Structural Characterization of Rare-Earth Doped Yttrium Aluminoborate Laser Glasses Using Solid State NMR


Autoria(s): DETERS, Heinz; CAMARGO, Andrea Simone Stucchi de; SANTOS, Cristiane N.; FERRARI, Cynthia R.; HERNANDES, Antonio Carlos; IBANEZ, Alain; RINKE, Matthias T.; ECKERT, Hellmut
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

The structure of laser glasses in the system (B(2)O(3))(0.6){(Al(2)O(3))(0.4-x)(Y(2)O(3))(x)} (0.1 <= x <= 0.25) has been investigated by means of (11)B, (27)Al, and (89)Y solid state NMR as well as Y-3d core-level X-ray photoelectron spectroscopy, (11)B magic-angle spinning (MAS) NMR spectra reveal that the majority of the boron atoms are three-coordinated, and a slight increase of four-coordinated boron content with increasing x can be noticed. (27)Al MAS NMR spectra show that the alumina species are present in the coordination states four, five and six. All of them are in intimate contact with both the three- and the four-coordinate boron species and vice versa, as indicated by (11)B/(27)Al rotational echo double resonance (REDOR) data. These results are consistent with the formation of a homogeneous, nonsegregated glass structure. For the first time, (89)Y solid state NMR has been used to probe the local environment of Y(3+) ions in a glass-forming system. The intrinsic sensitivity problem associated with (89)Y NMR has been overcome by combining the benefits of paramagnetic doping with those of signal accumulation via Carr-Purcell spin echo trains. Both the (89)Y chemical shifts and the Y-3d core level binding energies are found to be rather sensitive to the yttrium bonding state and reveal that the bonding properties of the yttrium atoms in these glasses are similar to those found in the model compounds YBO(3) and YAl(3)(BO(3))(4), Based on charge balance considerations as well as (11)B NMR line shape analyses, the dominant borate species are concluded to be meta- and pyroborate anions.

Deutsche Forschungsgemeinschaf (DFG)

Deutsche Forschungsgemeinschaft (DFG)

Brazilian Agencies FAPESP[04/00093-0]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES[455/04-1]

CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Alexandervon-Humboldt Foundation

Alexander von Humboldt Foundation (AvH)

NRW Forschungsschule

NRW Forschungsschule

CAPES-COFECUB project

Comité Français d´Evaluation de la Coopération Universitaire avec le Brésil (COFECUB)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Identificador

JOURNAL OF PHYSICAL CHEMISTRY C, v.113, n.36, p.16216-16225, 2009

1932-7447

http://producao.usp.br/handle/BDPI/29923

10.1021/jp9032904

http://dx.doi.org/10.1021/jp9032904

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Journal of Physical Chemistry C

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #NUCLEAR-MAGNETIC-RESONANCE #HIGH-RESOLUTION B-11 #Y-89 MAS-NMR #SITE CONNECTIVITIES #LOCAL-STRUCTURE #RANGE ORDER #O-17 MAS #BOROALUMINATE CRYSTALS #QUADRUPOLAR NUCLEI #SPECTROSCOPY #Chemistry, Physical #Nanoscience & Nanotechnology #Materials Science, Multidisciplinary
Tipo

article

original article

publishedVersion