H
Hajime Yamagata
Researcher at Temple University
Publications - 15
Citations - 1861
Hajime Yamagata is an academic researcher from Temple University. The author has contributed to research in topics: Exciton & Photoluminescence. The author has an hindex of 13, co-authored 15 publications receiving 1668 citations.
Papers
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Journal ArticleDOI
J-Aggregate Behavior in Poly-3-hexylthiophene Nanofibers
Edwards T. Niles,John D. Roehling,Hajime Yamagata,Adam J. Wise,Frank C. Spano,Adam J. Moulé,John K. Grey +6 more
TL;DR: In this article, a delicate interplay exists between intrachain order and inter-chain coupling as revealed through the emission 0−0/0−1 vibronic intensity ratios of poly-3-hexylthiophene (P3HT) assembled in toluene.
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Charge-transfer excitations steer the Davydov splitting and mediate singlet exciton fission in pentacene.
TL;DR: An admixture of charge-transfer excitations into the lowest singlet excited states form the origin of the Davydov splitting and mediate instantaneous singlet exciton fission by direct optical excitation of coherently coupled single and double exciton states, in agreement with recent experiments.
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Interplay between intrachain and interchain interactions in semiconducting polymer assemblies: the HJ-aggregate model.
Hajime Yamagata,Frank C. Spano +1 more
TL;DR: A new model for analyzing the photophysics of polymer aggregates is introduced taking into account exciton motion along a polymer chain and across polymer chains, and the predictions neatly account for the H-like dominance exhibited by the PL from spin-cast films and the J- like dominance exhibited from highly ordered P3HT nanofibers self-assembled in toluene.
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The nature of singlet excitons in oligoacene molecular crystals.
Hajime Yamagata,Joseph E. Norton,Eric Hontz,Yoann Olivier,David Beljonne,Jean-Luc Brédas,Robert J. Silbey,Frank C. Spano +7 more
TL;DR: A theory for polarized absorption in crystalline oligoacenes is presented, which includes Frenkel exciton coupling, the coupling between Frenkel and charge-transfer (CT) excitons, and the coupling of all neutral and ionic excited states to the dominant ring-breathing vibrational mode.
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Vibronic coupling in J-aggregates and beyond: a direct means of determining the exciton coherence length from the photoluminescence spectrum.
Frank C. Spano,Hajime Yamagata +1 more
TL;DR: In the presence of disorder and for T > 0 K, λ2S(R) is closely approximated by the exciton coherence number N( coh), thereby providing a simple and direct way of extracting N(coh) from the photoluminescence spectrum.