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Abstracts Book - IMRC 2018

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• SC3-O019 Invited Talk<br />

CONTSTRUCTIONS OF PHOTOCATALYTIC AND<br />

PHOTOELECTROCHEMICAL WATER SPLITTING SYSTEMS UNDER<br />

VISIBLE LIGHT<br />

Katayama Masao 1<br />

1 The University of Tokyo, Department of Chemical System Engineering, Japan.<br />

Photocatalytic and photoelectrochemical water splitting has attracted much<br />

attention as a means of sustainable solar hydrogen production. We have studied<br />

various semiconducting oxides, (oxy)nitrides, and (oxy)chalcogenides as<br />

photocatalysts and photoelectrodes for water splitting under visible light. In this<br />

talk, constructions of water splitting systems by using various photocatalysts are<br />

presented. LaMg1/3Ta2/3O2N, a solid solution of LaMg2/3Ta1/3O3 and LaTaON2,<br />

absorbs photons up to 600 nm and produces hydrogen and oxygen under<br />

visible light irradiation when being modified with Rh2-yCryO3 as a hydrogen<br />

evolution cocatalyst. However, nitrogen is also generated simultaneously<br />

because of the self-oxidation of the oxynitride. It was found that amorphous<br />

TiOx coating on LaMg1/3Ta2/3O2N suppressed the self-oxidation and enabled<br />

LaMg1/3Ta2/3O2N modified with Rh2-yCryO3 to split water stoichiometry. 2-step<br />

excitation system for water splitting reaction is also a promising approach<br />

because photocatalysts with narrow bandgaps that are active either for water<br />

reduction or oxidation are applicable. Recently we have developed<br />

photocatalyst sheets consisting of SrTiO3:La,Rh and BiVO4 embedded onto<br />

conductive layers. The conductive layers enable efficient charge transfer<br />

between the two kinds of photocatalysts. By using gold as conductive layers, the<br />

photocatalyst sheet showed significantly higher activity in the overall water<br />

splitting reaction than a conventional powder suspension system of<br />

SrTiO3:La,Rh and BiVO4.<br />

Keywords: Photocatalyst, Photoelectrochemistry, Water splitting<br />

Presenting authors email: katayama@chemsys.t.u-tokyo.ac.jp

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