2009 Annual Meeting

(447g) Synthetic Photoelectrochemical Complexes for Solar Energy Conversion That Self-Regenerate

Authors

Michael Strano - Presenter, Massachusetts Institute of Technology
Ardemis A. Boghossian - Presenter, Massachusetts Institute of Technology
Moon-Ho Ham - Presenter, Massachusetts Institute of Technology
Esther S. Jeng - Presenter, Massachusetts Institute of Technology
Rachel A. Graff - Presenter, University of Illinois at Urbana-Champaign
Daniel A. Heller - Presenter, Massachusetts Institute of Technology
Alice C. Chang - Presenter, Massachusetts Institute of Technology
Aidas Mattis - Presenter, University of Illinois Urbana-Champaign
Timothy H. Bayburt - Presenter, University of Illinois Urbana-Champaign
Yelena V. Grinkova - Presenter, University of Illinois Urbana-Champaign
Adam Scott Zeiger - Presenter, Massachusetts Institute of Technology
Erik K. Hobbie - Presenter, National Institute of Standards and Technology
Stephen G. Sligar - Presenter, University of Illinois Urbana-Champaign
Colin A. Wraight - Presenter, University of Illinois Urbana-Champaign


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.