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通过核磁共振(NMR)结合电化学测量对电解质成分的动态传输进行直接原位观察。

Direct in situ observation of dynamic transport for electrolyte components by NMR combined with electrochemical measurements.

作者信息

Hayamizu Kikuko, Seki Shiro, Miyashiro Hajime, Kobayashi Yo

出版信息

J Phys Chem B. 2006 Nov 16;110(45):22302-5. doi: 10.1021/jp065616a.

Abstract

Electrochemical studies provide broad, but not cation- or anion-specific information on the migration of charged ions. However, individual ion diffusion (as a weighted average of charged and neutral ions) can be measured using pulsed-gradient spin-echo (PGSE) NMR. In this paper, the lithium transport in an electrolyte including a lithium salt was measured using electrophoretic NMR (ENMR) with non-blocking electrodes. A propylene carbonate (PC) solution doped with LiN(SO(2)CF(3))(2) (LiTFSI) was inserted in a homemade NMR cell equipped with Li/Li electrodes. The drift migrations of lithium cation ((7)Li), anion ((19)F), and solvent ((1)H) were measured independently under potentials of up to 3.0 V. Greatly enhanced dynamic lithium transport was observed for the first time in the bulk electrolyte under an electric field closely related to real conditions in a rechargeable lithium battery.

摘要

电化学研究提供了关于带电离子迁移的广泛但非阳离子或阴离子特异性的信息。然而,单个离子扩散(作为带电和中性离子的加权平均值)可以使用脉冲梯度自旋回波(PGSE)核磁共振来测量。在本文中,使用带有非阻塞电极的电泳核磁共振(ENMR)测量了包含锂盐的电解质中的锂传输。将掺杂有双(三氟甲基磺酰)亚胺锂(LiTFSI)的碳酸丙烯酯(PC)溶液插入配备有锂/锂电极的自制核磁共振池中。在高达3.0 V的电位下独立测量了锂阳离子(⁷Li)、阴离子(¹⁹F)和溶剂(¹H)的漂移迁移。在与可充电锂电池实际条件密切相关的电场下,首次在本体电解质中观察到动态锂传输大大增强。

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