X-ray peak broadening analysis in LaMnO3+δ nano-particles with rhombohedral crystal structure

author

Abstract:

In this work, structural and magnetic properties of LaMnO3+δ compound prepared by citrate precursor method and annealed in presence of oxygen are investigated. The structural characterization of LaMnO3+δ by X-ray powder diffraction and using X’pert package and Fullprof program is evidence for a rhombohedral structure (R-3c space group) confirmed by FTIR measurement. The magnetic measurements show a super-paramagnetic behavior of LaMnO3+δ due to low values of coercive field and romance magnetization and also high value of saturation magnetization. In addition, a comparative study of the crystallite size of the compounds obtained from powder XRD is reported. The Williamson-Hall analysis, size-strain plot and Halder-Wagner methods were used to study the individual contributions of crystallite sizes and lattice micro-strain on isotropic line broadening of all the reflection peaks of the LaMnO3+δ compound. The results show the Halder-Wagner method is more accurate, with all data points touching the fitting line better than the other methods. The crystallite sizes estimated from XRD (30.86 nm) and particle size estimated from TEM method (36 nm) and also the magnetic core size (33.6 nm) estimated from magnetic measurement agree well, while a little difference reflects a spherical shape of the nanoparticles.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

X-Ray Peak Broadening Analysis in LaMnO3+δ Nano-Particles with RhombohedralCrystal Structure

Received 10 April 2015 Accepted 11 October 2015 Available online 30 September 2015 In this work, structural and magnetic properties of the LaMnO3+δ compound prepared by citrate precursor method and annealed in the presence of oxygen are investigated. The structural characterization of LaMnO3+δ by X-ray powder diffraction and X‟pert package and Fullprof program provides evidence for a rhombohedr...

full text

X-Ray, Crystal Structure and Solution Phase Studies of a Polymeric SrII Compound

In the crystal structure of the title polymeric compound, [C42H38N6O33Sr5.2(H2O)]n, five independent metal atoms (Sr1-Sr5) have different coordination environments. The Sr1 and Sr5 atoms are nine coordinated and feature distorted tricapped trigonal-prismatic and capped square-antiprismatic geometries, respectively....

full text

X-ray diffraction peak profile analysis of maraged Fe-Ni-Mn steels

X-ray diffraction peak profile analysis was used to identify changes in the lattice distortions during isothermal aging of Fe-10Ni-7Mn (wt. %) maraging steel. Integral peak breadths were analyzed using classical Williamson-Hall equation taking the elastic anisotropy into account. It was found that substantial lattice distortions rise during precipitation hardening which depend strongly on the s...

full text

The X-ray Transform and its Application in Nano Crystallography

In this article a review on the definition of the X- ray transform and some ofits applications in Nano crystallography is presented. We shall show that the X- raytransform is a special case of the Radon transform on homogeneous spaces when thetopological group E(n)- the Euclidean group - acts on ℝ2 transitively. First someproperties of the Radon transform are investigated then the relationship ...

full text

Analysis of Soil Structure Turnover with Garnet Particles and X-Ray Microtomography

Matter turnover in soil is tightly linked to soil structure which governs the heterogeneous distribution of habitats, reaction sites and pathways in soil. Thereby, the temporal dynamics of soil structure alteration is deemed to be important for essential ecosystem functions of soil but very little is known about it. A major reason for this knowledge gap is the lack of methods to study soil stru...

full text

Dislocation structure and crystallite size-distribution in hexagonal nanomaterials from X-ray peak profile analysis

The microstructure of three different nanocrystalline materials with hexagonal crystal structure are studied by X-ray diffraction peak profile analysis. The crystallite size distribution and the dislocation structure are determined in plasmathermal silicon nitride powder, sintered tungsten carbide and severely deformed titanium and are compared with transmission electron microscopy (TEM) result...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 3  issue 3

pages  71- 83

publication date 2015-09-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023