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Last updated January 31, 2026
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Lithium metal oxide particle morphology: BASFRecent Research Landscape

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.

What technical problems is BASF addressing in Lithium metal oxide particle morphology?

Structural instability and capacity decay

(32)evidences

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.

Inconsistent particle morphology

(32)evidences

Unprotected cathode surfaces react with electrolytes causing capacity loss and safety risks. Stabilizing the interface prevents chemical breakdown and extends cycle life.

Surface chemical instability

(21)evidences

Direct contact between high-voltage active materials and liquid electrolytes causes chemical instability and electrolyte decomposition. Preventing these surface reactions stops gas evolution and capacity fading.

Interfacial electrochemical instability

(18)evidences

Parasitic chemical reactions between the electrode surface and electrolyte cause rapid capacity loss. Mitigating these reactions prevents electrolyte decomposition and extends cycle life.