Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode
Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200...
Ausführliche Beschreibung
Autor*in: |
Sažinas, Rokas [verfasserIn] Andersen, Kjeld Bøhm [verfasserIn] Hansen, Kent Kammer [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Journal of solid state electrochemistry - Berlin : Springer, 1997, 24(2020), 3 vom: 18. Jan., Seite 609-621 |
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Übergeordnetes Werk: |
volume:24 ; year:2020 ; number:3 ; day:18 ; month:01 ; pages:609-621 |
Links: |
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DOI / URN: |
10.1007/s10008-020-04505-5 |
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Katalog-ID: |
SPR039021890 |
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520 | |a Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. | ||
650 | 4 | |a Silver |7 (dpeaa)DE-He213 | |
650 | 4 | |a Exsolution |7 (dpeaa)DE-He213 | |
650 | 4 | |a Nanoparticles |7 (dpeaa)DE-He213 | |
650 | 4 | |a SOFC |7 (dpeaa)DE-He213 | |
650 | 4 | |a Cathode |7 (dpeaa)DE-He213 | |
650 | 4 | |a LSF |7 (dpeaa)DE-He213 | |
650 | 4 | |a Oxygen reduction reaction |7 (dpeaa)DE-He213 | |
700 | 1 | |a Andersen, Kjeld Bøhm |e verfasserin |4 aut | |
700 | 1 | |a Hansen, Kent Kammer |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of solid state electrochemistry |d Berlin : Springer, 1997 |g 24(2020), 3 vom: 18. Jan., Seite 609-621 |w (DE-627)271175400 |w (DE-600)1478940-1 |x 1433-0768 |7 nnns |
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2020 |
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10.1007/s10008-020-04505-5 doi (DE-627)SPR039021890 (SPR)s10008-020-04505-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Sažinas, Rokas verfasserin aut Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 Andersen, Kjeld Bøhm verfasserin aut Hansen, Kent Kammer verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 24(2020), 3 vom: 18. Jan., Seite 609-621 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:24 year:2020 number:3 day:18 month:01 pages:609-621 https://dx.doi.org/10.1007/s10008-020-04505-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_267 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE 35.90 ASE AR 24 2020 3 18 01 609-621 |
spelling |
10.1007/s10008-020-04505-5 doi (DE-627)SPR039021890 (SPR)s10008-020-04505-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Sažinas, Rokas verfasserin aut Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 Andersen, Kjeld Bøhm verfasserin aut Hansen, Kent Kammer verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 24(2020), 3 vom: 18. Jan., Seite 609-621 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:24 year:2020 number:3 day:18 month:01 pages:609-621 https://dx.doi.org/10.1007/s10008-020-04505-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_267 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE 35.90 ASE AR 24 2020 3 18 01 609-621 |
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10.1007/s10008-020-04505-5 doi (DE-627)SPR039021890 (SPR)s10008-020-04505-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Sažinas, Rokas verfasserin aut Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 Andersen, Kjeld Bøhm verfasserin aut Hansen, Kent Kammer verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 24(2020), 3 vom: 18. Jan., Seite 609-621 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:24 year:2020 number:3 day:18 month:01 pages:609-621 https://dx.doi.org/10.1007/s10008-020-04505-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_267 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE 35.90 ASE AR 24 2020 3 18 01 609-621 |
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10.1007/s10008-020-04505-5 doi (DE-627)SPR039021890 (SPR)s10008-020-04505-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Sažinas, Rokas verfasserin aut Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 Andersen, Kjeld Bøhm verfasserin aut Hansen, Kent Kammer verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 24(2020), 3 vom: 18. Jan., Seite 609-621 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:24 year:2020 number:3 day:18 month:01 pages:609-621 https://dx.doi.org/10.1007/s10008-020-04505-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_267 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE 35.90 ASE AR 24 2020 3 18 01 609-621 |
allfieldsSound |
10.1007/s10008-020-04505-5 doi (DE-627)SPR039021890 (SPR)s10008-020-04505-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Sažinas, Rokas verfasserin aut Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 Andersen, Kjeld Bøhm verfasserin aut Hansen, Kent Kammer verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 24(2020), 3 vom: 18. Jan., Seite 609-621 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:24 year:2020 number:3 day:18 month:01 pages:609-621 https://dx.doi.org/10.1007/s10008-020-04505-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_267 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE 35.90 ASE AR 24 2020 3 18 01 609-621 |
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Journal of solid state electrochemistry |
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Sažinas, Rokas @@aut@@ Andersen, Kjeld Bøhm @@aut@@ Hansen, Kent Kammer @@aut@@ |
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The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. 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Sažinas, Rokas |
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Sažinas, Rokas ddc 540 bkl 35.14 bkl 35.90 misc Silver misc Exsolution misc Nanoparticles misc SOFC misc Cathode misc LSF misc Oxygen reduction reaction Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
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540 ASE 35.14 bkl 35.90 bkl Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode Silver (dpeaa)DE-He213 Exsolution (dpeaa)DE-He213 Nanoparticles (dpeaa)DE-He213 SOFC (dpeaa)DE-He213 Cathode (dpeaa)DE-He213 LSF (dpeaa)DE-He213 Oxygen reduction reaction (dpeaa)DE-He213 |
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ddc 540 bkl 35.14 bkl 35.90 misc Silver misc Exsolution misc Nanoparticles misc SOFC misc Cathode misc LSF misc Oxygen reduction reaction |
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Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
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Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
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facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
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Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
abstract |
Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. |
abstractGer |
Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. |
abstract_unstemmed |
Abstract Single-phase silver (Ag)-doped $ La_{0.85-x} %$ Sr_{0.15} %$ Ag_{x} %$ FeO_{3-δ} $ (x = 0–0.05) materials (LSAF) were synthesized by wet synthesis route and calcined at 800 °C in air. The materials exhibited no thermal degradation in Ar and synthetic air below sintering temperature at 1200 °C of the cathode for solid oxide fuel cells. Exsolution of Ag nanoparticles from the perovskite lattice at 420 °C in reducing 5% $ H_{2} $/$ N_{2} $ was investigated, and electrocatalytic activity of the cathodes towards oxygen reduction reaction for solid oxide fuel cells was demonstrated. Scanning electron microscopy confirmed exsolution of Ag nanoparticles with increased effective surface area, and the particles were distributed with a good contact on the surface of the perovskite. Electrochemical performance of novel materials was tested and compared. Enhanced cathode with Ag nanoparticles revealed the area specific resistance of 0.23 and 0.15 Ω $ cm^{2} $ at 800 °C in 20% $ O_{2} $/$ N_{2} $ before and after Ag exsolution, respectively. The area specific resistance of the cathode decreased with Ag exsolution, operation temperature, and increasing oxygen partial pressure. |
collection_details |
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container_issue |
3 |
title_short |
Facilitating oxygen reduction by silver nanoparticles on lanthanum strontium ferrite cathode |
url |
https://dx.doi.org/10.1007/s10008-020-04505-5 |
remote_bool |
true |
author2 |
Andersen, Kjeld Bøhm Hansen, Kent Kammer |
author2Str |
Andersen, Kjeld Bøhm Hansen, Kent Kammer |
ppnlink |
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isOA_txt |
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hochschulschrift_bool |
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doi_str |
10.1007/s10008-020-04505-5 |
up_date |
2024-07-03T21:25:38.109Z |
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score |
7.4004736 |