Synthesis and cathodic properties of LiCo1-yRhyO2 (0 <= y <= 0.2.) and LiRhO2

Citation
S. Madhavi et al., Synthesis and cathodic properties of LiCo1-yRhyO2 (0 <= y <= 0.2.) and LiRhO2, J ELCHEM SO, 148(11), 2001, pp. A1279-A1286
Citations number
63
Categorie Soggetti
Physical Chemistry/Chemical Physics","Material Science & Engineering
Journal title
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
ISSN journal
00134651 → ACNP
Volume
148
Issue
11
Year of publication
2001
Pages
A1279 - A1286
Database
ISI
SICI code
0013-4651(200111)148:11<A1279:SACPOL>2.0.ZU;2-V
Abstract
Compounds of the formula LiCo1-yRhyO2 (0.0 < y < 0.20 and y = 1.0) have bee n synthesized by high temperature solid-state reaction and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy, and infrared sp ectroscopy. Single-phase materials were obtained for y less than or equal t o 0.10 and y = 1.0 as observed by XRD. However, IR and electrochemical data indicate that the true solid solubility may be y less than or equal to 0.0 5. Their cathodic behavior in coin cells with Li metal as anode and a liqui d electrolyte has been examined. Cyclic voltammograms and galvanostatic cha rge/discharge curves show that for y = 0.05, the phase transformation occur ring at x = 0.5 in Li1-xCoO2 is suppressed and the deintercalation voltage is decreased. The compositions with y = 0.05 and 0.10 show improved cathodi c behavior and discharge capacity retention compared to LiCoO2 ( y = 0) at 0.14C rate in the voltage range 2.7-4.3 V up to 18 cycles. Electrochemical studies on LiRhO2 show that phase transitions occur on charge/discharge cyc ling (varying x in Li1-xRhO2) in the voltage window 3.2-3.7 V and these are reversible. This compound shows an initial charge capacity of 162 mAh/g wh en charged to 4.0 V (vs. Li metal), corresponding to x = 0.85 in Li1-xRhO2. After an initial loss of 40 mAh/g in capacity, the discharge capacity rete ntion corresponds to 90% after 18 cycles with respect to the initial discha rge capacity in the voltage window, 2.7-4.0 V. (C) 2001 The Electrochemical Society.