Part-II: Exchange current density and ionic diffusivity studies on the ordered and disordered spinel LiNi0.5Mn1.5O4 cathode

被引:47
作者
Amin, Ruhul [1 ]
Belharouak, Ilias [1 ,2 ]
机构
[1] Hamad Bin Khalifa Univ, Qatar Fdn, Qatar Environm & Energy Res Inst, Doha, Qatar
[2] Hamad Bin Khalifa Univ, Qatar Fdn, Coll Sci & Engn, Doha, Qatar
关键词
LiNi0.5Mn1.5O4; Ordered spinel; Disordered spinel; Exchange current density; Ionic diffusivity; ELECTROCHEMICAL IMPEDANCE; ELECTRODES; LITHIUM; INTERCALATION; CHARGE; TRANSPORT; KINETICS;
D O I
10.1016/j.jpowsour.2017.02.070
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Additive-free pellets of Li1-xNi0.5Mn1.5O4 have been prepared for the purpose of performing ionic diffusivity and exchange current density studies. Here we report on the characterization of interfacial charge transfer kinetics and ionic diffusivity of ordered (P4(3)32) and disordered (Fd (3) over barm)Li1-xNi0.5Mn1.5O4 as a function of lithium content at ambient temperature. The exchange current density at the electrode/ electrolyte interface is found to be continuously increased with increasing the degree of delithiation for ordered phase (similar to 0.21-6.5 mA/cm(2)) at (x = 0.01-0.60), in contrast the disordered phase exhibits gradually decrease of exchange current density in the initial delithiation at the 4 V plateau regime (x = 0.01 -0.04) and again monotonously increases (0.65-6.8 mA/cm(2)) with further delithiation at (x = 0.04 -0.60). The ionic diffusivity of ordered and disordered phase is found to be similar to 5 x 10(-10) cm(2)s(-1) and similar to 10(-9) cm(2)s(-1), respectively, and does not vary much with the degree of delithiation. From the obtained results it appears that the chemical diffusivity during electrochemical use is limited by lithium transport, but is fast enough over the entire state-of-charge range to allow charge/discharge of micron-scale particles at practical C-rates. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 325
页数:8
相关论文
共 39 条
[1]  
Amin R., J POWER SOURCES
[2]   Characterization of Electronic and Ionic Transport in Li1-xNi0.33Mn0.33Co0.33O2 (NMC333) and Li1-xNi0.50Mn0.20Co0.30O2 (NMC523) as a Function of Li Content [J].
Amin, Ruhul ;
Chiang, Ming .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2016, 163 (08) :A1512-A1517
[3]  
Amin R, 2015, J ELECTROCHEM SOC, V162, pA1163, DOI 10.1149/2.0171507jes
[4]   A new three-volt spinel Li1+xMn1.5Ni0.5O4 for secondary lithium batteries [J].
Amine, K ;
Tukamoto, H ;
Yasuda, H ;
Fujita, Y .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (05) :1607-1613
[5]  
[Anonymous], [No title captured]
[6]  
[Anonymous], THESIS
[7]  
[Anonymous], 2004, Physical Chemistry of Ionic Materials
[8]   On the electrochemistry of an anode stack for all-solid-state 3D-integrated batteries [J].
Baggetto, L. ;
Oudenhoven, J. F. M. ;
van Dongen, T. ;
Klootwijk, J. H. ;
Mulder, M. ;
Niessen, R. A. H. ;
de Croon, M. H. J. M. ;
Notten, P. H. L. .
JOURNAL OF POWER SOURCES, 2009, 189 (01) :402-410
[9]   Analysis of Lithium Insertion/Deinsertion in a Silicon Electrode Particle at Room Temperature [J].
Chandrasekaran, Rajeswari ;
Magasinski, Alexandre ;
Yushin, Gleb ;
Fuller, Thomas F. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (10) :A1139-A1151
[10]   Kinetic characterization of the electrochemical intercalation of lithium ions into graphite electrodes [J].
Chang, YC ;
Jong, JH ;
Fey, GTK .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (06) :2033-2038