Photocatalytic solar hydrogen production from water on a 100-m2 scale

The unprecedented impact of human activity on Earth’s climate and the ongoing increase in global energy demand have made the development of carbon-neutral energy sources ever more important. Hydrogen is an attractive and versatile energy carrier (and important and widely used chemical) obtainable fr...

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Published inNature (London) Vol. 598; no. 7880; pp. 304 - 307
Main Authors Nishiyama, Hiroshi, Yamada, Taro, Nakabayashi, Mamiko, Maehara, Yoshiki, Yamaguchi, Masaharu, Kuromiya, Yasuko, Nagatsuma, Yoshie, Tokudome, Hiromasa, Akiyama, Seiji, Watanabe, Tomoaki, Narushima, Ryoichi, Okunaka, Sayuri, Shibata, Naoya, Takata, Tsuyoshi, Hisatomi, Takashi, Domen, Kazunari
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 14.10.2021
Nature Publishing Group
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Abstract The unprecedented impact of human activity on Earth’s climate and the ongoing increase in global energy demand have made the development of carbon-neutral energy sources ever more important. Hydrogen is an attractive and versatile energy carrier (and important and widely used chemical) obtainable from water through photocatalysis using sunlight, and through electrolysis driven by solar or wind energy 1 , 2 . The most efficient solar hydrogen production schemes, which couple solar cells to electrolysis systems, reach solar-to-hydrogen (STH) energy conversion efficiencies of 30% at a laboratory scale 3 . Photocatalytic water splitting reaches notably lower conversion efficiencies of only around 1%, but the system design is much simpler and cheaper and more amenable to scale-up 1 , 2 —provided the moist, stoichiometric hydrogen and oxygen product mixture can be handled safely in a field environment and the hydrogen recovered. Extending our earlier demonstration of a 1-m 2 panel reactor system based on a modified, aluminium-doped strontium titanate particulate photocatalyst 4 , we here report safe operation of a 100-m 2 array of panel reactors over several months with autonomous recovery of hydrogen from the moist gas product mixture using a commercial polyimide membrane 5 . The system, optimized for safety and durability, and remaining undamaged on intentional ignition of recovered hydrogen, reaches a maximum STH of 0.76%. While the hydrogen production is inefficient and energy negative overall, our findings demonstrate that safe, large-scale photocatalytic water splitting, and gas collection and separation are possible. To make the technology economically viable and practically useful, essential next steps are reactor and process optimization to substantially reduce costs and improve STH efficiency, photocatalyst stability and gas separation efficiency. Carbon-neutral hydrogen can be produced through photocatalytic water splitting, as demonstrated here with a 100-m 2 array of panel reactors that reaches a maximum conversion efficiency of 0.76%.
AbstractList The unprecedented impact of human activity on Earth's climate and the ongoing increase in global energy demand have made the development of carbon-neutral energy sources ever more important. Hydrogen is an attractive and versatile energy carrier (and important and widely used chemical) obtainable from water through photocatalysis using sunlight, and through electrolysis driven by solar or wind energy1,2. The most efficient solar hydrogen production schemes, which couple solar cells to electrolysis systems, reach solar-to-hydrogen (STH) energy conversion efficiencies of 30% at a laboratory scale3. Photocatalytic water splitting reaches notably lower conversion efficiencies of only around 1%, but the system design is much simpler and cheaper and more amenable to scale-up1,2-provided the moist, stoichiometric hydrogen and oxygen product mixture can be handled safely in a field environment and the hydrogen recovered. Extending our earlier demonstration of a 1-m2 panel reactor system based on a modified, aluminium-doped strontium titanate particulate photocatalyst4, we here report safe operation of a 100-m2 array of panel reactors over several months with autonomous recovery of hydrogen from the moist gas product mixture using a commercial polyimide membrane5. The system, optimized for safety and durability, and remaining undamaged on intentional ignition of recovered hydrogen, reaches a maximum STH of 0.76%. While the hydrogen production is inefficient and energy negative overall, our findings demonstrate that safe, large-scale photocatalytic water splitting, and gas collection and separation are possible. To make the technology economically viable and practically useful, essential next steps are reactor and process optimization to substantially reduce costs and improve STH efficiency, photocatalyst stability and gas separation efficiency.
The unprecedented impact of human activity on Earth’s climate and the ongoing increase in global energy demand have made the development of carbon-neutral energy sources ever more important. Hydrogen is an attractive and versatile energy carrier (and important and widely used chemical) obtainable from water through photocatalysis using sunlight, and through electrolysis driven by solar or wind energy 1 , 2 . The most efficient solar hydrogen production schemes, which couple solar cells to electrolysis systems, reach solar-to-hydrogen (STH) energy conversion efficiencies of 30% at a laboratory scale 3 . Photocatalytic water splitting reaches notably lower conversion efficiencies of only around 1%, but the system design is much simpler and cheaper and more amenable to scale-up 1 , 2 —provided the moist, stoichiometric hydrogen and oxygen product mixture can be handled safely in a field environment and the hydrogen recovered. Extending our earlier demonstration of a 1-m 2 panel reactor system based on a modified, aluminium-doped strontium titanate particulate photocatalyst 4 , we here report safe operation of a 100-m 2 array of panel reactors over several months with autonomous recovery of hydrogen from the moist gas product mixture using a commercial polyimide membrane 5 . The system, optimized for safety and durability, and remaining undamaged on intentional ignition of recovered hydrogen, reaches a maximum STH of 0.76%. While the hydrogen production is inefficient and energy negative overall, our findings demonstrate that safe, large-scale photocatalytic water splitting, and gas collection and separation are possible. To make the technology economically viable and practically useful, essential next steps are reactor and process optimization to substantially reduce costs and improve STH efficiency, photocatalyst stability and gas separation efficiency. Carbon-neutral hydrogen can be produced through photocatalytic water splitting, as demonstrated here with a 100-m 2 array of panel reactors that reaches a maximum conversion efficiency of 0.76%.
Author Yamaguchi, Masaharu
Tokudome, Hiromasa
Okunaka, Sayuri
Nakabayashi, Mamiko
Akiyama, Seiji
Watanabe, Tomoaki
Shibata, Naoya
Takata, Tsuyoshi
Nishiyama, Hiroshi
Nagatsuma, Yoshie
Hisatomi, Takashi
Maehara, Yoshiki
Narushima, Ryoichi
Domen, Kazunari
Yamada, Taro
Kuromiya, Yasuko
Author_xml – sequence: 1
  givenname: Hiroshi
  orcidid: 0000-0003-2065-3773
  surname: Nishiyama
  fullname: Nishiyama, Hiroshi
  organization: Office of University Professors, The University of Tokyo
– sequence: 2
  givenname: Taro
  surname: Yamada
  fullname: Yamada, Taro
  organization: Office of University Professors, The University of Tokyo
– sequence: 3
  givenname: Mamiko
  orcidid: 0000-0001-6101-0382
  surname: Nakabayashi
  fullname: Nakabayashi, Mamiko
  organization: Institute of Engineering Innovation, School of Engineering, The University of Tokyo
– sequence: 4
  givenname: Yoshiki
  surname: Maehara
  fullname: Maehara, Yoshiki
  organization: Japan Technological Research Association of Artificial Photosynthetic Chemical Process (ARPChem), FUJIFILM Corporation, Ashigarakami-gun
– sequence: 5
  givenname: Masaharu
  surname: Yamaguchi
  fullname: Yamaguchi, Masaharu
  organization: Office of University Professors, The University of Tokyo
– sequence: 6
  givenname: Yasuko
  surname: Kuromiya
  fullname: Kuromiya, Yasuko
  organization: Office of University Professors, The University of Tokyo
– sequence: 7
  givenname: Yoshie
  surname: Nagatsuma
  fullname: Nagatsuma, Yoshie
  organization: Office of University Professors, The University of Tokyo
– sequence: 8
  givenname: Hiromasa
  orcidid: 0000-0001-6624-0515
  surname: Tokudome
  fullname: Tokudome, Hiromasa
  organization: Japan Technological Research Association of Artificial Photosynthetic Chemical Process (ARPChem), Research Institute, TOTO Ltd
– sequence: 9
  givenname: Seiji
  surname: Akiyama
  fullname: Akiyama, Seiji
  organization: Japan Technological Research Association of Artificial Photosynthetic Chemical Process (ARPChem), Mitsubishi Chemical Corporation, Science & Innovation Center
– sequence: 10
  givenname: Tomoaki
  surname: Watanabe
  fullname: Watanabe, Tomoaki
  organization: Department of Applied Chemistry, School of Science and Technology, Meiji University
– sequence: 11
  givenname: Ryoichi
  surname: Narushima
  fullname: Narushima, Ryoichi
  organization: Office of University Professors, The University of Tokyo
– sequence: 12
  givenname: Sayuri
  orcidid: 0000-0003-3888-7201
  surname: Okunaka
  fullname: Okunaka, Sayuri
  organization: Japan Technological Research Association of Artificial Photosynthetic Chemical Process (ARPChem), Research Institute, TOTO Ltd., Global Zero Emission Research Center (GZR), National Institution of Advanced Industrial Science and Technology (AIST)
– sequence: 13
  givenname: Naoya
  orcidid: 0000-0003-3548-5952
  surname: Shibata
  fullname: Shibata, Naoya
  organization: Institute of Engineering Innovation, School of Engineering, The University of Tokyo
– sequence: 14
  givenname: Tsuyoshi
  surname: Takata
  fullname: Takata, Tsuyoshi
  organization: Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University
– sequence: 15
  givenname: Takashi
  orcidid: 0000-0002-5009-2383
  surname: Hisatomi
  fullname: Hisatomi, Takashi
  organization: Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University
– sequence: 16
  givenname: Kazunari
  orcidid: 0000-0001-7995-4832
  surname: Domen
  fullname: Domen, Kazunari
  email: domen@chemsys.t.u-tokyo.ac.jp
  organization: Office of University Professors, The University of Tokyo, Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University
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Snippet The unprecedented impact of human activity on Earth’s climate and the ongoing increase in global energy demand have made the development of carbon-neutral...
The unprecedented impact of human activity on Earth's climate and the ongoing increase in global energy demand have made the development of carbon-neutral...
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SubjectTerms 639/301/299/890
639/4077/4072/4062
639/4077/909/4101/4102
Alternative energy
Aluminum
Bubbles
Carbon neutrality
Carbon sources
Climate and human activity
Efficiency
Electrolysis
Electrolytic cells
Energy conversion
Energy conversion efficiency
Energy demand
Energy sources
Gas separation
Gases
Glass
Human influences
Humanities and Social Sciences
Hydrogen
Hydrogen production
Hydrogen-based energy
multidisciplinary
Nanoparticles
Nuclear safety
Optimization
Oxygen
Photocatalysis
Photovoltaic cells
Product safety
Radiation
Reactors
Science
Science (multidisciplinary)
Solar cells
Solar energy
Strontium
Strontium titanates
Sunlight
Systems design
Water splitting
Title Photocatalytic solar hydrogen production from water on a 100-m2 scale
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