Photoelectrocatalysis of oxygen evolution on nTiO2
β Scribed by A.Q. Contractor; J.O'M. Bockris
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 237 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
Photoelectrochemical evolution of oxygen on n-TiO, is catalysed in basic medium by metal islets deposited on the electrode surface. The electrocatalytic effect increases linearly with D(M-H). However, no catalytic effect of the metal islets is observed in acidic solutions. Such findings are contrary to those expected on a Schottky barrier model. They are consistent with a model in which the overall rate of the photoelectrochemical reaction is controlled by the step at the metal-solution interface. * These were calculated from Born-Habcr cycle considerations similar to those of Ruetschi and Delahay[ll]. Acknowledgement+Discussions with Drs B. Au&n-Blajeni and M. Szklarcsyk of this laboratory and Dr A. J. Appleby of EPRI are gratefully acknowledged. The authors acknowledge gifts made to Texas A&M University by Dr Hampton Robinson, Jr, and his encouragement towards the development of a technology for storage of solar energy.
π SIMILAR VOLUMES
The oxygen evolution process on NiCo,,Rh,O, (0 Q x Q 0.5) spine1 system was studied in 5 mol dm-a KOH aqueous solution at room temperature. The electrodes ekctrocatalytical activity was analysed in terms of Tafel slope., exchange current density and overpotential vahnxs. The experimental results sho