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Published in 2019 at "Advanced Functional Materials"
DOI: 10.1002/adfm.201804839
Abstract: For donor–acceptor conjugated polymers, it is an effective strategy to improve their electron mobilities by introducing electron‐withdrawing groups (EWGs, such as F, Cl, or CF3) into the polymer backbone. However, the introduction of different EWGs…
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Keywords:
high performance;
electron withdrawing;
performance ambipolar;
annulated indigo ... See more keywords
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Published in 2025 at "Advanced Functional Materials"
DOI: 10.1002/adfm.202424259
Abstract: Diammonium derivatives with electron‐withdrawing cores of cyclohexyl or phenyl have demonstrated enormous potential in achieving high‐performance perovskite solar cells. Nevertheless, the critical role of these electron‐withdrawing cores of the diammonium passivation on device performance is…
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Keywords:
passivation;
withdrawing cores;
electron withdrawing;
high performance ... See more keywords
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Published in 2025 at "Advanced Materials"
DOI: 10.1002/adma.202500352
Abstract: Recently, benzene‐based solid additives (BSAs) have emerged as pivotal components in modulating the morphology of the blend film in organic solar cells (OSCs). However, since almost all substituents on BSAs are weak electron‐withdrawing groups and…
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Keywords:
non halogenated;
halogenated solvent;
efficiency;
organic solar ... See more keywords
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Published in 2025 at "Advanced Energy Materials"
DOI: 10.1002/aenm.202504572
Abstract: 2D/3D perovskite heterostructures have advanced the performance of perovskite solar cells. However, ion diffusion at the 2D/3D interface under illumination and prolonged heat affects device stability and scalability. Here, we studied the electron‐withdrawing strength of…
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Keywords:
solar cells;
engineering ligand;
ligand;
electron withdrawing ... See more keywords
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Published in 2018 at "European Journal of Organic Chemistry"
DOI: 10.1002/ejoc.201800051
Abstract: The use of a substoichiometric amount of molecular iodine in the presence of PPh3 and pyridine effects a direct deoxygenation of primary and secondary alcohols in positions α to a variety of activating electron‐withdrawing groups,…
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Keywords:
electron withdrawing;
withdrawing groups;
metal free;
free iodine ... See more keywords
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Published in 2019 at "European Journal of Organic Chemistry"
DOI: 10.1002/ejoc.201900530
Abstract: The introduction of functional groups into the mesoposition of dipyrromethanes, boron-dipyrromethenes (BODIPYs) and porphyrinoids, is of fundamental importance in designing such dye systems for material sciences or photomedicine. One route that has proven to be…
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Keywords:
electron withdrawing;
synthesis;
porphyrins corroles;
ruthenium ... See more keywords
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Published in 2022 at "Small"
DOI: 10.1002/smll.202207243
Abstract: Implementing a molecular modulation strategy for metallic phthalocyanines (MPc) without losing the activity of the metal center and inducing a multifunction characteristic in electrocatalytic remains a challenge. Herein, a series of 2D CuCo bimetallic polymerized…
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Keywords:
electron withdrawing;
active sites;
water;
withdrawing groups ... See more keywords
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Published in 2020 at "Structural Chemistry"
DOI: 10.1007/s11224-020-01504-0
Abstract: In this paper, polyvinyl carbazole fragments with side-hung chromogenic groups were used as the parent. The relationship between the structure and the properties of NLO was studied by changing the type of spacer groups on…
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Keywords:
electron withdrawing;
spacer;
spacer group;
group ... See more keywords
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Published in 2019 at "Macromolecular Research"
DOI: 10.1007/s13233-020-8002-7
Abstract: Three quinoxaline-based small molecules possessing multiple electron-withdrawing moieties were synthesized by the Suzuki coupling reaction for organic photovoltaic cells (OPVs). The electron-donating triarylamine units were linked to both ends of electron-accepting 2,3-diphenyl quinoxaline (DPQ) derivatives…
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Keywords:
electron withdrawing;
small molecules;
based small;
quinoxaline based ... See more keywords
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Published in 2019 at "Dyes and Pigments"
DOI: 10.1016/j.dyepig.2019.03.056
Abstract: Abstract In this work, two new donor-acceptor (D-A) copolymers (P32 and P33) for non-fullerene polymer solar cells (PSCs) have been synthesized based on a thiophene-fused benzotriazole (BTAZT) unit and thiophene substituted benzodithiophene (BDTT) unit, in…
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Keywords:
electron withdrawing;
solar cells;
thiophene;
polymer solar ... See more keywords
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Published in 2020 at "Dyes and Pigments"
DOI: 10.1016/j.dyepig.2020.108542
Abstract: Abstract Recent advances in non-fullerene acceptors have enabled the power conversion efficiencies of organic solar cells (OSCs) to exceed 16%. Fused-ring electron acceptors (FREAs) are some of the most widely investigated non-fullerene acceptors. Classical FREAs,…
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Keywords:
electron withdrawing;
non fullerene;
strong electron;
end groups ... See more keywords