Novel S-scheme 2D/2D BiOBr/g-C3N4 heterojunctions with enhanced photocatalytic activity

异质结 光催化 材料科学 复合数 催化作用 载流子 化学工程 辐照 方案(数学) 光电子学 纳米技术 化学 复合材料 物理 数学分析 生物化学 数学 核物理学 工程类
作者
Bin Zhang,Xiao Hu,Enzhou Liu,Jun Fan
出处
期刊:Chinese Journal of Catalysis [Elsevier BV]
卷期号:42 (9): 1519-1529 被引量:259
标识
DOI:10.1016/s1872-2067(20)63765-2
摘要

The design and construction of heterojunction photocatalysts, which possess a staggered energy band structure and appropriate interfacial contact, is an effective way to achieve outstanding photocatalytic performance. In this study, 2D/2D BiOBr/g-C3N4 heterojunctions were successfully obtained by a convenient in situ self-assembly route. Under simulated sunlight irradiation, 99% of RhB (10 mg·L−1, 100 mL) was efficiently degraded by 1.5-BiOBr/g-C3N4 within 30 min, which is better than the performance of both BiOBr and g-C3N4, and it has superior stability. In addition, the composite also exhibits enhanced photocatalytic activity for H2 production. The enhanced activity can be attributed to the intimate interface contact, the larger surface area, and the highly efficient separation of photoinduced electron–hole pairs. Based on the experimental results, a novel S-scheme model was proposed to illuminate the transfer process of charge carriers. This study presents a simple way to develop novel step-scheme photocatalysts for environmental and related applications.
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