440 research outputs found
Quantum confinement effects on the ordering of the lowest-lying excited states in conjugated chains
The symmetrized density matrix renormalization group approach is applied
within the extended Hubbard-Peierls model (with parameters U/t, V/t, and bond
alternation \delta) to study the ordering of the lowest one-photon
(1^{1}B^{-}_u) and two-photon (2^{1}A^{+}_g) states in one- dimensional
conjugated systems with chain lengths, N, up to N=80 sites. Three different
types of crossovers are studied, as a function of U/t, \delta, and N. The
U-crossover emphasizes the larger ionic character of the 2A_g state compared to
the lowest triplet excitation. The \delta crossover shows strong dependence on
both N and U/t. The N-crossover illustrates the more localized nature of the
2A_g excitation relative to the 1B_u excitation at intermediate correlation
strengths.Comment: Latex file; figures available upon request. Submitted to PR
Quantum inelastic conductance through molecular wires
We calculate non-perturbatively the inelastic effects on the conductance
through a conjugated molecular wire-metal heterojunction, including realistic
electron-phonon coupling. We show that at sub-band-gap energies the current is
dominated by quantum coherent transport of virtual polarons through the
molecule. In this regime, the tunneling current is strongly increased relative
to the case of elastic scattering. It is essential to describe the full quantum
coherence of the polaron formation and transport in order to obtain correct
physics. Our results are generally applicable to one-dimensional atomic or
molecular wires.Comment: 4 pages, 4 figures, accepted for publication in Physical Review
Letter
Unification of trap-limited electron transport in semiconducting polymers
Electron transport in semiconducting polymers is usually inferior to hole transport, which is ascribed to charge trapping on isolated defect sites situated within the energy bandgap. However, a general understanding of the origin of these omnipresent charge traps, as well as their energetic position, distribution and concentration, is lacking. Here we investigate electron transport in a wide range of semiconducting polymers by current-voltage measurements of single-carrier devices. We observe for this materials class that electron transport is limited by traps that exhibit a Gaussian energy distribution in the bandgap. Remarkably, the electron-trap distribution is identical for all polymers considered: the number of traps amounts to 3 × 1023 traps per m3 centred at an energy of ∼3.6 eV below the vacuum level, with a typical distribution width of ∼0.1 eV. This indicates that the electron traps have a common origin that, we suggest, is most likely related to hydrated oxygen complexes. A consequence of this finding is that the trap-limited electron current can be predicted for any polymer. © 2012 Macmillan Publishers Limited. All rights reserved
Strong Suppression of Thermal Conductivity in the Presence of Long Terminal Alkyl Chains in Low-Disorder Molecular Semiconductors
While the charge transport properties of organic semiconductors have been extensively studied over the recent years, the field of organics-based thermoelectrics is still limited by a lack of experimental data on thermal transport and of understanding of the associated structure–property relationships. To fill this gap, a comprehensive experimental and theoretical investigation of the lattice thermal conductivity in polycrystalline thin films of dinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene (Cn-DNTT-Cn with n = 0, 8) semiconductors is reported. Strikingly, thermal conductivity appears to be much more isotropic than charge transport, which is confined to the 2D molecular layers. A direct comparison between experimental measurements (3ω–Völklein method) and theoretical estimations (approach-to-equilibrium molecular dynamics (AEMD) method) indicates that the in-plane thermal conductivity is strongly reduced in the presence of the long terminal alkyl chains. This evolution can be rationalized by the strong localization of the intermolecular vibrational modes in C8-DNTT-C8 in comparison to unsubstituted DNTT cores, as evidenced by a vibrational mode analysis. Combined with the enhanced charge transport properties of alkylated DNTT systems, this opens the possibility to decouple electron and phonon transport in these materials, which provides great potential for enhancing the thermoelectric figure of merit ZT
Valence bands of poly(methylmethacrylate) and photoion emission in vacuum ultraviolet region
Photoion and photoelectron yields were measured for poly(methylmethacrylate) in the photon energy region of 8–40 eV using synchrotron radiation. Further, the valence‐band structure was investigated with ultraviolet photoelectron spectra and valence effective Hamiltonian calculations. A significant difference was observed between the photon energy dependencies of photoion and photoelectron yields. The threshold energy for photoion emission was found to be 10.5 eV, while that for photoelectron emission was 8.5 eV, indicating holes created near the valence‐band top do not contribute to the ion emission. At the higher‐energy region, the ion emission efficiency was found to be enhanced in the photon energy region of 17–28 eV. The difference between the threshold energies of photoion and photoelectron emission and the enhancement of the photoion emission are discussed in conjunction with the valence‐band [email protected] ; [email protected]
Photoinduced absorption and photoluminescence in poly(2,5-dimethoxy-p- phenylene vinylene)
We report a study of the photoexcited states in the conjugated polymer poly(2,5-dimethoxy-p-phenylene vinylene). Photoluminescence due to radiative recombination of singlet excitons is observed at energiesjust below the onset of the pi-pi* absorption band at 2.1 eV. Photoinduced absorption at 80 K shows bands peaking at 0.68, 1.35, and 1.80 eV. The features at 0.68 and 1.8 eV are associated with the same excited state which we propose is a doubly charged bipolaron, while the third at 1.35 eV is unrelated. We assign this 1.35-eV absorption to a triplet-triplet transition of a triplet exciton. The bipolarons are long lived with significant numbers surviving in excess of 100 ms at 80 K, and have a weak temperature dependence such that photoinduced absorption is readily detectable even at room temperature. The triplet exciton has a lifetime of order 2.5 ms at 80 K but this falls rapidly at higher temperature and the response is not detected at room temperature. We contrast these results with those obtained previously for the related poly(arylene vinylene) polymers poly(p-phenylene vinylene), and poly(2,5-thienylene vinylene) and for other conjugated polymers, and draw attention to the important role played in the photophysics of these materials by neutral excited states
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