Yb:Y2O3 submicrometric particles were synthesized through co-precipitation of Yb and Y nitrate in water. Microwave heating and controlled release of ammonia through urea decomposition at reaction temperature leaded to the formation of disaggregated, monosized spherical particles of carbo-hydroxy-nitrate precursors. Pure crystalline Yb:Y2O3 powder that preserved the described morphology was obtained after calcination in air at 800°C for 30 min. This powder mixed with commercial alumina powder was used to produce transparent Yb:YAG ceramics. Improved properties in terms of powder morphology and reactivity were presented in comparison with powders obtained by traditional heating.

Microwave assisted synthesis of Yb:Y2O3 based materials for laser source application

Anna Luisa Costa;Magda Blosi;Elisa Mercadelli;Laura Esposito;Andreana Piancastelli;Alessandra Sanson
2010

Abstract

Yb:Y2O3 submicrometric particles were synthesized through co-precipitation of Yb and Y nitrate in water. Microwave heating and controlled release of ammonia through urea decomposition at reaction temperature leaded to the formation of disaggregated, monosized spherical particles of carbo-hydroxy-nitrate precursors. Pure crystalline Yb:Y2O3 powder that preserved the described morphology was obtained after calcination in air at 800°C for 30 min. This powder mixed with commercial alumina powder was used to produce transparent Yb:YAG ceramics. Improved properties in terms of powder morphology and reactivity were presented in comparison with powders obtained by traditional heating.
2010
Istituto di Scienza, Tecnologia e Sostenibilità per lo Sviluppo dei Materiali Ceramici - ISSMC (ex ISTEC)
Microwave synthesis
Yb:Y2O3
Laser source application
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/439926
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