Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution
Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are de...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Marchesi, L. F. [verfasserIn] Freitas, R. G. [verfasserIn] Spada, E. R. [verfasserIn] Paula, F. R. [verfasserIn] Góes, M. S. [verfasserIn] Garcia, J. R. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2015 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of solid state electrochemistry - Berlin : Springer, 1997, 19(2015), 8 vom: 22. Apr., Seite 2205-2211 |
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| Übergeordnetes Werk: |
volume:19 ; year:2015 ; number:8 ; day:22 ; month:04 ; pages:2205-2211 |
| Links: |
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| DOI / URN: |
10.1007/s10008-015-2848-1 |
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| Katalog-ID: |
SPR007983832 |
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| 520 | |a Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. | ||
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| 650 | 4 | |a electrodes |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Cathodic electrodeposition |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Electrochemical impedance spectroscopy |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Freitas, R. G. |e verfasserin |4 aut | |
| 700 | 1 | |a Spada, E. R. |e verfasserin |4 aut | |
| 700 | 1 | |a Paula, F. R. |e verfasserin |4 aut | |
| 700 | 1 | |a Góes, M. S. |e verfasserin |4 aut | |
| 700 | 1 | |a Garcia, J. R. |e verfasserin |4 aut | |
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10.1007/s10008-015-2848-1 doi (DE-627)SPR007983832 (SPR)s10008-015-2848-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Marchesi, L. F. verfasserin aut Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 Freitas, R. G. verfasserin aut Spada, E. R. verfasserin aut Paula, F. R. verfasserin aut Góes, M. S. verfasserin aut Garcia, J. R. verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 19(2015), 8 vom: 22. Apr., Seite 2205-2211 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:19 year:2015 number:8 day:22 month:04 pages:2205-2211 https://dx.doi.org/10.1007/s10008-015-2848-1 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 19 2015 8 22 04 2205-2211 |
| spelling |
10.1007/s10008-015-2848-1 doi (DE-627)SPR007983832 (SPR)s10008-015-2848-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Marchesi, L. F. verfasserin aut Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 Freitas, R. G. verfasserin aut Spada, E. R. verfasserin aut Paula, F. R. verfasserin aut Góes, M. S. verfasserin aut Garcia, J. R. verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 19(2015), 8 vom: 22. Apr., Seite 2205-2211 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:19 year:2015 number:8 day:22 month:04 pages:2205-2211 https://dx.doi.org/10.1007/s10008-015-2848-1 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 19 2015 8 22 04 2205-2211 |
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10.1007/s10008-015-2848-1 doi (DE-627)SPR007983832 (SPR)s10008-015-2848-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Marchesi, L. F. verfasserin aut Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 Freitas, R. G. verfasserin aut Spada, E. R. verfasserin aut Paula, F. R. verfasserin aut Góes, M. S. verfasserin aut Garcia, J. R. verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 19(2015), 8 vom: 22. Apr., Seite 2205-2211 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:19 year:2015 number:8 day:22 month:04 pages:2205-2211 https://dx.doi.org/10.1007/s10008-015-2848-1 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 19 2015 8 22 04 2205-2211 |
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10.1007/s10008-015-2848-1 doi (DE-627)SPR007983832 (SPR)s10008-015-2848-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Marchesi, L. F. verfasserin aut Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 Freitas, R. G. verfasserin aut Spada, E. R. verfasserin aut Paula, F. R. verfasserin aut Góes, M. S. verfasserin aut Garcia, J. R. verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 19(2015), 8 vom: 22. Apr., Seite 2205-2211 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:19 year:2015 number:8 day:22 month:04 pages:2205-2211 https://dx.doi.org/10.1007/s10008-015-2848-1 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 19 2015 8 22 04 2205-2211 |
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10.1007/s10008-015-2848-1 doi (DE-627)SPR007983832 (SPR)s10008-015-2848-1-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl 35.90 bkl Marchesi, L. F. verfasserin aut Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 Freitas, R. G. verfasserin aut Spada, E. R. verfasserin aut Paula, F. R. verfasserin aut Góes, M. S. verfasserin aut Garcia, J. R. verfasserin aut Enthalten in Journal of solid state electrochemistry Berlin : Springer, 1997 19(2015), 8 vom: 22. Apr., Seite 2205-2211 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:19 year:2015 number:8 day:22 month:04 pages:2205-2211 https://dx.doi.org/10.1007/s10008-015-2848-1 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 19 2015 8 22 04 2205-2211 |
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F.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Photoanodes</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ITO/TiO</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">electrodes</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cathodic electrodeposition</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Electrochemical impedance spectroscopy</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Freitas, R. G.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Spada, E. R.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Paula, F. R.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Góes, M. S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Garcia, J. 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|
| author |
Marchesi, L. F. |
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Marchesi, L. F. ddc 540 bkl 35.14 bkl 35.90 misc Photoanodes misc ITO/TiO misc electrodes misc Cathodic electrodeposition misc Electrochemical impedance spectroscopy Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
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Marchesi, L. F. |
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540 ASE 35.14 bkl 35.90 bkl Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution Photoanodes (dpeaa)DE-He213 ITO/TiO (dpeaa)DE-He213 electrodes (dpeaa)DE-He213 Cathodic electrodeposition (dpeaa)DE-He213 Electrochemical impedance spectroscopy (dpeaa)DE-He213 |
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ddc 540 bkl 35.14 bkl 35.90 misc Photoanodes misc ITO/TiO misc electrodes misc Cathodic electrodeposition misc Electrochemical impedance spectroscopy |
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ddc 540 bkl 35.14 bkl 35.90 misc Photoanodes misc ITO/TiO misc electrodes misc Cathodic electrodeposition misc Electrochemical impedance spectroscopy |
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ddc 540 bkl 35.14 bkl 35.90 misc Photoanodes misc ITO/TiO misc electrodes misc Cathodic electrodeposition misc Electrochemical impedance spectroscopy |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
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(DE-627)SPR007983832 (SPR)s10008-015-2848-1-e |
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Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
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Marchesi, L. F. |
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Journal of solid state electrochemistry |
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Journal of solid state electrochemistry |
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Marchesi, L. F. Freitas, R. G. Spada, E. R. Paula, F. R. Góes, M. S. Garcia, J. R. |
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19 |
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540 ASE 35.14 bkl 35.90 bkl |
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Elektronische Aufsätze |
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Marchesi, L. F. |
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10.1007/s10008-015-2848-1 |
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540 |
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verfasserin |
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photoelectrochemical characterization of ito/$ tio_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
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Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
| abstract |
Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. |
| abstractGer |
Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. |
| abstract_unstemmed |
Abstract In the present work, the photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes electrosynthesized at two distinct $ TiO_{2} $ film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay. |
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Photoelectrochemical characterization of ITO/$ TiO_{2} $ electrodes obtained by cathodic electrodeposition from aqueous solution |
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https://dx.doi.org/10.1007/s10008-015-2848-1 |
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Freitas, R. G. Spada, E. R. Paula, F. R. Góes, M. S. Garcia, J. R. |
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Freitas, R. G. Spada, E. R. Paula, F. R. Góes, M. S. Garcia, J. R. |
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10.1007/s10008-015-2848-1 |
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| score |
7.4011183 |