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Identifying Charge-Transfer States in Polymer:Fullerene Heterojunctions by Their Emission Polarization Anisotropy

Arndt, Andreas P. 1; Gerhard, Marina; Koch, Martin; Lemmer, Uli 1,2; Howard, Ian A. 2
1 Lichttechnisches Institut (LTI), Karlsruher Institut für Technologie (KIT)
2 Institut für Mikrostrukturtechnik (IMT), Karlsruher Institut für Technologie (KIT)

Abstract (englisch):

We investigate the time-resolved photoluminescence (PL) polarization anisotropy of the organic photovoltaic model systems P3HT:PC61BM and PTB7:PC71BM, and their corresponding neat polymer films. Both blends show a strong emission from interfacial charge-transfer states (CTSs); the CTS emission can be uniquely identified by its negative polarization anisotropy, which is indicative of a significant rotation of the transition dipole moment upon charge transfer at the donor–acceptor interface. We also observe a spectral region showing negative anisotropy in the PL of the neat PTB7 film; this spectral region is at slightly higher energy than the blend CTS emission. This negative anisotropy is not observed in the emission spectrum of the polymer in solution. This suggests that some emissive states in the pristine PTB7 film have transition dipole moments rotated relative to the absorbing states; we interpret these to be states with a significant interchain charge-transfer character.


Originalveröffentlichung
DOI: 10.1021/acs.jpcc.6b12853
Web of Science
Zitationen: 8
Dimensions
Zitationen: 8
Zugehörige Institution(en) am KIT Institut für Mikrostrukturtechnik (IMT)
Universität Karlsruhe (TH) – Interfakultative Einrichtungen (Interfakultative Einrichtungen)
Karlsruhe School of Optics & Photonics (KSOP)
Lichttechnisches Institut (LTI)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2017
Sprache Englisch
Identifikator ISSN: 1932-7447, 1932-7455
KITopen-ID: 1000070137
HGF-Programm 43.23.04 (POF III, LK 01) Nanophotonics for Energy Conversion
Erschienen in The journal of physical chemistry <Washington, DC> / C
Verlag American Chemical Society (ACS)
Band 121
Heft 11
Seiten 6357–6364
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