期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 5, 期 14, 页码 2402-2407出版社
AMER CHEMICAL SOC
DOI: 10.1021/jz5008164
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资金
- PRESTO (Japan Science and Technology Agency, JST)
- Tatematsu
- Takahashi
- Hibi Foundation
- AOARD
- Grants-in-Aid for Scientific Research [23655196, 26440139] Funding Source: KAKEN
Hydrogenases are powerful catalysts for light-driven H-2 production using a combination of photosensitizers. However, except oxygen-tolerant hydrogenases, they are immediately deactivated under aerobic conditions. We report a light-driven H-2 evolution system that works stably even under aerobic conditions. A [NiFe]-hydrogenase from Desulfovibrio vulgaris Miyazaki F was immobilized inside nanoporous glass plates (PGPs) with a pore diameter of 50 nm together with a ruthenium complex and methyl viologen as a photosensitizer and an electron mediator, respectively. After immersion of PGP into the medium containing the catalytic components, an anaerobic environment automatically established inside the nanopores even under aerobic external conditions upon irradiation with solar-simulated light; this system constantly evolved H-2 with an efficiency of 3.7 mu mol H-2 m(-2) s(-1). The PGP system proposed in this work represents a promising first step toward the development of an O-2-tolerant solar energy conversion system.
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