Biologically templated photocatalytic nanostructures for sustained light-driven water oxidation

被引:2
|
作者
Nam, Yoon Sung [1 ]
Magyar, Andrew P. [2 ]
Lee, Daeyeon [3 ]
Kim, Jin-Woong [3 ]
Yun, Dong Soo [2 ]
Park, Heechul [2 ]
Pollom, Thomas S., Jr. [1 ]
Weitz, David A. [3 ,4 ]
Belcher, Angela M. [1 ,2 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[4] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
COLLOIDAL IRIDIUM OXIDE; OXYGEN EVOLUTION; ELECTRON-TRANSFER; CATALYSTS; PORPHYRINS; NANOWIRES; HYDROSOLS; EFFICIENT; SYSTEMS; SILICA;
D O I
10.1038/NNANO.2010.57
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Over several billion years, cyanobacteria and plants have evolved highly organized photosynthetic systems to shuttle both electronic and chemical species for the efficient oxidation of water(1). In a similar manner to reaction centres in natural photosystems, molecular(2) and metal oxide(3) catalysts have been used to photochemically oxidize water. However, the various approaches involving the molecular design of ligands(4), surface modification(5) and immobilization(6,7) still have limitations in terms of catalytic efficiency and sustainability. Here, we demonstrate a biologically templated nanostructure for visible light-driven water oxidation that uses a genetically engineered M13 virus scaffold to mediate the co-assembly of zinc porphyrins (photosensitizer) and iridium oxide hydrosol clusters (catalyst). Porous polymer microgels are used as an immobilization matrix to improve the structural durability of the assembled nanostructures and to allow the materials to be recycled. Our results suggest that the biotemplated nanoscale assembly of functional components is a promising route to significantly improved photocatalytic water-splitting systems.
引用
收藏
页码:340 / 344
页数:5
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