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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) 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 K, 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.
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http://dx.doi.org/10.1002/adma.202502426 | DOI Listing |
J Am Chem Soc
September 2025
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China.
Compared with the conventionally used strong acid/electrophile initiators, carboxylic acids are much more compatible with other functional groups but are incapable of initiating cationic polymerization for the one-step synthesis of end-functionalized polymers. Using lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as a catalyst, we realized carboxylic acid-initiated cationic ring-opening polymerization (CROP) of 2-ethyl-2-oxazoline (EtOx). The dynamic exchange between carboxylate and TFSI anions, driven by Li-carboxylate interaction, significantly enhances the activity of oxazolinium propagating species and ensures uniform chain growth, as shown by both experiments and calculations.
View Article and Find Full Text PDFMater Horiz
September 2025
State Key Laboratory of Fluorine & Nitrogen Chemicals, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, China.
Despite the prevalence of zeolitic imidazolate framework (ZIF-67)-derived catalysts for the hydrogen evolution reaction (HER), the catalytic potential of pristine ZIF-67 remains obscured by its inherent inertness. In this work, we address this gap by developing an annealing-free strategy to implant atomically dispersed noble metals (Ru, Rh, and Pd) into the intact ZIF-67 framework. Remarkably, Ru single-atom modification reduces the HER overpotential of ZIF-67/CC by 252 mV at 10 mA cm (from 331 mV to 79 mV) and slashes the Tafel slope by 70%, representing the most significant activation of pristine ZIF-67 reported for the HER.
View Article and Find Full Text PDFPLoS One
September 2025
School of Economics and Management, Shanghai University of Sport, Shanghai, China.
The rise of the "sports fandom circle" has become a significant phenomenon in the digital media era, reshaping the emotional and social dynamics of sports fan communities. This study employs grounded theory methodology to analyze web-scraped data from 40 selected accounts on major Chinese social media platforms [Weibo, Xiaohongshu, and Bilibili] over a two-year period. These accounts were identified based on their focus on celebrity athletes [e.
View Article and Find Full Text PDFSmall Methods
September 2025
Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, School of Materials Science & Engineering and Hubei Key Laboratory of Polymer Materials, Hubei University, Wuhan, 430062, China.
Photocatalytic technology has garnered considerable attention in wastewater treatment, but its application to complex wastewater remains challenged by particle aggregation and the difficulty of separating the catalyst from water. In this study, the heterojunction composite catalyst ZnS@BiS and halloysite nanotubes (HNTs) are immobilized onto a sponge substrate to enhance photocatalytic performance. SEM, XRD, XPS, FTIR, and UV-Vis analyses are conducted to characterize the morphology and evaluate the organic degradation performance of PPG/HNTs/ZnS@BiS.
View Article and Find Full Text PDFSmall
September 2025
School of Chemistry, University of New South Wales, Sydney, 2052, Australia.
Oxygen reduction reaction (ORR) performance of platinum can be improved through alloying transition metals, with L1-PtCo emerging as a standout option due to its balanced catalytic performance, durability, and manufacturability. However, traditional carbon supports often fail to stabilize nanoparticles, leading to performance degradation. This study introduces a mesoporous Co-N-C supported ordered L1-PtCo catalyst to overcome the above limitations.
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