Title of article
Photocatalytic hydrogen evolution over delafossite
Author/Authors
Koriche، نويسنده , , N. and Bouguelia، نويسنده , , A. and Aider، نويسنده , , A. and Trari، نويسنده , , M.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
7
From page
693
To page
699
Abstract
The small band gap CuAlO 2 , as prepared, is a p-type semiconductor with a low mobility polarons. Its catalytic ability for H 2 production upon visible light was studied in connection with its synthesis method. The potential of the conduction band ( - 1.63 V sce ) lies below H 2 O / H 2 level leading to a spontaneous H 2 -evolution. An enhancement has been made in the preparation of active oxide by coprecipitation. The highest H 2 production, with a generation rate of 0.19 ml h - 1 mg - 1 , has been obtained in a 0.1 M S 2 - solution at pH 13.72 and increases parallel to polysulfide S n 2 - formation ( n S 2 - + 2 ( n - 1 ) H 2 O → S n 2 - + ( n - 1 ) H 2 + 2 ( n - 1 ) OH - ) ; both reactions occur simultaneously and no photoactivity was observed below pH 7 indicating that S 2 - is a determining specie. The carriersʹ exchange between CuAlO 2 and electrolyte occurs iso-energetically; the exchange is possible through induced band gap states acting as efficient relays. The global reaction is governed by the arrival rate of electrons to the interface and the thermal improvement of photoactivity is attributed to an increase in electronic mobility. The decrease of the rate of H 2 -evolution over time results from produced S n 2 - that act as light filter and interfere with H 2 O reduction.
Keywords
delafossite , CuAlO 2 , H 2 -evolution , Coprecipitation , Polysulfides
Journal title
International Journal of Hydrogen Energy
Serial Year
2005
Journal title
International Journal of Hydrogen Energy
Record number
1650551
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