Photosystem I/molecular wire/metal nanoparticle bioconjugates for the photocatalytic production of H2

被引:118
作者
Grimme, Rebecca A. [1 ]
Lubner, Carolyn E. [1 ]
Bryant, Donald A. [2 ]
Golbeck, John H. [1 ,2 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
关键词
D O I
10.1021/ja800923y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photosystem I (PS I) is a robust photosynthetic complex that adeptly captures photons to create a charge-separated state with a quantum efficiency that approaches 1.0. This charge-separated state is stable for similar to 100 ms, and the low-potential reductant that is produced is poised at a redox potential favorable for H-2 evolution. PS I has been covalently linked to Pt and Au nanoparticle surfaces by 1,6-hexanedithiol which serves as a molecular wire to both connect PS I to the particles and transfer electrons from the terminal electron transfer cofactor of PS I, F-B, to the nanoparticle. Illumination of these Photosystem I/molecular wire/nanoparticle bioconjugates is able to catalyze the reaction: 2H(+) + 2e(-) -> H-2. Transfer of the electrons from PS I to the nanoparticle through the molecular wire is not rate-limiting for H-2 evolution. Supplying the system with more efficient donor-side electron donating species results in a 5-fold increase in the rate of H-2 evolution.
引用
收藏
页码:6308 / +
页数:3
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