Wiring of Photosystem II to Hydrogenase for Photoelectrochemical Water-splitting
Authors
Mersch, Dirk
Lee, Chong Yong
Brinkert, Katharina
Fontecilla-Camps, Juan C
Rutherford, A William
Publication Date
2015-06-05Journal Title
Journal of the American Chemical Society
ISSN
0002-7863
Publisher
American Chemical Society
Volume
137
Pages
8541-8549
Language
English
Type
Article
Metadata
Show full item recordCitation
Mersch, D., Lee, C. Y., Zhang, J., Brinkert, K., Fontecilla-Camps, J. C., Rutherford, A. W., & Reisner, E. (2015). Wiring of Photosystem II to Hydrogenase for Photoelectrochemical Water-splitting. Journal of the American Chemical Society, 137 8541-8549. https://doi.org/10.1021/jacs.5b03737
Abstract
In natural photosynthesis, light is used for the production of chemical energy carriers to fuel biological activity. The re-engineering of natural photosynthetic pathways can provide inspiration for sustainable fuel production and insights for understanding the process itself. Here, we employ a semi-artificial approach to study photo-biological water-splitting via a pathway unavailable to nature: the direct coupling of the water-oxidation enzyme, Photosystem II, to the H2 evolving enzyme, hydrogenase. Essential to this approach is the integration of the isolated enzymes into the artificial circuit of a photoelectrochemical cell. We therefore developed a tailor-made hierarchically structured porous indium-tin oxide electrode that gives rise to the excellent integration of both Photosystem II and hydrogenase for performing the anodic and cathodic half reactions, respectively. When connected together with the aid of an applied bias, the semi-artificial cell demonstrated quantitative electron flow from Photosystem II to the hydrogenase with the production of H2 and O2 being in the expected two-to-one ratio, and a light-to-hydrogen conversion efficiency of 5.4% under low intensity red light irradiation. We thereby demonstrate efficient light-driven water-splitting using a pathway inaccessible to biology, and report on a widely applicable in vitro platform for the controlled coupling of enzymatic redox processes to meaningfully study photocatalytic reactions.
Sponsorship
This work was supported by the U.K. Engineering and Physical Sciences Research Council (EP/H00338X/2 to E.R. and EP/G037221/1, nanoDTC, to D.M.), the UK Biology and Biotechnological Sciences Research Council (BB/K002627/1 to A.W.R. and BB/K010220/1 to E.R.), a Marie Curie Intra-European Fellowship (PIEF-GA-2013-625034 to C.Y.L), a Marie Curie International Incoming Fellowship (PIIF-GA-2012-328085 RPSII to J.J.Z) and the CEA and the CNRS (to J.C.F.C.). A.W.R. holds a Wolfson Merit Award from the Royal Society.
Funder references
BBSRC (BB/K010220/1)
EPSRC (EP/H00338X/2)
Identifiers
External DOI: https://doi.org/10.1021/jacs.5b03737
This record's URL: https://www.repository.cam.ac.uk/handle/1810/248630