Steric hindrance induced low exciton binding energy enables low-driving-force organic solar cells
Journal article, 2024

Exciton 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.

organic solar cells

exciton dissociation

exciton binding energy

steric hindrance

Author

Tianyu Hu

Jianghan University

Xufan Zheng

Jianghan University

T. Wang

Jianghan University

Aziz Saparbaev

National University of Uzbekistan named after Mirzo Ulugbek

Bowen Gao

Wuhan Institute of Technology

Jingnan Wu

Chalmers, Chemistry and Chemical Engineering, Applied Chemistry

Jingyi Xiong

Wuhan Institute of Technology

Ming Wan

Jianghan University

Tingting Cong

Jianghan University

Yuda Li

Wuhan Institute of Technology

Ergang Wang

Chalmers, Chemistry and Chemical Engineering, Applied Chemistry

Xunchang Wang

Jianghan University

Renqiang Yang

Jianghan University

Aggregate

2766-8541 (ISSN) 2692-4560 (eISSN)

Vol. 5 5 e632

Subject Categories

Physical Chemistry

Theoretical Chemistry

Condensed Matter Physics

DOI

10.1002/agt2.632

More information

Latest update

11/6/2024