Magnetic properties of pseudo-ideal cubic La0.6−xCaxBa0.4CoO3 with hole doping
Creators
- 1. Inner Mongolia Key Lab of Nanoscience and Nanotechnology, Hohhot 010021 (China)
- 2. School of Physics, Inner Mongolia University, Hohhot 010021 (China)
Description
The La0.6−xCaxBa0.4CoO3 (x=0.03, 0.04, 0.05, 0.075, 0.1 and 0.15) compounds are synthesized. The cubic La0.6Ba0.4CoO3 has the strongest ferromagnetic (FM) double exchange interaction among all the La–Ba–Co–O compounds due to the straight Co–O–Co bond. The variation of the lattice parameter versus the calcium content exhibits a non-linear dependence and has the lowest value at x=0.05. In La0.6−xCaxBa0.4CoO3 compounds with x≤0.05, the magnetic frustration is observed below about 190 K, and the substitution of Ca2+ for La3+ enhances the FM interaction due to the increasing double exchange through Co3+–O2−–Co4+ bond. The analysis based on the measured magnetization at 50 kOe and the calculated value indicates that Co3+ ions are almost equally distributed at the low spin state and the intermediate spin state, and the Co4+ ions are at the low spin state. La0.55Ca0.05Ba0.4CoO3 has the lowest coercivity. As the composition deviates from x=0.05, the coercivity is enhanced. For the samples with θCW, the substitution of Ca2+ ions enhances the antiferromagnetic (AFM) interaction, and it is strong enough to make the long range AFM interaction appear. The percentage of the FM domains is calculated, and it decreases very quickly with the Ca2+ content x≥0.05. The sample with x=0.15 is mostly composed of AFM domains, and its AFM–FM transition temperature is 120 K. Another FM interaction with a low magnetic moment at the low temperature is also observed. - Graphical abstract: The thermal magnetization at 200 Oe at the ZFC and the FC states. - Highlights: • We studied the hole doping on the magnetic properties of La0.6−xCaxBa0.4CoO3. • With x≤0.05, Ca2+ enhances the ferromagnetic interaction. • With θCW, Ca2+ induces long range antiferromagnetic interaction. x=0.15 is mostly AFM. • Co3+ ions are equally distributed at LS and IS state, and Co4+ are at LS state. • We analyzed the development of the magnetic interaction with the doping Ca2+
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2014.04.007Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2014.04.007;
- PII
- S0022-4596(14)00164-9;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry
- Journal Volume
- 215
- Journal Page Range
- p. 241-244
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46040572
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANTIFERROMAGNETISM; ATOMIC FORCE MICROSCOPY; CALCIUM IONS; COBALT IONS; COERCIVE FORCE; EXCHANGE INTERACTIONS; LANTHANUM IONS; LATTICE PARAMETERS; MAGNETIC MOMENTS; MAGNETIC PROPERTIES; MAGNETIZATION; PEROVSKITE; SPIN; TRANSITION TEMPERATURE
- Descriptors DEC
- ANGULAR MOMENTUM; CHARGED PARTICLES; INTERACTIONS; IONS; MAGNETISM; MICROSCOPY; MINERALS; OXIDE MINERALS; PARTICLE PROPERTIES; PEROVSKITES; PHYSICAL PROPERTIES; THERMODYNAMIC PROPERTIES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.