1. Diffusion-Limited Crystallization: A Rationale for the Thermal Stability of Non-Fullerene Solar Cells
- Author
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Feng Gao, Johannes Benduhn, Deping Qian, Detlef-M. Smilgies, Ferry Anggoro Ardy Nugroho, Sandra Hultmark, Anna I. Hofmann, Anirudh Sharma, Jaime Martín, Liyang Yu, Koen Vandewal, Christoph Langhammer, Sara Marina, Renee Kroon, Christian Müller, and Mats Andersson
- Subjects
Solid-state chemistry ,Nanostructure ,Materials science ,Fullerene ,Organic solar cell ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Acceptor ,0104 chemical sciences ,law.invention ,Chemical engineering ,law ,General Materials Science ,Thermal stability ,Crystallization ,0210 nano-technology ,Glass transition ,organic solar cell ,thermally stable photovoltaics ,glass-transition temperature ,diffusion-limited crystallization ,non-fullerene acceptor - Abstract
Organic solar cells are thought to suffer from poor thermal stability of the active layer nanostructure, a common belief that is based on the extensive work that has been carried out on fullerene-based systems. We show that a widely studied non-fullerene acceptor, the indacenodithienothiophene-based acceptor ITIC, crystallizes in a profoundly different way as compared to fullerenes. Although fullerenes are frozen below the glass-transition temperature T-g of the photovoltaic blend, ITIC can undergo a glass-crystal transition considerably below its high T-g of similar to 180 degrees C. Nanoscopic crystallites of a low-temperature polymorph are able to form through a diffusion-limited crystallization process. The resulting fine-grained nanostructure does not evolve further with time and hence is characterized by a high degree of thermal stability. Instead, above T-g, the low temperature polymorph melts, and micrometer-sized crystals of a high-temperature polymorph develop, enabled by more rapid diffusion and hence long-range mass transport. This leads to the same detrimental decrease in photovoltaic performance that is known to occur also in the case of fullerene-based blends. Besides explaining the superior thermal stability of non-fullerene blends at relatively high temperatures, our work introduces a new rationale for the design of bulk heterojunctions that is not based on the selection of high-T-g materials per se but diffusion-limited crystallization. The planar structure of ITIC and potentially other non-fullerene acceptors readily facilitates the desired glass-crystal transition, which constitutes a significant advantage over fullerenes, and may pave the way for truly stable organic solar cells. We acknowledge financial support from the Knut and Alice Wallenberg Foundation through the project "Mastering Morphology for Solution-borne Electronics", the Swedish Research Council (grant agreement no. 2016-06146), and the Swedish Foundation for Strategic Research (grant agreement no. RMA15-0052). We thank the Cornell High Energy Synchrotron Source (CHESS), supported by the NSF under award DMR-1332208, for providing time for GIWAXS measurements. J.B. and K.V. acknowledge funding from the German Federal Ministry for Education and Research (BMBF) through the InnoProfile project "Organische p-i-n Bauelemente 2.2" (03IPT602X).
- Published
- 2019