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Measurement of Ultrafast Photoinduced Electron Transfer from Chemically Anchored Ru-Dye Molecules into Empty Electronic States in a Colloidal Anatase TiO2 Film
Electron transfer from the excited electronic singlet state of chemisorbed ruthenium(II) cis-di(isothiocyanato)bis(2,2‘-bipyridyl-4,4‘-dicarboxylate) into empty electronic states in a colloidal anatase TiO2 film was measured as a transient absorption signal of the injected hot electrons with a rise...
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Published in: | The journal of physical chemistry. B 1997-08, Vol.101 (35), p.6799-6802 |
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container_end_page | 6802 |
container_issue | 35 |
container_start_page | 6799 |
container_title | The journal of physical chemistry. B |
container_volume | 101 |
creator | Hannappel, Thomas Burfeindt, Bernd Storck, Winfried Willig, Frank |
description | Electron transfer from the excited electronic singlet state of chemisorbed ruthenium(II) cis-di(isothiocyanato)bis(2,2‘-bipyridyl-4,4‘-dicarboxylate) into empty electronic states in a colloidal anatase TiO2 film was measured as a transient absorption signal of the injected hot electrons with a rise time |
doi_str_mv | 10.1021/jp971581q |
format | article |
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Optical absorption of the anchored dye molecules led to the excited singlet state of the dye with a small admixture of charge transfer states. The electron transfer reaction reported here did not involve redistribution of vibrational excitation energy and was thus completely different from the well-known Marcus−Levich−Jortner−Gerischer type of electron transfer in the case of weak electronic interaction. It was also not a direct optical charge transfer transition from the donor to the acceptor level but rather an electron transfer reaction with an ultrashort but finite reaction time.</description><identifier>ISSN: 1520-6106</identifier><identifier>EISSN: 1520-5207</identifier><identifier>DOI: 10.1021/jp971581q</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>The journal of physical chemistry. 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B</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hannappel, Thomas</au><au>Burfeindt, Bernd</au><au>Storck, Winfried</au><au>Willig, Frank</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measurement of Ultrafast Photoinduced Electron Transfer from Chemically Anchored Ru-Dye Molecules into Empty Electronic States in a Colloidal Anatase TiO2 Film</atitle><jtitle>The journal of physical chemistry. B</jtitle><addtitle>J. Phys. Chem. B</addtitle><date>1997-08-28</date><risdate>1997</risdate><volume>101</volume><issue>35</issue><spage>6799</spage><epage>6802</epage><pages>6799-6802</pages><issn>1520-6106</issn><eissn>1520-5207</eissn><abstract>Electron transfer from the excited electronic singlet state of chemisorbed ruthenium(II) cis-di(isothiocyanato)bis(2,2‘-bipyridyl-4,4‘-dicarboxylate) into empty electronic states in a colloidal anatase TiO2 film was measured as a transient absorption signal of the injected hot electrons with a rise time <25 fs. Optical absorption of the anchored dye molecules led to the excited singlet state of the dye with a small admixture of charge transfer states. The electron transfer reaction reported here did not involve redistribution of vibrational excitation energy and was thus completely different from the well-known Marcus−Levich−Jortner−Gerischer type of electron transfer in the case of weak electronic interaction. It was also not a direct optical charge transfer transition from the donor to the acceptor level but rather an electron transfer reaction with an ultrashort but finite reaction time.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp971581q</doi><tpages>4</tpages></addata></record> |
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title | Measurement of Ultrafast Photoinduced Electron Transfer from Chemically Anchored Ru-Dye Molecules into Empty Electronic States in a Colloidal Anatase TiO2 Film |
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