Impact of Different π-Bridges on the Photovoltaic Performance of A-D-D'-D-A Small Molecule-Based Donors.

Molecules

Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, Department of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China.

Published: September 2024

AI Article Synopsis

  • Three small donor molecule materials were synthesized using methods like Vilsmeier-Haack reaction and Stille coupling, focusing on their optical properties and photovoltaic performance.
  • Incorporating thiophene π-bridges helped achieve a blue shift in UV absorption and improved energy levels, resulting in a maximum open circuit voltage of 0.75 V and a power conversion efficiency (PCE) of 3%.
  • Adding alkyl chains improved solubility and led to better performance, achieving a short-circuit current of 10.59 mA/cm and a PCE of 4.25%, suggesting strategies for designing future small donor molecules.

Article Abstract

Three small donor molecule materials (, , ) based on dithiophene [2,3-d:2',3'-d']dithiophene [1,2-b:4,5-b']dithiophene (DTBDT) utilized in this study were synthesized using the Vilsmeier-Haack reaction, traditional Stille coupling, and Knoevenagel condensation. Then, a variety of characterization methods were applied to study the differences in optical properties and photovoltaic devices among the three. By synthesizing using a thiophene π-bridge based on , the blue shift in ultraviolet absorption can be enhanced, the band gap and energy level can be reduced, the open circuit voltage () can be increased to 0.75 V using the : device, and a power conversion efficiency (PCE) of 3% can be achieved. Also, after developing the device using , introduced the alkyl chain of thiophene π-bridge to , which improved the solubility of tiny donor molecules, achieved the maximum short-circuit current ( = 10.59 mA/cm), filling factor (FF = 49.72%), and PCE (4.25%). Thus, a viable option for future design and synthesis of small donor molecule materials is to incorporate thiophene π-bridges into these materials, along with alkyl chains, in order to enhance the device's morphology and charge transfer behavior.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11396980PMC
http://dx.doi.org/10.3390/molecules29174231DOI Listing

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