Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation
Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochem...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Yue, Ruirui [verfasserIn] Yao, Zhangquan [verfasserIn] Geng, Jingyi [verfasserIn] Du, Yukou [verfasserIn] Xu, Jingkun [verfasserIn] Yang, Ping [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2012 |
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| Schlagwörter: |
3,4-Ethylenedioxythiophene (EDOT) |
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| Übergeordnetes Werk: |
Enthalten in: Journal of solid state electrochemistry - Berlin : Springer, 1997, 17(2012), 3 vom: 28. Okt., Seite 751-760 |
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| Übergeordnetes Werk: |
volume:17 ; year:2012 ; number:3 ; day:28 ; month:10 ; pages:751-760 |
| Links: |
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| DOI / URN: |
10.1007/s10008-012-1922-1 |
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| Katalog-ID: |
SPR007974507 |
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| 520 | |a Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. | ||
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| 650 | 4 | |a 3,4-Ethylenedioxythiophene (EDOT) |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Electrochemical copolymerization |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Electrocatalysis |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Platinum |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Formic acid |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Yao, Zhangquan |e verfasserin |4 aut | |
| 700 | 1 | |a Geng, Jingyi |e verfasserin |4 aut | |
| 700 | 1 | |a Du, Yukou |e verfasserin |4 aut | |
| 700 | 1 | |a Xu, Jingkun |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Ping |e verfasserin |4 aut | |
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| allfields |
10.1007/s10008-012-1922-1 doi (DE-627)SPR007974507 (SPR)s10008-012-1922-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Yue, Ruirui verfasserin aut Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 Yao, Zhangquan verfasserin aut Geng, Jingyi verfasserin aut Du, Yukou verfasserin aut Xu, Jingkun verfasserin aut Yang, Ping verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 17(2012), 3 vom: 28. Okt., Seite 751-760 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:17 year:2012 number:3 day:28 month:10 pages:751-760 https://dx.doi.org/10.1007/s10008-012-1922-1 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 35.14 ASE 35.90 ASE AR 17 2012 3 28 10 751-760 |
| spelling |
10.1007/s10008-012-1922-1 doi (DE-627)SPR007974507 (SPR)s10008-012-1922-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Yue, Ruirui verfasserin aut Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 Yao, Zhangquan verfasserin aut Geng, Jingyi verfasserin aut Du, Yukou verfasserin aut Xu, Jingkun verfasserin aut Yang, Ping verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 17(2012), 3 vom: 28. Okt., Seite 751-760 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:17 year:2012 number:3 day:28 month:10 pages:751-760 https://dx.doi.org/10.1007/s10008-012-1922-1 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 35.14 ASE 35.90 ASE AR 17 2012 3 28 10 751-760 |
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10.1007/s10008-012-1922-1 doi (DE-627)SPR007974507 (SPR)s10008-012-1922-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Yue, Ruirui verfasserin aut Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 Yao, Zhangquan verfasserin aut Geng, Jingyi verfasserin aut Du, Yukou verfasserin aut Xu, Jingkun verfasserin aut Yang, Ping verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 17(2012), 3 vom: 28. Okt., Seite 751-760 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:17 year:2012 number:3 day:28 month:10 pages:751-760 https://dx.doi.org/10.1007/s10008-012-1922-1 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 35.14 ASE 35.90 ASE AR 17 2012 3 28 10 751-760 |
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10.1007/s10008-012-1922-1 doi (DE-627)SPR007974507 (SPR)s10008-012-1922-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Yue, Ruirui verfasserin aut Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 Yao, Zhangquan verfasserin aut Geng, Jingyi verfasserin aut Du, Yukou verfasserin aut Xu, Jingkun verfasserin aut Yang, Ping verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 17(2012), 3 vom: 28. Okt., Seite 751-760 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:17 year:2012 number:3 day:28 month:10 pages:751-760 https://dx.doi.org/10.1007/s10008-012-1922-1 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 35.14 ASE 35.90 ASE AR 17 2012 3 28 10 751-760 |
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10.1007/s10008-012-1922-1 doi (DE-627)SPR007974507 (SPR)s10008-012-1922-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Yue, Ruirui verfasserin aut Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 Yao, Zhangquan verfasserin aut Geng, Jingyi verfasserin aut Du, Yukou verfasserin aut Xu, Jingkun verfasserin aut Yang, Ping verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 17(2012), 3 vom: 28. Okt., Seite 751-760 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:17 year:2012 number:3 day:28 month:10 pages:751-760 https://dx.doi.org/10.1007/s10008-012-1922-1 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 35.14 ASE 35.90 ASE AR 17 2012 3 28 10 751-760 |
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Enthalten in Journal of solid state electrochemistry 17(2012), 3 vom: 28. Okt., Seite 751-760 volume:17 year:2012 number:3 day:28 month:10 pages:751-760 |
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Enthalten in Journal of solid state electrochemistry 17(2012), 3 vom: 28. Okt., Seite 751-760 volume:17 year:2012 number:3 day:28 month:10 pages:751-760 |
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5-Aminoindole 3,4-Ethylenedioxythiophene (EDOT) Electrochemical copolymerization Electrocatalysis Platinum Formic acid |
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Journal of solid state electrochemistry |
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Yue, Ruirui @@aut@@ Yao, Zhangquan @@aut@@ Geng, Jingyi @@aut@@ Du, Yukou @@aut@@ Xu, Jingkun @@aut@@ Yang, Ping @@aut@@ |
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2012-10-28T00:00:00Z |
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The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">5-Aminoindole</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">3,4-Ethylenedioxythiophene (EDOT)</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electrochemical copolymerization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electrocatalysis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Platinum</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Formic acid</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yao, Zhangquan</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Geng, Jingyi</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Du, Yukou</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Xu, Jingkun</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yang, Ping</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of solid state electrochemistry</subfield><subfield code="d">Berlin : Springer, 1997</subfield><subfield code="g">17(2012), 3 vom: 28. 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|
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Yue, Ruirui |
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Yue, Ruirui ddc 540 bkl 35.14 bkl 35.90 misc 5-Aminoindole misc 3,4-Ethylenedioxythiophene (EDOT) misc Electrochemical copolymerization misc Electrocatalysis misc Platinum misc Formic acid Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation |
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540 ASE 35.14 bkl 35.90 bkl Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation 5-Aminoindole (dpeaa)DE-He213 3,4-Ethylenedioxythiophene (EDOT) (dpeaa)DE-He213 Electrochemical copolymerization (dpeaa)DE-He213 Electrocatalysis (dpeaa)DE-He213 Platinum (dpeaa)DE-He213 Formic acid (dpeaa)DE-He213 |
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ddc 540 bkl 35.14 bkl 35.90 misc 5-Aminoindole misc 3,4-Ethylenedioxythiophene (EDOT) misc Electrochemical copolymerization misc Electrocatalysis misc Platinum misc Formic acid |
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ddc 540 bkl 35.14 bkl 35.90 misc 5-Aminoindole misc 3,4-Ethylenedioxythiophene (EDOT) misc Electrochemical copolymerization misc Electrocatalysis misc Platinum misc Formic acid |
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ddc 540 bkl 35.14 bkl 35.90 misc 5-Aminoindole misc 3,4-Ethylenedioxythiophene (EDOT) misc Electrochemical copolymerization misc Electrocatalysis misc Platinum misc Formic acid |
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Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation |
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Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation |
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Yue, Ruirui Yao, Zhangquan Geng, Jingyi Du, Yukou Xu, Jingkun Yang, Ping |
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facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and edot and its use as pt catalyst support for formic acid electrooxidation |
| title_auth |
Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation |
| abstract |
Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. |
| abstractGer |
Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. |
| abstract_unstemmed |
Abstract 5-Aminoindole and 3,4-ethylenedioxythiophene (EDOT) were copolymerized electrochemically on a carbon cloth (CC) electrode in an aqueous sulfuric acid solution. The as-prepared copolymer was characterized by cyclic voltammogram, SEM, and UV-vis and FT-IR spectra through which the electrochemical properties, structure, and composition of the as-obtained copolymer were determined. The electrochemical activity and stability of the as-formed copolymer are significantly improved in comparison with poly(5-aminoindole) due to the incorporation of EDOT units into the conjugated chain. The copolymer film-modified CC electrode was used as substrate for Pt particle deposition (denoted as Pt/copolymer/CC), and then, its catalytic activity towards formic acid electrooxidation was studied. Experimental results indicate that the catalytic activity of Pt/copolymer/CC towards formic acid electrooxidation is enhanced in comparison with that of Pt/homopolymer/CC, which can be attributed to the homogeneous distribution of Pt nanoparticles on the copolymer/CC substrate and the improved electrochemical activity of the copolymer film. |
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Facile electrochemical synthesis of a conducting copolymer from 5-aminoindole and EDOT and its use as Pt catalyst support for formic acid electrooxidation |
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| score |
7.3984165 |