Related Experiment Video
Updated: May 16, 2025

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Expanding the Electrochemical Stability Window: Unraveling the Role of Solvent Polarity and a WiSE-Compatible
Guobin Lai1,2, Jinguo Lin1, Weixing Mo1
1State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Abstract:
Expanding the electrochemical stability window (ESW) of aqueous batteries significantly enhances their safety and energy density, addressing performance limitations and elevating their position in energy storage systems. Over the past decade, water-in-salt electrolyte (WiSE) has led to groundbreaking advancement in this field. However, a pressing question arises: can we further broaden the ESW through novel approaches? This study delves into this question, leveraging atomistic simulation along with ESW estimation and WiSE continuum theory to uncover that interfacial solvent polarity, subtly modulated by adding minor organic solvents, expands the ESW as well as promotes ion intercalation and transport. The strategy of incorporating minor organic solvents is compatible with WiSE, which not only advances our comprehension but also forges new research paths for post-WiSE era aqueous battery innovation. More importantly, our study provides a systematic way for theoretically estimating ESW and analyzing its enhancement mechanism in aqueous batteries.
More Related Videos
07:05Author Spotlight: Eco-Friendly Extraction of Bioactive Compounds Using Polyol-Based Microwave-Assisted Techniques
Published on: August 23, 2024
11:04Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
Published on: December 20, 2016
Related Concept Videos
Solvating Effects
Leveling Effect
Entropy and Solvation
Molecular Shape and Polarity
Solvents
A...
Leveling Effect and Non-Aqueous Acid-Base Solutions
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):