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Copolymerized Plasticizer Enables Halogen-Free Processing Toward 20.78% and 17.83% Efficient Organic Solar Cells and
Jiachen Zhang1, Hongxiang Li2, Junyuan Ding1
1Laboratory of Advanced Optoelectronic Materials, Suzhou Key Laboratory of Novel Semiconductor-Optoelectronics Materials and Devices, State Key Laboratory of Bioinspired Interfacial Materials Science, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, China.
Researchers developed a copolymerized plasticizer strategy to improve the solubility of donor polymers in nonhalogenated solvents for organic solar cells (OSCs). This breakthrough enhances processability and achieves record power conversion efficiencies in OSCs and modules.
Area of Science:
- Materials Science
- Organic Electronics
- Polymer Chemistry
Background:
- Nonhalogenated solvents are ideal for scalable organic solar cell (OSC) fabrication.
- High-molecular-weight donor polymers with crystalline backbones exhibit poor solubility in these solvents, hindering OSC performance.
- The pinnacle donor material (D18) exemplifies this challenge, limiting morphology development.
Purpose of the Study:
- To enhance the solubility and processability of high-molecular-weight donor polymers in nonhalogenated solvents.
- To improve the morphology evolution and device performance of organic solar cells (OSCs).
- To develop a strategy that maintains the polymer's intrinsic properties while improving solvation.
Main Methods:
- A copolymerized "plasticizer" strategy was employed, integrating a specific plasticizing comonomer into the D18 polymer backbone, creating D18-O.
- The plasticizing unit (bis(2-(2-methoxyethoxy)ethyl) thieno[3,2-b]thiophene-3,6-dicarboxylate) was designed to enhance dipolar interactions with toluene.
- The effects of this modification on polymer solubility, aggregation, crystallization kinetics, and morphology were investigated.
Main Results:
- D18-O demonstrated significantly enhanced solubility in toluene due to improved solvation via dipolar interactions.
- The plasticizing units effectively suppressed excessive pre-aggregation and slowed down donor crystallization kinetics.
- This led to the formation of well-defined nanocrystals and optimized hierarchical morphologies during nonhalogenated processing.
Conclusions:
- The copolymerized plasticizer strategy successfully overcomes the solubility limitations of high-performance donor polymers in nonhalogenated solvents.
- This approach enables high power conversion efficiencies (PCEs) in organic solar cells (OSCs) and modules processed from toluene.
- Record certified PCEs of 20.40% for OSCs and 17.29% for modules were achieved, alongside exceptional stability.
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