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离子液体辅助制备金属有机框架衍生的氧化铟/氧化铋碘 p-n 结光催化剂用于高效光催化酚类污染物。

Ionic liquid-assisted fabrication of metal-organic framework-derived indium oxide/bismuth oxyiodide p-n junction photocatalysts for robust photocatalysis against phenolic pollutants.

机构信息

School of Water Conservancy and Environment, University of Jinan, Jinan 250022, PR China.

School of Water Conservancy and Environment, University of Jinan, Jinan 250022, PR China.

出版信息

J Colloid Interface Sci. 2022 Jan 15;606(Pt 2):1261-1273. doi: 10.1016/j.jcis.2021.08.132. Epub 2021 Aug 25.

DOI:10.1016/j.jcis.2021.08.132
PMID:34492464
Abstract

Constructing a p-n heterojunction is a feasible strategy to manipulate the dynamic behaviors of photogenerated carriers through an internal electric field. Herein, a novel highly efficient indium oxide/bismuth oxyiodide (InO/BiOI) p-n junction photocatalyst was fabricated using a facile ionic liquid-assisted precipitation method for the first time. The morphologies were modified by adding different amounts of acetic acid solution. Their hierarchical architecture was beneficial for adsorbing contaminants in wastewater, while the in-situ formed p-n heterojunction between BiOI and InO facilitated interfacial charge transfer and improved the quantum efficiency. Their visible light-responsive photocatalytic activities were systematically investigated by photocatalytic o-phenylphenol (OPP) and 4-tert-butylphenol (PTBP) oxidation. The degradation rate of OPP over InO/BiOI-2 was up to 5.67 times higher than that for BiOI. The excellent activity of InO/BiOI should be attributed to the rapid interfacial charge transfer, depressed carrier recombination, and proper band potentials. Trapping experiments and electron paramagnetic resonance characterizations confirmed the generation of hydroxyl radicals (•OH) and superoxide radicals (•O), which have played a key role in decomposing pollutants. The intermediate products generated during the photocatalytic degradation of OPP were detected and identified by liquid chromatography-mass spectrometry. Meanwhile, their possible molecular structures and degradation pathways have also been inferred.

摘要

构建 p-n 异质结是通过内电场来操纵光生载流子动态行为的一种可行策略。在此,首次使用简便的离子液体辅助沉淀法制备了一种新型高效的氧化铟/碘氧化铋(InO/BiOI)p-n 结光催化剂。通过添加不同量的乙酸溶液来改变形貌。其分级结构有利于吸附废水中的污染物,而 InO 和 BiOI 之间原位形成的 p-n 异质结则有利于界面电荷转移,提高量子效率。通过光催化邻苯基苯酚(OPP)和 4-叔丁基苯酚(PTBP)氧化对它们的可见光响应光催化活性进行了系统研究。InO/BiOI-2 对 OPP 的降解速率比 BiOI 高 5.67 倍。InO/BiOI 的优异活性应归因于快速的界面电荷转移、抑制的载流子复合和合适的能带势。捕获实验和电子顺磁共振特性证实了羟基自由基(•OH)和超氧自由基(•O)的生成,它们在分解污染物方面发挥了关键作用。通过液相色谱-质谱检测并鉴定了 OPP 光催化降解过程中生成的中间产物。同时,还推断了它们可能的分子结构和降解途径。

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