SYNTHESIS, REDOX POTENTIAL EVALUATION AND ELECTROCHEMICAL CHARACTERISTICS OF NASICON-RELATED-3D FRAMEWORK COMPOUNDS

Citation
Ks. Nanjundaswamy et al., SYNTHESIS, REDOX POTENTIAL EVALUATION AND ELECTROCHEMICAL CHARACTERISTICS OF NASICON-RELATED-3D FRAMEWORK COMPOUNDS, Solid state ionics, 92(1-2), 1996, pp. 1-10
Citations number
32
Categorie Soggetti
Physics, Condensed Matter","Chemistry Physical
Journal title
ISSN journal
01672738
Volume
92
Issue
1-2
Year of publication
1996
Pages
1 - 10
Database
ISI
SICI code
0167-2738(1996)92:1-2<1:SRPEAE>2.0.ZU;2-P
Abstract
The framework compounds M(2)(SO4)(3) with M = (Ti Fe), (V Fe), Fe and Li(x)M(2)(PO4)(3) with M = Ti, (V Fe), Fe, were synthesized and electr ochemically characterized by the coin-cell method. Use of larger (XO(4 ))(n-), polyanions not only allows fast Li+-ion conduction in an open three-dimensional framework that is selective for the working alkali i on on discharge; it also stabilizes operative redox potentials Fe3+/Fe 2+, Ti4+/Ti3+ and V3+/V2+ that give open-circuit voltages V-oc > 2.5 V as well as access to V4+/V3+, Ti3+/Ti2+ and Fe2+/Fe+ couples. Separat ion of the V4+/V3+ and V3+/V2+ couples were found to be 2.0 V. Fe-2(SO 4)(3) has both monoclinic and rhombohedral modifications that give a f lat open-circuit voltage V-oc = 3.6 V versus Li and a reversible capac ity for similar to 1.8 lithium atoms per formula unit. LixFe2(SO4)(3) shows an abrupt voltage drop occurring for x > 2 that can be held in c heck by the addition of buffers such as Li3Fe2(PO4)(3), FeV(SO4)(3) an d LiTi2(PO4)(3). Changing the polyanion group from (SO4)(2-) to (PO4)( 3-) in these framework compounds decreases the redox potentials from 3 .2 to 2.5 V for the Ti4+/Ti3+ couple, 2.5 to 1.7 V for the V3+/V2+ cou ple and 3.6 to 2.8 V for the Fe3+/Fe2+ couple. Comparative advantages and disadvantages of framework cathodes for Li rechargeable battery ap plications are discussed.