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High Voltage Mg-Doped Na0.67Ni0.3–xMgxMn0.7O2 (x = 0.05, 0.1) Na-Ion Cathodes with Enhanced Stability and Rate Capability
Author(s) -
Gurpreet Singh,
Nuria TapiaRuiz,
Juan Miguel López del Amo,
Urmimala Maitra,
James Somerville,
A. Robert Armstrong,
Jaione Martínez de Ilarduya,
Teófilo Rojo,
Peter G. Bruce
Publication year - 2016
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.6b01935
Subject(s) - doping , materials science , scanning electron microscope , analytical chemistry (journal) , electrochemistry , ion , phase (matter) , sodium , metal , nuclear chemistry , chemistry , electrode , metallurgy , optoelectronics , organic chemistry , chromatography , composite material
Magnesium substituted P2-structure Na0.67Ni0.3Mn0.7O2 materials have been prepared by a facile solid-state method and investigated as cathodes in sodium-ion batteries. The Mg-doped materials described here were characterized by X-ray diffraction (XRD), 23Na solid-state nuclear magnetic resonance (SS-NMR), and scanning electron microscopy (SEM). The electrochemical performance of the samples was tested in half cells vs Na metal at room temperature. The Mg-doped materials operate at a high average voltage of ca. 3.3 V vs Na/Na+ delivering specific capacities of ∼120 mAh g–1, which remain stable up to 50 cycles. Mg doping suppresses the well-known P2–O2 phase transition observed in the undoped composition by stabilizing the reversible OP4 phase during charging (during Na removal). GITT measurements showed that the Na-ion mobility is improved by 2 orders of magnitude with respect to the parent P2–Na0.67Ni0.3Mn0.7O2 material. The fast Na-ion mobility may be the cause of the enhanced rate performance

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