Polymer Molecular-Weight Engineering Enables 19.56%-Efficient Organic Solar Cells Based on Y6 Acceptors

As the prototypical Y-series nonfullerene acceptor, Y6 exhibits outstanding optoelectronic properties but its limited solubility and strong crystallization tendency have long been regarded as constraints on the device performance. Here, we propose a strategy distinct from conventional acceptor molecular engineering: by tuning the molecular weight of the donor polymer D18, the film formation kinetics of Y6 can be substantially reshaped, enabling highly efficient devices without relying on molecular redesign of the acceptor. We find that an intermediate polymer molecular weight effectively slows down the rapid crystallization of Y6 during spin-coating, prolongs the duration of the intermediate metastable state, suppresses premature phase separation, and facilitates the formation of a more uniform and interpenetrating bulk heterojunction morphology. In situ UV–vis absorption and fluorescence spectroscopy provide direct evidence for this kinetic control mechanism. The device based on this strategy achieved 19.56% photoelectric conversion efficiency, indicating that polymer molecular-weight engineering can overcome the limitation of low solubility acceptors.

Authors

Institutions

Publication Details

Journal
Macromolecules
Published
2026-05-21
DOI
https://doi.org/10.1021/acs.macromol.6c00614
Primary Topic
Organic Electronics and Photovoltaics
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Polymer Molecular-Weight Engineering Enables 19.56%-Efficient Organic Solar Cells Based on Y6 Acceptors

Guangliu Ran, Liu Y, Yonghuan Li, Bohan Shang et al.
Macromolecules
Organic Electronics and Photovoltaics
article

Polymer Molecular-Weight Engineering Enables 19.56%-Efficient Organic Solar Cells Based on Y6 Acceptors

Guangliu Ran, Liu Y, Yonghuan Li, Bohan Shang, X D Yan, Hao Lu, Luyao Yang, Zhishan Bo
article en

Abstract

As the prototypical Y-series nonfullerene acceptor, Y6 exhibits outstanding optoelectronic properties but its limited solubility and strong crystallization tendency have long been regarded as constraints on the device performance. Here, we propose a strategy distinct from conventional acceptor molecular engineering: by tuning the molecular weight of the donor polymer D18, the film formation kinetics of Y6 can be substantially reshaped, enabling highly efficient devices without relying on molecular redesign of the acceptor. We find that an intermediate polymer molecular weight effectively slows down the rapid crystallization of Y6 during spin-coating, prolongs the duration of the intermediate metastable state, suppresses premature phase separation, and facilitates the formation of a more uniform and interpenetrating bulk heterojunction morphology. In situ UV–vis absorption and fluorescence spectroscopy provide direct evidence for this kinetic control mechanism. The device based on this strategy achieved 19.56% photoelectric conversion efficiency, indicating that polymer molecular-weight engineering can overcome the limitation of low solubility acceptors.

Macromolecules
Qingdao University (CN), Beijing Normal University (CN), Division of Materials Science and Engineering (AU)
National Natural Science Foundation of China
Affordable and clean energy
Openalex Percentile: Top 9%
Organic Electronics and Photovoltaics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.