Synthetic Photoelectrochemical Complexes for Solar Energy Conversion That Self-Regenerate

Wednesday, November 11, 2009: 5:15 PM
Tennessee A (Gaylord Opryland Hotel)

Michael Strano, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Jong Hyun Choi, Mechanical Engineering, Purdue University, West Lafayette, IN
Moon-Ho Ham, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Ardemis A. Boghossian, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Esther S. Jeng, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Rachel A. Graff, Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL
Daniel A. Heller, Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Alice C. Chang, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Aidas Mattis, Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL
Timothy H. Bayburt, Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL
Yelena V. Grinkova, Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL
Adam Scott Zeiger, Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA
Krystyn J. Van Vliet, Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA
Erik K. Hobbie, Polymers Division, National Institute of Standards and Technology, Gaithersburg, MD
Stephen G. Sligar, Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL
Colin A. Wraight, Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL

Naturally occurring photosynthetic systems in plants are supported by elaborate pathways of self-repair that limit the impact of photo-damage and degradation. Despite advantages in stability and fault tolerance, synthetic photoelectrochemical systems have to date been invariably static. Herein, we demonstrate a complex consisting of two recombinant proteins, phospholipid and a carbon nanotube that reversibly assembles into a particular configuration, forming an array of 4 nm lipid bilayers housing light-converting proteins orientated perpendicular such that the hole conducting site is in close proximity to the nanotube conductor. The complex can reversibly self-assemble into this useful configuration, and disassemble to free components upon the addition of sodium cholate, over an indefinite number of cycles. The assembly is thermodynamically meta-stable and can only transition reversibly between free components and assembled state if the rate of surfactant removal exceeds about 10-5 sec-1. In the assembled state only, the complexes exhibit high photoelectrochemical activity using a dual Fe(CN)63-/ubiquinone mediator with external efficiencies near 40% that are repeatedly recoverable even after continuous cycles of disassembly and regeneration. By mimicking natural repair processes, such systems may lead to more robust and facile solar conversion systems.
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See more of this Session: Chemical Processing for Advanced Photovoltaics
See more of this Group/Topical: Topical H: Solar Topical