Novel discrete architecture for quantum dots modified ultrathin hollow nanotube Bi2Sn2O7/Bi4O5I2 S-scheme heterojunction for ultra-efficient photocatalytic degradation of bisphenol A

Huizhong Wu, Jiana Jing, ShaSha Li, Shuaishuai Li, Jingyang Liu, Ruiheng Liang, Yican Zhang, Zehua Xia, Minghua Zhou
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Abstract

Designing and constructing novel discrete architecture for quantum dots modified ultrathin hollow nanotube BiSnO/BiOI S-scheme heterojunctions for the first time in this work is an ideal strategy to improve the photocatalytic activity. As expected, the BiSnO/BiOI heterojunction exhibited outstanding performance of degradation bisphenol A (BPA), the rate constant of BiSnO/BiOI heterojunction was 1.7 and 41.8 times higher than that of BiOI and BiSnO, respectively. The promoted activity could be attributed to the spatial separation of photogenerated carriers as well as redox reaction sites due to the discrete structure, and the enhanced charge separation due to the S-scheme mechanism via Bi-O channels as derived from DFT calculations. Furthermore, BiSnO/BiOI heterojunction exhibited unprecedented ultra-efficient in BPA degradation compared to other published Bi-based catalysts, and excellent performance under actual sunlight contributes to its prospective practical application. This strategy affords a novel approach for fabricating discrete S-scheme heterojunctions photocatalysts with high-efficiency, strong-stable, and sustainable.
用于超高效光催化降解双酚 A 的量子点修饰超薄中空纳米管 Bi2Sn2O7/Bi4O5I2 S 型异质结的新型离散结构
本研究首次设计并构建了新型离散结构的量子点修饰超细空心纳米管 BiSnO/BiOI S 型异质结,是提高光催化活性的理想策略。不出所料,BiSnO/BiOI异质结在降解双酚A(BPA)方面表现突出,BiSnO/BiOI异质结的速率常数分别是BiOI和BiSnO的1.7倍和41.8倍。活性的提高可归因于离散结构导致的光生载流子和氧化还原反应位点的空间分离,以及 DFT 计算得出的通过 Bi-O 通道的 S 型机制导致的电荷分离增强。此外,与其他已发表的铋基催化剂相比,BiSnO/BiOI 异质结在降解双酚 A 方面表现出前所未有的超高效率,而且在实际日照下的优异性能也为其实际应用前景做出了贡献。这种策略为制造高效、强稳定、可持续的离散 S 型异质结光催化剂提供了一种新方法。
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