Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst
Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offer...
Ausführliche Beschreibung
Autor*in: |
Ju, HyungKuk [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2017 |
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Anmerkung: |
© Springer-Verlag GmbH Germany, part of Springer Nature 2017 |
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Übergeordnetes Werk: |
Enthalten in: Ionics - Berlin : Springer, 1995, 24(2017), 8 vom: 05. Dez., Seite 2367-2378 |
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Übergeordnetes Werk: |
volume:24 ; year:2017 ; number:8 ; day:05 ; month:12 ; pages:2367-2378 |
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DOI / URN: |
10.1007/s11581-017-2371-8 |
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Katalog-ID: |
SPR020870248 |
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520 | |a Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. | ||
650 | 4 | |a Electrolysis |7 (dpeaa)DE-He213 | |
650 | 4 | |a Methanol oxidation |7 (dpeaa)DE-He213 | |
650 | 4 | |a Renewable energy |7 (dpeaa)DE-He213 | |
650 | 4 | |a Transport fuel |7 (dpeaa)DE-He213 | |
650 | 4 | |a Hydrogen fueling station |7 (dpeaa)DE-He213 | |
700 | 1 | |a Giddey, Sarbjit |4 aut | |
700 | 1 | |a Badwal, Sukhvinder P. S. |4 aut | |
700 | 1 | |a Mulder, Roger J. |4 aut | |
700 | 1 | |a Gengenbach, Thomas R. |4 aut | |
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10.1007/s11581-017-2371-8 doi (DE-627)SPR020870248 (SPR)s11581-017-2371-8-e DE-627 ger DE-627 rakwb eng Ju, HyungKuk verfasserin aut Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 Giddey, Sarbjit aut Badwal, Sukhvinder P. S. aut Mulder, Roger J. aut Gengenbach, Thomas R. aut Enthalten in Ionics Berlin : Springer, 1995 24(2017), 8 vom: 05. Dez., Seite 2367-2378 (DE-627)509398944 (DE-600)2226746-3 1862-0760 nnns volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 https://dx.doi.org/10.1007/s11581-017-2371-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 24 2017 8 05 12 2367-2378 |
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10.1007/s11581-017-2371-8 doi (DE-627)SPR020870248 (SPR)s11581-017-2371-8-e DE-627 ger DE-627 rakwb eng Ju, HyungKuk verfasserin aut Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 Giddey, Sarbjit aut Badwal, Sukhvinder P. S. aut Mulder, Roger J. aut Gengenbach, Thomas R. aut Enthalten in Ionics Berlin : Springer, 1995 24(2017), 8 vom: 05. Dez., Seite 2367-2378 (DE-627)509398944 (DE-600)2226746-3 1862-0760 nnns volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 https://dx.doi.org/10.1007/s11581-017-2371-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 24 2017 8 05 12 2367-2378 |
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10.1007/s11581-017-2371-8 doi (DE-627)SPR020870248 (SPR)s11581-017-2371-8-e DE-627 ger DE-627 rakwb eng Ju, HyungKuk verfasserin aut Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 Giddey, Sarbjit aut Badwal, Sukhvinder P. S. aut Mulder, Roger J. aut Gengenbach, Thomas R. aut Enthalten in Ionics Berlin : Springer, 1995 24(2017), 8 vom: 05. Dez., Seite 2367-2378 (DE-627)509398944 (DE-600)2226746-3 1862-0760 nnns volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 https://dx.doi.org/10.1007/s11581-017-2371-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 24 2017 8 05 12 2367-2378 |
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10.1007/s11581-017-2371-8 doi (DE-627)SPR020870248 (SPR)s11581-017-2371-8-e DE-627 ger DE-627 rakwb eng Ju, HyungKuk verfasserin aut Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 Giddey, Sarbjit aut Badwal, Sukhvinder P. S. aut Mulder, Roger J. aut Gengenbach, Thomas R. aut Enthalten in Ionics Berlin : Springer, 1995 24(2017), 8 vom: 05. Dez., Seite 2367-2378 (DE-627)509398944 (DE-600)2226746-3 1862-0760 nnns volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 https://dx.doi.org/10.1007/s11581-017-2371-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 24 2017 8 05 12 2367-2378 |
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10.1007/s11581-017-2371-8 doi (DE-627)SPR020870248 (SPR)s11581-017-2371-8-e DE-627 ger DE-627 rakwb eng Ju, HyungKuk verfasserin aut Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 Giddey, Sarbjit aut Badwal, Sukhvinder P. S. aut Mulder, Roger J. aut Gengenbach, Thomas R. aut Enthalten in Ionics Berlin : Springer, 1995 24(2017), 8 vom: 05. Dez., Seite 2367-2378 (DE-627)509398944 (DE-600)2226746-3 1862-0760 nnns volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 https://dx.doi.org/10.1007/s11581-017-2371-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 24 2017 8 05 12 2367-2378 |
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Enthalten in Ionics 24(2017), 8 vom: 05. Dez., Seite 2367-2378 volume:24 year:2017 number:8 day:05 month:12 pages:2367-2378 |
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Ju, HyungKuk @@aut@@ Giddey, Sarbjit @@aut@@ Badwal, Sukhvinder P. S. @@aut@@ Mulder, Roger J. @@aut@@ Gengenbach, Thomas R. @@aut@@ |
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Ju, HyungKuk |
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Ju, HyungKuk misc Electrolysis misc Methanol oxidation misc Renewable energy misc Transport fuel misc Hydrogen fueling station Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst |
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Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst Electrolysis (dpeaa)DE-He213 Methanol oxidation (dpeaa)DE-He213 Renewable energy (dpeaa)DE-He213 Transport fuel (dpeaa)DE-He213 Hydrogen fueling station (dpeaa)DE-He213 |
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Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst |
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methanol-water co-electrolysis for sustainable hydrogen production with ptru/c-$ sno_{2} $ electro-catalyst |
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Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst |
abstract |
Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. © Springer-Verlag GmbH Germany, part of Springer Nature 2017 |
abstractGer |
Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. © Springer-Verlag GmbH Germany, part of Springer Nature 2017 |
abstract_unstemmed |
Abstract Hydrogen at present is mainly produced from fossil fuels for use in ammonia synthesis, the petrochemical industry, and chemical production. In the future, hydrogen will be increasingly used as an energy vector. Although water electrolysis to produce hydrogen with renewable electricity offers a clean process, the approach is energy intensive, requiring a large renewable resource footprint. Methanol-water co-electrolysis can reduce the energy input by > 50%; its electrochemical oxidation poses complex issues such as poisoning of the catalyst, sluggish oxidation kinetics, and degradation over time. The addition of nano-sized $ SnO_{2} $ to PtRu/C catalyst, to reduce noble metal loading, has been shown here to reduce catalyst leaching and increase the chemical, micro-structural, and performance stability of the methanol-water co-electrolysis process during extended periods of testing. The electrochemical characterization, analysis of the methanol solution, and exit gases, post-cell testing, revealed complete oxidation of methanol with little performance degradation. This is further supported by the stability of the catalyst composition and structure as revealed by the post-mortem XRD and XPS analysis of the cell. The energy balance calculations show that methanol-water co-electrolysis can significantly reduce the renewable energy footprint, and the process can become carbon neutral if bio-methanol is used with renewable electricity. © Springer-Verlag GmbH Germany, part of Springer Nature 2017 |
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title_short |
Methanol-water co-electrolysis for sustainable hydrogen production with PtRu/C-$ SnO_{2} $ electro-catalyst |
url |
https://dx.doi.org/10.1007/s11581-017-2371-8 |
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Giddey, Sarbjit Badwal, Sukhvinder P. S. Mulder, Roger J. Gengenbach, Thomas R. |
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Giddey, Sarbjit Badwal, Sukhvinder P. S. Mulder, Roger J. Gengenbach, Thomas R. |
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up_date |
2024-07-03T18:47:44.208Z |
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|
score |
7.398587 |