Size Effects Observed via the Electrical Response of BaTiO3 Nanoparticles in a Cavity

Barium titanate (BaTiO3) is one of the most widely used electronic materials. The origin of changing structural and electronic behavior between larger and smaller nanoparticles in BaTiO3 has been extensively investigated. Here, the dielectric loss measured for BaTiO3 or BaZrO3 particles in a cavity...

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Published inJournal of physical chemistry. C Vol. 116; no. 44; pp. 23742 - 23748
Main Authors Lomax, Joseph F, Fontanella, John J, Edmondson, Charles A, Wintersgill, Mary C, Westgate, Mark A, Eker, Sitki
Format Journal Article
LanguageEnglish
Published Columbus, OH American Chemical Society 08.11.2012
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Summary:Barium titanate (BaTiO3) is one of the most widely used electronic materials. The origin of changing structural and electronic behavior between larger and smaller nanoparticles in BaTiO3 has been extensively investigated. Here, the dielectric loss measured for BaTiO3 or BaZrO3 particles in a cavity at audio frequencies (10–105 Hz) and low temperatures (5.5–350 K) is reported. Distinct differences were found between small (50–100 nm diameter/cubic) and large (>200 nm diameter/tetragonal at room temperature) BaTiO3 particles. Isochronal relaxation features observed around 20 K showed differing shape and dynamics (50–100 nm particles: broad peak, E act ≈ 0.04 eV, log10(f pre(s)) ≈ 14.7; >200 nm particles: sharp peak, E act ≈ 0.025 eV and log10(f pre(s)) ≈ 12, with a shoulder). The low-temperature relaxations are attributed to the motion of off-center titanium ions. In support of this identification, low-temperature relaxations were not observed in BaZrO3 nanoparticles. Finally, structural change features were observed at about 180 and 270 K in the larger BaTiO3 particles (rhombohedral at low temperature) but not in the smaller particles (cubic at all temperatures). The results provide a new set of testable bounds that should contribute to the understanding of nanoparticle-sized BaTiO3, in particular, and ferroelectric behavior in perovskites, in general.
ISSN:1932-7447
1932-7455
DOI:10.1021/jp307218v