TY - JOUR
T1 - Auto-combustion synthesis and characterization of perovskite-type LaFeO3 nanocrystals prepared via different routes
AU - Gabal, M. A.
AU - Al-Solami, F.
AU - Al Angari, Y. M.
AU - Ali, A. A.
AU - Al-Juaid, A. A.
AU - Huang, Kuo-Wei
AU - Alsabban, Merfat
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2019/5/18
Y1 - 2019/5/18
N2 - LaFeO3 was prepared via simple, economical and environmentally friendly auto-combustion methods using different fuels, including citrate, urea, sucrose, egg whites, gelatin and chitosan. The prepared ferrites were systematically characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, high resolution transmission electron microscopy (HRTEM), vibrating sample magnetometry (VSM) and electrical measurements to study the impact of the synthetic routes on the various properties. XRD showed the formation of a single orthorhombic phase, except for the samples prepared via egg white, gelatin and urea methods, which indicated a secondary La2O2CO3 phase. The FT-IR and TEM studies confirmed the formation of the phase. Differential thermal analysis-thermogravimetry techniques (DTA-TG) were used to characterize the auto-combustion process up to ferrite formation. The obtained unsaturated magnetization for all of the samples suggested the presence of anti-ferromagnetic ordering in addition to weak ferromagnetic ordering. The egg white method showed higher magnetization (1.78 emu/g), while the urea and chitosan methods indicated lower magnetization (0.13 emu/g). The coercivity measurements confirmed the presence of ferromagnetic/anti-ferromagnetic interfaces with higher values than those reported in the literature. The AC-conductivity measurements indicated semiconducting characteristics and exhibited a change in the conduction mechanism from hopping to polaron conduction by increasing the temperature. LaFeO3 prepared via the egg white method indicated an anti-ferromagnetic/paramagnetic transition at approximately 715 K. The dielectric measurements confirmed the AC-conductivity results and exhibited values higher than those reported in the literature.
AB - LaFeO3 was prepared via simple, economical and environmentally friendly auto-combustion methods using different fuels, including citrate, urea, sucrose, egg whites, gelatin and chitosan. The prepared ferrites were systematically characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, high resolution transmission electron microscopy (HRTEM), vibrating sample magnetometry (VSM) and electrical measurements to study the impact of the synthetic routes on the various properties. XRD showed the formation of a single orthorhombic phase, except for the samples prepared via egg white, gelatin and urea methods, which indicated a secondary La2O2CO3 phase. The FT-IR and TEM studies confirmed the formation of the phase. Differential thermal analysis-thermogravimetry techniques (DTA-TG) were used to characterize the auto-combustion process up to ferrite formation. The obtained unsaturated magnetization for all of the samples suggested the presence of anti-ferromagnetic ordering in addition to weak ferromagnetic ordering. The egg white method showed higher magnetization (1.78 emu/g), while the urea and chitosan methods indicated lower magnetization (0.13 emu/g). The coercivity measurements confirmed the presence of ferromagnetic/anti-ferromagnetic interfaces with higher values than those reported in the literature. The AC-conductivity measurements indicated semiconducting characteristics and exhibited a change in the conduction mechanism from hopping to polaron conduction by increasing the temperature. LaFeO3 prepared via the egg white method indicated an anti-ferromagnetic/paramagnetic transition at approximately 715 K. The dielectric measurements confirmed the AC-conductivity results and exhibited values higher than those reported in the literature.
UR - http://hdl.handle.net/10754/656476
UR - https://linkinghub.elsevier.com/retrieve/pii/S0272884219313008
UR - http://www.scopus.com/inward/record.url?scp=85065895572&partnerID=8YFLogxK
U2 - 10.1016/j.ceramint.2019.05.187
DO - 10.1016/j.ceramint.2019.05.187
M3 - Article
SN - 0272-8842
VL - 45
SP - 16530
EP - 16539
JO - Ceramics International
JF - Ceramics International
IS - 13
ER -