Charge localization in one-dimensional tetramerized organic conductors: the special case of (tTTF)2ClO4
We report a detailed structural and spectroscopic study of the 1D 2:1 cation radical salt (tTTF)ClO, where tTTF = trimethylenetetrathiafulvalene, which exhibits a semiconductor-semiconductor phase transition at ca. T = 137 K. Crystal structures are determined above and below the transition; the...
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Veröffentlicht in: | Journal of physics. Condensed matter 2019-02, Vol.31 (15) |
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container_title | Journal of physics. Condensed matter |
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creator | Frąckowiak, Arkadiusz Świetlik, Roman Jeannin, Olivier Fourmigué, Marc Li, Weiwu Dressel, Martin |
description | We report a detailed structural and spectroscopic study of the 1D 2:1 cation radical salt (tTTF)ClO, where tTTF = trimethylenetetrathiafulvalene, which exhibits a semiconductor-semiconductor phase transition at ca. T = 137 K. Crystal structures are determined above and below the transition; the tTTF molecules in stacks are grouped into weakly interacting tetramers. The reorganization of tTTF stacks is accompanied with an order-disorder transition in anion sublattice. Polarized infrared and Raman spectra of (tTTF)ClO are measured in the broad frequency range as a function of the temperature (10-293 K). The structural and vibrational features are investigated to elucidate the origin of the semiconductor-semiconductor phase transition. We discuss the electron-intramolecular vibration coupling effects in the vibrational spectra of (tTTF)ClO and identify signatures of high- and low-temperature states of charge localization in the tetramerized system. Both the C=C and C-S stretching modes of tTTF give evidence of strong charge distribution fluctuations in conducting stacks for T > 137 K, which are responsible for the appearance of molecules with charge +1e, and charge localization in tTTF tetramers for T |
doi_str_mv | 10.1088/1361-648X/ab00b5 |
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T = 137 K. Crystal structures are determined above and below the transition; the tTTF molecules in stacks are grouped into weakly interacting tetramers. The reorganization of tTTF stacks is accompanied with an order-disorder transition in anion sublattice. Polarized infrared and Raman spectra of (tTTF)ClO are measured in the broad frequency range as a function of the temperature (10-293 K). The structural and vibrational features are investigated to elucidate the origin of the semiconductor-semiconductor phase transition. We discuss the electron-intramolecular vibration coupling effects in the vibrational spectra of (tTTF)ClO and identify signatures of high- and low-temperature states of charge localization in the tetramerized system. Both the C=C and C-S stretching modes of tTTF give evidence of strong charge distribution fluctuations in conducting stacks for T > 137 K, which are responsible for the appearance of molecules with charge +1e, and charge localization in tTTF tetramers for T < 137 K. The uniqueness of the salt (tTTF)ClO in comparison with other tetramerized 1D systems is discussed.</description><identifier>ISSN: 0953-8984</identifier><identifier>EISSN: 1361-648X</identifier><identifier>DOI: 10.1088/1361-648X/ab00b5</identifier><identifier>PMID: 30669131</identifier><language>eng</language><publisher>IOP Publishing [1989-....]</publisher><subject>Chemical Sciences ; Condensed Matter ; Material chemistry ; Materials Science ; Physics</subject><ispartof>Journal of physics. 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Condensed matter</title><description>We report a detailed structural and spectroscopic study of the 1D 2:1 cation radical salt (tTTF)ClO, where tTTF = trimethylenetetrathiafulvalene, which exhibits a semiconductor-semiconductor phase transition at ca. T = 137 K. Crystal structures are determined above and below the transition; the tTTF molecules in stacks are grouped into weakly interacting tetramers. The reorganization of tTTF stacks is accompanied with an order-disorder transition in anion sublattice. Polarized infrared and Raman spectra of (tTTF)ClO are measured in the broad frequency range as a function of the temperature (10-293 K). The structural and vibrational features are investigated to elucidate the origin of the semiconductor-semiconductor phase transition. We discuss the electron-intramolecular vibration coupling effects in the vibrational spectra of (tTTF)ClO and identify signatures of high- and low-temperature states of charge localization in the tetramerized system. Both the C=C and C-S stretching modes of tTTF give evidence of strong charge distribution fluctuations in conducting stacks for T > 137 K, which are responsible for the appearance of molecules with charge +1e, and charge localization in tTTF tetramers for T < 137 K. 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Condensed matter</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frąckowiak, Arkadiusz</au><au>Świetlik, Roman</au><au>Jeannin, Olivier</au><au>Fourmigué, Marc</au><au>Li, Weiwu</au><au>Dressel, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Charge localization in one-dimensional tetramerized organic conductors: the special case of (tTTF)2ClO4</atitle><jtitle>Journal of physics. Condensed matter</jtitle><date>2019-02-18</date><risdate>2019</risdate><volume>31</volume><issue>15</issue><issn>0953-8984</issn><eissn>1361-648X</eissn><abstract>We report a detailed structural and spectroscopic study of the 1D 2:1 cation radical salt (tTTF)ClO, where tTTF = trimethylenetetrathiafulvalene, which exhibits a semiconductor-semiconductor phase transition at ca. T = 137 K. Crystal structures are determined above and below the transition; the tTTF molecules in stacks are grouped into weakly interacting tetramers. The reorganization of tTTF stacks is accompanied with an order-disorder transition in anion sublattice. Polarized infrared and Raman spectra of (tTTF)ClO are measured in the broad frequency range as a function of the temperature (10-293 K). The structural and vibrational features are investigated to elucidate the origin of the semiconductor-semiconductor phase transition. We discuss the electron-intramolecular vibration coupling effects in the vibrational spectra of (tTTF)ClO and identify signatures of high- and low-temperature states of charge localization in the tetramerized system. Both the C=C and C-S stretching modes of tTTF give evidence of strong charge distribution fluctuations in conducting stacks for T > 137 K, which are responsible for the appearance of molecules with charge +1e, and charge localization in tTTF tetramers for T < 137 K. The uniqueness of the salt (tTTF)ClO in comparison with other tetramerized 1D systems is discussed.</abstract><pub>IOP Publishing [1989-....]</pub><pmid>30669131</pmid><doi>10.1088/1361-648X/ab00b5</doi><orcidid>https://orcid.org/0000-0002-1411-5656</orcidid><orcidid>https://orcid.org/0000-0002-3796-4802</orcidid><orcidid>https://orcid.org/0000-0002-3796-4802</orcidid><orcidid>https://orcid.org/0000-0002-1411-5656</orcidid><oa>free_for_read</oa></addata></record> |
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title | Charge localization in one-dimensional tetramerized organic conductors: the special case of (tTTF)2ClO4 |
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