-based S-scheme heterojunctions photocatalytic materials with high quality atomic co-sharing interfaces. The S-scheme BiOBr/AgBr heterojunction with co-sharing Br atoms had been successfully designed, the synergistic effects of the S-scheme heterojunctions and atomic-level interfacial channels result in enhancing the separation and utilization efficiency of photoinduced carriers, and enhancing the photocatalytic. • A novel BiOBr/AgBr S-scheme heterojunction was established via the interface co-sharing of Br using an ion-exchange method. • Co-sharing Br atom heterointerface promote interfacial charge transfer. • S-scheme heterojunctions promote the migration of carriers and retain photogenerated carriers with high redox potentials. • The photocatalytic degradation of organic pollutants by BiOBr/AgBr S-scheme heterojunctions are significantly improved.
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