Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $
Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was inves...
Ausführliche Beschreibung
Autor*in: |
Lu, Sheng-li [verfasserIn] Geng, Rui [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2013 |
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Enthalten in: Chemical Research in Chinese Universities - Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012, 29(2013), 6 vom: 15. Nov., Seite 1208-1213 |
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Übergeordnetes Werk: |
volume:29 ; year:2013 ; number:6 ; day:15 ; month:11 ; pages:1208-1213 |
Links: |
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DOI / URN: |
10.1007/s40242-013-3116-5 |
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SPR03291007X |
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10.1007/s40242-013-3116-5 doi (DE-627)SPR03291007X (SPR)s40242-013-3116-5-e DE-627 ger DE-627 rakwb eng Lu, Sheng-li verfasserin aut Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 Geng, Rui verfasserin aut Enthalten in Chemical Research in Chinese Universities Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012 29(2013), 6 vom: 15. Nov., Seite 1208-1213 (DE-627)SPR03290777X nnns volume:29 year:2013 number:6 day:15 month:11 pages:1208-1213 https://dx.doi.org/10.1007/s40242-013-3116-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA AR 29 2013 6 15 11 1208-1213 |
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10.1007/s40242-013-3116-5 doi (DE-627)SPR03291007X (SPR)s40242-013-3116-5-e DE-627 ger DE-627 rakwb eng Lu, Sheng-li verfasserin aut Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 Geng, Rui verfasserin aut Enthalten in Chemical Research in Chinese Universities Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012 29(2013), 6 vom: 15. Nov., Seite 1208-1213 (DE-627)SPR03290777X nnns volume:29 year:2013 number:6 day:15 month:11 pages:1208-1213 https://dx.doi.org/10.1007/s40242-013-3116-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA AR 29 2013 6 15 11 1208-1213 |
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10.1007/s40242-013-3116-5 doi (DE-627)SPR03291007X (SPR)s40242-013-3116-5-e DE-627 ger DE-627 rakwb eng Lu, Sheng-li verfasserin aut Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 Geng, Rui verfasserin aut Enthalten in Chemical Research in Chinese Universities Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012 29(2013), 6 vom: 15. Nov., Seite 1208-1213 (DE-627)SPR03290777X nnns volume:29 year:2013 number:6 day:15 month:11 pages:1208-1213 https://dx.doi.org/10.1007/s40242-013-3116-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA AR 29 2013 6 15 11 1208-1213 |
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10.1007/s40242-013-3116-5 doi (DE-627)SPR03291007X (SPR)s40242-013-3116-5-e DE-627 ger DE-627 rakwb eng Lu, Sheng-li verfasserin aut Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 Geng, Rui verfasserin aut Enthalten in Chemical Research in Chinese Universities Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012 29(2013), 6 vom: 15. Nov., Seite 1208-1213 (DE-627)SPR03290777X nnns volume:29 year:2013 number:6 day:15 month:11 pages:1208-1213 https://dx.doi.org/10.1007/s40242-013-3116-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA AR 29 2013 6 15 11 1208-1213 |
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10.1007/s40242-013-3116-5 doi (DE-627)SPR03291007X (SPR)s40242-013-3116-5-e DE-627 ger DE-627 rakwb eng Lu, Sheng-li verfasserin aut Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 Geng, Rui verfasserin aut Enthalten in Chemical Research in Chinese Universities Jilin University and The Editorial Department of Chemical Research in Chinese Universities, 2012 29(2013), 6 vom: 15. Nov., Seite 1208-1213 (DE-627)SPR03290777X nnns volume:29 year:2013 number:6 day:15 month:11 pages:1208-1213 https://dx.doi.org/10.1007/s40242-013-3116-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA AR 29 2013 6 15 11 1208-1213 |
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Lu, Sheng-li misc electrochemical polymerization misc Hybrid photovoltaic device misc Photovoltaic characterization Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ |
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Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ electrochemical polymerization (dpeaa)DE-He213 Hybrid photovoltaic device (dpeaa)DE-He213 Photovoltaic characterization (dpeaa)DE-He213 |
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efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ tio_{2} $ |
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Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ |
abstract |
Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. |
abstractGer |
Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. |
abstract_unstemmed |
Abstract Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. The mechanism of overall photovoltaic parameter improvement was discussed. |
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Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $ |
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10.1007/s40242-013-3116-5 |
up_date |
2024-07-03T15:24:42.304Z |
_version_ |
1803571987548733440 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR03291007X</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519171535.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201007s2013 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s40242-013-3116-5</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR03291007X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s40242-013-3116-5-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Lu, Sheng-li</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Efficient hybrid photovoltaic devices based on in-situ electrochemical copolymerization of 3-methylthiophene and bithiophene into pores of nanocrystalline $ TiO_{2} $</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2013</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 Novel organic and inorganic hybrid photovoltaic devices were fabricated by in-situ electrochemical copolymerization of 3-methylthiophene(3MT) and bithiophene(BT) into the pores of nanostructured $ TiO_{2} $ sintered on fluorine-doped tin oxide(FTO) substrate. The photoactive layer was investigated by Fourier transform infrared(FTIR) spectroscopy, ultraviolet-visable(UV-Vis) spectrometer, scanning electron microscope(SEM) and cyclic voltammogram characterization. Device efficiency based on different molar feed ratios of 3MT and BT during electrochemical polymerization, and the effect of in-situ copolymer state(doped by electrolyte and de-doped) were measured and compared. Under the solar illumination of 100 mW/$ cm^{2} $(AM1.5), an optimized device efficiency of 0.938% was obtained when the molar ratio of 3MT to BT was 500:1, polymerization time was 500 s and the system was in doped copolymer state, respectively. 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7.3984594 |