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Related Concept Videos

π Molecular Orbitals of the Allyl Cation and Anion01:18

π Molecular Orbitals of the Allyl Cation and Anion

An allyl group is a three-carbon conjugated system where the sp³-hybridized allylic carbon is bonded to a CH=CH2 group via a single bond. Allyl anions can be obtained by treating propene with a strong base that can deprotonate methyl groups. Allyl cations are formed as intermediates during substitution reactions involving allylic halides. In both cases, the hybridization of the allylic carbon changes from sp3 to sp2, giving rise to a carbon chain with three sp2-hybridized carbons, each with an...
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In organic synthesis, the formation of products can be altered by changing the reaction conditions. For example, a dibromo addition product is formed when propene is treated with bromine at room temperature. In contrast, propene undergoes allylic substitution in non-polar solvents at high temperatures to give 3-bromopropene. In order to avoid the addition reaction, the bromine concentration must be kept as low as possible throughout the reaction. This can be achieved using N-bromosuccinimide...

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Efficient all-small-molecule organic solar cells processed with non-halogen solvent.

Wei Gao1, Ruijie Ma2, Top Archie Dela Peña3,4

  • 1Xiamen Key Laboratory of Optoelectronic Materials and Advanced Manufacturing, Institute of Luminescent Materials and Information Displays, College of Materials Science and Engineering, Huaqiao University, Xiamen, 361021, China.

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|March 2, 2024
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Researchers developed a new small molecule donor for organic solar cells, achieving high power conversion efficiencies using non-halogen solvents. This breakthrough enhances the commercial viability of these eco-friendly solar technologies.

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Area of Science:

  • Materials Science
  • Organic Electronics
  • Photovoltaics

Background:

  • All-small-molecule organic solar cells (SMOSCs) offer commercialization potential due to reproducibility and non-halogen solvent processing.
  • Improving power conversion efficiencies (PCEs) in non-halogen processed SMOSCs remains a significant challenge.

Purpose of the Study:

  • To design and synthesize a small molecule donor (BM-ClEH) that enhances molecular pre-aggregation and film morphology in non-halogen solvents.
  • To investigate the impact of intramolecular chlorine-sulfur non-covalent interactions on SMOSC performance.

Main Methods:

  • Synthesis of small molecule donor BM-ClEH utilizing intramolecular chlorine-sulfur non-covalent interactions.
  • Fabrication of binary and ternary SMOSCs using tetrahydrofuran (THF) as a non-halogen solvent.
  • Performance characterization of solar cells including power conversion efficiency (PCE) measurements.

Main Results:

  • Tetrahydrofuran-processed SMOSCs based on BM-ClEH:BO-4Cl achieved high PCEs of 15.0% (binary) and 16.1% (ternary) after thermal annealing.
  • The chlorine-sulfur interaction in BM-ClEH promoted beneficial pre-aggregation and improved film micromorphology.
  • A control molecule (BM-HEH) lacking this interaction showed poor performance due to disordered molecular packing and inefficient exciton dissociation.

Conclusions:

  • The designed small molecule donor BM-ClEH enables efficient non-halogen solvent processing for SMOSCs.
  • Intramolecular non-covalent interactions are crucial for optimizing molecular aggregation and device performance.
  • This study advances the development of eco-friendly SMOSCs and provides insights for future material design.