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The influence of phosphonic acid protonation state on the efficiency of bis(diimine)copper() dye-sensitized solar cells

We present an investigation of the effects of a change in the protonation state of the phosphonic acid anchoring ligand in the dye [Cu(H 4 1 )( 2 )][PF 6 ] (H 4 1 = ((6,6′-dimethyl-[2,2′-bipyridine]-4,4′-diyl)bis(4,1-phenylene))bis(phosphonic acid), 2 = 4,4′-bis(4-bromophenyl)-6,6′-dimethyl-2,2′-bip...

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Published in:Sustainable energy & fuels 2018, Vol.2 (4), p.786-794
Main Authors: Stephens, Alexander J, Malzner, Frederik J, Constable, Edwin C, Housecroft, Catherine E
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description We present an investigation of the effects of a change in the protonation state of the phosphonic acid anchoring ligand in the dye [Cu(H 4 1 )( 2 )][PF 6 ] (H 4 1 = ((6,6′-dimethyl-[2,2′-bipyridine]-4,4′-diyl)bis(4,1-phenylene))bis(phosphonic acid), 2 = 4,4′-bis(4-bromophenyl)-6,6′-dimethyl-2,2′-bipyridine) on the performance of n-type dye-sensitized solar cells (DSCs). FTO/TiO 2 electrodes were immersed in solutions of H 4 1 in the presence of base (0-4 equivalents). TiO 2 -anchored heteroleptic copper( i ) sensitizers were subsequently formed by ligand exchange between the homoleptic complex [Cu( 2 ) 2 ][PF 6 ] and the anchored ligand [H 4− n 1 ] n − . The results demonstrate that the addition of one equivalent of base during the initial surface functionalization can afford up to a 26% increase in DSC efficiency, while the addition of ≥3 equivalents of base significantly hinders DSC performance. Deprotonation of H 4 1 has been investigated using 1 H and 31 P NMR spectroscopic titrations. Further insight into DSC performance has been gained by using electrochemical impedance spectroscopy, and a comparison is made between DSCs in which the working electrodes are either pre-treated with a base, or exposed to a base post heteroleptic copper( i ) dye-assembly. The effects of a change in the protonation state of the phosphonic acid anchoring ligand in a heteroleptic copper( i ) sensitizer on the performance of n-type dye-sensitized solar cells are presented.
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FTO/TiO 2 electrodes were immersed in solutions of H 4 1 in the presence of base (0-4 equivalents). TiO 2 -anchored heteroleptic copper( i ) sensitizers were subsequently formed by ligand exchange between the homoleptic complex [Cu( 2 ) 2 ][PF 6 ] and the anchored ligand [H 4− n 1 ] n − . The results demonstrate that the addition of one equivalent of base during the initial surface functionalization can afford up to a 26% increase in DSC efficiency, while the addition of ≥3 equivalents of base significantly hinders DSC performance. Deprotonation of H 4 1 has been investigated using 1 H and 31 P NMR spectroscopic titrations. Further insight into DSC performance has been gained by using electrochemical impedance spectroscopy, and a comparison is made between DSCs in which the working electrodes are either pre-treated with a base, or exposed to a base post heteroleptic copper( i ) dye-assembly. 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source Royal Society of Chemistry
subjects Acids
Anchoring
Copper
Dye-sensitized solar cells
Dyes
Electrochemical impedance spectroscopy
Electrochemistry
Electrodes
Equivalence
Ligands
NMR
Nuclear magnetic resonance
Photovoltaic cells
Protonation
Solar cells
Spectroscopy
Titanium dioxide
title The influence of phosphonic acid protonation state on the efficiency of bis(diimine)copper() dye-sensitized solar cells
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