Influence of magnetic field upon electrode kinetics and ionic transport

Performance properties in lithium-ion, sodium-ion, and zero excess metal batteries are currently limited by the sluggish ion diffusion and inhomogeneity of the transport ion flux, resulting in poor formation, low rates, and short cycle lives. In this work, a magnetic field is applied to the cell by the incorporation of a NdFeB magnetic spacer, and the effect upon the kinetics and transport properties at each electrode is studied using galvanic charge and discharge, electrochemical impedance spectroscopy, and intermittent titration techniques. Stabilization of the anode-free or zero excess sodium and lithium metal cells is achieved during formation, and upon cycling. Reduced cell overpotential is observed with resulting higher areal capacities, with improved ionic diffusion through the electrode. Upon cycling metallic dendritic structures are suppressed due to the inhomogeneity of ion flux, and the likely competing kinetics of plating at a metallic tip and the surrounding surface. At the NMC electrode, improved kinetics are observed with lower charge-transfer resistance (Rct) due to the reshaped and aligned domain in the ferromagnetic Ni of NMC cathode. Pulsed current methods further confirm enhanced cationic diffusion in the anode graphite materials, particularly at high mass loading of 4 mA h cm−2 and high C rates. Consequently, the combination of enhanced reaction kinetics on the ferromagnetic cathode and improved diffusion kinetics in the porous anode leads to excellent full-cell performance compared to control groups. This study highlights the potential of magnetic fields in enhancing diffusion and reaction kinetics for rechargeable batteries (Li, Na, K, Mg, etc.), and may provide routes for extending cycle life, reconditioning cells, and improving formation protocols.