Research conducted by Purdue’s Vilas Pol Energy Research (ViPER) Group shows promise for developing high-energy-density rechargeable Lithium (Li)-metal batteries (LMB) and addressing the electrochemical oxidation instability of ether-based electrolytes.
The research was published in the Feb. 10, 2023 issue of Nature Communications, a peer-reviewed, open access, scientific journal published by Nature Portfolio. Zheng Li, a graduate research assistant in the Davidson School of Chemical Engineering, was the lead author.
The focus of the ViPER Group is the design and fabrication of high-capacity materials for next generation safer Lithium-ion, Lithium-sulfur, Sodium-ion, Solid-state and ultralow temperature battery systems. “The rapid growth of energy storage technologies aimed at reducing proposed carbon emission targets, and huge demands of energy storage systems also exist in the consumer electronic and electric vehicle markets. They call for next-generation Li batteries with higher energy density with enhanced safety,” says Vilas Pol, a professor of chemical engineering who has led Purdue’s premier laboratories for battery fabrication, electrochemical and thermal safety testing since 2014.
Replacing the conventional graphite anode material with high-energy lithium metal is a very promising approach. However, this “holy grail” anode material suffers from challenging drawbacks of low cyclability and safety, etc.
“From the perspective of fundamental research on new LMB technologies, it is critical to meticulously develop suitable liquid electrolyte chemistry that works with promising anodes and cathodes,” said Pol.
In their study, the researchers demonstrated that low concentration ether-based electrolyte can successfully endure the long-term high voltage (4.3 V) operation of practical LMB under industry viable configurations, when using the highly nonpolar dipropyl ether as the electrolyte solvent.
“Realizing the long-term cycling of Li metal anode and high-voltage cathode simultaneously with dilute ether-based electrolyte is the main challenge in this study,” said Li. “Ethers have poor oxidation stability despite their reasonable compatibilities to the Li metal anode. It was thus our target to extend their high-voltage capabilities. From the molecular level, we confirmed the essential correlations between the solvation behaviors of dilute ether-based electrolytes and their performance on high-voltage positive electrode.”
The correlations were further interpreted via detailed classical molecular dynamics (MD) simulations and density functional theory (DFT) calculations coupled with multimodal experimental analyses. It was demonstrated that regulating the solvation structure of ether-based electrolytes can rearrange the degradation order of solvation species and selectively form a robust protection on the cathode surface. It also adjusts the composition of surficial electric double layer to prevent the ether oxidation.
This unique kinetic-suppression approach differs from the conventional strategies such as using ultra-high concentration electrolyte or introducing molecular fluorination to improve the electrolyte stability, which dramatically increase the battery cost. The developed LMB by the ViPER group is expected to improve 40% of energy density, compared to the conventional Li-ion batteries.
The research work is funded by the Naval Enterprise Partnership Teaming with Universities for National Excellence (NEPTUNE), Office of Naval Research.
ABSTRACT
Non-polar ether-based electrolyte solutions for stable high-voltage non-aqueous lithium metal batteries
Zheng Li, lead author; Vilas G. Pol
Purdue University, Davidson School of Chemical Engineering
The electrochemical instability of ether-based electrolyte solutions hinders their practical applications in high-voltage Li metal batteries. To circumvent this issue, here, we propose a dilution strategy to lose the Li+/solvent interaction and use the dilute non-aqueous electrolyte solution in high-voltage lithium metal batteries. We demonstrate that in a non-polar dipropyl ether (DPE)-based electrolyte solution with lithium bis(fluorosulfonyl) imide salt, the decomposition order of solvated species can be adjusted to promote the Li+/salt-derived anion clusters decomposition over free ether solvent molecules. This selective mechanism favors the formation of a robust cathode electrolyte interphase (CEI) and a solvent-deficient electric double-layer structure at the positive electrode interface. When the DPE-based electrolyte is tested in combination with a Li metal negative electrode (50 μm thick) and a LiNi0.8Co0.1Mn0.1O2-based positive electrode (3.3 mAh/cm2) in pouch cell configuration at 25 °C, a specific discharge capacity retention of about 74% after 150 cycles (0.33 and 1 mA/cm2 charge and discharge, respectively) is obtained.
For more on Pol’s research, visit Purdue Engineers Create Safer Solid State Lithium Ion Batteries from New Composite Materials
