Related Experiment Video
Updated: Sep 20, 2025

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Ether-Oxygen Groups Modified Carboxylic Ester Enabling High-Voltage Lithium Metal Batteries
Shuang Li1,2, Hongliang Xie1, Pushpendra Kumar3
1State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, China.
Propylene glycol monomethyl ether acetate (PMA) is a new solvent for lithium metal batteries (LMBs). PMA-based electrolytes enable stable high-voltage cycling and retain capacity at elevated temperatures.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Storage
Background:
- Lithium metal batteries (LMBs) offer high energy density but face capacity degradation due to electrolyte decomposition at high voltages.
- Developing stable electrolytes is crucial for advancing high-performance LMBs.
Purpose of the Study:
- To introduce propylene glycol monomethyl ether acetate (PMA) as a novel solvent for LMB electrolytes.
- To investigate the impact of PMA on electrolyte solvation structure and interfacial behavior.
- To enhance the stability and performance of LMBs at high cut-off voltages.
Main Methods:
- Formulation of PMA-based electrolytes with dual salts.
- Electrochemical cycling of Li||LiNi0.8Co0.1Mn0.1O2 (NCM811) batteries at 4.5 V and 60 °C.
- Molecular interfacial modeling to elucidate electrolyte-electrode interactions.
Main Results:
- The PMA-based electrolyte demonstrated stable cycling performance for over 100 cycles at a high cut-off voltage of 4.5 V.
- The battery retained 90.1% of its initial capacity at 60 °C.
- The unique ether-oxygen functionality of PMA promotes contact ion pairs (CIPs), enhancing electrolyte stability.
Conclusions:
- PMA is a promising solvent for developing high-performance LMB electrolytes.
- The study provides insights into electrolyte design for stable high-voltage lithium metal batteries.
- The findings contribute to advancing energy storage technologies.
More Related Videos
Related Concept Videos
Batteries and Fuel Cells
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Crown Ethers
Reactivity of Enolate Ions
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...

