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Journal ArticleDOI

Side-Chain Effect on Cyclopentadithiophene/Fluorobenzothiadiazole-Based Low Band Gap Polymers and Their Applications for Polymer Solar Cells

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TLDR
In this paper, a series of cyclopentadithiophene-based low band gap conjugated polymers with varied side-chain patterns and F-substituents were synthesized.
Abstract
A series of cyclopentadithiophene-based low band gap conjugated polymers with varied side-chain patterns and F-substituents were synthesized. By replacing the shorter 2-ethylhexyl (EH) side-chain with the longer 3,7-dimethyloctyl (DMO) side-chain, it resulted in significant changes to the optical, electrochemical, and morphological properties of the polymers, as well as the subsequent performance of devices made from these materials. Solar cells fabricated from polymer with 2-ethylhexyl (EH) side-chain and monofluoro substituent exhibits increased open circuit voltage, short circuit current and fill factor, resulting in the highest power conversion efficiency (5.5%) in this series of polymers. This finding provides valuable insight for making more efficient low band gap polymers.

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Citations
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Journal ArticleDOI

High Efficiency Near-Infrared and Semitransparent Non-Fullerene Acceptor Organic Photovoltaic Cells

TL;DR: The absence of near-infrared (NIR) solar cells with high open circuit voltage (Voc) and external quantum efficiency (EQE) has impeded progress toward achieving organic photovoltaic (OPV) power conversion efficiency PCE > 15%.
Journal ArticleDOI

Recent progress of high performance polymer OLED and OPV materials for organic printed electronics

TL;DR: The basic guidelines for material design and the recent progress of polymer-based organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs) are reported.
Journal ArticleDOI

A near-infrared non-fullerene electron acceptor for high performance polymer solar cells

TL;DR: In this article, a low-bandgap (143 eV) non-fullerene electron acceptor (BT-IC) bearing a fused 7-heterocyclic ring with absorption edge extending to the near-infrared (NIR) region was specially designed and synthesized.
References
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Journal ArticleDOI

Synthesis of Conjugated Polymers for Organic Solar Cell Applications

TL;DR: Fluorene-Based Copolymers ContainingPhosphorescent Complexes and Carbazole-Based Conjugated Polymers R5.1.3.
Journal ArticleDOI

Enhanced power-conversion efficiency in polymer solar cells using an inverted device structure

TL;DR: In this article, the authors showed that PFN can be incorporated into polymer light-emitting devices (PLEDs) to enhance electron injection from high-work-function metals such as aluminium (work function w of 4.3 eV) and gold (w ¼ 5.2 eV).
Journal ArticleDOI

Fluorine Substituted Conjugated Polymer of Medium Band Gap Yields 7% Efficiency in Polymer-Fullerene Solar Cells

TL;DR: The resulting fluorinated polymer PBnDT-FTAZ outperforms poly(3-hexylthiophene), the current medium band gap polymer of choice, and thus is a viable candidate for use in highly efficient tandem cells.
Journal ArticleDOI

Rational Design of High Performance Conjugated Polymers for Organic Solar Cells

TL;DR: The research community has made great progress in the field of bulk heterojunction (BHJ) polymer solar cells since its inception in 1995 as mentioned in this paper and the power conversion efficiency (PCE) has increased from 1% in the 1990s to over 8% just recently.
Journal ArticleDOI

Development of fluorinated benzothiadiazole as a structural unit for a polymer solar cell of 7 % efficiency.

TL;DR: F fluorine is the mostelectronegative element, with a Pauling electronegativity of 4.0, which is much larger than that of hydrogen (2.2), and these fluorine atoms often have a great influence on inter- and intramolecular interaction.
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