Regiospecific Incorporation of Acetylene Linker in High‐Electron Mobility Dimerized Acceptors for Organic Solar Cells with High Efficiency (18.8%) and Long 1‐Sun Lifetime (> 5000 h)

Author:

Sun Cheng12,Lee Jin‐Woo3ORCID,Tan Zhengping3,Phan Tan Ngoc‐Lan3,Han Daehee3,Lee Heung‐Goo3,Lee Seungjin4,Kwon Soon‐Ki5,Kim Bumjoon J.3ORCID,Kim Yun‐Hi1

Affiliation:

1. Department of Chemistry and RINS Gyeongsang National University Jinju 52828 Republic of Korea

2. Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao 266101 China

3. Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST) Daejeon 34141 Republic of Korea

4. Energy Materials Research Center Korea Research Institute of Chemical Technology (KRICT) Daejeon 34114 Republic of Korea

5. Department of Materials Engineering and Convergence Technology and ERI Gyeongsang National University Jinju 52828 Republic of Korea

Abstract

AbstractThe commercialization of organic solar cells (OSCs) requires both high power conversion efficiency (PCE) and long‐term stability. However, the lifetime of the OSCs containing small‐molecule acceptors (SMA) should be significantly enhanced. In this study, a series of planarity‐controlled is developed, high electron mobility dimerized SMAs (DSMAs) and realize OSCs with high‐performance (PCE = 18.8%) and high‐stability (t80% lifetime = 5380 h under 1‐Sun illumination). An acetylene linker with a planar triple bond is designed for dimerization of SMA units to afford the high backbone planarity necessary to achieve high crystallinity and electron mobility. To further engineer the molecular conformation and electron mobility of the DSMAs, different regioisomers of a Y‐based SMA are dimerized to yield three regioisomerically distinct DSMAs, denoted as DYA‐I, DYA‐IO, and DYA‐O, respectively. It is found that the crystallinity, electron mobility, and glass transition temperature of the DSMAs gradually increase in the order of DYA‐O, DYA‐IO, and DYA‐I, which, in turn, enhance the PCE and device stability of the resulting OSCs; DYA‐O (PCE = 16.45% and t80% lifetime = 3337 h) < DYA‐IO (PCE = 17.54% and t80% lifetime = 4255 h) < DYA‐I (PCE = 18.83% and t80% lifetime = 5380 h).

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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