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基于废弃生物质衍生的碳量子点耦合BiWO在可见光下对土霉素抗生素的增强降解

Enhanced Degradation of Oxytetracycline Antibiotic Under Visible Light over BiWO Coupled with Carbon Quantum Dots Derived from Waste Biomass.

作者信息

Ren Haitao, Qi Fan, Zhao Ke, Lv Du, Ma Hao, Ma Cheng, Padervand Mohsen

机构信息

Technological Institute of Materials & Energy Science (TIMES), Xijing University, Xi'an 710123, China.

School of Environmental Science and Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China.

出版信息

Molecules. 2024 Dec 4;29(23):5725. doi: 10.3390/molecules29235725.

DOI:10.3390/molecules29235725
PMID:39683884
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11643479/
Abstract

Improving the photogenerated carrier separation efficiency of individual semiconductor materials has always been a key challenge in photocatalysis. In this study, we synthesized a novel photocatalytic material, N-CQDs/UBWO, in situ by combining nitrogen-doped carbon quantum dots (N-CQDs) derived from discarded corn stover with ultrathin BiWO nanosheets (UBWO). Detailed characterization indicates that the random distribution of N-CQDs on the UBWO surface increases the specific surface area of UBWO, which is beneficial for the adsorption and degradation of oxytetracycline (OTC). More importantly, N-CQDs act as electron acceptors, promoting the effective separation of photogenerated charges, prolonging the lifetime of charge carriers in UBWO, and thereby enhancing the degradation efficiency of OTC. As a result, the optimized 3wt%N-CQDs/UBWO could degrade 85% of OTC within 40 min under visible light, with a removal rate four times that of pure BiWO. The performance of photocatalytic degradation over OTC by 3wt%N-CQDs/UBWO exceeds that of most reported BiWO-based photocatalysts. The EPR analysis confirmed that ∙O and ∙OH are the main active species in the photocatalytic degradation of OTC on 3wt%N-CQDs/UBWO. This study provides insight into designing green, low-cost, and efficient photocatalysts using CQDs derived from waste biomass and the degradation of emerging pollutants like antibiotics.

摘要

提高单个半导体材料的光生载流子分离效率一直是光催化领域的关键挑战。在本研究中,我们通过将废弃玉米秸秆衍生的氮掺杂碳量子点(N-CQDs)与超薄BiWO纳米片(UBWO)原位合成了一种新型光催化材料N-CQDs/UBWO。详细表征表明,N-CQDs在UBWO表面的随机分布增加了UBWO的比表面积,有利于土霉素(OTC)的吸附和降解。更重要的是,N-CQDs作为电子受体,促进了光生电荷的有效分离,延长了UBWO中载流子的寿命,从而提高了OTC的降解效率。结果,优化后的3wt%N-CQDs/UBWO在可见光下40分钟内可降解85%的OTC,去除率是纯BiWO的四倍。3wt%N-CQDs/UBWO对OTC的光催化降解性能超过了大多数报道的BiWO基光催化剂。电子顺磁共振(EPR)分析证实,∙O和∙OH是3wt%N-CQDs/UBWO上OTC光催化降解的主要活性物种。本研究为利用废弃生物质衍生的CQDs设计绿色、低成本、高效的光催化剂以及降解抗生素等新兴污染物提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/2ba4b43e6a17/molecules-29-05725-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/576bae7ca706/molecules-29-05725-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/8a86509ade2b/molecules-29-05725-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/ce6a0fb4d980/molecules-29-05725-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/c7ca8510e36a/molecules-29-05725-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/91685cafb51a/molecules-29-05725-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/954c7b19a6bd/molecules-29-05725-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/f705f3c60b13/molecules-29-05725-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/2ba4b43e6a17/molecules-29-05725-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/576bae7ca706/molecules-29-05725-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/8a86509ade2b/molecules-29-05725-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/ce6a0fb4d980/molecules-29-05725-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/c7ca8510e36a/molecules-29-05725-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/91685cafb51a/molecules-29-05725-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/954c7b19a6bd/molecules-29-05725-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/f705f3c60b13/molecules-29-05725-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80a/11643479/2ba4b43e6a17/molecules-29-05725-sch001.jpg

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