Diffusion-Limited Crystallization: A Rationale for the Thermal Stability of Non-Fullerene Solar Cells
Artikel i vetenskaplig tidskrift, 2019

© 2019 American Chemical Society. 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 Tg of the photovoltaic blend, ITIC can undergo a glass-crystal transition considerably below its high Tg of ∼180 °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 Tg, 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-Tg 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.

diffusion-limited crystallization

thermally stable photovoltaics

non-fullerene acceptor

organic solar cell

glass-transition temperature

Författare

Liyang Yu

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Sichuan University

D. P. Qian

Linköpings universitet

Sara Marina

Institute for Polymer Materials, San Sebastian

Ferry Nugroho

Chalmers, Fysik, Kemisk fysik

A. Sharma

Université de Bordeaux

Flinders University

Sandra Hultmark

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Anna Hofmann

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Renee Kroon

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Johannes Benduhn

Technische Universität Dresden

Detlef M. Smilgies

Cornell University

K. Vandewal

Institute for Materials Research Hasselt University

Mats Andersson

Flinders University

Christoph Langhammer

Chalmers, Fysik, Kemisk fysik

Jaime Martín

Basque Foundation for Science (Ikerbasque)

Institute for Polymer Materials, San Sebastian

Feng Gao

Linköpings universitet

Christian Müller

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

ACS Applied Materials & Interfaces

1944-8244 (ISSN) 1944-8252 (eISSN)

Ämneskategorier

Oorganisk kemi

Materialkemi

Den kondenserade materiens fysik

DOI

10.1021/acsami.9b04554

Mer information

Senast uppdaterat

2019-07-08