{"title":"通过协同界面调节提高富锂二元氧化物阴极的可逆性,以改善高深度充放电时的电荷转移动力学","authors":"Qing Zhang, Jiaoyang Cheng, Jinxin Cao, Fang Lian","doi":"10.1002/celc.202500045","DOIUrl":null,"url":null,"abstract":"<p>Lithium-rich manganese-based oxides are accepted as a promising cathode material for high-energy density batteries. However, they suffer from irreversible structural transformations and detrimental interfacial reactions, especially under deep charge/discharge states, causing severe voltage fade and capacity degradation. Herein, Li-rich binary oxide Li<sub>1.16</sub>(Ni<sub>0.25</sub>Mn<sub>0.75</sub>)<sub>0.84</sub>O<sub>2</sub> is proposed to dual-coated by superionic conductor Li<sub>1.4</sub>Al<sub>0.4</sub>Ti<sub>1.6</sub>(PO<sub>4</sub>)<sub>3</sub> and conductive polymer polyaniline, displaying nearly two orders of magnitude promotion for lithium ion transmission coefficient (10<sup>−9.5</sup> cm<sup>2</sup> S<sup>−1</sup>) at the end of charge/discharge. COMSOL Multiphysics simulation indicates the synergistic interfacial coating elevates the homogeneous distribution of lithium–ions and current density, improving utilization rates of lithium–ions, mitigating irreversible structural transformation, and suppressing the dissolution of transition metal ions and side reactions between the cathode and electrolyte. 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引用次数: 0
摘要
富锂锰基氧化物是一种很有前途的高能密度电池正极材料。然而,它们遭受不可逆的结构转变和有害的界面反应,特别是在深充放电状态下,导致严重的电压衰减和容量退化。本文提出了由超离子导体Li1.4Al0.4Ti1.6(PO4)3和导电聚合物聚苯胺双包覆的富锂二元氧化物Li1.16(Ni0.25Mn0.75)0.84O2,在充放电结束时,锂离子传输系数(10−9.5 cm2 S−1)提高了近两个数量级。COMSOL Multiphysics模拟表明,协同界面涂层提高了锂离子的均匀分布和电流密度,提高了锂离子的利用率,减轻了不可逆的结构转变,抑制了过渡金属离子的溶解和阴极与电解质之间的副反应。因此,在2.0-4.8 V范围内,在20 mA g−1条件下,Li1.16(Ni0.25Mn0.75)0.84O2的电荷转移动力学得到了显著提升,比容量达到293.6 mAh g−1,初始库仑效率提高了84.42%,150次循环容量保持率提高了88.94%,同时具有低电压衰减(150次循环0.23 V)和5℃时160 mAh g−1的高倍率容量。
Enhanced Reversibility of Li-Rich Binary Oxide Cathodes through Synergistic Interfacial Regulation for Improved Charge Transfer Kinetics at High Depth of Charge/Discharge
Lithium-rich manganese-based oxides are accepted as a promising cathode material for high-energy density batteries. However, they suffer from irreversible structural transformations and detrimental interfacial reactions, especially under deep charge/discharge states, causing severe voltage fade and capacity degradation. Herein, Li-rich binary oxide Li1.16(Ni0.25Mn0.75)0.84O2 is proposed to dual-coated by superionic conductor Li1.4Al0.4Ti1.6(PO4)3 and conductive polymer polyaniline, displaying nearly two orders of magnitude promotion for lithium ion transmission coefficient (10−9.5 cm2 S−1) at the end of charge/discharge. COMSOL Multiphysics simulation indicates the synergistic interfacial coating elevates the homogeneous distribution of lithium–ions and current density, improving utilization rates of lithium–ions, mitigating irreversible structural transformation, and suppressing the dissolution of transition metal ions and side reactions between the cathode and electrolyte. Therefore, Li1.16(Ni0.25Mn0.75)0.84O2 with the significantly promoted charge transfer kinetics exhibits greatly strengthened specific capacity of 293.6 mAh g−1 at 20 mA g−1 within the range of 2.0–4.8 V, with an increased initial Coulombic efficiency of 84.42% and capacity retention of 88.94% in 150 cycles, alongside with a low voltage decay (0.23 V within 150 cycles) and a high rate capability of 160 mAh g−1 at 5 C.
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.