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通过面耦合和 s 型结构,用 Bi-MOF 原位构建 Ag/BiO/BiOI 异质结以提高双酚 A 的光催化效率。

In situ construction of Ag/BiO/BiOI heterojunction with Bi-MOF for enhance the photocatalytic efficiency of bisphenol A by facet-coupling and s-scheme structure.

机构信息

College of Biological and Chemical Engineering, Changsha University, Changsha, 410022, China; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, China.

College of Biological and Chemical Engineering, Changsha University, Changsha, 410022, China.

出版信息

J Environ Manage. 2024 Jun;362:121342. doi: 10.1016/j.jenvman.2024.121342. Epub 2024 Jun 3.

Abstract

In this study, Ag/BiO/BiOI with s-scheme heterostructures were successfully synthesized in situ by nano-silver modification of CUA-17 and halogenated hydrolysis.The growth rate of BiO crystals was effectively controlled by adjusting the doping amount of Ag, resulting in the formation of a facet-coupling heterojunctions. Through the investigation of the microstructure and compositional of catalysts, it has been confirmed that an intimate facet coupling between the BiO (120) facet and the BiOI (312) facet, which provides robust support for charge transfer. Under visible light irradiation, the AgBOI.3 heterojunction photocatalyst exhibited an outstanding degradation rate of 98.2% for Bisphenol A (BPA) with excellent stability. Further characterization using optical, electrochemical, impedance spectroscopy, and electron spin resonance techniques revealed significantly enhanced efficiency in photogenerated charge separation and transfer, and confirming the s-scheme structure of the photocatalyst. Density functional theory calculations was employed to elucidate the mechanism of BPA degradation and the degradation pathway of BPA was investigated by LC-MS. Finally, the toxicity of the degradation intermediates was evaluated using T.E.S.T software.

摘要

在这项研究中,通过 CUA-17 的纳米银修饰和卤化水解,成功原位合成了具有 s 型异质结构的 Ag/BiO/BiOI。通过调节 Ag 的掺杂量,有效地控制了 BiO 晶体的生长速率,从而形成了面-面耦合异质结。通过对催化剂的微观结构和组成的研究,证实了 BiO(120)面和 BiOI(312)面之间的紧密面-面耦合,为电荷转移提供了有力的支持。在可见光照射下,AgBOI.3 异质结光催化剂对双酚 A(BPA)表现出 98.2%的优异降解率和出色的稳定性。进一步的光学、电化学、阻抗谱和电子顺磁共振技术的表征表明,光生载流子的分离和转移效率显著提高,并证实了光催化剂的 s 型结构。通过密度泛函理论计算,阐明了 BPA 降解的机制,并通过 LC-MS 研究了 BPA 的降解途径。最后,使用 T.E.S.T 软件评估了降解中间体的毒性。

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