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Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels
Electrolysis of water to generate hydrogen fuel is an attractive renewable energy storage technology. However, grid-scale freshwater electrolysis would put a heavy strain on vital water resources. Developing cheap electrocatalysts and electrodes that can sustain seawater splitting without chloride c...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452679/ https://www.ncbi.nlm.nih.gov/pubmed/30886092 http://dx.doi.org/10.1073/pnas.1900556116 |
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author | Kuang, Yun Kenney, Michael J. Meng, Yongtao Hung, Wei-Hsuan Liu, Yijin Huang, Jianan Erick Prasanna, Rohit Li, Pengsong Li, Yaping Wang, Lei Lin, Meng-Chang McGehee, Michael D. Sun, Xiaoming Dai, Hongjie |
author_facet | Kuang, Yun Kenney, Michael J. Meng, Yongtao Hung, Wei-Hsuan Liu, Yijin Huang, Jianan Erick Prasanna, Rohit Li, Pengsong Li, Yaping Wang, Lei Lin, Meng-Chang McGehee, Michael D. Sun, Xiaoming Dai, Hongjie |
author_sort | Kuang, Yun |
collection | PubMed |
description | Electrolysis of water to generate hydrogen fuel is an attractive renewable energy storage technology. However, grid-scale freshwater electrolysis would put a heavy strain on vital water resources. Developing cheap electrocatalysts and electrodes that can sustain seawater splitting without chloride corrosion could address the water scarcity issue. Here we present a multilayer anode consisting of a nickel–iron hydroxide (NiFe) electrocatalyst layer uniformly coated on a nickel sulfide (NiSx) layer formed on porous Ni foam (NiFe/NiSx-Ni), affording superior catalytic activity and corrosion resistance in solar-driven alkaline seawater electrolysis operating at industrially required current densities (0.4 to 1 A/cm(2)) over 1,000 h. A continuous, highly oxygen evolution reaction-active NiFe electrocatalyst layer drawing anodic currents toward water oxidation and an in situ-generated polyatomic sulfate and carbonate-rich passivating layers formed in the anode are responsible for chloride repelling and superior corrosion resistance of the salty-water-splitting anode. |
format | Online Article Text |
id | pubmed-6452679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-64526792019-04-11 Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels Kuang, Yun Kenney, Michael J. Meng, Yongtao Hung, Wei-Hsuan Liu, Yijin Huang, Jianan Erick Prasanna, Rohit Li, Pengsong Li, Yaping Wang, Lei Lin, Meng-Chang McGehee, Michael D. Sun, Xiaoming Dai, Hongjie Proc Natl Acad Sci U S A Physical Sciences Electrolysis of water to generate hydrogen fuel is an attractive renewable energy storage technology. However, grid-scale freshwater electrolysis would put a heavy strain on vital water resources. Developing cheap electrocatalysts and electrodes that can sustain seawater splitting without chloride corrosion could address the water scarcity issue. Here we present a multilayer anode consisting of a nickel–iron hydroxide (NiFe) electrocatalyst layer uniformly coated on a nickel sulfide (NiSx) layer formed on porous Ni foam (NiFe/NiSx-Ni), affording superior catalytic activity and corrosion resistance in solar-driven alkaline seawater electrolysis operating at industrially required current densities (0.4 to 1 A/cm(2)) over 1,000 h. A continuous, highly oxygen evolution reaction-active NiFe electrocatalyst layer drawing anodic currents toward water oxidation and an in situ-generated polyatomic sulfate and carbonate-rich passivating layers formed in the anode are responsible for chloride repelling and superior corrosion resistance of the salty-water-splitting anode. National Academy of Sciences 2019-04-02 2019-03-18 /pmc/articles/PMC6452679/ /pubmed/30886092 http://dx.doi.org/10.1073/pnas.1900556116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Physical Sciences Kuang, Yun Kenney, Michael J. Meng, Yongtao Hung, Wei-Hsuan Liu, Yijin Huang, Jianan Erick Prasanna, Rohit Li, Pengsong Li, Yaping Wang, Lei Lin, Meng-Chang McGehee, Michael D. Sun, Xiaoming Dai, Hongjie Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title | Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title_full | Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title_fullStr | Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title_full_unstemmed | Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title_short | Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
title_sort | solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452679/ https://www.ncbi.nlm.nih.gov/pubmed/30886092 http://dx.doi.org/10.1073/pnas.1900556116 |
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