Preventing Benzoquinone‐Based Catalyst Aggregation Enables the One‐Step Synthesis of Highly Conductive Poly(benzodifurandione) without Post‐Reaction Purification

J Jun‐Da Huang (Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden) Q Qifan Li (Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping Sweden) Q Qingqing Wang (Institute of Immunology, Zhejiang University School of Medicine) T Tiefeng Liu (College of Chemical and Biological Engineering) S Sang Young Jeong (Department of Chemistry, Korea University, Anamro 145, Seoul 02841, Republic of Korea) S Sri Harish Kumar Paleti (Department of Chemistry and Chemical Engineering Chalmers University of Technology Göteborg 41296 Sweden) T Tom P. A. van der Pol (Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden) K Kai Xu H Han‐Yan Wu (Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping Sweden) N Natalie Pinchin (n‐Ink AB Källvindsgatan 5 Norrköping SE‐60240 Sweden) M Marc‐Antoine Stoeckel (Wallenberg Initiative Materials Science for Sustainability Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden) W Wenlong Jin A Aleksandr Perevedentsev (Department of Nanostructured Materials Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra E‐08193 Spain) X Xianjie Liu (Laboratory of Organic Electronics Department of Science and Technology (ITN) Linköping University Norrköping Sweden) J Juan Sebastián Reparaz (Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra Spain) M Mariano Campoy‐Quiles (Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra Spain) H Han Young Woo C Christian Müller M Mats Fahlman C Chi‐Yuan Yang (n‐ink AB Norrköping SE‐60221 Sweden) S Simone Fabiano (Laboratory of Organic Electronics, Department of Science and Technology, Linköping University)

Abstract

Abstract Conductive polymers have become crucial in advancing various electronic applications. While p‐type materials like poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) are widely used and produced at scale, the development of high‐performance n‐type polymers has lagged due to challenges in synthesis and scalability. In this work, a novel method is introduced to synthesize the highly conductive n‐type polymer poly(benzodifurandione) (PBFDO) using α‐tocopherylquinone (α‐TQ) as a catalyst. This approach eliminates the need for post‐reaction dialysis, a major obstacle to large‐scale PBFDO production. By preventing catalyst aggregation, high electrical conductivity (>1320 S cm −1 ) is achieved, which remains stable in air for over 180 d, significantly simplifying the process. The α‐TQ‐synthesized PBFDO also exhibits excellent thermoelectric properties, with a power factor exceeding 100 µW m −1 K −2 , placing it among the highest‐performing n‐type thermoelectric polymers. Additionally, residual α‐TQ acts as a plasticizer, reducing the elastic modulus by over tenfold while maintaining high conductivity, making this material suitable for mechanically compliant electronics. Similarly, residual α‐TQ lowers the thermal conductivity of PBFDO by more than an order of magnitude. The process is scalable, as demonstrated by producing high‐conductivity ink in a 20 L reactor. This work presents an efficient and sustainable approach for large‐scale n‐type polymer production.

Article Details

Volume / Issue Vol. 37, Issue 17
Published April 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (21)

J

Jun‐Da Huang

Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden

Q

Qifan Li

Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping Sweden

Q

Qingqing Wang

Institute of Immunology, Zhejiang University School of Medicine

T

Tiefeng Liu

College of Chemical and Biological Engineering

S

Sang Young Jeong

Department of Chemistry, Korea University, Anamro 145, Seoul 02841, Republic of Korea

S

Sri Harish Kumar Paleti

Department of Chemistry and Chemical Engineering Chalmers University of Technology Göteborg 41296 Sweden

T

Tom P. A. van der Pol

Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden

K

Kai Xu

H

Han‐Yan Wu

Laboratory of Organic Electronics Department of Science and Technology Linköping University Norrköping Sweden

N

Natalie Pinchin

n‐Ink AB Källvindsgatan 5 Norrköping SE‐60240 Sweden

M

Marc‐Antoine Stoeckel

Wallenberg Initiative Materials Science for Sustainability Department of Science and Technology Linköping University Norrköping SE‐60174 Sweden

W

Wenlong Jin

A

Aleksandr Perevedentsev

Department of Nanostructured Materials Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra E‐08193 Spain

X

Xianjie Liu

Laboratory of Organic Electronics Department of Science and Technology (ITN) Linköping University Norrköping Sweden

J

Juan Sebastián Reparaz

Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra Spain

M

Mariano Campoy‐Quiles

Institut de Ciència de Materials de Barcelona ICMAB‐CSIC Bellaterra Spain

H

Han Young Woo

C

Christian Müller

M

Mats Fahlman

C

Chi‐Yuan Yang

n‐ink AB Norrköping SE‐60221 Sweden

S

Simone Fabiano

Laboratory of Organic Electronics, Department of Science and Technology, Linköping University