Cargando…

Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites

Direct electrocatalytic oxidation of benzene has been regarded as a promising approach for achieving high‐value phenol product, but remaining a huge challenge. Here an oxygen‐coordinated nickel single‐atom catalyst (Ni–O–C) is reported with bifunctional electrocatalytic activities toward the two‐ele...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Shengbo, Jin, Meng, Xu, Hui, Li, Wenyi, Ye, Yixing, Shi, Tongfei, Zhou, Hongjian, Chen, Chun, Wang, Guozhong, Zhang, Yunxia, Lin, Yue, Zheng, Lirong, Zhang, Haimin, Zhao, Huijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762286/
https://www.ncbi.nlm.nih.gov/pubmed/36310149
http://dx.doi.org/10.1002/advs.202204043
_version_ 1784852832329924608
author Zhang, Shengbo
Jin, Meng
Xu, Hui
Li, Wenyi
Ye, Yixing
Shi, Tongfei
Zhou, Hongjian
Chen, Chun
Wang, Guozhong
Zhang, Yunxia
Lin, Yue
Zheng, Lirong
Zhang, Haimin
Zhao, Huijun
author_facet Zhang, Shengbo
Jin, Meng
Xu, Hui
Li, Wenyi
Ye, Yixing
Shi, Tongfei
Zhou, Hongjian
Chen, Chun
Wang, Guozhong
Zhang, Yunxia
Lin, Yue
Zheng, Lirong
Zhang, Haimin
Zhao, Huijun
author_sort Zhang, Shengbo
collection PubMed
description Direct electrocatalytic oxidation of benzene has been regarded as a promising approach for achieving high‐value phenol product, but remaining a huge challenge. Here an oxygen‐coordinated nickel single‐atom catalyst (Ni–O–C) is reported with bifunctional electrocatalytic activities toward the two‐electron oxygen reduction reaction (2e(−) ORR) to H(2)O(2) and H(2)O(2)‐assisted benzene oxidation to phenol. The Ni–(O–C(2))(4) sites in Ni–O–C ar proven to be the catalytic active centers for bifunctional 2e(−) ORR and H(2)O(2)‐assisted benzene oxidation processes. As a result, Ni–O–C can afford a benzene conversion as high as 96.4 ± 3.6% with a phenol selectivity of 100% and a Faradaic efficiency (FE) of 80.2 ± 3.2% with the help of H(2)O(2) in 0.1 m KOH electrolyte at 1.5 V (vs RHE). A proof of concept experiment with Ni–O–C concurrently as cathode and anode in a single electrochemical cell demonstrates a benzene conversion of 33.4 ± 2.2% with a phenol selectivity of 100% and a FE of 44.8 ± 3.0% at 10 mA cm(−2).
format Online
Article
Text
id pubmed-9762286
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-97622862022-12-20 Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites Zhang, Shengbo Jin, Meng Xu, Hui Li, Wenyi Ye, Yixing Shi, Tongfei Zhou, Hongjian Chen, Chun Wang, Guozhong Zhang, Yunxia Lin, Yue Zheng, Lirong Zhang, Haimin Zhao, Huijun Adv Sci (Weinh) Research Articles Direct electrocatalytic oxidation of benzene has been regarded as a promising approach for achieving high‐value phenol product, but remaining a huge challenge. Here an oxygen‐coordinated nickel single‐atom catalyst (Ni–O–C) is reported with bifunctional electrocatalytic activities toward the two‐electron oxygen reduction reaction (2e(−) ORR) to H(2)O(2) and H(2)O(2)‐assisted benzene oxidation to phenol. The Ni–(O–C(2))(4) sites in Ni–O–C ar proven to be the catalytic active centers for bifunctional 2e(−) ORR and H(2)O(2)‐assisted benzene oxidation processes. As a result, Ni–O–C can afford a benzene conversion as high as 96.4 ± 3.6% with a phenol selectivity of 100% and a Faradaic efficiency (FE) of 80.2 ± 3.2% with the help of H(2)O(2) in 0.1 m KOH electrolyte at 1.5 V (vs RHE). A proof of concept experiment with Ni–O–C concurrently as cathode and anode in a single electrochemical cell demonstrates a benzene conversion of 33.4 ± 2.2% with a phenol selectivity of 100% and a FE of 44.8 ± 3.0% at 10 mA cm(−2). John Wiley and Sons Inc. 2022-10-30 /pmc/articles/PMC9762286/ /pubmed/36310149 http://dx.doi.org/10.1002/advs.202204043 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Shengbo
Jin, Meng
Xu, Hui
Li, Wenyi
Ye, Yixing
Shi, Tongfei
Zhou, Hongjian
Chen, Chun
Wang, Guozhong
Zhang, Yunxia
Lin, Yue
Zheng, Lirong
Zhang, Haimin
Zhao, Huijun
Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title_full Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title_fullStr Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title_full_unstemmed Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title_short Hydrogen Peroxide Assisted Electrooxidation of Benzene to Phenol over Bifunctional Ni–(O–C(2))(4) Sites
title_sort hydrogen peroxide assisted electrooxidation of benzene to phenol over bifunctional ni–(o–c(2))(4) sites
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762286/
https://www.ncbi.nlm.nih.gov/pubmed/36310149
http://dx.doi.org/10.1002/advs.202204043
work_keys_str_mv AT zhangshengbo hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT jinmeng hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT xuhui hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT liwenyi hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT yeyixing hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT shitongfei hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT zhouhongjian hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT chenchun hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT wangguozhong hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT zhangyunxia hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT linyue hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT zhenglirong hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT zhanghaimin hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites
AT zhaohuijun hydrogenperoxideassistedelectrooxidationofbenzenetophenoloverbifunctionalnioc24sites