LaMn/sub 1-y//sup 3+/Mn/sub y//sup 4+/O/sub 3+or-d/ and La/sub 0.67/R/sub 0.33/Mn/sub 1-y//sup 3+/Mn/sub y//sup 4+/O/sub 3+or-d/ (R=Ca, Sr, Ba) phases were synthesized at 350 degrees C by using very reactive, amorphous precursors obtained from the stoichiometric citrate solutions. The chemical process was optimized with respect to the solution concentration, pH, and additives. The precursor reactions were investigated as a function of the cation stoichiometry and the additive by simultaneous thermal and thermogravimetric analysis and X-ray diffraction. The reaction pathway was found to be independent of the cation stoichiometry, but related to the acid or base additive. The annealing temperature was systematically increased in the 350-1200 degrees C interval and the La/sub 0.67/Sr/sub 0.33/MnO/sub 3+or-d/ properties (i.e., crystal sizes, Mn average valence, Curie temperature, magnetization, magnetic susceptibility) were measured and found to vary consistently as a function of it.

Low-temperature synthesis and properties of LaMnO/sub 3+or-d/ and La/sub 0.67/R/sub 0.33/MnO/sub 3+or-d/ (R=Ca, Sr, Ba) from citrate precursors

Licci F;Ferro P;
2003

Abstract

LaMn/sub 1-y//sup 3+/Mn/sub y//sup 4+/O/sub 3+or-d/ and La/sub 0.67/R/sub 0.33/Mn/sub 1-y//sup 3+/Mn/sub y//sup 4+/O/sub 3+or-d/ (R=Ca, Sr, Ba) phases were synthesized at 350 degrees C by using very reactive, amorphous precursors obtained from the stoichiometric citrate solutions. The chemical process was optimized with respect to the solution concentration, pH, and additives. The precursor reactions were investigated as a function of the cation stoichiometry and the additive by simultaneous thermal and thermogravimetric analysis and X-ray diffraction. The reaction pathway was found to be independent of the cation stoichiometry, but related to the acid or base additive. The annealing temperature was systematically increased in the 350-1200 degrees C interval and the La/sub 0.67/Sr/sub 0.33/MnO/sub 3+or-d/ properties (i.e., crystal sizes, Mn average valence, Curie temperature, magnetization, magnetic susceptibility) were measured and found to vary consistently as a function of it.
2003
Istituto dei Materiali per l'Elettronica ed il Magnetismo - IMEM
86
413
419
Sintesi chimica
Materiali magnetici
Manganiti
Nell'articolo viene riportata la preparazione dei precursori di manganito NaMn7O12 per reazioni in alta pressione. A causa principalmente della elevata tensione di vapore di Na, NaMn7O12 comincia a decomporsi a temperature inferiori a quella di formazione del composto dagli ossidi metallici. L’aumentata reattività del precursore riduce l’energia di attivazione del processo ed accelera la velocità della reazione, rendendone possibile il completamento prima della decomposizione. La comprensione di questo meccanismo e la soluzione dei problemi connessi mediante l’uso del precursore metallorganico hanno reso possibile ottenere il composto NaMn7O12 in forma monofasica, adatto allo studio delle proprietà intrinseche, ed hanno consentito di conseguire gli interessanti risultati tutt’ora in fase di studio.
4
info:eu-repo/semantics/article
262
Licci, F; Turilli, G; Ferro, P; Ciccarone, A
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/52726
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