Dielectric properties of strontium iron holmium niobate ceramics

Strontium iron holmium niobate (Sr(Fe 1-x Ho x ) 0.5 Nb 0.5 O 3 ) ceramics were synthesized via a solid-state reaction technique. The undoped ceramic showed an orthorhombic phase, but it transformed to a pseudocubic phase for higher Ho concentrations. A low solubility limit of Ho in SFN caused a for...

Full description

Saved in:
Bibliographic Details
Main Authors: K. Sanjoom, T. Tunkasiri, K. Pengpat, S. Eitssayeam, G. Rujijanagul
Format: Journal
Published: 2018
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875736132&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/47953
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-47953
record_format dspace
spelling th-cmuir.6653943832-479532018-04-25T08:45:59Z Dielectric properties of strontium iron holmium niobate ceramics K. Sanjoom T. Tunkasiri K. Pengpat S. Eitssayeam G. Rujijanagul Strontium iron holmium niobate (Sr(Fe 1-x Ho x ) 0.5 Nb 0.5 O 3 ) ceramics were synthesized via a solid-state reaction technique. The undoped ceramic showed an orthorhombic phase, but it transformed to a pseudocubic phase for higher Ho concentrations. A low solubility limit of Ho in SFN caused a formation of second phase for the x=0.15 ceramic. Dielectric behavior of undoped ceramic exhibited high dielectric constant over a wide temperature range. However, the doping shifted this region to a higher temperature. The doping also shifted the peak of dielectric loss to a higher temperature. Activation energy of dielectric relaxation increased with increasing Ho concentration. In addition, complex impedance analysis was applied to determine the behaviors of grain boundary and grain after doping. © 2012 Elsevier Ltd and Techna Group S.r.l. 2018-04-25T08:45:59Z 2018-04-25T08:45:59Z 2013-05-01 Journal 02728842 2-s2.0-84875736132 10.1016/j.ceramint.2012.10.067 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875736132&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/47953
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description Strontium iron holmium niobate (Sr(Fe 1-x Ho x ) 0.5 Nb 0.5 O 3 ) ceramics were synthesized via a solid-state reaction technique. The undoped ceramic showed an orthorhombic phase, but it transformed to a pseudocubic phase for higher Ho concentrations. A low solubility limit of Ho in SFN caused a formation of second phase for the x=0.15 ceramic. Dielectric behavior of undoped ceramic exhibited high dielectric constant over a wide temperature range. However, the doping shifted this region to a higher temperature. The doping also shifted the peak of dielectric loss to a higher temperature. Activation energy of dielectric relaxation increased with increasing Ho concentration. In addition, complex impedance analysis was applied to determine the behaviors of grain boundary and grain after doping. © 2012 Elsevier Ltd and Techna Group S.r.l.
format Journal
author K. Sanjoom
T. Tunkasiri
K. Pengpat
S. Eitssayeam
G. Rujijanagul
spellingShingle K. Sanjoom
T. Tunkasiri
K. Pengpat
S. Eitssayeam
G. Rujijanagul
Dielectric properties of strontium iron holmium niobate ceramics
author_facet K. Sanjoom
T. Tunkasiri
K. Pengpat
S. Eitssayeam
G. Rujijanagul
author_sort K. Sanjoom
title Dielectric properties of strontium iron holmium niobate ceramics
title_short Dielectric properties of strontium iron holmium niobate ceramics
title_full Dielectric properties of strontium iron holmium niobate ceramics
title_fullStr Dielectric properties of strontium iron holmium niobate ceramics
title_full_unstemmed Dielectric properties of strontium iron holmium niobate ceramics
title_sort dielectric properties of strontium iron holmium niobate ceramics
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875736132&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/47953
_version_ 1681423159267426304