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J Colloid Interface Sci ; 608(Pt 3): 3013-3021, 2022 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-34802768

RESUMO

P2-type materials are regarded as competitive cathodes for next generation sodium ion batteries. However, the unfavorable P2 â†’ O2 phase transition usually leads to severe capacity decay. Moreover, the cathode material always suffers from destruction of surface crystal structure caused by trace amount of HF. In this study, a dual-modification method containing Mg/Ti co-doping and MgO surface coating is designed to solve the defects of P2-type Na0.67Ni0.17Co0.17Mn0.66O2 cathode. Results turn out that the P2 structure can be stabilized via Mg/Ti co-substitution and MgO layer could effectively prevent the surface from corroding by HF and promote migration of Na+. Moreover, the as-prepared MgO-coated Na0.67Ni0.17Co0.17Mn0.66Mg0.1O2 exhibits improved electrochemical performance than the raw material. It delivers 111.6 mAh g-1 initial discharge capacity and maintains 90.6% at high current density of 100 mA g-1 within 2-4.5 V, which has been obviously enhanced than that of Na0.67Ni0.17Co0.17Mn0.66O2. The significant improvement can be attributed to the synergistic effect of Mg/Ti co-substitution and MgO surface coating. This dual-modification strategy based on the synergetic effect of Mg/Ti co-doping and MgO surface coating might be a resultful step forward to develop cathode materials for sodium ion batteries.

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