Angewandte Chemie International Edition · 2021 · 201 citations · 52 references
Natural SciencesMaterials EngineeringMaterials ScienceElectrochemistryInorganic ChemistryMaterials ChemistryBattery MaterialsCathode MaterialsElectrochemical Energy StorageEnergy Storage MaterialsMetal OxidesRedox-active MaterialsBand GapCapacity FadingCapacity MechanismHigh-voltage Cathode MaterialsHigh-voltage CathodesLithium-ion Battery Cathode MaterialsLithium-ion Battery MaterialsSurface Integrity
Abstract High‐voltage LiCoO 2 delivers a high capacity but sharp fading is a critical issue, and the capacity decay mechanism is also poorly understood. Herein, we clarify that the escape of surface oxygen and Li‐insulator Co 3 O 4 formation are the main causes for the capacity fading of 4.6 V LiCoO 2 . We propose the inhibition of the oxygen escape for achieving stable 4.6 V LiCoO 2 by tailoring the Co3d and O2p band center and enlarging their band gap with MgF 2 doping. This enhances the ionicity of the Co−O bond and the redox activity of Co and improves cation migration reversibility. The inhibition of oxygen escape suppresses the formation of Li‐insulator Co 3 O 4 and maintains the surface structure integrity. Mg acts as a pillar, providing a stable and enlarged channel for fast Li + intercalation/extraction. The modulated LiCoO 2 shows almost zero strain and achieves a record capacity retention at 4.6 V: 92 % after 100 cycles at 1C and 86.4 % after 1000 cycles at 5C.
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Naoaki Yabuuchi, Kazuhiro Yoshii, Seung‐Taek Myung et al. · Journal of the American Chemical Society · 2011 · 1.2K citations
Natural Sciences, Materials Engineering, Materials Science +15