Crystalline 1D Linear Conjugated Polymers with a Quinoidal Unit As Metal‐Free Electrocatalysts for Oxygen Reduction

Author:

Fan Renzhen1,Wang Cheng2,Zhang Xiaofei3,Zhang Xuwen2,Dong Weijia2,Xu Yiyang2,Xu Chenhui2,Chi Chunyan4,Zhu Jun3,Deng Yunfeng12ORCID,Geng Yanhou12

Affiliation:

1. Joint School of National University of Singapore and Tianjin University International Campus of Tianjin University Binhai New City Fuzhou 350207 China

2. School of Materials Science and Engineering and Tianjin Key Laboratory of Molecular Optoelectronic Science Tianjin University and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin 300072 China

3. Institute of Materials Research and Engineering (IMRE) Agency for Science, Technology and Research (A*STAR) 2 Fusionopolis Way Singapore 138634 Singapore

4. Department of Chemistry National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore

Abstract

AbstractCrystalline and soluble 1D linear conjugated polymers (LCPs) have garnered considerable interest as cost‐effective and efficient metal‐free electrocatalysts for the oxygen reduction reaction (ORR) due to their high exposure of catalytic sites and ease of processing. However, difficulties remain in achieving excellent ORR performance for 1D LCPs by conventional molecular design. Herein, it is demonstrated the utilization of quinoidal units as a promising strategy to develop 1D LCPs for ORR. The incorporation of quinoidal unit not only results in polymers with strong inter‐ and intra‐molecular interactions and low‐lying LUMO (lowest unoccupied molecular orbital) energy levels, but also provides polymers with good crystallinity and commendable charge carrier mobilities. The electronic properties of these polymers are fine‐tuned through the introduction of additional heteroatoms and/or substituents in the monomers and comonomers to understand and optimize their ORR catalytic activity. Evaluation of their catalytic performances reveals a remarkable half‐wave potential and limiting current density of up to 0.74 V (vs reversible hydrogen electrod) and 7.50 mA cm−2, respectively. Notably, these performances are achieved without the addition of carbon nanomaterials as support. This study offers a new insight into the design of highly efficient metal‐free organic electrocatalysts.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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