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Molecular Engineering of D-D-?-A-Based Organic Sensitizers for Enhanced Dye-Sensitized Solar Cell Performance.


ABSTRACT: A series of molecularly engineered and novel dyes WS1, WS2, WS3, and WS4, based on the D35 donor, 1-(4-hexylphenyl)-2,5-di(thiophen-2-yl)-1H-pyrrole and 4-(4-hexylphenyl)-4H-dithieno[3,2-b:2',3'-d]pyrrole as ?-conjugating linkers, were synthesized and compared to the well-known LEG4 dye. The performance of the dyes was investigated in combination with an electrolyte based on Co(II/III) complexes as redox shuttles. The electron recombination between the redox mediators in the electrolyte and the TiO2 interface decreases upon the introduction of 4-hexylybenzene entities on the 2,5-di(thiophen-2-yl)-1H-pyrrole and 4H-dithieno[3,2-b:2',3'-d]pyrrole linker units, probably because of steric hindrance. The open circuit photovoltage of WS1-, WS2-, WS3-, and WS4-based devices in combination with the Co(II/III)-based electrolyte are consistently higher than those based on a I-/I3 - electrolyte by 105, 147, 167, and 75 mV, respectively. The WS3-based devices show the highest power conversion efficiency of 7.4% at AM 1.5 G 100 mW/cm2 illumination mainly attributable to the high open-circuit voltage (V OC).

SUBMITTER: Sharmoukh W 

PROVIDER: S-EPMC6641492 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Molecular Engineering of D-D-π-A-Based Organic Sensitizers for Enhanced Dye-Sensitized Solar Cell Performance.

Sharmoukh Walid W   Cong Jiayan J   Gao Jiajia J   Liu Peng P   Daniel Quentin Q   Kloo Lars L  

ACS omega 20180404 4


A series of molecularly engineered and novel dyes WS1, WS2, WS3, and WS4, based on the D35 donor, 1-(4-hexylphenyl)-2,5-di(thiophen-2-yl)-1<i>H</i>-pyrrole and 4-(4-hexylphenyl)-4<i>H</i>-dithieno[3,2-<i>b</i>:2',3'-<i>d</i>]pyrrole as π-conjugating linkers, were synthesized and compared to the well-known LEG4 dye. The performance of the dyes was investigated in combination with an electrolyte based on Co(II/III) complexes as redox shuttles. The electron recombination between the redox mediators  ...[more]

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