Influence of spacer and donor groups as tetraphenylethylene or triphenylamine in asymmetric zinc phthalocyanine dyes for dye-sensitized solar cells

dc.contributor.authorCelik, Gizem Gumusgoz
dc.contributor.authorTunc, Gulenay
dc.contributor.authorLafzi, Ferruh
dc.contributor.authorSaracoglu, Nurullah
dc.contributor.authorArslan, Baris Seckin
dc.contributor.authorNebioglu, Mehmet
dc.contributor.authorSisman, Ilkay
dc.date.accessioned2025-10-29T11:26:06Z
dc.date.issued2023
dc.departmentFakülteler, Temel Bilimler Fakültesi, Kimya Bölümü
dc.description.abstractBased on the available literature, the carboxylic acid is a suitable electron-withdrawing group for the develop-ment of push-pull type AB3 phthalocyanines that can be used in dye-sensitized solar cell (DSSC). This study aims to assess the impact of carboxylic acid groups on solar cell energy conversion efficiency. Two types of carboxylic acid groups were selected as electron-withdrawing groups for this purpose. These groups were attached to the phthalocyanine (Pc) core either directly or via conjugated linker groups. Two novel push-pull zinc phthalocy-anine dyes (GT-52 and GGC-22) containing tetraphenylethylene (TPE) or triphenylamine (TPA) substituents as electron donor groups and carboxylic acid or phenoxy carboxylic acid as anchoring groups, respectively, have been synthesized to construct DSSCs. The optical, electrochemical, and photovoltaic properties of the effect of the spacer and electron donor groups in these phthalocyanines are evaluated. Both dyes exhibit good anti-aggregation ability owing to the presence of the bulky donor groups. On the other hand, the DSSC based on GGC-22 showed a significantly higher power conversion efficiency (PCE) of 2.15% than that of GT-52 (0.26%) under AM 1.5G solar conditions. The superior performance of GGC-22 is attributed to the introduction of a phenoxy spacer, which results in a longer distance between the donor groups and the TiO2 surface compared to GT-52 without any spacer. This allows for higher dye loading, resulting in higher JSC, VOC, and PCE for GGC-22. As a result, the presence of a longer anchoring group for the donor groups is an important synthetic strategy for efficient phthalocyanine-based DSSCs.
dc.identifier.doi10.1016/j.jphotochem.2023.114962
dc.identifier.issn1010-6030
dc.identifier.issn1873-2666
dc.identifier.orcid0000-0002-1504-7480
dc.identifier.orcid0000-0002-2603-3906
dc.identifier.orcid0000-0003-4816-7419
dc.identifier.orcid0000-0002-3371-0899
dc.identifier.scopus2-s2.0-85162954131
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.jphotochem.2023.114962
dc.identifier.urihttps://hdl.handle.net/20.500.14854/10126
dc.identifier.volume444
dc.identifier.wosWOS:001055970300001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofJournal of Photochemistry and Photobiology A-Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectAsymmetric zinc phthalocyanine
dc.subjectTriphenylamine
dc.subjectTetraphenylethylene
dc.subjectCarboxylic acid
dc.subjectDye-sensitized solar cell (DSSC)
dc.titleInfluence of spacer and donor groups as tetraphenylethylene or triphenylamine in asymmetric zinc phthalocyanine dyes for dye-sensitized solar cells
dc.typeArticle

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