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首页> 外文期刊>Advanced energy materials >High-Voltage-Driven Surface Structuring and Electrochemical Stabilization of Ni-Rich Layered Cathode Materials for Li Rechargeable Batteries
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High-Voltage-Driven Surface Structuring and Electrochemical Stabilization of Ni-Rich Layered Cathode Materials for Li Rechargeable Batteries

机译:用于LI可充电电池的Ni富含Ni的层状阴极材料的高压驱动的表面结构和电化学稳定

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摘要

Layered lithium-nickel-cobalt-manganese oxide (NCM) materials have emerged as promising alternative cathode materials owing to their high energy density and electrochemical stability. Although high reversible capacity has been achieved for Ni-rich NCM materials when charged beyond 4.2 V versus Li+/Li, full lithium utilization is hindered by the pronounced structural degradation and electrolyte decomposition. Herein, the unexpected realization of sustained working voltage as well as improved electrochemical performance upon electrochemical cycling at a high operating voltage of 4.9 V in the Ni-rich NCM LiNi0.895Co0.085Mn0.02O2 is presented. The improved electrochemical performance at a high working voltage at 4.9 V is attributed to the removal of the resistive Ni2+O rock-salt surface layer, which stabilizes the voltage profile and improves retention of the energy density during electrochemical cycling. The manifestation of the layered Ni2+O rock-salt phase along with the structural evolution related to the metal dissolution are probed using in situ X-ray diffraction, neutron diffraction, transmission electron microscopy, and X-ray absorption spectroscopy. The findings help unravel the structural complexities associated with high working voltages and offer insight for the design of advanced battery materials, enabling the realization of fully reversible lithium extraction in Ni-rich NCM materials.
机译:由于其高能量密度和电化学稳定性,层状锂 - 钴 - 锰氧化物(NCM)材料被出现为有前途的替代阴极材料。尽管在超过4.2V的富含NCM材料与Li + / Li的充电时已经实现了高可逆能力,但是通过明显的结构降解和电解质分解来阻碍全锂利用。在此,持续工作电压以及在电化学循环改进的电化学性能的在富Ni NCM LiNi0.895Co0.085Mn0.02O2 4.9 V的工作电压高的意想不到的实现被呈现。在4.9V的高工作电压下改善的电化学性能归因于去除电阻Ni2 + O岩盐表面层,其稳定电压曲线并改善电化学循环期间能量密度的保留。使用原位X射线衍射,中子衍射,透射电子显微镜和X射线吸收光谱法探测层状Ni2 + O岩盐相和与金属溶解相关的结构演进的表现。该研究结果有助于解开与高工作电压相关的结构复杂性,并为高级电池材料设计提供洞察力,从而实现富含Ni的NCM材料中的完全可逆锂萃取。

著录项

  • 来源
    《Advanced energy materials》 |2020年第23期|2000521.1-2000521.10|共10页
  • 作者单位

    Korea Atom Energy Res Inst KAERI Neutron Sci Ctr 111 Daedeok Daero 989 Beon Gil Daejeon 34057 South Korea|Korea Univ Dept Chem & Biol Engn 145 Anam Ro Seoul 02841 South Korea;

    Korea Atom Energy Res Inst KAERI Neutron Sci Ctr 111 Daedeok Daero 989 Beon Gil Daejeon 34057 South Korea;

    Res Inst Ind Sci & Technol RIST Battery Mat Res Ctr 67 Cheongam Ro Pohang 37673 South Korea;

    Max Planck POSTECH Hsinchu Ctr Complex Phase Mat 67 Cheongam Ro Pohang 37673 South Korea|Pohang Univ Sci & Technol Dept Phys 67 Cheongam Ro Pohang 37673 South Korea;

    Max Planck POSTECH Hsinchu Ctr Complex Phase Mat 67 Cheongam Ro Pohang 37673 South Korea|Pohang Univ Sci & Technol Dept Phys 67 Cheongam Ro Pohang 37673 South Korea|Korea Basic Sci Inst KBSI Res Ctr Mat Anal 169-148 Gwahak Ro Daejeon 34133 South Korea;

    Korea Inst Sci & Technol KIST Ctr Energy Mat Res 5 Hwarang Ro 14 Gil Seoul 02792 South Korea;

    Sejong Univ Dept Nanotechnol & Adv Mat Engn 209 Neungdong Ro Seoul 05006 South Korea;

    Samsung Elect Co Ltd Samsung Adv Inst Technol SAIT Mat Res Ctr Next Generat Battery Lab 130 Samsung Ro Suwon 16678 Gyeonggi Do South Korea;

    Australian Nucl Sci & Technol Org ANSTO New Illawarra Rd Lucas Heights NSW 2232 Australia;

    Korea Atom Energy Res Inst KAERI Neutron Sci Ctr 111 Daedeok Daero 989 Beon Gil Daejeon 34057 South Korea;

    Korea Atom Energy Res Inst KAERI Neutron Sci Ctr 111 Daedeok Daero 989 Beon Gil Daejeon 34057 South Korea;

    Korea Univ Dept Chem & Biol Engn 145 Anam Ro Seoul 02841 South Korea;

    Korea Atom Energy Res Inst KAERI Neutron Sci Ctr 111 Daedeok Daero 989 Beon Gil Daejeon 34057 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    cathodes; high voltages; Li-ion batteries; Ni-rich NCM; surface stabilization;

    机译:阴极;高电压;锂离子电池;Ni-Rich NCM;表面稳定;

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