Performance enhancement of high-temperature polymer electrolyte membrane fuel cells using Pt pulse electrodeposition
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作者:
Kim, Don Kwon
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Chung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South KoreaChung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
Kim, Don Kwon
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Kim, Hoyoung
[1
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Park, Hyanjoo
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Chung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South KoreaChung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
Park, Hyanjoo
[1
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Oh, SeonHwa
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Chung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South KoreaChung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
Oh, SeonHwa
[1
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Ahn, Sang Hyun
[2
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Kim, Hyoung-Juhn
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Korea Inst Sci & Technol, Fuel Cell Res Ctr, 5 Hwarang Ro 14 Gil, Seoul 02792, South KoreaChung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
Kim, Hyoung-Juhn
[3
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Kim, Soo-Kil
[1
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[1] Chung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
[2] Chung Ang Univ, Sch Chem Engn & Mat Sci, 84 Heukseok Ro, Seoul 06974, South Korea
[3] Korea Inst Sci & Technol, Fuel Cell Res Ctr, 5 Hwarang Ro 14 Gil, Seoul 02792, South Korea
The development of high-performance polymer electrolyte membrane fuel cells that operate at elevated temperatures is urgently required to overcome the technical problems associated with operation at low temperatures. Here, we report an effective way to enhance electrode performance via simple Pt pulse electrodeposition at room temperature. This electrodeposition process enables both the formation of additional Pt electrocatalysts with extremely low loading (i.e., similar to 0.05 mg cm(-2) for 100 pulse cycles) as a function of pulse number and control of the wetting properties of commercial Pt-based electrodes. Following optimization of the electrode conditions and configurations, the controlled hydrophilicity of the anode enhances the phosphoric acid distribution and the formation of a triple phase boundary in the catalyst layer, resulting in lowered ohmic and charge transfer resistances, respectively. The mass activities of the membrane electrode assembly with the anode modified by Pt pulse electrodeposition is 437.2 mW mg(Pt)(-1) (H-2/O-2), which is approximately 1.36 times higher than that of the pristine membrane electrode assembly. The controlled hydrophilicity allows moderate improvement of the performance, even without additional Pt. The results presented herein demonstrate the importance of surface property control for electrode preparation to achieve enhanced performance of high-performance polymer electrolyte membrane fuel cells.
机构:
Gwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South Korea
Natl Inst Green Technol, Ctr Technol Anal, Div Policy Res, Seoul 04513, South KoreaGwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South Korea
Kim, Do-Hyung
Jung, Hyeon-Seung
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Gwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South KoreaGwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South Korea
Jung, Hyeon-Seung
Kim, Dong Hee
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Gwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South KoreaGwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South Korea
Kim, Dong Hee
Pak, Chanho
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Gwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South KoreaGwangju Inst Sci & Technol, Inst Integrated Technol, Grad Sch Energy Convergence, Gwangju 61005, South Korea
机构:
China Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R ChinaChina Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R China
Zhang, Quan
Ling, Ying
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China Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R ChinaChina Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R China
Ling, Ying
Cai, Weiwei
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China Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R ChinaChina Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R China
Cai, Weiwei
Yu, Xinxin
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China Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R ChinaChina Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R China
Yu, Xinxin
Yang, Zehui
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China Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R ChinaChina Univ Geosci Wuhan, Sustainable Energy Lab, Fac Mat Sci & Chem, 388 Lumo RD, Wuhan 430074, Peoples R China
机构:
Univ Porto, Fac Engn, LEPAE, P-4200465 Oporto, Portugal
Univ Tras Os Montes & Alto Douro, Escola Ciencias Vida & Ambiente, Dept Quim, P-5001801 Vila Real Codex, PortugalUniv Porto, Fac Engn, LEPAE, P-4200465 Oporto, Portugal