Local probing of ionic diffusion by electrochemical strain microscopy: Spatial resolution and signal formation mechanisms

被引:122
作者
Morozovska, A. N. [1 ]
Eliseev, E. A. [2 ]
Balke, N. [3 ]
Kalinin, S. V. [3 ]
机构
[1] Natl Acad Sci Ukraine, Inst Semicond Phys, UA-03028 Kiev, Ukraine
[2] Natl Acad Sci Ukraine, Inst Problems Mat Sci, UA-03142 Kiev, Ukraine
[3] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37922 USA
关键词
ATOMIC-FORCE MICROSCOPY; IN-SITU AFM; INTERCALATION-INDUCED STRESS; LITHIUM-ION; THIN-FILMS; DYNAMIC-BEHAVIOR; SURFACE; LI; BATTERIES; LICOO2;
D O I
10.1063/1.3460637
中图分类号
O59 [应用物理学];
学科分类号
摘要
Electrochemical insertion-deintercalation reactions are typically associated with significant change in molar volume of the host compound. This strong coupling between ionic currents and strains underpins image formation mechanisms in electrochemical strain microscopy (ESM), and allows exploring the tip-induced electrochemical processes locally. Here we analyze the signal formation mechanism in ESM, and develop the analytical description of operation in frequency and time domains. The ESM spectroscopic modes are compared to classical electrochemical methods including potentiostatic and galvanostatic intermittent titration, and electrochemical impedance spectroscopy. This analysis illustrates the feasibility of spatially resolved studies of Li-ion dynamics on the sub-10-nm level using electromechanical detection. (C) 2010 American Institute of Physics. [doi :10.1063/1.3460637]
引用
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页数:21
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