Exfoliated Boron Nitride (e-BN) Tailored Exfoliated Graphitic Carbon Nitride (e-CN): An Improved Visible Light Mediated Photocatalytic Approach towards TCH Degradation and H2 Evolution

化学 石墨氮化碳 氮化硼 光催化 降级(电信) 纳米复合材料 光致发光 可见光谱 氮化碳 异质结 光电流 光化学 化学工程 纳米技术 光电子学 有机化学 催化作用 材料科学 工程类 电信 计算机科学
作者
Lopamudra Acharya,Sambhu Prasad Pattnaik,Arjun Behera,Rashmi Acharya,Kulamani Parida
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:60 (7): 5021-5033 被引量:70
标识
DOI:10.1021/acs.inorgchem.1c00062
摘要

A series of 2D/2D exfoliated boron nitride/exfoliated g-C3N4 nanocomposites denoted as e-BN/e-CN have been successfully prepared using a simple in situ technique. The successful deposition of e-BN on e-CN was confirmed from high-resolution transmission electron microscopy analysis. According to electrochemical measurements, 1.5 wt % e-BN/e-CN nanocomposites showed 1.5 times more photocurrent than e-CN, which indicates the successful formation of an e-BN/e-CN heterostructure. The photocatalytic activities of the e-CN and e-BN/e-CN composites were investigated through photocatalytic tetracycline hydrochloride (TCH) degradation and H2 evolution under visible light illumination. The 1.5 wt % e-BN/e-CN composite demonstrated the highest photocatalytic activities, which are about 21 and 1.5 fold greater than e-CN towards H2 generation with an apparent conversion efficiency of 2.34% and TCH degradation, respectively. The improved photocatalytic activities of e-BN/e-CN photocatalysts were ascribed to the augmented light-harvesting ability and enhanced separation efficiency of charge carriers. Lower photoluminescence intensity and a smaller arc value in the impedance spectra again proved the reduced recombination of the e–-h+ pairs in the e-BN/e-CN nanocomposites. Trapping experiments show that •O2–, h+, and •OH radicals are the predominant reactive species that accelerated the photocatalytic activities of e-BN/e-CN composites. This study opens up a new window towards the fabrication of such 2D/2D nanocomposites in the field of photocatalysis.
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