4.7 Article

Dibenzo[a,e]Cyclooctatetraene-Functionalized Polymers as Potential Battery Electrode Materials

期刊

MACROMOLECULAR RAPID COMMUNICATIONS
卷 42, 期 18, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202000725

关键词

anode materials; cyclooctatetraene; molecular actuators; organic batteries; redox polymers; Wittig reaction

资金

  1. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [230408635, 398214985]
  2. German Federal Ministry of Education and Research [03XP0140]
  3. Projekt DEAL

向作者/读者索取更多资源

Organic redox polymers show promise as electrode materials for rechargeable batteries, with dibenzo[a,e]cyclooctatetraene (DBCOT) identified as a particularly attractive redox-active group. The synthesis of aliphatic DBCOT-polymers and their electrochemical properties were investigated, demonstrating their potential as battery electrode materials. Further research is needed to optimize electrode composition and fabrication processes to fully utilize the redox activity of DBCOT polymers.
Organic redox polymers are attractive electrode materials for more sustainable rechargeable batteries. To obtain full-organic cells with high operating voltages, redox polymers with low potentials (<2 V versus Li|Li+) are required for the negative electrode. Dibenzo[a,e]cyclooctatetraene (DBCOT) is a promising redox-active group in this respect, since it can be reversibly reduced in a two-electron process at potentials below 1 V versus Li|Li+. Upon reduction, its conformation changes from tub-shaped to planar, rendering DBCOT-based polymers also of interest to molecular actuators. Here, the syntheses of three aliphatic DBCOT-polymers and their electrochemical properties are presented. For this, a viable three-step synthetic route to 2-bromo-functionalized DBCOT as polymer precursor is developed. Cyclic voltammetry (CV) measurements in solution and of thin films of the DBCOT-polymers demonstrate their potential as battery electrode materials. Half-cell measurements in batteries show pseudo capacitive behavior with Faradaic contributions, which demonstrate that electrode composition and fabrication will play an important role in the future to release the full redox activity of the DBCOT polymers.

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