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Zhu, Baikang Dong, Qinbing Huang, Jianghua Song, Debin Chen, Lihui Chen, Qingguo Zhai, Chunyang Wang, Bohong Klemes, Jiri Jaromir Tao, Hengcong
Originální název
Visible-light driven p-n heterojunction formed between a-Bi2O3 and Bi2O2CO3 for efficient photocatalytic degradation of tetracycline
Typ
článek v časopise ve Web of Science, Jimp
Jazyk
angličtina
Originální abstrakt
To improve the efficiency of photocatalytic oxidative degradation of antibiotic pollutants, it is essential to develop an efficient and stable photocatalyst. In this study, a polymer-assisted facile synthesis strategy is proposed for the polymorph-controlled alpha-Bi2O3/Bi2O2CO3 heterojunction retained at elevated calcination temperatures. The p-n heterojunction can effectively separate and migrate electron-hole pairs, which improves visible-light-driven photocatalytic degradation from tetracycline (TC). The BO-400@PAN-140 photocatalyst achieves the highest pollutant removal efficiency of 98.21% for photocatalytic tetracycline degradation in 1 h (lambda > 420 nm), and the degradation efficiency was maintained above 95% after 5 cycles. The morphology, crystal structure, and chemical state of the composites were analysed by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. Ultraviolet-visible diffuse reflection, transient photocurrent response, and electrochemical impedance spectroscopy were adopted to identify the charge transfer and separation efficiency of photogenerated electron-hole pairs. The EPR results verified h(+) and OH radicals as the primary active species in the photocatalytic oxidation reactions. This observation was also consistent with the results of radical trapping experiments. In addition, the key intermediate products of the photocatalytic degradation of TC over BO-400@PAN-140 were identified via high-performance liquid chromatography-mass spectrometry, which is compatible with two possible photocatalytic reaction pathways. This work provides instructive guidelines for designing heterojunction photocatalysts via a polymer-assisted semiconductor crystallographic transition pathway for TC degradation into cleaner production.
Klíčová slova
Charge transfer; Crystal structure; Efficiency; Electrochemical impedance spectroscopy; Free radicals; Heterojunctions; High performance liquid chromatography; Mass spectrometry; Photocatalytic activity; Photodegradation; Reaction intermediates; Scanning electron microscopy; X ray photoelectron spectroscopy; Calcination temperature; Electron hole pairs; Facile synthesis; Oxidative degradation; P-n heterojunctions; Photo-catalytic; Photocatalytic degradation; Polymer-assisted; Synthesis strategy; Visible-light-driven; Bismuth compounds
Autoři
Zhu, Baikang; Dong, Qinbing; Huang, Jianghua; Song, Debin; Chen, Lihui; Chen, Qingguo; Zhai, Chunyang; Wang, Bohong; Klemes, Jiri Jaromir; Tao, Hengcong
Vydáno
6. 1. 2023
Nakladatel
ROYAL SOC CHEMISTRYTHOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND
Místo
ISSN
2046-2069
Periodikum
RSC Advances
Ročník
13
Číslo
3
Stát
Spojené království Velké Británie a Severního Irska
Strany od
1594
Strany do
1605
Strany počet
12
URL
https://pubs.rsc.org/en/content/articlelanding/2023/ra/d2ra08162h
BibTex
@article{BUT187264, author="Zhu, Baikang and Dong, Qinbing and Huang, Jianghua and Song, Debin and Chen, Lihui and Chen, Qingguo and Zhai, Chunyang and Wang, Bohong and Klemes, Jiri Jaromir and Tao, Hengcong", title="Visible-light driven p-n heterojunction formed between a-Bi2O3 and Bi2O2CO3 for efficient photocatalytic degradation of tetracycline", journal="RSC Advances", year="2023", volume="13", number="3", pages="1594--1605", doi="10.1039/d2ra08162h", issn="2046-2069", url="https://pubs.rsc.org/en/content/articlelanding/2023/ra/d2ra08162h" }