Enhancing the photoelectric performance of TiO2-based heterojunction using the hydrothermal decomposition of MIL-125 strategy for sensitive detection of Bisphenol A

热液循环 光电效应 异质结 吸收(声学) 检出限 材料科学 三元运算 带隙 可见光谱 纳米技术 化学工程 光电子学 计算机科学 化学 复合材料 工程类 色谱法 程序设计语言
作者
Shaohui Yu,Haizhong Lin,Xiaoshan Liu,Jian‐Ji Zhong,Liangsheng Hu,Fushen Lu,Zhong Hu,Wenhua Gao
出处
期刊:Sensors and Actuators B-chemical [Elsevier BV]
卷期号:413: 135881-135881 被引量:5
标识
DOI:10.1016/j.snb.2024.135881
摘要

Due to its outstanding conductive properties, TiO2-based heterojunctions have extensive applications in the field of photoelectrochemical sensors. However, due to surface energy and van der Waals forces, TiO2 tends to aggregate and presents an uneven distribution, which reduces the overall performance of these heterostructures. To overcome these challenges and achieve a uniform distribution of TiO2 within the heterojunction, the characteristic of gradual decomposition of the metal-organic framework MIL-125 under hydrothermal conditions was employed. This process gradually generates TiO2 particles that slowly participate in the construction of the heterojunction. By combining the exceptional light absorption properties and appropriate bandgap widths of CdS and CdIn2S4, a uniformly distributed flower-globular ternary heterojunction CdS/CdIn2S4/TiO2-FG was successfully synthesized. In comparison to the disordered heterojunction CdS/CdIn2S4/TiO2-DO, CdS/CdIn2S4/TiO2-FG exhibits enhanced visible light absorption properties and photoelectric conversion efficiency. Taking Bisphenol A (BPA) as a model, a signal-off photoelectrochemical (PEC) aptasensor based on the CdS/CdIn2S4/TiO2-FG was established and exhibited a high sensitive detection for BPA with a linear response range from 10-1 to 107 pM, as well as an ultralow detection limit of 0.015 pM, revealing vivid selectivity, stability, and reproducibility. Therefore, this study offers an efficient and straightforward approach for the preparation of TiO2-based heterojunctions with superior photoelectric activity.
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