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Hydrogen evolution and iodine reduction on an illuminated n-p junction silicon electrode and its application to efficient solar photoelectrolysis of hydrogen iodide

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j150663a006· OSTI ID:6167697
A p-type silicon electrode, highly doped with phosphorus from the surface (hereafter abbreviated as an n/sup +//p-Si electrode), generated a photocurrent corresponding to iodine (or triiodide) reduction in a hydrogen iodide/iodine solution at potentials much more positive than those at platinum and p-Si electrodes. The photocurrent-potential curve did not change when the electrode was illuminated for 60 h at a sufficiently cathodic potential, but changed due to the formation of a thin silicon oxide layer at the surface when illuminated near the onset potential of the photocurrent. The kinetics of the photoevolution of hydrogen on the n/sup +//p-Si electrode in acid solutions were improved by depositing a 0.5-3 nm thick platinum layer on the surface. The hydrogen-evolution photocurrent at the Pt-coated n/sup +//p-Si electrode gradually decayed under prolonged illumination, but was restored to the initial value by keeping the electrode in an oxidative condition. This suggests that the decay is due to the formation of a reduced surface species. Photoelectrochemical cells constructed with a Pt-deposited n/sup +//p-Si electrode and a Pt counterelectrode separated by a commercial cation-exchange membrane electrolyzed hydrogen iodide into hydrogen and triiodide ions under no externally applied voltage with an encouragingly high solar-to-chemical energy conversion efficiency (phi/sub chem//sup s/) of 7.8% under simulated solar AM 1 radiation. 30 references, 8 figures.
Research Organization:
Osaka Univ., Toyonaka, Japan
OSTI ID:
6167697
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 88:19; ISSN JPCHA
Country of Publication:
United States
Language:
English