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非共价BPTCD/g-CN异质结光催化剂的制备及在太阳辐射下对有机染料的光降解

Preparation of Non-Covalent BPTCD/g-CN Heterojunction Photocatalysts and Photodegradation of Organic Dyes Under Solar Irradiation.

作者信息

Wei Xing, Jia Gaopeng, Chen Ru, Zhang Yalong

机构信息

Faculty of Environmental Science and Engineering, Yancheng Institute of Technology, Yancheng 224051, China.

Institute of Textile and Apparel, Yancheng Institute of Technology, Yancheng 224051, China.

出版信息

Nanomaterials (Basel). 2025 Jul 21;15(14):1131. doi: 10.3390/nano15141131.

Abstract

In this study, the BPTCD/g-CN heterojunction photocatalyst was successfully prepared by the hydrothermal method. BPTCD (3,3',4,4'-benzophenone tetracarboxylic dianhydride) is immobilised on the surface of g-CN by non-covalent π-π stacking. The BPTCD/g-CN heterojunction photocatalyst is an all-organic photocatalyst with significantly improved photocatalytic performance compared with g-CN. BPTCD/g-CN-60% was able to effectively degrade MO solution (10 mg/L) to 99.9% and 82.8% in 60 min under full spectrum and visible light. The TOC measurement results indicate that MO can ultimately be decomposed into HO and CO through photocatalytic action. The photodegradation of methyl orange by BPTCD/g-CN composite materials under sunlight is mainly attributed to the successful construction of the heterojunction structure and its excellent π-π stacking effect. Superoxide radicals (O) were found to be the main active species, while OH and h played a secondary role. The synthesised BPTCD/g-CN also showed excellent stability in the activity of photodegradation of MO in wastewater, with the performance remaining above 90% after three cycles. The mechanism of the photocatalytic removal of MO dyes was also investigated by the trap agent experiments. Additionally, BPTCD/g-CN-60% demonstrated exceptional photodegradation performance in the degradation of methylene blue (MB). BPTCD/g-CN heterojunctions have great potential to degrade organic pollutants in wastewater under solar irradiation conditions.

摘要

在本研究中,通过水热法成功制备了BPTCD/g-CN异质结光催化剂。BPTCD(3,3',4,4'-二苯甲酮四羧酸二酐)通过非共价π-π堆积固定在g-CN表面。BPTCD/g-CN异质结光催化剂是一种全有机光催化剂,与g-CN相比,其光催化性能有显著提高。BPTCD/g-CN-60%在全光谱和可见光下60分钟内能够将MO溶液(10mg/L)有效降解至99.9%和82.8%。TOC测量结果表明,MO最终可通过光催化作用分解为HO和CO。BPTCD/g-CN复合材料在阳光下对甲基橙的光降解主要归因于异质结结构的成功构建及其优异的π-π堆积效应。发现超氧自由基(O)是主要活性物种,而OH和h起次要作用。合成的BPTCD/g-CN在废水中MO的光降解活性方面也表现出优异的稳定性,三个循环后性能保持在90%以上。还通过捕获剂实验研究了MO染料的光催化去除机理。此外,BPTCD/g-CN-60%在亚甲基蓝(MB)的降解中表现出优异的光降解性能。BPTCD/g-CN异质结在太阳辐射条件下对废水中有机污染物的降解具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf1a/12298509/5c8f0617fa0c/nanomaterials-15-01131-g001.jpg

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