Methanol, being a high energy density liquid fuel, with 12.5 wt% hydrogen content, is an attractive energy storage and energy transport media. Methanol assisted water electrolysis for hydrogen production has the potential to reduce the electric energy input by more than 50% compared to conventional electrolysis. However, high electro-catalytic activity and stable performance are key factors for sustainable hydrogen production by this route. In this paper, a number of Pt based catalysts with or without the addition of nano-sized SnO2 and CeO2 to reduce noble metal loading have been investigated for methanol assisted water electrolysis. A controlled spraying technique was used for catalyst deposition on the catalyst supports in a polymer electrolyte membrane-based zero-gap electrolysis cell. The performance has been investigated under different cell operating conditions of temperatute, methanol concentration and current loading. The V-I curves extrapolated to zero current density showed that the cell approach the thermo-neutral voltage of 0.22 V for the methanol assisted water electtolysis compared with 1.48 V for conventional electrolysis. Electrochemical impedance spectroscopy was used to elucidate information on the methanol oxidation reaction. Although the PtRu/C catalyst showed the best performance, SnO2-modified Pt/C catalyst was found to be superior to Pt/C as well as PtRu/C-SnO2 catalysts with low degradation rates. This approach for pure hydrogen generation has the potential to drastically decrease the electric energy input by similar to 60%. (C) 2017 Elsevier Ltd. All rights reserved.
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Hanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, VietnamHanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, Vietnam
Duoc, Vo Thanh
Nguyen, Hugo
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Uppsala Univ, Dept Mat Sci & Engn, Lagerhyddsvagen 1, S-75121 Uppsala, SwedenHanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, Vietnam
Nguyen, Hugo
Ngoc, Trinh Minh
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Hanoi Med Univ, Dept Phys, 1 Ton That Tung, Hanoi, VietnamHanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, Vietnam
Ngoc, Trinh Minh
Xuan, Chu Thi
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Hanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, VietnamHanoi Univ Sci & Technol HUST, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, Vietnam
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Chinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R ChinaChinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
Fu, Mingkai
Xu, Huajun
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Univ Washington, Dept Chem, Seattle, WA 98195 USAChinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
Xu, Huajun
Ma, Haitao
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Chinese Acad Sci, CAS Res Educ Ctr Excellence Mol Sci, Inst Chem, Beijing 100190, Peoples R ChinaChinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
Ma, Haitao
Li, Xin
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Chinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
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Institute of Electrical Engineering, Chinese Academy of SciencesInstitute of Electrical Engineering, Chinese Academy of Sciences
Mingkai Fu
Huajun Xu
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Department of Chemistry, University of WashingtonInstitute of Electrical Engineering, Chinese Academy of Sciences
Huajun Xu
Haitao Ma
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CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of SciencesInstitute of Electrical Engineering, Chinese Academy of Sciences
Haitao Ma
Xin Li
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Institute of Electrical Engineering, Chinese Academy of Sciences
University of Chinese Academy of SciencesInstitute of Electrical Engineering, Chinese Academy of Sciences