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Light-induced electrolyte improvement in cobalt tris(bipyridine)-mediated dye-sensitized solar cells

Lithium-ion-free tris(2,2′-bipyridine) Co( ii / iii )-mediated electrolytes have previously been proposed for long-term stable dye-sensitized solar cells (DSSCs). Such redox systems also offer an impressive DSSC performance improvement under light soaking exposure, manifested by an increase in photo...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (33), p.19495-1955
Main Authors: Gao, Jiajia, Yang, Wenxing, El-Zohry, Ahmed M, Prajapati, Govind Kumar, Fang, Yuan, Dai, Jing, Hao, Yan, Leandri, Valentina, Svensson, Per H, Furó, István, Boschloo, Gerrit, Lund, Torben, Kloo, Lars
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cited_by cdi_FETCH-LOGICAL-c465t-1c6de4f2085e2690b55b1461a0d028c3b5ad94ab88b4867931b4fa3186bce42d3
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container_end_page 1955
container_issue 33
container_start_page 19495
container_title Journal of materials chemistry. A, Materials for energy and sustainability
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creator Gao, Jiajia
Yang, Wenxing
El-Zohry, Ahmed M
Prajapati, Govind Kumar
Fang, Yuan
Dai, Jing
Hao, Yan
Leandri, Valentina
Svensson, Per H
Furó, István
Boschloo, Gerrit
Lund, Torben
Kloo, Lars
description Lithium-ion-free tris(2,2′-bipyridine) Co( ii / iii )-mediated electrolytes have previously been proposed for long-term stable dye-sensitized solar cells (DSSCs). Such redox systems also offer an impressive DSSC performance improvement under light soaking exposure, manifested by an increase in photocurrent and fill factor without the expense of decreasing photovoltage. Kinetic studies show that charge transfer and ion diffusion at the electrode/electrolyte interface are improved due to the light exposure. Control experiments reveal that the light effect is unambiguously associated with electrolyte components, [Co(bpy) 3 ] 3+ and the Lewis-base additive tert -butylpyridine (TBP). Electrochemical and spectroscopic investigation of the [Co(bpy) 3 ] 3+ /TBP mixtures points out that the presence of TBP, which retards the electrolyte diffusion, however causes an irreversible redox reaction of [Co(bpy) 3 ] 3+ upon light exposure that improves the overall conductivity. This discovery not only provides a new strategy to mitigate the typical J sc - V oc trade-off in Co( ii / iii )-mediated DSSCs but also highlights the importance of investigating the photochemistry of a photoelectrochemical system. We observe a light-induced performance improvement in Co( ii / iii )-mediated DSSCs, and attribute this to an irreversible light effect on the electrolyte system containing Co( iii ) together with tert-butylpyridine (TBP).
doi_str_mv 10.1039/c9ta07198a
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subjects Absorption spectra
Charge transfer
Cobalt
Control experiments
Dye-sensitized solar cells
Dyes
Economic and social effects
Electrochemistry
Electrode/electrolyte interfaces
Electrolytes
Electrolytic cells
Exposure
Infrared absorption
Infrared spectra
Ion charge
Ion diffusion
Light effects
Light exposure
Lithium
Lithium ions
NMR
Nuclear magnetic resonance
Photo-voltage
Photochemistry
Photoelectric effect
Photoelectric emission
Photoelectrochemical system
Photovoltaic cells
Photovoltaics
Redox reactions
Redox systems
Regeneration
Solar cells
Spectroscopic investigations
title Light-induced electrolyte improvement in cobalt tris(bipyridine)-mediated dye-sensitized solar cells
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