Interfacial degradation at the cathode-electrolyte boundary triggers capacity fade and thermal instability. Controlled surface modification of active particles stabilizes the electrochemical interface to extend cycle life.
Polycrystalline secondary particles suffer from anisotropic volume expansion during cycling, leading to micro-cracks and electrolyte penetration. Transitioning to single-crystalline or modified multi-element structures prevents structural disintegration and rapid capacity fade.