B-derived charge carrier transfer in SnO2/g-C3N4 heterostructures towards enhanced photocatalytic H2O2 production and tetracycline removal

IF 5.8 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Journal of Alloys and Compounds Pub Date : 2024-11-19 DOI:10.1016/j.jallcom.2024.177659
Peihao Song, Ping Yang, Xiao Zhang
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Abstract

To improve photocatalytic hydrogen peroxide (H2O2) generation and antibiotic degradation, SnO2 nanocrystals were embedded in boron-doped graphitic carbon nitride (g-C3N4) nanosheets. Superior thin B-g-C3N4 nanosheets were created via two-step thermal polymerization at 550 and 700 °C in Ar atmosphere. SnO2 nanocrystals less than 5 nm were homogeneously embedded in nanosheets by mechano-chemical pre-reaction and heat-treatment at 400 °C in air condition to form SnO2/B-g-C3N4 composites. The mechano-chemical pre-treatment and B doping were crucial for the homogeneous distribution of SnO2 nanocrystals. The formation of heterostructure, well-developed interfaces, introduced B components, and decent conductivity of SnO2 components resulted in efficient charge separation/transfer during photocatalysis. B-doping played key role in enhancing photoinduced charge separation/transfer to enhance H2O2 generation and tetracycline degradation. After embedding SnO2 nanocrystals in B-g-C3N4, the photocatalytic activity was drastically enhanced. A SnO2/B-g-C3N4 sample prepared using optimized conditions revealed a H2O2 production rate of 9287.0 μM g-1 h-1 which was 3.8 times of that of g-C3N4 (2449.8 μM g-1 h-1). The photocatalytic tetracycline degradation rate constant of the SnO2/B-g-C3N4 composites was 0.018 min-1 using first-order kinetic fitting, which was 6 times of that of g-C3N4 (0.003 min-1). These results provide novel insight for the application of photocatalytic technology in environmental field.
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在 SnO2/g-C3N4 异质结构中实现 B 源电荷载流子转移,从而增强光催化 H2O2 生成和四环素去除能力
为了改善光催化过氧化氢(H2O2)生成和抗生素降解,SnO2 纳米晶体被嵌入到掺硼氮化石墨碳(g-C3N4)纳米片中。超薄的 B-g-C3N4 纳米片是在 550 ℃ 和 700 ℃ 的氩气环境中通过两步热聚合反应生成的。通过机械化学预反应将小于 5 nm 的 SnO2 纳米晶体均匀地嵌入纳米片中,并在 400 °C 空气条件下进行热处理,形成 SnO2/B-g-C3N4 复合材料。机械化学预处理和掺杂 B 对 SnO2 纳米晶体的均匀分布至关重要。异质结构的形成、发达的界面、B 组份的引入以及二氧化锡组份的良好导电性,使得光催化过程中电荷分离/转移变得高效。B 掺杂在增强光诱导的电荷分离/转移以促进 H2O2 生成和四环素降解方面发挥了关键作用。在 B-g-C3N4 中嵌入 SnO2 纳米晶体后,光催化活性显著增强。在优化条件下制备的 SnO2/B-g-C3N4 样品的 H2O2 生成率为 9287.0 μM g-1 h-1,是 g-C3N4 (2449.8 μM g-1 h-1)的 3.8 倍。采用一阶动力学拟合,SnO2/B-g-C3N4 复合材料的光催化四环素降解速率常数为 0.018 min-1,是 g-C3N4 (0.003 min-1)的 6 倍。这些结果为光催化技术在环境领域的应用提供了新的见解。
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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