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Preparation of Novel C/N-Doped LaFeO(3) Type Perovskite for Efficient Photocatalytic Degradation of Sodium Humate
[Image: see text] LaFeO(3) chalcocite precursor was prepared by solid-phase milling method, and LaFeO(3)-type chalcocite composite catalyst, referred to as LFCN catalyst, was synthesized by in situ doping of carbon and nitrogen (urea, melamine, dicyandiamide, and carbon powder), The catalytic perfor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10633878/ https://www.ncbi.nlm.nih.gov/pubmed/37970008 http://dx.doi.org/10.1021/acsomega.3c06161 |
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author | Hao, Pengcheng Suo, Yanli Shi, Rui Zhang, Juan Li, Bo Yan, Zhen Wang, Jing Liu, Bo Wang, Zhongzhi Qiao, Xin |
author_facet | Hao, Pengcheng Suo, Yanli Shi, Rui Zhang, Juan Li, Bo Yan, Zhen Wang, Jing Liu, Bo Wang, Zhongzhi Qiao, Xin |
author_sort | Hao, Pengcheng |
collection | PubMed |
description | [Image: see text] LaFeO(3) chalcocite precursor was prepared by solid-phase milling method, and LaFeO(3)-type chalcocite composite catalyst, referred to as LFCN catalyst, was synthesized by in situ doping of carbon and nitrogen (urea, melamine, dicyandiamide, and carbon powder), The catalytic performance of the catalysts was investigated by the different mass ratios of LaFeO(3) chalcocite precursor and carbon and nitrogen (1:1, 1:2, and 2:1) and the degradation mechanism. Various characterization analyses, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET), showed that the doped composite LFCN catalysts exhibited a hemispherical network structure with a larger specific surface area than that of the pure phase LaFeO(3) material. In addition, the LaFeO(3) material adjusted the electronic structure of the original LaFeO(3) chalcogenide material to a certain extent after in situ doping with organic C and N elements, which enhanced its lattice oxygen oxidation ability. In the study of the catalytic degradation of sodium humate solution under natural light conditions, the catalytic performance was significantly improved compared to that of the pure phase LaFeO(3), and 10 mg of the catalyst degraded 30 mg/L of sodium humate solution in 50 min, with a degradation rate increasing from 40 to 98%. The degradation rate increased from 40 to 98% after 4 applications, indicating that the LFCN catalyst has good stability and significant catalytic degradation performance. |
format | Online Article Text |
id | pubmed-10633878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106338782023-11-15 Preparation of Novel C/N-Doped LaFeO(3) Type Perovskite for Efficient Photocatalytic Degradation of Sodium Humate Hao, Pengcheng Suo, Yanli Shi, Rui Zhang, Juan Li, Bo Yan, Zhen Wang, Jing Liu, Bo Wang, Zhongzhi Qiao, Xin ACS Omega [Image: see text] LaFeO(3) chalcocite precursor was prepared by solid-phase milling method, and LaFeO(3)-type chalcocite composite catalyst, referred to as LFCN catalyst, was synthesized by in situ doping of carbon and nitrogen (urea, melamine, dicyandiamide, and carbon powder), The catalytic performance of the catalysts was investigated by the different mass ratios of LaFeO(3) chalcocite precursor and carbon and nitrogen (1:1, 1:2, and 2:1) and the degradation mechanism. Various characterization analyses, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET), showed that the doped composite LFCN catalysts exhibited a hemispherical network structure with a larger specific surface area than that of the pure phase LaFeO(3) material. In addition, the LaFeO(3) material adjusted the electronic structure of the original LaFeO(3) chalcogenide material to a certain extent after in situ doping with organic C and N elements, which enhanced its lattice oxygen oxidation ability. In the study of the catalytic degradation of sodium humate solution under natural light conditions, the catalytic performance was significantly improved compared to that of the pure phase LaFeO(3), and 10 mg of the catalyst degraded 30 mg/L of sodium humate solution in 50 min, with a degradation rate increasing from 40 to 98%. The degradation rate increased from 40 to 98% after 4 applications, indicating that the LFCN catalyst has good stability and significant catalytic degradation performance. American Chemical Society 2023-10-26 /pmc/articles/PMC10633878/ /pubmed/37970008 http://dx.doi.org/10.1021/acsomega.3c06161 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Hao, Pengcheng Suo, Yanli Shi, Rui Zhang, Juan Li, Bo Yan, Zhen Wang, Jing Liu, Bo Wang, Zhongzhi Qiao, Xin Preparation of Novel C/N-Doped LaFeO(3) Type Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title | Preparation of
Novel C/N-Doped LaFeO(3) Type
Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title_full | Preparation of
Novel C/N-Doped LaFeO(3) Type
Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title_fullStr | Preparation of
Novel C/N-Doped LaFeO(3) Type
Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title_full_unstemmed | Preparation of
Novel C/N-Doped LaFeO(3) Type
Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title_short | Preparation of
Novel C/N-Doped LaFeO(3) Type
Perovskite for Efficient Photocatalytic Degradation of Sodium Humate |
title_sort | preparation of
novel c/n-doped lafeo(3) type
perovskite for efficient photocatalytic degradation of sodium humate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10633878/ https://www.ncbi.nlm.nih.gov/pubmed/37970008 http://dx.doi.org/10.1021/acsomega.3c06161 |
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