Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst
Fabrication of effective photocatalyst for the U(VI) reduction is a promising approach to disposing the great challenges posed by rising the rapid development of nuclear energy. Herein, it rationally designed a single-atom Fe anchored g-C3N4 support (Fe-g-C3N4, Fe-N4 moiety), showing the ultrahigh p...
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2024
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2-s2.0-85201502899 Hu Z.; Liu Z.; Tay C.C.; Bao L.; Qiu M. Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst 2024 Journal of Molecular Liquids 411 10.1016/j.molliq.2024.125774 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85201502899&doi=10.1016%2fj.molliq.2024.125774&partnerID=40&md5=206b2d4e92f643a8210083353b21bc6b Fabrication of effective photocatalyst for the U(VI) reduction is a promising approach to disposing the great challenges posed by rising the rapid development of nuclear energy. Herein, it rationally designed a single-atom Fe anchored g-C3N4 support (Fe-g-C3N4, Fe-N4 moiety), showing the ultrahigh photocatalytic performance towards over wide pH range of 3.0–8.0, outer-performing pristine g-C3N4 by 82 times. Combination with X-ray photoelectron spectroscopy and X-ray absorption near-edge structure spectroscopy, the highly photoreduction of U(VI) could be attributed to the highly activity of g-C3N4 and Fe2+. According to quenching experiments and EPR spectra, it is demonstrated that the superoxide (·O2–) radicals played an important role in the photoreduction of U(VI) on Fe-g-C3N4 rather than ·OH and 1O2 species. These findings are crucial for the actual application of single-atom photocatalyst in environmental remediation. © 2024 Elsevier B.V. Elsevier B.V. 1677322 English Article |
author |
Hu Z.; Liu Z.; Tay C.C.; Bao L.; Qiu M. |
spellingShingle |
Hu Z.; Liu Z.; Tay C.C.; Bao L.; Qiu M. Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
author_facet |
Hu Z.; Liu Z.; Tay C.C.; Bao L.; Qiu M. |
author_sort |
Hu Z.; Liu Z.; Tay C.C.; Bao L.; Qiu M. |
title |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
title_short |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
title_full |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
title_fullStr |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
title_full_unstemmed |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
title_sort |
Investigating the photocatalytic reduction of U(VI) over a single-atom Fe complex catalyst |
publishDate |
2024 |
container_title |
Journal of Molecular Liquids |
container_volume |
411 |
container_issue |
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doi_str_mv |
10.1016/j.molliq.2024.125774 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85201502899&doi=10.1016%2fj.molliq.2024.125774&partnerID=40&md5=206b2d4e92f643a8210083353b21bc6b |
description |
Fabrication of effective photocatalyst for the U(VI) reduction is a promising approach to disposing the great challenges posed by rising the rapid development of nuclear energy. Herein, it rationally designed a single-atom Fe anchored g-C3N4 support (Fe-g-C3N4, Fe-N4 moiety), showing the ultrahigh photocatalytic performance towards over wide pH range of 3.0–8.0, outer-performing pristine g-C3N4 by 82 times. Combination with X-ray photoelectron spectroscopy and X-ray absorption near-edge structure spectroscopy, the highly photoreduction of U(VI) could be attributed to the highly activity of g-C3N4 and Fe2+. According to quenching experiments and EPR spectra, it is demonstrated that the superoxide (·O2–) radicals played an important role in the photoreduction of U(VI) on Fe-g-C3N4 rather than ·OH and 1O2 species. These findings are crucial for the actual application of single-atom photocatalyst in environmental remediation. © 2024 Elsevier B.V. |
publisher |
Elsevier B.V. |
issn |
1677322 |
language |
English |
format |
Article |
accesstype |
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record_format |
scopus |
collection |
Scopus |
_version_ |
1812871793214488576 |