scholarly journals Galvanostatic Intermittent Titration Technique Reinvented: Part I. A Critical Review

2021 ◽  
Vol 168 (12) ◽  
pp. 120504
Author(s):  
Stephen Dongmin Kang ◽  
William C. Chueh

The galvanostatic intermittent titration technique (GITT), introduced in 1977 by Weppner and Huggins, provided a readily accessible means to measuring the chemical diffusion coefficient of electrochemical electrode materials. The method continues to be widely used today, but the reported diffusivity values are highly inconsistent, ranging as much as four orders of magnitude for some Li layered oxide compositions. Even qualitative trends of diffusivity are inconsistent, suggesting significant flaws in the implementation of the method. Other variants of the GITT method also suffer from similar inconsistency problems. Here we identify numerous sources of significant error including composition-dependent reaction overpotentials, mathematical flaws in the relaxation analysis methods, finite-size and non-planar geometry effects, inter-particle inhomogeneity issues, early transient effects, and surface area uncertainties. We propose a simple relaxation analysis scheme using the time variable t relax + τ − t relax , where t relax is relaxation time and τ is the galvanostatic pulse duration. We also propose to use dense diffusion-limited samples to isolate the bulk-diffusion process in the time domain. Chemical diffusivity can be extracted much more reliably with this improved implementation of the GITT method.

1995 ◽  
Vol 393 ◽  
Author(s):  
Takashi Miura ◽  
Tomiya Kishi

ABSTRACTIn a series of fundamental studies on the cathode active materials for a lithium secondary cell using geometrically well-defined sample electrodes, thin films of spinel LiMn204on a platinum plate were investigated in this work in an LiCl04/propylene carbonate solution. These pyrolytically prepared films exihibit reversible extraction/insertion behavior for lithium under galvanostatic charge/discharge cycling between 4.3-3.5 V. The chemical diffusion coefficient of lithium in LixMn204determined by the galvanostatic intermittent titration technique (GITT) was in the order of 10−7-10−10cm2- s−1within a spinel single-phase region of 0.6<x<1.0 and increased with increasingx.


2003 ◽  
Vol 02 (06) ◽  
pp. 461-468
Author(s):  
D. G. W. PARFITT ◽  
M. E. PORTNOI

The anyon exciton model, which describes an exciton against the background of an incompressible quantum liquid, is generalized to the case of an arbitrary number of anyons. Some mathematical aspects of this quantum-mechanical few-particle problem are considered and several exact solutions are obtained. The four-particle case is also considered in the classical limit in both planar and spherical geometries. Such a classical approach gives an adequate description of an anyon exciton at large separation between the valence hole and the two-dimensional electron gas. It is shown that in this limit in a planar geometry the anyon exciton is always energetically more favorable than a charged anyon ion. This indicates that the appearance of fractionally-charged anyon ions reported in recent numerical calculations is an artefact apparently caused by finite-size effects in a spherical geometry.


2010 ◽  
Vol 181 (35-36) ◽  
pp. 1611-1615 ◽  
Author(s):  
J. Xie ◽  
N. Imanishi ◽  
A. Hirano ◽  
Y. Takeda ◽  
O. Yamamoto ◽  
...  

2015 ◽  
Vol 8 (1) ◽  
pp. 182-187 ◽  
Author(s):  
Z. H. Cui ◽  
X. X. Guo ◽  
H. Li

Key thermodynamic and kinetic properties of the Li–O2battery are studied by the GITT technique for the first time.


2005 ◽  
Vol 237-240 ◽  
pp. 1022-1030
Author(s):  
Junichi Shirakawa ◽  
H. Ikuta ◽  
Y. Uchimoto ◽  
M. Wakihara

Lithium diffusion properties of Li1-2yCo1+yVO4 (y = 0, 0.05, 0.1) with inverse spinel structure as cathode materials for a Li-ion battery were investigated in view of lithium vacancies. >From galvanostatic intermittent titration technique (GITT) analysis, it is evaluated that diffusion coefficients of lithium ion DLi in Li1-xCoVO4 were decreasing from about 10-10 cm2 s-1 (x = 0.05) to 10-12 cm2 s-1 (x = 0.4), and also decreasing for Li1-2y-xCo1+yVO4 in spite of production for lithium vacancies that is related to pre-exponential factor D0. EXAFS analysis revealed that the Debye-Waller factors which corresponded to the local distortion of each V-O and Co-O bonds were increasing by production of cation vacancies, indicating that the large local distortion of the lattice around vanadium and cobalt ions occurred. The result suggested that lithium diffusion path in these materials was disturbed by the local distortion and caused increasing the activation energy DG‡.


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