Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites

Detalhes bibliográficos
Autor(a) principal: Yu, Zhipeng
Data de Publicação: 2022
Outros Autores: Li, Yifan, Martin‐Diaconescu, Vlad, Simonelli, Laura, Ruiz Esquius, Jonathan, Amorim, Isilda, Araujo, Ana, Meng, Lijian, Faria, Joaquim Luis, Liu, Lifeng
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/20797
Resumo: Direct seawater electrolysis is proposed as a potential low-cost approach to green hydrogen production, taking advantage of the vastly available seawater and large-scale offshore renewable energy being deployed. However, developing efficient, earth-abundant electrocatalysts that can survive under harsh corrosive conditions for a long time is still a significant technical challenge. Herein, the fabrication of a self-supported nickel-iron phosphosulfide (NiFeSP) nanotube array electrode through a two-step sulfurization/phosphorization approach is reported. The as-obtained NiFeSP nanotubes comprise abundant NiFeS/NiFeP heterointerfaces and under-coordinated metal sites, exhibiting outstanding activity and durability for the hydrogen and oxygen evolution reactions (HER and OER) in simulated alkaline-seawater solution (KOH + NaCl), with an overpotential of 380 (HER) and 260 mV (OER) at 500 mA cm-2 and outstanding durability of 1000 h. Theoretical calculations support the observed outstanding performance, showing that the heterointerface and under-coordinated metal sites synergistically lower the energy barrier of the rate-determining step reactions. The NiFeSP electrode also shows good catalytic performance for the urea oxidation reaction (UOR). By coupling UOR with HER, the bifunctional NiFeSP electrode pair can efficiently catalyze the overall urea-mediated alkaline-saline water electrolysis at 500 mA cm-2 under 1.938 V for 1000 h without notable performance degradation.
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spelling Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active SitesDirect seawater electrolysis is proposed as a potential low-cost approach to green hydrogen production, taking advantage of the vastly available seawater and large-scale offshore renewable energy being deployed. However, developing efficient, earth-abundant electrocatalysts that can survive under harsh corrosive conditions for a long time is still a significant technical challenge. Herein, the fabrication of a self-supported nickel-iron phosphosulfide (NiFeSP) nanotube array electrode through a two-step sulfurization/phosphorization approach is reported. The as-obtained NiFeSP nanotubes comprise abundant NiFeS/NiFeP heterointerfaces and under-coordinated metal sites, exhibiting outstanding activity and durability for the hydrogen and oxygen evolution reactions (HER and OER) in simulated alkaline-seawater solution (KOH + NaCl), with an overpotential of 380 (HER) and 260 mV (OER) at 500 mA cm-2 and outstanding durability of 1000 h. Theoretical calculations support the observed outstanding performance, showing that the heterointerface and under-coordinated metal sites synergistically lower the energy barrier of the rate-determining step reactions. The NiFeSP electrode also shows good catalytic performance for the urea oxidation reaction (UOR). By coupling UOR with HER, the bifunctional NiFeSP electrode pair can efficiently catalyze the overall urea-mediated alkaline-saline water electrolysis at 500 mA cm-2 under 1.938 V for 1000 h without notable performance degradation.Repositório Científico do Instituto Politécnico do PortoYu, ZhipengLi, YifanMartin‐Diaconescu, VladSimonelli, LauraRuiz Esquius, JonathanAmorim, IsildaAraujo, AnaMeng, LijianFaria, Joaquim LuisLiu, Lifeng2022-07-132031-01-01T00:00:00Z2022-07-13T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/20797eng10.1002/adfm.202206138metadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T13:16:20Zoai:recipp.ipp.pt:10400.22/20797Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:40:52.834187Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
title Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
spellingShingle Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
Yu, Zhipeng
title_short Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
title_full Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
title_fullStr Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
title_full_unstemmed Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
title_sort Highly Efficient and Stable Saline Water Electrolysis Enabled by Self‐Supported Nickel‐Iron Phosphosulfide Nanotubes With Heterointerfaces and Under‐Coordinated Metal Active Sites
author Yu, Zhipeng
author_facet Yu, Zhipeng
Li, Yifan
Martin‐Diaconescu, Vlad
Simonelli, Laura
Ruiz Esquius, Jonathan
Amorim, Isilda
Araujo, Ana
Meng, Lijian
Faria, Joaquim Luis
Liu, Lifeng
author_role author
author2 Li, Yifan
Martin‐Diaconescu, Vlad
Simonelli, Laura
Ruiz Esquius, Jonathan
Amorim, Isilda
Araujo, Ana
Meng, Lijian
Faria, Joaquim Luis
Liu, Lifeng
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Yu, Zhipeng
Li, Yifan
Martin‐Diaconescu, Vlad
Simonelli, Laura
Ruiz Esquius, Jonathan
Amorim, Isilda
Araujo, Ana
Meng, Lijian
Faria, Joaquim Luis
Liu, Lifeng
description Direct seawater electrolysis is proposed as a potential low-cost approach to green hydrogen production, taking advantage of the vastly available seawater and large-scale offshore renewable energy being deployed. However, developing efficient, earth-abundant electrocatalysts that can survive under harsh corrosive conditions for a long time is still a significant technical challenge. Herein, the fabrication of a self-supported nickel-iron phosphosulfide (NiFeSP) nanotube array electrode through a two-step sulfurization/phosphorization approach is reported. The as-obtained NiFeSP nanotubes comprise abundant NiFeS/NiFeP heterointerfaces and under-coordinated metal sites, exhibiting outstanding activity and durability for the hydrogen and oxygen evolution reactions (HER and OER) in simulated alkaline-seawater solution (KOH + NaCl), with an overpotential of 380 (HER) and 260 mV (OER) at 500 mA cm-2 and outstanding durability of 1000 h. Theoretical calculations support the observed outstanding performance, showing that the heterointerface and under-coordinated metal sites synergistically lower the energy barrier of the rate-determining step reactions. The NiFeSP electrode also shows good catalytic performance for the urea oxidation reaction (UOR). By coupling UOR with HER, the bifunctional NiFeSP electrode pair can efficiently catalyze the overall urea-mediated alkaline-saline water electrolysis at 500 mA cm-2 under 1.938 V for 1000 h without notable performance degradation.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-13
2022-07-13T00:00:00Z
2031-01-01T00:00:00Z
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.1002/adfm.202206138
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