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Site-Selective In Situ Electrochemical Doping for Mn-Rich Layered Oxide Cathode Materials in Lithium-Ion Batteries

机译:锂离子电池中锰含量高的层状氧化物阴极材料的定点原位电化学掺杂

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摘要

Various doped materials have been investigated to improve the structural stability of layered transition metal oxides for lithium-ion batteries. Most doped materials are obtained through solid state methods, in which the doping of cations is not strictly site selective. This paper demonstrates, for the first time, an in situ electrochemical site-selective doping process that selectively substitutes Li+ at Li sites in Mn-rich layered oxides with Mg2+. Mg2+ cations are electrochemically intercalated into Li sites in delithiated Mn-rich layered oxides, resulting in the formation of [Li1-xMgy][Mn1-zMz]O-2 (M = Co and Ni). This Mg2+ intercalation is irreversible, leading to the favorable doping of Mg2+ at the Li sites. More interestingly, the amount of intercalated Mg2+ dopants increases with the increasing amount of Mn in Li1-x[Mn1-zMz]O-2, which is attributed to the fact that the Mn-to-O electron transfer enhances the attractive interaction between Mg2+ dopants and electronegative O(delta-)atoms. Moreover, Mg2+ at the Li sites in layered oxides suppresses cation mixing during cycling, resulting in markedly improved capacity retention over 200 cycles. The first-principle calculations further clarify the role of Mg2+ in reduced cation mixing during cycling. The new concept of in situ electrochemical doping provides a new avenue for the development of various selectively doped materials.
机译:已经研究了各种掺杂材料以改善用于锂离子电池的层状过渡金属氧化物的结构稳定性。大多数掺杂材料是通过固态方法获得的,其中阳离子的掺杂并非严格地选择性。本文首次展示了一种现场电化学位点选择性掺杂工艺,该工艺可以选择性地用Mg2 +替代富锰层状氧化物中Li位的Li +。 Mg2 +阳离子被电化学嵌入到脱锂的富锰层状氧化物中的锂位点中,导致形成[Li1-xMgy] [Mn1-zMz] O-2(M = Co和Ni)。 Mg2 +的嵌入是不可逆的,从而导致Li位上的Mg2 +掺杂良好。更有趣的是,随着Li1-x [Mn1-zMz] O-2中Mn含量的增加,嵌入的Mg2 +掺杂剂的数量也会增加,这归因于Mn到O的电子转移增强了Mg2 +之间的吸引作用。掺杂剂和负电O(δ)原子。此外,层状氧化物中Li位置的Mg2 +抑制了循环过程中的阳离子混合,从而在200个循环中显着提高了容量保持率。第一性原理计算进一步阐明了Mg2 +在循环过程中减少阳离子混合中的作用。原位电化学掺杂的新概念为各种选择性掺杂材料的开发提供了新途径。

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  • 来源
    《Advanced energy materials》 |2018年第11期|1702514.1-1702514.10|共10页
  • 作者单位

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Dongguk Univ Seoul, Dept Energy & Mat Engn, 26 Pil Dong,3 Ga, Seoul 100715, South Korea;

    Pukyong Natl Univ, Dept Phys, Busan 48513, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Dongguk Univ Seoul, Dept Energy & Mat Engn, 26 Pil Dong,3 Ga, Seoul 100715, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

    Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
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  • 关键词

    cathode materials; in situ electrochemical doping; lithium-ion batteries; Mn-rich layered oxides; structural stability;

    机译:阴极材料;原位电化学掺杂;锂离子电池;富锰层状氧化物;结构稳定性;

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