Cited by 102Organic Electronics and PhotovoltaicsPorphyrin and Phthalocyanine ChemistryPhotodynamic Therapy Research Studies

Enhanced performance of solution-processed solar cells based on porphyrin small molecules with a diketopyrrolopyrrole acceptor unit and a pyridine additive

Li, Lisheng, Huang, Yuying, Peng, Junbiao, Cao, Yong, Peng, Xiaobin·2013·J. Mater. Chem. A

Abstract

A conjugated donor–acceptor porphyrin small molecule was designed and synthesized with diketopyrrolopyrrole as the acceptor unit. The new porphyrin-based small molecule exhibits broad and intense absorption in the visible and near IR regions, and the hole mobility and the power conversion efficiency of the bulk heterojunction devices based on the porphyrin : [6,6]-phenyl-C-61-butyric acid methyl ester (1 : 1, w/w) are increased up to 4.6 × 10−5 cm2 V−1 s−1 and 3.71%, respectively, which are further enhanced to 1.6 × 10−4 cm2 V−1 s−1 and 4.78%, respectively, upon the introduction of 3.0 vol% of pyridine additive. Further studies show that the performance of the solar cells based on other zinc porphyrins could also be improved by the pyridine additive.

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Crossref · 10.1039/c2ta00858k

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  • Porphyrins are extensively used for dye sensitized solar cells, and numerous research articles and several review papers have been published.

    “In fact, porphyrins are extensively used for dye sensitized solar cells (DSSCs), and numerous research articles and several review papers have been published. 9 -17”
  • Pyridine as a solvent additive improved the D1-based device PCE to 4.78% and balanced charge carrier mobilities by enhancing hole mobility while slightly decreasing electron mobility.

    “further device optimization using pyridine as a solvent additive led to an improved PCE of 4.78%, where pyridine addition showed a balancing e ff ect on the charge carrier mobilities: enhanced the hole mobility while slightly decreasing the electron mobility.”
  • The BHJ OSC based on the D1:PC61BM (1:1) blend realized a PCE of 3.71%.

    “The BHJ OSC based on the D1 : PC61BM (1 : 1) blend realized a PCE of 3.71% (Table 4).”
  • D1 realized a broad absorption spectrum spanning the near-IR region with a high absorption coefficient.

    “D1 realized a broad absorption spectrum which spanned the near-IR region with a high absorption coe ffi cient.”

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Authors
Li, L., Huang, Y., Peng, J., Cao, Y., & Peng, X.
Affiliations
State Key Laboratory of Luminescent Materials and Devices (CN)
Corresponding author
Peng, Xiaobin
Venue
J. Mater. Chem. A
Published
2013
Volume
1
Issue
6
Pages
2144-2150
ISSN
  • 2050-7488 (ISSN-L)
  • 2050-7496
OpenAlex
W2044308573
Cited by
102
References
0
Citations by year
2026: 3 · 2025: 1 · 2024: 5 · 2023: 2 · 2022: 1 · 2021: 4 · 2020: 9 · 2019: 8 · 2018: 4 · 2017: 12 · 2016: 22 · 2015: 14 · 2014: 12 · 2013: 5
FWCI
6.34
Type
journal article
Language
en
Open access
closed
Locations
Journal of Materials Chemistry A (publishedVersion)
Funders
National Natural Science Foundation of China
Topics
  • Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Electronics and Photovoltaics
  • Physical Sciences › Materials Science › Materials Chemistry › Porphyrin and Phthalocyanine Chemistry
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Photodynamic Therapy Research Studies
Keywords
pyridine additive, organic solar cells, bulk heterojunction, zinc porphyrin, hole mobility, power conversion efficiency, solution processing, donor-acceptor materials

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