Effect of paramagnetic manganese ions doping on frequency and high temperature dependence dielectric response of layered Na1.9Li 0.1Ti3O7 ceramics

12Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The manganese doped layered ceramic samples (Na1.9Li 0.1)Ti3O7 : XMn(0-01 ≤X≤0-1) have been prepared using high temperature solid state reaction. The room temperature electron paramagnetic resonance (EPR) investigations exhibit that at lower percentage of doping the substitution of manganese ions occur as Mn3+ at Ti4+ sites, whereas for higher percentage of doping Mn 2+ ions occupy the two different interlayer sodium/lithium sites. In both cases, the charge compensation mechanism should operate to maintain the overall charge neutrality of the lattice. The manganese doped derivatives of layered Na1.9Li0.1Ti3O7 (SLT) ceramics have been investigated through frequency dependence dielectric spectroscopy in this work. The results indicate that the dielectric losses in these ceramics are the collective contribution of electric conduction, dipole orientation and space charge polarization. Smeared peaks in temperature dependence of permittivity plots suggest diffuse nature of high temperature ferroelectric phase transition. The light manganese doping in SLT enhances the dielectric constant. However, manganese doping decreases dielectric loss due to inhibition of domain wall motion, enhances electron-hopping conduction, and impedes the interlayer ionic conduction as well. Manganese doping also gives rise to contraction of interlayer space. © Indian Academy of Sciences.

Cite

CITATION STYLE

APA

Pal, D., & Pandey, J. L. (2010). Effect of paramagnetic manganese ions doping on frequency and high temperature dependence dielectric response of layered Na1.9Li 0.1Ti3O7 ceramics. Bulletin of Materials Science, 33(6), 691–696. https://doi.org/10.1007/s12034-011-0139-8

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free