期刊
NATURE
卷 598, 期 7880, 页码 304-+出版社
NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03907-3
关键词
-
资金
- New Energy and Industrial Technology Development Organization (NEDO), Japan
- Nanotechnology Platform project by the Ministry of Education, Culture, Sports, Science and Technology of Japan [JPMXP09A20UT0004]
Hydrogen, as an energy carrier, can be obtained through photocatalysis and electrolysis, making it a carbon-neutral energy source. While photocatalytic water splitting efficiency is low, large-scale safe production and collection of hydrogen is feasible. The essential next steps for economic viability and practical use are reactor and process optimization to reduce costs and improve efficiency and stability.
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.
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