Abstract
Layered transition metal oxides hold promise as cathode materials for sodium-ion batteries (SIBs). The P2-type Na2/3Ni1/3Mn2/3O2 cathode presents a high theoretical capacity and energy density, yet rapid capacity degradation occurs when the high-voltage plateau corresponding to the nominal Ni4+/Ni3+ redox is activated. Mitigating this degradation is necessary to realize the theoretical capacity of this material. While surface modification is a common strategy to improve the stability of cathode materials at high voltages, its effectiveness on the layered transition metal oxides for SIBs remains elusive. In this work, we investigated the role of surface coating on the reversibility of the high-voltage plateau through a suite of surface, bulk, and electrochemical characterizations. The surface modification of the P2-type Na2/3Ni1/3Mn2/3O2 cathode suppresses the growth of high-voltage polarization with minimal impact on the detrimental structure disorder induced by the P2-O2 phase transition. Our study highlights the limited effect of surface modification on capacity retention, which is predominantly driven by bulk structure degradation.
Supplementary materials
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Supporting Information
Description
Figures S1-5:
XRD patterns of Pristine Na2/3Ni1/3Mn2/3O2; Voltage profiles of Pristine and Al-NaNMO-400 for EIS measurements; Specific discharge capacity vs cycle numbers for Pristine and Al-NaNMOs; Specific capacity vs cycle numbers of pristine and Al-NaNMO-400 for Operando XRD; GITT profile of Pristine.
Tables S1-3:
Elemental compositions of Pristine and Al-NaNMO-400 by ICP-OES and HAADF-EDS mapping; XPS spectra Al peak fitting of Pristine and Al-NaNMOs; EIS fitting of Pristine and Al-NaNMO-400.
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