Steric hindrance induced low exciton binding energy enables low‐driving‐force organic solar cells

Author:

Hu Tianyu1ORCID,Zheng Xufan1,Wang Ting1,Saparbaev Aziz2,Gao Bowen3,Wu Jingnan4,Xiong Jingyi3,Wan Ming1,Cong Tingting1,Li Yuda3,Wang Ergang4,Wang Xunchang1,Yang Renqiang1

Affiliation:

1. Key Laboratory of Optoelectronic Chemical Materials and Devices (Ministry of Education) School of Optoelectronic Materials & Technology Jianghan University Wuhan China

2. Institute of Ion‐Plasma and Laser Technologies National University of Uzbekistan Tashkent Uzbekistan

3. Key Laboratory of Novel Biomass‐Based Environmental and Energy Materials in Petroleum and Chemical Industry Key Laboratory for Green Process of Ministry of Education School of Chemical Engineering and Pharmacy Wuhan Institute of Technology Wuhan China

4. Department of Chemistry and Chemical Engineering Chalmers University of Technology Göteborg Sweden

Abstract

AbstractExciton binding energy (Eb) has been regarded as a critical parameter in charge separation during photovoltaic conversion. Minimizing the Eb of the photovoltaic materials can facilitate the exciton dissociation in low‐driving force organic solar cells (OSCs) and thus improve the power conversion efficiency (PCE); nevertheless, diminishing the Eb with deliberate design principles remains a significant challenge. Herein, bulky side chain as steric hindrance structure was inserted into Y‐series acceptors to minimize the Eb by modulating the intra‐ and intermolecular interaction. Theoretical and experimental results indicate that steric hindrance‐induced optimal intra‐ and intermolecular interaction can enhance molecular polarizability, promote electronic orbital overlap between molecules, and facilitate delocalized charge transfer pathways, thereby resulting in a low Eb. The conspicuously reduced Eb obtained in Y‐ChC5 with pinpoint steric hindrance modulation can minimize the detrimental effects on exciton dissociation in low‐driving‐force OSCs, achieving a remarkable PCE of 19.1% with over 95% internal quantum efficiency. Our study provides a new molecular design rationale to reduce the Eb.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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