Photocatalytic water oxidation at soft interfaces

被引:59
作者
Hansen, Malte [1 ]
Li, Fei [2 ]
Sun, Licheng [2 ,3 ]
Koenig, Burkhard [1 ]
机构
[1] Univ Regensburg, Inst Organ Chem, D-93040 Regensburg, Germany
[2] Dalian Univ Technol, DUT KTH Joint Educ & Res Ctr Mol Devices, State Key Lab Fine Chem, Dalian 116012, Peoples R China
[3] KTH Royal Inst Technol, Dept Chem, S-10044 Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
MONONUCLEAR RUTHENIUM COMPLEXES; LIGHT-DRIVEN; ENERGY; CATALYSTS; MECHANISM;
D O I
10.1039/c4sc01018c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular water oxidation catalysts have been, for the first time, co-embedded with a photosensitizer into phospholipid membranes. The functionalized small unilamellar vesicles produce molecular oxygen by photocatalysis when irradiated with visible light in aqueous buffer. The two dimensional assembly of the catalysts at the lipid-water interface mimics photoactive membranes in biology and allows photocatalytic water oxidation at very low catalyst concentrations of 500 nM, which cannot be reached in homogeneous systems. Highest TONs are obtained below the membrane's main transition temperature indicating that phase separation, clustering and a limited dynamic enhance the photocatalytic activity of the assembly. The concept of membrane co- embedding can be applied to various combinations, ratios and concentrations of photosensitizers and water oxidizing catalysts, providing a new approach for artificial photosynthesis.
引用
收藏
页码:2683 / 2687
页数:5
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