Drying Temperature and Capillarity-Driven Crack Formation in Aqueous Processing of Li-Ion Battery Electrodes

Kelsey Rollag, Daniel Juarez-Robles, Zhijia Du, David L. Wood, Partha P. Mukherjee

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Unlike conventional electrode processing for Li-ion batteries, which uses the expensive and highly toxic organic N-methyl-2-pyrrolidone (NMP) solvent, aqueous processing simply employs deionized water as the solvent. However, thick aqueous processed cathodes have been found to crack during drying. In this study, the influence of electrode drying temperature and thickness on cracking was investigated. LiNi1/3Mn1/3Co1/3O2 cathodes prepared with a hydrophilic binder, modified styrene-butadiene rubber (SBR), were coated at various thicknesses and dried at temperatures ranging from 20 to 70 °C. Experiments revealed cracking worsens with increased electrode thickness and elevated drying temperatures. Cracks were formed during the capillarity-driven phase during drying. Strong evaporation and weak diffusion played a critical role in the nonuniform distribution of the inactive phase. Images of electrode surfaces were processed to quantify crack dimensions and crack intensity factor (CIF). The average crack length and width, as well as CIF, increased with drying temperature and electrode thickness. Electrochemical performance revealed a strong and negative correlation between the crack density and performance in terms of specific capacity. Transport limitations associated with the presence of cracks adversely affect the advantage of high volume ratio of active materials in the thick electrodes.

Original languageEnglish
Pages (from-to)4464-4476
Number of pages13
JournalACS Applied Energy Materials
Volume2
Issue number6
DOIs
StatePublished - Jun 24 2019

Bibliographical note

Publisher Copyright:
© Copyright 2019 American Chemical Society.

Funding

This research was supported in part by NSF Grant 1438431/ 1759651 and a summer internship award to K.R. at Oak Ridge National Laboratory, a U.S. Department of Energy laboratory. The use of the Microscopy and Imaging Center (MIC) facility at Texas A&M University (TAMU) is acknowledged. Mukherjee’s group recently moved from TAMU to Purdue University.

FundersFunder number
National Science Foundation1438431/ 1759651
U.S. Department of Energy
Oak Ridge National Laboratory

    Keywords

    • aqueous processing
    • capillarity
    • crack formation
    • drying temperature
    • hydrophilic binder
    • thick cathode

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