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Influence of Lattice Polarizability on the Ionic Conductivity in the Lithium Superionic Argyrodites Li_6PS_5X (X = Cl, Br, I)

机译:晶格极化率对锂超离子菱形锂Li_6PS_5X(X = Cl,Br,I)中离子电导率的影响

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摘要

In the search for novel solid electrolytes for solid-state batteries, thiophosphate ionic conductors have been in recent focus owing to their high ionic conductivities, which are believed to stem from a softer, more polarizable anion framework. Inspired by the oft-cited connection between a soft anion lattice and ionic transport, this work aims to provide evidence on how changing the polarizability of the anion sublattice in one structure affects ionic transport. Here, we systematically alter the anion framework polarizability of the superionic argyrodites Li_6PS_5X by controlling the fractional occupancy of the halide anions (X = Cl, Br, I). Ultrasonic speed of sound measurements are used to quantify the variation in the lattice stiffness and Debye frequencies. In combination with electrochemical impedance spectroscopy and neutron diffraction, these results show that the lattice softness has a striking influence on the ionic transport: the softer bonds lower the activation barrier and simultaneously decrease the prefactor of the moving ion. Due to the contradicting influence of these parameters on ionic conductivity, we find that it is necessary to tailor the lattice stiffness of materials in order to obtain an optimum ionic conductivity.
机译:在寻找用于固态电池的新型固体电解质时,由于其高离子电导率,硫代磷酸酯离子导体已成为最近的焦点,据信这些离子电导率源于更柔软,更可极化的阴离子骨架。受到经常引用的软阴离子晶格与离子迁移之间的联系的启发,这项工作旨在提供证据,证明在一种结构中改变阴离子亚晶格的极化率如何影响离子迁移。在这里,我们通过控制卤化物阴离子的分数占有率(X = Cl,Br,I),系统地改变了超离子菱锰矿Li_6PS_5X的阴离子骨架极化率。声音测量的超声波速度用于量化晶格刚度和德拜频率的变化。结合电化学阻抗谱和中子衍射,这些结果表明,晶格柔软度对离子迁移具有显着影响:较软的键降低了活化势垒,同时降低了移动离子的前置因子。由于这些参数对离子电导率的矛盾影响,我们发现有必要调整材料的晶格刚度以获得最佳的离子电导率。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第31期|10909-10918|共10页
  • 作者单位

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany;

    Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI, United States;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany;

    Heinz Maier-Leibnitz Zentrum, Technische Universität München, Garching, Germany;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany,Center for Materials Research (LaMa), Justus-Liebig-University Giessen, Heinrich-Buff-Ring 16, Giessen, Germany;

    Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI, United States;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany,Center for Materials Research (LaMa), Justus-Liebig-University Giessen, Heinrich-Buff-Ring 16, Giessen, Germany;

    Institute of Physical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, Germany,Center for Materials Research (LaMa), Justus-Liebig-University Giessen, Heinrich-Buff-Ring 16, Giessen, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:08:00

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