4.7 Article

Polybenzimidazole-reinforced polyethylene oxide-based polymer-in-salt electrolytes enabling excellent structural stability and superior electrochemical performance for lithium metal batteries

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 465, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.142794

Keywords

Lithium metal battery; PEO-based electrolyte; Polymer-in-salt electrolyte; Cycling performance; Rate capability

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A flexible and robust polymer-in-salt electrolyte based on a composite of polybenzimidazole (PBI) and polyethylene oxide (PEO) has been developed for room-temperature lithium metal batteries. The PBI's rigid structure and dense hydrogen bonds with PEO enhance the structural stability of the electrolyte and suppress lithium dendrite growth. The thermal stability and fire resistance of the electrolyte have also been improved. The PEO-based polymer-in-salt electrolyte demonstrates high room temperature ionic conductivity, wide electrochemical window, and large lithium transference number, leading to improved cycling performance and rate capability in lithium-ion batteries.
Polyethylene oxide (PEO)-based solid polymer electrolyte (SPEs) is full of attraction due to its exceptional lithium ion dissolubility and strong resistance toward lithium metal reduction. Nevertheless, it still suffers from the unfulfilling room temperature ionic conductivity and poor mechanical properties. Herein, a flexible and robust polymer-in-salt electrolyte based on composite of polybenzimidazole (PBI) and PEO via a facile prepa-ration approach has been developed for room-temperature lithium metal batteries (LMBs). The rigid framework structure of PBI and dense hydrogen bonds formed between PBI and PEO jointly reinforce the structural stability of SPEs at high lithium salt concentration, which makes the SPEs possess sufficient mechanical properties to resist the lithium dendrites growth. The thermal stability and fire resistance of SPEs have also been improved relying on the distinctive flame retardancy and incombustibility of PBI. Besides, PBI is prone to forming hydrogen bonds with lithium salt anions to limit their mobility, while the rich N atoms on PBI chains can promote the dissociation of lithium salt through electrostatic attraction interaction. Their synergistic effects make the PEO-based polymer-in-salt electrolytes achieve the high room temperature ionic conductivity of 5.7 x 10-4 S cm-1, wide electrochemical window of 4.45 V, and large lithium transference number of 0.639. When applied to LMBs with LiFePO4 or LiNi0.88Co0.06Mn0.06O2 cathode, both coin cells exhibit improved cycling performance and rate capability. Furthermore, the LiNi0.88Co0.06Mn0.06O2/SiOx-C pouch cells using the SPEs demonstrate remarkable flexibility and safety, clarifying that the PEO-based polymer-in-salt electrolytes possess a promising application prospect for safe and high-performance LMBs.

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