1989 Fiscal Year Final Research Report Summary
Synthesis and Water Adsorption Properties of Perovskite-type Oxides Containing Manganese
Project/Area Number |
63470062
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Research Category |
Grant-in-Aid for General Scientific Research (B)
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Allocation Type | Single-year Grants |
Research Field |
無機工業化学
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Research Institution | Okayama University |
Principal Investigator |
NAGAO Mahiko Okayama University, Faculty of Science Professor, 理学部, 教授 (30032816)
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Project Period (FY) |
1988 – 1989
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Keywords | Perovskite / Metal oxide / Electrical property / Solid state reaction / Co-precipitation / Hopping conduction / Adsorption / Sintering |
Research Abstract |
Perovskite-type (Ln_<1-x>Ca_x)MnO_3 (Ln: La, Nd, Gd) were synthesized at 1300-1350゚C in the flow of pure oxygen gas. X-ray powder diffraction patterns of these manganates were indexed as the perovskite-type structure. At low temperature, manganates are n-type semiconductors and the electrical resistivity follows Mott's T^<-1/4> law, indicating the possible occurrence of variable range hopping of electron due to Anderson localization. Above room temperature, manganates have positive temperature coefficient, and exhibit a metal-insulator transition without any crystallographic change. The magnetic susceptibility measurement suggests that spin state of Mn^<3+> ions change from low to high at the metal-insulator transition temperature. From these results, it is considered that the metal-insulator transition is caused by a change in the spin state of Mn^<3+> ion in (Ln_<1-X> Ca_X)MnO_3. Fine particle (La^<1-x> Ca_x)MnO_3 was synthesized as follows: one is the decomposition of the precursor a
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nd the other is the solid state reaction by using acetates. The precursor was prepared from the co-precipitation method and its formula was found to be (Ca_<0.5> Mn_<0.5>)CO_3. Fine particle (La_<1-X> Ca_X)MnO_3 was synthesized as follows: one is the decomposition of the precursor and the other is the solid state reaction by using acetated. The precursor was prepared from the co-precipitation method and its formula was found to be (Ca_<0.5> Mn_<0.5>)CO_3. Firing this precursor at 950゚C, CaMnO_3 was obtained. On the other hand, acetates were weighted and mixed, then fired at 900゚C. The particle size of manganates thus obtained was 0.8-0.9 m, and the specific surface area was 3-5 m^2/g. By using these methods, the synthesis temperature of (La_<1-x> Ca_x)MnO_3 was lowered by 300-400゚C compared with the conventional solid state reaction. The electrical resistivity of (La_<1-x> Ca_x)MnO_3 under various relative pressure of H_2O vapor was measured. Only the electrical resistivity of CaMnO_3 decreased with increasing vapor pressure of H_2O, and this decrease was assumed to be ascribed to the ionic conductivity of water layer adsorbed on CaMnO_3. Less
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