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一种双表面无机分子印迹 BiWO-CuO/AgO 杂化结构,对目标污染物的光催化降解具有增强的活性和选择性。

A dual surface inorganic molecularly imprinted BiWO-CuO/AgO heterostructure with enhanced activity-selectivity towards the photocatalytic degradation of target contaminantst.

机构信息

Chemistry Department, Yasouj University, 75918-74831, Yasouj, Iran.

Department of Gas and Petroleum, Yasouj University, 75918-74831, Gachsaran, Iran.

出版信息

Photochem Photobiol Sci. 2020 Jul;19(7):943-955. doi: 10.1039/d0pp00008f. Epub 2020 Oct 27.

Abstract

In this work, a high-surface-area dual inorganic molecularly imprinted (DIMI) BiWO/CuO/AgO photo-catalyst was developed for the selective photocatalytic degradation of methyl green (MG) and auramine O (AO) dyes as target pollutants. The DIMI-BiWO/CuO/AgO heterojunction was synthesized by a sono-chemically assisted sol-gel method by coating a layer of molecularly imprinted AgO/CuO on the surface of BiWO nanocubes with MG and AO as the templates. This was followed by calcination for the removal of target molecules and annealing for Ag/Cu oxide preparation. This novel photocatalyst was prepared to overcome the challenge of the co-existing non-target molecules, which has limited the photocatalytic degradation performance. The surface DIMI sites could act as surface defects for accelerating the separation of photogenerated holes and electrons, which led to the increased generation of OH radicals. Moreover, the DIMI sites had increased binding affinity toward MG and AO via the formation of multiple H bonds and electrostatic bonds, which were confirmed by FTIR spectroscopy, PL and EIS studies. The surface DIMI sites led to the increased adsorption and improved local concentration of MG and AO on BiWO/CuO/AgO. Consequently, the heterojunction properties of the final DIMI product accelerated the transfer and separation of photogenerated carriers. The high binding affinity of the DIMI sites to MG and AO confirmed the selective recognition, which was tested in the presence of coexisting pollutant dyes. The other characterizations confirmed the successful fabrication and high photocatalytic activity of the high-surface-area DIMI-BiWO/CuO/AgO heterostructured composite. In general, the superior interfacial electronic interactions, high migration efficiency of photoinduced charge carriers, and strong visible light absorption of the prepared photocatalyst resulted in good photocatalytic performance.

摘要

在这项工作中,开发了一种高比表面积的双无机分子印迹(DIMI)BiWO/CuO/AgO 光催化剂,用于选择性光催化降解甲基绿(MG)和吖啶橙(AO)作为目标污染物的染料。通过超声辅助溶胶-凝胶法在 BiWO 纳米立方体表面涂覆一层印迹 AgO/CuO 层,以 MG 和 AO 为模板,合成了 DIMI-BiWO/CuO/AgO 异质结。然后进行煅烧以去除目标分子并进行退火以制备 Ag/Cu 氧化物。制备这种新型光催化剂是为了克服共存的非目标分子的挑战,这限制了光催化降解性能。表面 DIMI 位点可以作为表面缺陷,加速光生空穴和电子的分离,从而增加 OH 自由基的生成。此外,通过形成多个氢键和静电键,DIMI 位点对 MG 和 AO 具有增加的结合亲和力,这通过 FTIR 光谱、PL 和 EIS 研究得到证实。表面 DIMI 位点导致 MG 和 AO 在 BiWO/CuO/AgO 上的吸附增加和局部浓度提高。因此,最终 DIMI 产物的异质结特性加速了光生载流子的转移和分离。DIMI 位点对 MG 和 AO 的高结合亲和力证实了选择性识别,这在共存污染物染料的存在下进行了测试。其他特征证实了高表面积 DIMI-BiWO/CuO/AgO 杂化结构复合材料的成功制备和高光催化活性。总的来说,制备的光催化剂具有优越的界面电子相互作用、光生载流子的高效迁移效率和强可见光吸收,因此具有良好的光催化性能。

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