Formation of perovskite phase mixed metal oxides via thermal decomposition of metal-organic complexes with bifunctional ligands

1994 ◽  
Vol 2 (1-3) ◽  
pp. 305-309 ◽  
Author(s):  
C. D. Chandler ◽  
L. B. Archer ◽  
M. J. Hampden-Smith ◽  
R. W. Schwartz
1992 ◽  
Vol 271 ◽  
Author(s):  
Clive D. Chandlertw ◽  
M. J. Hampden-Smitht ◽  
C. J. Brinker

ABSTRACTCrystalline perovskite phase mixed metal oxides have been prepared at low temperatures from single-component mixed metal-organic precursors specifically designed for this purpose. Pyridine solutions of divalent metal α-hydroxycarboxylates of general empirical formula A(O2CMe2OH)2 where A = Pb, Ca, Sr, Ba; Me = methyl, react with metal alkoxide compounds such as B(OR')4, where B = Ti, Zr, Sn with the elimination of two equivalents of alcohol to form species with a fixed A:B stoichiometry of 1:1 according to the equation below.


1993 ◽  
Vol 93 (3) ◽  
pp. 1205-1241 ◽  
Author(s):  
Clive D. Chandler ◽  
Christophe. Roger ◽  
Mark J. Hampden-Smith

2018 ◽  
Vol 813 ◽  
pp. 127-133 ◽  
Author(s):  
Leticia Mirella da Silva ◽  
Géssica de Oliveira Santiago Santos ◽  
Marilia Moura de Salles Pupo ◽  
Katlin Ivon Barrios Eguiluz ◽  
Giancarlo Richard Salazar-Banda

RSC Advances ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 3979-3986 ◽  
Author(s):  
Magdalena Jabłońska ◽  
Miren Agote Arán ◽  
Andrew M. Beale ◽  
Kinga Góra-Marek ◽  
Gérard Delahay ◽  
...  

Cu–Al–Ox mixed metal oxides with intended molar ratios of Cu/Al = 85/15, 78/22, 75/25, 60/30, were prepared by thermal decomposition of precursors at 600 °C and tested for the decomposition of nitrous oxide (deN2O).


1995 ◽  
Vol 5 (1) ◽  
pp. 151 ◽  
Author(s):  
Leo B. Archer ◽  
Clive D. Chandler ◽  
Richard Kingsborough ◽  
Mark J. Hampden-Smith

1991 ◽  
Vol 243 ◽  
Author(s):  
Clive D. Chandler ◽  
Mark J. Hampden-Smith ◽  
Jeffrey Brinker

AbstractWe are developing strategies to form single-component precursors to perovskite phase mixed metal oxides where the stoichiometry of the precursor is fixed at the molecular level to be that of the final desired phase. These strategies ean be applied to the formation of perovskite phase thin films. Two such methods are described herein, relying on ester elimination and alcohol elimination reactions. We have found the reaction between lead(II) acetate and titanium(IV) isopropoxide in ethanol results in ligand redistribution at room temperature. Reactions between (β-diketonate)2M(OR)2 where M = Ti, Zr and Sn and lead(II) acetate do not result in any detectable ester elimination under the reaction conditions employed, and this approach was not successful. Alcohol elimination experiments have been explored as an alternative strategy using a bifunctional glycolate ligand. Lead carbonate reacted with glycolic acid to form the corresponding lead glycolate complex Pb(O2CCH2OH)2. This compound reacted with (β-diketonate)2M(OR)2, M = Ti and Sn, to eliminate two equivalents of alcohol and form the corresponding single component (β-diketonate)2M(OCH2CO2)2Pb complexes. These complexes start to thermally decompose at 150°C and loss of weight is complete by 450°C to yield a product whose weight loss corresponds to the formation of PbTiO3 for M = Ti. Bulk thermolysis of a sample of (dpm)2Ti(OCH2CO2)2Pb at 400°C resulted in formation of crystalline perovskite phase lead titanate together with PbO, massicot and α-PbO phases.


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