Synthesis of Zinc Porphyrin Sensitizers for Dye‐Sensitized Solar Cells by Tuning Electron‐Donor Group

ABSTRACT Dye‐sensitized solar cells (DSSCs) are considered a promising solution to current energy challenges. In this study, three porphyrin sensitizers ZnP1–ZnP3 with donor‐π‐acceptor (D‐π‐A) configurations were synthesized. The donors included 9,9‐dimethylfluorene, 4‐biphenyl, and 1,1′:3′,1″‐terphenyl groups, whereas alkynylbenzoic acid was used as the acceptor. The modification of the side alkyl chain addressed the poor solubility of the porphyrin sensitizer. The synthesized porphyrin sensitizers were structurally characterized by nuclear magnetic resonance, high‐resolution mass spectrometry, and ultraviolet absorption spectroscopy. The introduction of electron donor groups into 1,1′:3′,1″‐terphenyl and alkynylbenzoic acid into the acceptor group improved the light‐harvesting ability of the sensitizer, increased the short‐circuit photocurrent density, and enhanced cell efficiency ( η = 3.6%). Finally, density functional theory was used to verify the experimental results.

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Publication Details

Journal
Applied Organometallic Chemistry
Published
2024-11-21
DOI
https://doi.org/10.1002/aoc.7902
Citations
2
Primary Topic
TiO2 Photocatalysis and Solar Cells
Type
article
Field-Weighted Citation Impact
0.20
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article

Synthesis of Zinc Porphyrin Sensitizers for Dye‐Sensitized Solar Cells by Tuning Electron‐Donor Group

Wen‐Le Zhang, Yuhuai Li, Wenyuan Zhang, Jia‐Cheng Liu et al.
2 citations
Applied Organometallic Chemistry
TiO2 Photocatalysis and Solar Cells
0.20
article

Synthesis of Zinc Porphyrin Sensitizers for Dye‐Sensitized Solar Cells by Tuning Electron‐Donor Group

Wen‐Le Zhang, Yuhuai Li, Wenyuan Zhang, Jia‐Cheng Liu, Yong Hu, Bo Wang, Xueqin Sun
article en
2 citations

Abstract

ABSTRACT Dye‐sensitized solar cells (DSSCs) are considered a promising solution to current energy challenges. In this study, three porphyrin sensitizers ZnP1–ZnP3 with donor‐π‐acceptor (D‐π‐A) configurations were synthesized. The donors included 9,9‐dimethylfluorene, 4‐biphenyl, and 1,1′:3′,1″‐terphenyl groups, whereas alkynylbenzoic acid was used as the acceptor. The modification of the side alkyl chain addressed the poor solubility of the porphyrin sensitizer. The synthesized porphyrin sensitizers were structurally characterized by nuclear magnetic resonance, high‐resolution mass spectrometry, and ultraviolet absorption spectroscopy. The introduction of electron donor groups into 1,1′:3′,1″‐terphenyl and alkynylbenzoic acid into the acceptor group improved the light‐harvesting ability of the sensitizer, increased the short‐circuit photocurrent density, and enhanced cell efficiency ( η = 3.6%). Finally, density functional theory was used to verify the experimental results.

Applied Organometallic ChemistryVol. 39(3)
Tarim University (CN), Chengdu Organic Chemicals (China) (CN), Urumqi Vocational University (CN), Northwest Normal University (CN)
Affordable and clean energy
Openalex Percentile: Top 57%
TiO2 Photocatalysis and Solar Cells
0.20
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