4.6 Article

Performance comparison of electro-polymerized polypyrrole and polyaniline as cathodes for iodine redox reaction in zinc-iodine batteries

Journal

ELECTROCHIMICA ACTA
Volume 415, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2022.140206

Keywords

Polyaniline; Polypyrrloe; Shuttling effect; Zinc-iodine battery; Long cycle life

Funding

  1. Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China [2021ZR137]
  2. Fujian Provincial Department of Science and Technology [2018H0042, 2020H0040, 2019T3017, 2020T3004, 2020T3030, 2021T3036]
  3. STS science andtechnology project of Chinese Academy of Sciences [KFJSTS-QYZD-2021-09-001]
  4. Quanzhou science and technology project [2020G17]

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The electro-polymerization of polyaniline and polypyrrole on carbon felt was studied for zinc-iodine batteries, with the former showing better performance due to its porous structure compared to the dense structure of the latter. The porous PANI electrode proved to have higher capacity, stronger ability to suppress polyiodide ions shuttling, and better cyclic stability than the dense PPy electrode. Ultimately, the PANI@CF electrode demonstrated promising long-term performance and stability for actual application in Zn//I batteries.
At present, Zinc-iodine (Zn//I) batteries have attracted much attention due to their high safety and capacity. However, how to suppress the shuttling of polyiodide ions generated during charging processes is still a tricky problem. Herein, polyaniline (PANI) and polypyrrole (PPy) are electro-polymerized on carbon felt (CF) by constant current and used as cathodes for zinc-iodine (Zn//I) batteries. Electrochemical tests of the PANI@CF and PPy@CF electrodes prove that the PANI@CF electrode has a higher capacity, a stronger ability to suppress shuttling of polyiodine ions, and more excellent cyclic stability than the PPy@CF electrode. According to the material characterizations, the differences of both electrodes in electrochemical performances are mainly caused by the microstructures of PANI and PPy in both electrodes. The PANI has a micro-nano porous structure while the PPy is very dense. The porous PANI not only has more channels for the infiltration of electrolyte, but also can provide more active adsorption sites to minimize the shuttling of polyiodide ions to anode, ensuring the excellent performances of the PANI@CF. However, dense PPy seriously hinders the electrolyte diffusion and triggers the formation of an insulating dense iodine film, bringing poor performances to the PPy@CF. Ultimately, the PANI@CF electrodes achieves the most specific capacity of 235.9 mAh g(-1) at 0.35 A g(-1) (similar to 1.7 C) and performs out long cycle life with high stability (75.7% capacitiy rention after 10,000 cycles) at 3.5 A g(-1) (similar to 17 C) in Zn//I battery, manifesting the porous PANI@CF electrode is a greatly promising candidate as cathode for Zn//I batteries in actual application.

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