兴奋剂
动力学
材料科学
钠
阴极
无机化学
离子
氧化物
化学工程
化学
冶金
光电子学
物理化学
有机化学
工程类
物理
量子力学
作者
Jinxun Yu,Haifeng Yu,Linlin Zhou,Qilin Cheng,Hao Jiang
标识
DOI:10.1016/j.apsusc.2023.159121
摘要
O3-type layered oxide cathodes are identified as a promising cathode material for sodium-ion batteries (SIBs) due to their high specific capacity and moderate operating voltage, yet it usually suffers from sluggish Na-ion diffusion and structure instability. Herein, we demonstrate the synthesis of a trace Ti/Mg co-doped NaNi1/3Fe1/3Mn1/3O2 (TiMg-NFM) cathode, in which Ti-ion is distributed in transition metal layers and Mg-ion is doped into sodium layers. The co-doping can enlarge the Na-layer spacing inside the layered structure to reduce Na-ion diffusion barrier. Meanwhile, the structural stability is effectively reinforced via the stronger Ti-O bond and the pillar effect of Mg-ions, further reducing surface side reaction with electrolyte. These merits endow a high reversible capacity of the TiMg-NFM cathode with 144.5 mAh g−1 at 0.1C, and much higher capacity retention of 111.4 mAh g−1 at 5C versus the pristine NFM (62.1 mAh g−1). More impressively, 80.1% of initial capacity can be maintained after 300 cycles at 2C. This work presents a feasible strategy to enhance the reaction kinetics and structure stability for developing advanced O3-type layered oxide cathodes.
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