| Full text | |
| Author(s): |
Santagneli, Silvia H.
;
Baldacim, Helio V. A.
;
Ribeiro, Sidney J. L.
;
Kundu, Swarup
;
Martins Rodrigues, Ana Candida
;
Doerenkamp, Carsten
;
Eckert, Hellmut
Total Authors: 7
|
| Document type: | Journal article |
| Source: | Journal of Physical Chemistry C; v. 120, n. 27, p. 14556-14567, JUL 14 2016. |
| Web of Science Citations: | 8 |
| Abstract | |
Highly ion conducting glass-ceramics, crystallizing in the Na-superionic conducting (NASICON) structure, have been prepared in the system Li1+xAlxSnyGe2-(x+y)(PO4)(3) by crystallization of glassy precursor samples. For modest substitution levels (y = 0.25), these crystalline solid solutions show slightly higher electrical conductivity than corresponding samples-without Sn, supporting the rationale that the lattice expansion associated with the substitution of Ge by its larger homologue Sn can enhance ionic conductivity. Higher Sn substitution levels (y = 0.45) do not result in any improvement. The glass-to-crystal transition has been characterized in detail by multinuclear single and double resonance NMR experiments. While substantial changes in the P-31 and Al-27 MAS NMR spectra indicate that the crystallization of the glasses is accompanied by significant modifications in the local environments of the phosphate and the aluminum species, the dipolar solid state NMR experiments indicate that the structures of both phases are dominated by Ge-O-P, Sn-O-P, and Al-O-P connectivities. Substitution of Ge by Al and Sn in the crystalline NASICON structure results in a binomial distribution of multiple phosphate environments, which differ in the number of P-O-Ge, P-O-Al, and P-O-Sn linkages. While there is no chemical shift discrimination between P-O-Al and P-O-Sn linkages, an unambiguous distinction is possible on the basis of P-31[Al-27] rotational echo adiabatic passage double resonance (REAPDOR) experiments. (AU) | |
| FAPESP's process: | 13/02456-1 - Structural and dynamic study in disordered materials by nuclear magnetic resonance |
| Grantee: | Silvia Helena Santagneli |
| Support Opportunities: | Regular Research Grants |