Microporous Metal-Organic Framework (MOF)-Based Composite Polymer Electrolyte (CPE) Mitigating Lithium Dendrite Formation in All-Solid-State-Lithium Batteries

N Angulakshmi; Yingke Zhou; Shruti Suriyakumar; R Baby Dhanalakshmi; M Satishrajan; Subbiah Alwarappan; Mohamed H Alkordi; A Manuel Stephan

doi:10.1021/acsomega.9b04133

Microporous Metal-Organic Framework (MOF)-Based Composite Polymer Electrolyte (CPE) Mitigating Lithium Dendrite Formation in All-Solid-State-Lithium Batteries

ACS Omega. 2020 Apr 1;5(14):7885-7894. doi: 10.1021/acsomega.9b04133. eCollection 2020 Apr 14.

Authors

N Angulakshmi¹, Yingke Zhou¹, Shruti Suriyakumar², R Baby Dhanalakshmi², M Satishrajan², Subbiah Alwarappan², Mohamed H Alkordi³, A Manuel Stephan²

Affiliations

¹ The State Key Laboratory of Refractories and Metallurgy, Institute of Advanced Materials and Nanotechnology, College of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan 430 081, P.R.China.
² Electrochemical Power Sources Division, CSIR - Central Electrochemical Research Institute, Karaikudi 630 006, India.
³ Center for Materials Science, Zewail City of Science and Technology, October Gardens, Giza 12578, Egypt.

Abstract

Poly(ethylene oxide) (PEO)-based composite polymer electrolytes (CPEs) containing the amine-functionalized, zirconium-based metal-organic framework @silica (UiO-66-NH₂@SiO₂) and lithium, LiN(CF₃SO₂)₂ salt (LiTFSI) are prepared using a simple hot press method. The electrochemical properties such as compatibility of the electrolyte with the Li metal anode, Li transference number, and ionic conductivity are investigated for the different systems containing different relative concentrations of the additives. The incorporation of UiO-66-NH₂@SiO₂ in the PEO-LiTFSI matrix not only enhanced ionic conductivity by one order of magnitude but also offered better compatibility and suppressed the formation of lithium dendrites appreciably. X-ray photoelectron spectroscopy studies on post-cycled materials revealed the formation of lithium alkoxide (RO-Li) on the cathode and Li₂O on the anode. The coin cell (2032-type) consisting of LiFePO₄/CPE/Li with UiO-66-NH₂@SiO₂ as filler provided a discharge capacity of 151 mA h g^-1 at 0.1 C-rate at 60 °C, measurably higher than control experiments utilizing SiO₂ and UiO-66-NH₂. The notable enhancement of electrochemical properties when incorporating the UiO-66-NH₂@SiO₂ at the CPE was attributed to formation of more uniform ion conduction pockets and channels within the PEO matrix, facilitated by the presence of the microporous UiO-66-NH₂@SiO₂. The enhanced distribution of microporous channels, where Li ions are assumed to percolate through within the matrix, is assumed to desirably reduce formation of Li dendrites by increasing diffusion channels and therefore reducing crystallization and growth of dendrites at the electrode surface.