Solvent-Induced Covalent Bond Softening Boosts Battery Voltage

Angew Chem Int Ed Engl. 2026 Apr 14:e9887882. doi: 10.1002/anie.9887882. Online ahead of print.

Abstract

Increasing cell voltage is a key strategy for enhancing the energy density of lithium batteries. Previously, this was mainly achieved by adjusting the redox potentials of transition-metal-based cathode materials through inductive effects that altered the covalency of metal-oxygen bonds. Here, we present a novel strategy for increasing battery voltage that consists of acting on the redox potential of the electrochemically active electrode through charge transfer with the electrolyte. To demonstrate this new concept, we used CFx-type electrodes, which are found in commercial primary batteries, and successfully achieved an impressive increase in redox potential of over 250 mV. This was done by increasing the ionicity of the C─F bond via a lactam-based electrolyte with high electron-donating capability. This finding, which was extended to other electrodes, namely I2, was rationalized through an array of analytical techniques and computational methods. Contrary to common belief, we clearly demonstrate that the electrolyte itself can significantly impact the bulk redox properties of electrodes, such as voltage. The new proposed inductive effect, driven by interactions between the solvent and the redox center, opens up new avenues of research in chemical bond regulation. It would also be highly valuable in energy-related systems, including electrocatalyst and beyond.

Keywords: Solvent/redox center interactions; bond elongation; charge transfer; covalent bond weakening.