The behavior of semiconducting electrodes for photoelectrolysis of water is examined in terms of the physical properties of the semiconductor. The semiconductor-electrolyte junction is treated as a simple Schottky barrier, and the photocurrent is described using this model. The approach is appropriate since large-band-gap semiconductors have an intrinsic oxygen overpotential which removes the electrode reaction kinetics as the rate-limiting step. The model is successful in describing the wavelength and potential dependence of the photocurrent in WO3 and allows a determination of the band gap, optical absorption depth, minority-carrier diffusion length, flat-band potential, and the nature of the fundamental optical transition (direct or indirect). It is shown for WO3 that minority-carrier diffusion plays a limited role in determining the photoresponse of the semiconductor-electrolyte junction. There are indications that the diffusion length in this low carrier mobility material is determined by diffusion-controlled bulk recombination processes rather than the more common trap-limited recombination. It is also shown that the fundamental optical transition is indirect and that the band-gap energy depends relatively strongly on applied potential and electrolyte. This effect seems to be the result of field-induced crystallographic distortions in antiferroelectric WO3.
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M. A. Butler (1977) studied this question.
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