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Träfflista för sökning "WFRF:(Cai Tianqi) srt2:(2010-2014)"

Sökning: WFRF:(Cai Tianqi) > (2010-2014)

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1.
  • Cai, Tianqi, et al. (författare)
  • Low bandgap polymers synthesized by FeCl(3) oxidative polymerization
  • 2010
  • Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248. ; 94:7, s. 1275-1281
  • Tidskriftsartikel (refereegranskat)abstract
    • Four low bandgap polymers, combining an alkyl thiophene donor with benzo[c][1,2,5]thiadiazole, 2,3-diphenylquinoxaline, 2,3-diphenylthieno[3,4-b]pyrazine and 6,7-diphenyl-[1,2,5]thiadiazolo[3,4-g] quinoxaline acceptors in a donor-acceptor-donor architecture, were synthesized via FeCl3 oxidative polymerization. The molecular weights of the polymers were improved by introducing o-dichlor-obenzene (ODCB) as the reaction solvent instead of the commonly used solvent, chloroform. The photophysical, electrochemical and photovoltaic properties of the resulting polymers were investigated and compared. The optical bandgaps of the polymers vary between 1.0 and 1.9 eV, which is promising for solar cells. The devices spin-coated from an ODCB solution of P1DB:[70]PCBM showed a power conversion efficiency of 1.08% with an open-circuit voltage of 0.91 V and a short-circuit current density of 3.36 mA cm(-2) under irradiation from an AM1.5G solar simulator (100 mW cm(-2)). (C) 2010 Elsevier B.V. All rights reserved.
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2.
  • Hellström, Stefan, 1978, et al. (författare)
  • Influence of side chains on electrochromic properties of green donor-acceptor-donor polymers
  • 2011
  • Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686. ; 56:10, s. 3454-3459
  • Tidskriftsartikel (refereegranskat)abstract
    • Three solution processable cathodically coloring green electrochromic polymers, based on 2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine, have been synthesized by oxidative FeCl3 polymerization. The polymers were designed with solubilizing alkyl and oligoethylene oxide side chains to achieve solubility and processability. All three polymers have a small electrochemical bandgap (1.8-1.9 eV) and low oxidation potentials. Spectroelectrochemical studies of polymer films on ITO reveal that the alkyl side chains in head-to-head position on the polymer backbone promote a defined high-energy absorption peak and suppress tailing of charge-carrier absorption into the visible region. Kinetic studies, based on transmission measurements applying a square-wave potential between reduced and oxidized states, show that the polymer with exclusively oligoethylene oxide side chains (P3) had the fastest response times, monitored at the low-energy absorption maxima. The best performing polymer (P1) showed a good optical contrast in the visible region with a Delta T of 26% at 700 nm. An initial test of the electrochemical stability showed that the oligoethylene oxide containing polymers had superior stability over 500 full switches.
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