Modulation of Alkyl Chain Length on the Thiazole Side Group Enables Over 17% Efficiency in All‐Small‐Molecule Organic Solar Cells

Author:

Ma Kangqiao1,Feng Wanying1,Liang Huazhe1,Chen Hongbin1,Wang Yuxin1,Wan Xiangjian1,Yao Zhaoyang1,Li Chenxi1,Kan Bin2,Chen Yongsheng1ORCID

Affiliation:

1. State Key Laboratory and Institute of Elemento‐Organic Chemistry The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials Renewable Energy Conversion and Storage Center (RECAST) College of Chemistry Nankai University Tianjin 300071 China

2. School of Materials Science and Engineering National Institute for Advanced Materials Nankai University Tianjin 300350 China

Abstract

AbstractMolecular innovation is highly desirable to achieve efficient all‐small‐molecule organic solar cells (SM‐OSCs). Herein, three small‐molecule donors (SMDs) with alkylated thiazole side groups (namely BO‐1, HD‐1, and OD‐1), which differ only in the alkyl side chain are reported. Although these SMDs possess similar absorption profiles and molecular energy levels, their crystallinity and miscibility with BTP‐eC9 slightly decrease along with the elongation of the alkyl side chain. After blending with BTP‐eC9, different miscibility leads to different degrees of phase separation. Among these SM‐OSCs, the HD‐1‐based device shows a decent bulk‐heterojunction (BHJ) morphology with proper phase separation and more dynamic carrier behavior. Thus, compared to the BO‐1 and OD‐1‐based devices, the HD‐1‐based device achieves a higher short‐circuit current of 26.04 mA cm−2 and a fill factor of 78.46%, leading to an outstanding PCE of 17.19%, which is one of the highest values among SM‐OSCs. This work provides a rational design strategy of SMDs for highly efficient SM‐OSCs.

Funder

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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