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
Link To Document :
بازگشت