Photocatalytic hydrogen evolution from CdS-ZnO-CdO systems under visible light irradiation: Effect of thermal treatment and presence of Pt and Ru cocatalysts
被引:135
作者:
Navarro, R. M.
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机构:
CSIC, Inst Catalisis & Petr Quim, Madrid 28049, SpainCSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
Navarro, R. M.
[1
]
del Valle, F.
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机构:
CSIC, Inst Catalisis & Petr Quim, Madrid 28049, SpainCSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
del Valle, F.
[1
]
Fierro, J. L. G.
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机构:
CSIC, Inst Catalisis & Petr Quim, Madrid 28049, SpainCSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
Fierro, J. L. G.
[1
]
机构:
[1] CSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
Cadmium sulphide;
Platinum;
Ruthenium;
Photocatalysts;
Hydrogen;
Water splitting;
D O I:
10.1016/j.ijhydene.2008.05.048
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A CdS-CdO-ZnO mixture annealed at different temperatures and loaded with Ru or Pt cocatalysts has been investigated in the production of hydrogen from aqueous solutions containing SO32- + S2- as sacrificial reagents under visible light. The physicochemical characterization of the CdS-CdO-ZnO catalyst revealed significant changes in the crystalline structure and visible light absorption capacity as a result of thermal treatments. Catalytic activity was found to be strongly dependent on physicochemical changes associated with thermal annealing. Hydrogen evolution over the CdS-CdO-ZnO catalyst was enhanced in the sample annealed at 773 K by the better contact between the CdS and CdO-ZnO phases, which improved physical charge separation. CdS-CdO-ZnO catalyst activity was significantly improved by the addition of Pt or Ru cocatalysts. Among the noble metals studied, activity promotion was higher for the sample loaded with Ru. The enhancement of activity associated with Ru loading is linked to a good interaction between Ru oxide particles and CdS, which reduces the possibility of electron-hole recombination, thus resulting in more efficient water splitting. (C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER
SPANHEL, L
WELLER, H
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机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER
WELLER, H
HENGLEIN, A
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h-index: 0
机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER
机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER
SPANHEL, L
WELLER, H
论文数: 0引用数: 0
h-index: 0
机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER
WELLER, H
HENGLEIN, A
论文数: 0引用数: 0
h-index: 0
机构:
HAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GERHAHN MEITNER INST KERNFORSCH BERLIN GMBH,BEREICH STRAHLENCHEM,D-1000 BERLIN 39,FED REP GER