Abstract

The photocatalytic reaction in an aqueous TiO 2 suspension has been found to be enhanced by the additiona of some metal powders such as copper, silver, nickel and cobalt into the suspension. Just mixing a metal powder into the suspension gave nearly the same efficiency as metal-loading on the semiconductor particles. The effect is attributed to the rapid transfer of the photogenerated electrons from the TiO 2 to the metal particles, resulting in the effective separation of the electrons and holes. The photo-current measurements were performed using inert collecting electrodes in the suspensions of TiO 2, where formate was added as a hole scavenger, with and without a metal powder. Higher anodic photocurrent was obtained in the presence of a metal than in its absence, indicating that the metal-mediated electron transfer reaction occurs more effectively from the electron-rich TiO 2 particles to the collecting electrode than the direct discharge of the electron-rich TiO 2 on the collecting electrode.

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