Promoting solution phase discharge in Li-O2 batteries containing weakly solvating electrolyte solutions
Related Experiment Video
Updated: Mar 22, 2026

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Xiangwen Gao1, Yuhui Chen1, Lee Johnson1
1Departments of Materials and Chemistry, Parks Road, University of Oxford, Oxford OX1 3PH, UK.
Abstract:
On discharge, the Li-O2 battery can form a Li2O2 film on the cathode surface, leading to low capacities, low rates and early cell death, or it can form Li2O2 particles in solution, leading to high capacities at relatively high rates and avoiding early cell death. Achieving discharge in solution is important and may be encouraged by the use of high donor or acceptor number solvents or salts that dissolve the LiO2 intermediate involved in the formation of Li2O2. However, the characteristics that make high donor or acceptor number solvents good (for example, high polarity) result in them being unstable towards LiO2 or Li2O2. Here we demonstrate that introduction of the additive 2,5-di-tert-butyl-1,4-benzoquinone (DBBQ) promotes solution phase formation of Li2O2 in low-polarity and weakly solvating electrolyte solutions. Importantly, it does so while simultaneously suppressing direct reduction to Li2O2 on the cathode surface, which would otherwise lead to Li2O2 film growth and premature cell death. It also halves the overpotential during discharge, increases the capacity 80- to 100-fold and enables rates >1 mA cmareal(-2) for cathodes with capacities of >4 mAh cmareal(-2). The DBBQ additive operates by a new mechanism that avoids the reactive LiO2 intermediate in solution.
Related Concept Videos
Weak Acid Solutions
The Electrical Double Layer
Electrolyte and Nonelectrolyte Solutions
Electrochemical Systems
Ostwald’s Dilution Law
Electrolysis

