Title of article :
A review and recent developments in photocatalytic water-splitting using for hydrogen production
Author/Authors :
Ni، نويسنده , , Meng and Leung، نويسنده , , Michael K.H. and Leung، نويسنده , , Dennis Y.C. and Sumathy، نويسنده , , K.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
25
From page :
401
To page :
425
Abstract :
Nano-sized TiO 2 photocatalytic water-splitting technology has great potential for low-cost, environmentally friendly solar-hydrogen production to support the future hydrogen economy. Presently, the solar-to-hydrogen energy conversion efficiency is too low for the technology to be economically sound. The main barriers are the rapid recombination of photo-generated electron/hole pairs as well as backward reaction and the poor activation of TiO 2 by visible light. In response to these deficiencies, many investigators have been conducting research with an emphasis on effective remediation methods. Some investigators studied the effects of addition of sacrificial reagents and carbonate salts to prohibit rapid recombination of electron/hole pairs and backward reactions. Other research focused on the enhancement of photocatalysis by modification of TiO 2 by means of metal loading, metal ion doping, dye sensitization, composite semiconductor, anion doping and metal ion-implantation. This paper aims to review the up-to-date development of the above-mentioned technologies applied to TiO 2 photocatalytic hydrogen production. Based on the studies reported in the literature, metal ion-implantation and dye sensitization are very effective methods to extend the activating spectrum to the visible range. Therefore, they play an important role in the development of efficient photocatalytic hydrogen production.
Keywords :
Dye sensitization , Hydrogen production , Metal ion-implantation , photocatalysis , Solar
Journal title :
Renewable and Sustainable Energy Reviews
Serial Year :
2007
Journal title :
Renewable and Sustainable Energy Reviews
Record number :
1498054
Link To Document :
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