A Rigid Polymer Donor Based on a Simple Benzodithiophene–Thiazole Backbone for Organic Photovoltaics

We report a new polymer donor, PBDTTz, featuring a simple benzo[1,2-b:4,5-b']dithiophene-thiazole backbone for organic photovoltaics (OPVs). Introduction of thiazole units induces intramolecular N···S interactions that lock the backbone conformation, yielding a rigid and coplanar structure. This design not only enhances intermolecular π-π interactions but also balances crystallinity with miscibility. As a result, PBDTTz exhibited a deeper highest occupied molecular orbital energy level, stronger π-π stacking, and improved blend morphology with the nonfullerene acceptor L8-BO, significantly outperforming its thiophene analog PBDTT in OPV performance. Optimized cells achieved a power conversion efficiency of 15.3%, which is quite high considering its simple chemical structure. These results highlight thiazole incorporation as an effective strategy to simultaneously control backbone rigidity, crystallinity, and miscibility, providing a straightforward route to high-performance polymer donors for OPVs.

Authors

Institutions

Publication Details

Journal
ChemSusChem
Published
2025-12-03
DOI
https://doi.org/10.1002/cssc.202501961
Citations
1
Primary Topic
Organic Electronics and Photovoltaics
Type
article
Field-Weighted Citation Impact
0.73

Funders

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

A Rigid Polymer Donor Based on a Simple Benzodithiophene–Thiazole Backbone for Organic Photovoltaics

Hyung Do Kim, Hideo Ohkita, Itaru Osaka, Yuki Sato et al.
1 citations
ChemSusChem
Organic Electronics and Photovoltaics
0.73
article

A Rigid Polymer Donor Based on a Simple Benzodithiophene–Thiazole Backbone for Organic Photovoltaics

Hyung Do Kim, Hideo Ohkita, Itaru Osaka, Yuki Sato, Tsubasa Mikie, Kodai Yamanaka, Yoshikazu Teshima, Masahiko Saito, Jihun Jeon
article en
1 citations

Abstract

We report a new polymer donor, PBDTTz, featuring a simple benzo[1,2-b:4,5-b']dithiophene-thiazole backbone for organic photovoltaics (OPVs). Introduction of thiazole units induces intramolecular N···S interactions that lock the backbone conformation, yielding a rigid and coplanar structure. This design not only enhances intermolecular π-π interactions but also balances crystallinity with miscibility. As a result, PBDTTz exhibited a deeper highest occupied molecular orbital energy level, stronger π-π stacking, and improved blend morphology with the nonfullerene acceptor L8-BO, significantly outperforming its thiophene analog PBDTT in OPV performance. Optimized cells achieved a power conversion efficiency of 15.3%, which is quite high considering its simple chemical structure. These results highlight thiazole incorporation as an effective strategy to simultaneously control backbone rigidity, crystallinity, and miscibility, providing a straightforward route to high-performance polymer donors for OPVs.

ChemSusChemVol. 19(1)
Hiroshima University (JP), Kyoto University (JP)
Japan Society for the Promotion of Science, Japan Science and Technology Agency, Advanced Low Carbon Technology Research and Development Program, JST-Mirai Program
Openalex Percentile: Top 21%
Organic Electronics and Photovoltaics
0.73
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.

A Rigid Polymer Donor Based on a Simple Benzodithiophene–Thiazole Backbone for Organic Photovoltaics — Hyung Do Kim, Hideo Ohkita, et al. · ChemSusChem (2025) | TGRS Research Map | TGRS