4.8 Article

Bioinspired Catechol-Grafting PEDOT Cathode for an All-Polymer Aqueous Proton Battery with High Voltage and Outstanding Rate Capacity

Journal

ADVANCED SCIENCE
Volume 9, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1002/advs.202103896

Keywords

all-organic batteries; aqueous proton batteries; catechol; poly(3; 4-ethylenedioxythiophene); polymer electrodes

Funding

  1. National Natural Science Foundation of China [521032089, 21774046]
  2. Department of Science and Technology of Jilin Province [20210508046RQ, 20200801057GH]
  3. China Postdoctoral Science Foundation [2021T140253, 2021M691188]
  4. Science and Technology Research Project of the Education Department of Jilin Province [JJKH20211048KJ]

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By designing a capacitive-type polymer cathode material and coupling it with a diffusion-type anode, this study demonstrates enhanced output voltage, rate capability, and cycling stability in aqueous all-polymer proton batteries compared to all-organic proton batteries.
Aqueous all-polymer proton batteries (APPBs) consisting of redox-active polymer electrodes are considered safe and clean renewable energy storage sources. However, there remain formidable challenges for APPBs to withstand a high current rate while maximizing high cell output voltage within a narrow electrochemical window of aqueous electrolytes. Here, a capacitive-type polymer cathode material is designed by grafting poly(3,4-ethylenedioxythiophene) (PEDOT) with bioinspired redox-active catechol pendants, which delivers high redox potential (0.60 V vs Ag/AgCl) and remarkable rate capability. The pseudocapacitive-dominated proton storage mechanism illustrated by the density functional theory (DFT) calculation and electrochemical kinetics analysis is favorable for delivering fast charge/discharge rates. Coupled with a diffusion-type anthraquinone-based polymer anode, the APPB offers a high cell voltage of 0.72 V, outstanding rate capability (64.8% capacity retention from 0.5 to 25 A g(-1)), and cycling stability (80% capacity retention over 1000 cycles at 2 A g(-1)), which is superior to the state-of-the-art all-organic proton batteries. This strategy and insight provided by DFT and ex situ characterizations offer a new perspective on the delicate design of polymer electrode patterns for high-performance APPBs.

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