Show simple item record

dc.contributor.authorPoelking, Carl
dc.contributor.authorCho, Eunkyung
dc.contributor.authorMalafeev, Alexander
dc.contributor.authorIvanov, Viktor
dc.contributor.authorKremer, Kurt
dc.contributor.authorRisko, Chad
dc.contributor.authorBrédas, Jean-Luc
dc.contributor.authorAndrienko, Denis
dc.date.accessioned2016-02-25T12:56:11Z
dc.date.available2016-02-25T12:56:11Z
dc.date.issued2013-01-31
dc.identifier.citationPoelking C, Cho E, Malafeev A, Ivanov V, Kremer K, et al. (2013) Characterization of Charge-Carrier Transport in Semicrystalline Polymers: Electronic Couplings, Site Energies, and Charge-Carrier Dynamics in Poly(bithiophene- alt -thienothiophene) [PBTTT] . The Journal of Physical Chemistry C 117: 1633–1640. Available: http://dx.doi.org/10.1021/jp311160y.
dc.identifier.issn1932-7447
dc.identifier.issn1932-7455
dc.identifier.doi10.1021/jp311160y
dc.identifier.urihttp://hdl.handle.net/10754/597757
dc.description.abstractWe establish a link between the microscopic ordering and the charge-transport parameters for a highly crystalline polymeric organic semiconductor, poly(2,5-bis(3-tetradecylthiophen-2-yl)thieno[3,2-b]thiophene) (PBTTT). We find that the nematic and dynamic order parameters of the conjugated backbones, as well as their separation, evolve linearly with temperature, while the side-chain dynamic order parameter and backbone paracrystallinity change abruptly upon the (also experimentally observed) melting of the side chains around 400 K. The distribution of site energies follows the behavior of the backbone paracrystallinity and can be treated as static on the time scale of a single-charge transfer reaction. On the contrary, the electronic couplings between adjacent backbones are insensitive to side-chain melting and vary on a much faster time scale. The hole mobility, calculated after time-averaging of the electronic couplings, reproduces well the value measured in a short-channel thin-film transistor. The results underline that to secure efficient charge transport in lamellar arrangements of conjugated polymers: (i) the electronic couplings should present high average values and fast dynamics, and (ii) the energetic disorder (paracrystallinity) should be small. © 2013 American Chemical Society.
dc.description.sponsorshipThe work in Maim was partly supported by the DFG programs IRTG 1328 and SPP 1355, and BMBF grants MESOMERIE and MEDOS. The work at Georgia Tech was supported by the Center for Advanced Molecular Photovoltaics funded through the King Abdullah University of Science and Technology (KAUST). We are grateful to Bjorn Baumeier, Pascal Kordt, Anton Melnyk, Kostas Daoulas, Patrick Gemunden, and Mara Jochum for critical reading of the manuscript.
dc.publisherAmerican Chemical Society (ACS)
dc.titleCharacterization of Charge-Carrier Transport in Semicrystalline Polymers: Electronic Couplings, Site Energies, and Charge-Carrier Dynamics in Poly(bithiophene- alt -thienothiophene) [PBTTT]
dc.typeArticle
dc.identifier.journalThe Journal of Physical Chemistry C
dc.contributor.institutionMax Planck Institute for Polymer Research, Mainz, Germany
dc.contributor.institutionGeorgia Institute of Technology, Atlanta, United States
dc.contributor.institutionLomonosov Moscow State University, Moscow, Russian Federation
kaust.grant.fundedcenterCenter for Advanced Molecular Photovoltaics (CAMP)


This item appears in the following Collection(s)

Show simple item record