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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 |
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creator | Stephens, Alexander J Malzner, Frederik J Constable, Edwin C Housecroft, Catherine E |
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. |
doi_str_mv | 10.1039/c7se00586e |
format | article |
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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.</description><identifier>ISSN: 2398-4902</identifier><identifier>EISSN: 2398-4902</identifier><identifier>DOI: 10.1039/c7se00586e</identifier><language>eng</language><publisher>London: Royal Society of Chemistry</publisher><subject>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</subject><ispartof>Sustainable energy & fuels, 2018, Vol.2 (4), p.786-794</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-80644727ae8702922965dff618cfc9de56303415de50c45ba5a82d80d15832ae3</citedby><cites>FETCH-LOGICAL-c281t-80644727ae8702922965dff618cfc9de56303415de50c45ba5a82d80d15832ae3</cites><orcidid>0000-0003-4916-4041 ; 0000-0002-6554-8136 ; 0000-0002-8074-0089</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>Stephens, Alexander J</creatorcontrib><creatorcontrib>Malzner, Frederik J</creatorcontrib><creatorcontrib>Constable, Edwin C</creatorcontrib><creatorcontrib>Housecroft, Catherine E</creatorcontrib><title>The influence of phosphonic acid protonation state on the efficiency of bis(diimine)copper() dye-sensitized solar cells</title><title>Sustainable energy & fuels</title><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.</description><subject>Acids</subject><subject>Anchoring</subject><subject>Copper</subject><subject>Dye-sensitized solar cells</subject><subject>Dyes</subject><subject>Electrochemical impedance spectroscopy</subject><subject>Electrochemistry</subject><subject>Electrodes</subject><subject>Equivalence</subject><subject>Ligands</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Photovoltaic cells</subject><subject>Protonation</subject><subject>Solar cells</subject><subject>Spectroscopy</subject><subject>Titanium dioxide</subject><issn>2398-4902</issn><issn>2398-4902</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpNkM1LAzEQxYMoWGov3oWAl1ZYTbKb3exRSv2AggfreUmTCY2syZqkSP3rTa2oh2He4fdmeA-hc0quKSnbG9VEIISLGo7QiJWtKKqWsON_-hRNYnwlhDDKKsabEfpYbQBbZ_otOAXYGzxsfMzjrMJSWY2H4JN3MlnvcEwyZcjhlF1gjFU223Z729rGqbb2zTqYKT8MEKYzrHdQRHDRJvsJGkffy4AV9H08QydG9hEmP3uMXu4Wq_lDsXy6f5zfLgvFBE2FIHVVNayRIBrCWsbammtjaiqUUa0GXpekrCjPiqiKryWXgmlBNOWiZBLKMbo83M0x3rcQU_fqt8Hllx0jtCV1K2idqasDpYKPMYDphmDfZNh1lHT7brt587z47naR4YsDHKL65f66L78ANTp2SQ</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Stephens, Alexander J</creator><creator>Malzner, Frederik J</creator><creator>Constable, Edwin C</creator><creator>Housecroft, Catherine E</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7SP</scope><scope>7ST</scope><scope>7U6</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>L7M</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0003-4916-4041</orcidid><orcidid>https://orcid.org/0000-0002-6554-8136</orcidid><orcidid>https://orcid.org/0000-0002-8074-0089</orcidid></search><sort><creationdate>2018</creationdate><title>The influence of phosphonic acid protonation state on the efficiency of bis(diimine)copper() dye-sensitized solar cells</title><author>Stephens, Alexander J ; Malzner, Frederik J ; Constable, Edwin C ; Housecroft, Catherine E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-80644727ae8702922965dff618cfc9de56303415de50c45ba5a82d80d15832ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acids</topic><topic>Anchoring</topic><topic>Copper</topic><topic>Dye-sensitized solar cells</topic><topic>Dyes</topic><topic>Electrochemical impedance spectroscopy</topic><topic>Electrochemistry</topic><topic>Electrodes</topic><topic>Equivalence</topic><topic>Ligands</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Photovoltaic cells</topic><topic>Protonation</topic><topic>Solar cells</topic><topic>Spectroscopy</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stephens, Alexander J</creatorcontrib><creatorcontrib>Malzner, Frederik J</creatorcontrib><creatorcontrib>Constable, Edwin C</creatorcontrib><creatorcontrib>Housecroft, Catherine E</creatorcontrib><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Sustainable energy & fuels</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stephens, Alexander J</au><au>Malzner, Frederik J</au><au>Constable, Edwin C</au><au>Housecroft, Catherine E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The influence of phosphonic acid protonation state on the efficiency of bis(diimine)copper() dye-sensitized solar cells</atitle><jtitle>Sustainable energy & fuels</jtitle><date>2018</date><risdate>2018</risdate><volume>2</volume><issue>4</issue><spage>786</spage><epage>794</epage><pages>786-794</pages><issn>2398-4902</issn><eissn>2398-4902</eissn><abstract>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.</abstract><cop>London</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c7se00586e</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4916-4041</orcidid><orcidid>https://orcid.org/0000-0002-6554-8136</orcidid><orcidid>https://orcid.org/0000-0002-8074-0089</orcidid></addata></record> |
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ispartof | Sustainable energy & fuels, 2018, Vol.2 (4), p.786-794 |
issn | 2398-4902 2398-4902 |
language | eng |
recordid | cdi_rsc_primary_c7se00586e |
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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