Origin of Suppressed Photovoltage Loss in Organic Solar Cells With Additive Engineering

S Shilin Li W Weichao Zhang X Xuning Zhang H Hong Zhang J Jiawei Qiao Y Yingyu Zhang (Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University) S Shengli Yue (School of Chemistry Beijing Advanced Innovation Center for Biomedical Engineering Beihang University Beijing People's Republic of China) L Linge Xiao (CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology Beijing People's Republic of China) Y Yanxun Li Y Ya‐Nan Jing (School of Chemistry Beijing Advanced Innovation Center for Biomedical Engineering Beihang University Beijing People's Republic of China) X Xiao‐Tao Hao (School of Physics State Key Laboratory of Crystal Materials Shandong University Jinan People's Republic of China) H Hui Wang Y Yuan Zhang H Huiqiong Zhou (CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology Beijing People's Republic of China)

Abstract

ABSTRACT Additive engineering has become widely adopted for tuning morphology and photovoltaic behaviors of organic solar cells (OSCs), while the resultant increase in delocalization of charge transfer (CT) excitons is often accompanied by a reduced CT‐state energy of additive‐processed blend films, which impairs photovoltage and restrains further improvements of photovoltaic efficiencies. Here, we achieve mitigation of photovoltage loss ( V loss ) over 30 meV while remaining high charge generation/transport efficiencies in a range of OSCs with A‐D‐A’‐D‐A type acceptors after additive treatment. Combined experimental and molecular dynamics simulation analyses reveal that additive treatments suppress voltage loss primarily by increasing the dielectric constant ( ε r ) in the CT state and reducing energetic disorder. These changes help inhibit back charge transfer from charge‐separated states to CT states, thereby decreasing non‐radiative recombination (Δ V non‐rad ) and improving device open‐circuit voltage. We further establish a universal ε r ‐dependent relationship for voltage loss, showing that both the increase in photovoltage and the reduction in Δ V non‐rad scale linearly with the enhancement of the blend dielectric constant. These findings deepen our insights into the voltage loss in organic solar cells, paving a way for surpassing the current photovoltage limits toward higher‐performance devices.

Article Details

Volume / Issue Vol. 65, Issue 32
Published August 03, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

S

Shilin Li

W

Weichao Zhang

X

Xuning Zhang

H

Hong Zhang

J

Jiawei Qiao

Y

Yingyu Zhang

Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University

S

Shengli Yue

School of Chemistry Beijing Advanced Innovation Center for Biomedical Engineering Beihang University Beijing People's Republic of China

L

Linge Xiao

CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology Beijing People's Republic of China

Y

Yanxun Li

Y

Ya‐Nan Jing

School of Chemistry Beijing Advanced Innovation Center for Biomedical Engineering Beihang University Beijing People's Republic of China

X

Xiao‐Tao Hao

School of Physics State Key Laboratory of Crystal Materials Shandong University Jinan People's Republic of China

H

Hui Wang

Y

Yuan Zhang

H

Huiqiong Zhou

CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology Beijing People's Republic of China