Solar water splitting to generate hydrogen fuel—a photothermal electrochemical analysis

Theory11From a similar paper reprinted with permission from S. Licht, J. Phys. Chem., B 107 (2003) 4253. Copyright 2003 American Chemical Society. xperiment22From a similar paper reprinted with permission from S. Licht, Halperin, L. Kalina, M. Halperin, N. Chem. Commun. 2003, 3006—Reproduced by permission of The Royal Society of Chemistry. erived for highly efficient photothermal electrochemical solar water splitting to provide clean, renewable sources of hydrogen fuel. The theory derives semiconductor band-gap-restricted, thermal enhanced, solar water splitting efficiencies, combining photodriven charge transfer, with excess sub-band-gap insolation to lower the water potential. Fundamental water thermodynamics and solar photosensitizer constraints determine solar to hydrogen fuel conversion efficiencies in the 50% range over a wide range of insolation, temperature, pressure and photosensitizer band-gap conditions. Experimentally, a novel physical chemical process within molten NaOH is demonstrated, in which an external single, small band-gap photosentizer, such as Si, can drive the energetics of water cleavage. This is accomplished by tuning (decreasing) the water splitting electrochemical potential, EH2O, rather than tuning the photosensitizer band gap; this diminished potential is due to (i) thermodynamic temperature induced decrease of EH2O with increasing temperature, and (ii) partial recombination of the cleavage products.