This technology involves doping the ZnMn2O4 spinel structure—a cathode active material for aqueous zinc-ion batteries—with nickel. This process converts the crystal structure from tetragonal to cubic and reduces the Mn3+ content, thereby suppressing manganese dissolution and improving ion diffusion pathways.
Conventional ZnMn2O4 cathode materials suffer from manganese dissolution into the electrolyte due to the disproportionation reaction of Mn3+. Furthermore, electrostatic repulsion between zinc ions within the lattice leads to poor rate capability and reduced cycle life.
This technology utilizes a co-precipitation method to synthesize ZnMn2-xNixO4 (1.0≤x≤1.5), which replaces Mn3+ with Mn4+, mitigates Jahn-Teller distortion, and expands the lattice volume to facilitate smoother zinc-ion transport. Suitable for residential and industrial ESS using non-flammable aqueous electrolytes as well as safety-critical wearable power sources, it achieves a specific capacity of over 70mAh/g and rapid charge-discharge performance without capacity degradation caused by manganese dissolution.
N/A