Abstract

The effects of the A-site transition from Ca 2+ to Cd 2+ on the microstructure, morphology, and electrical properties of Ca 1–x Cd x Cu 3 Ti 4 O 12 thin films were studied. The film surfaces are smooth, compact, and without cracks. The CaCu 3 Ti 4 O 12 and CdCu 3 Ti 4 O 12 films had similar morphologies and electrical properties. The grain size initially increased and subsequently decreased with the transition from Ca 2+ to Cd 2+ at the A site. The change in Ca sites has an obvious effect on Cu sites. The film with more copper-rich phases at the grain boundaries had the largest grain size when Ca 2+ and Cd 2+ equally occupied the A sites. The dielectric constant of Ca 1–x Cd x Cu 3 Ti 4 O 12 was closely related to the copper oxide secondary phase. The dielectric loss tangent and nonlinearity coefficient were associated with the compact structure, copper oxide secondary phase, copper vacancies and improved grain boundary response. The simultaneous occupancy of the A sites by Ca 2+ and Cd 2+ improves the dielectric and nonlinear properties of Ca 1–x Cd x Cu 3 Ti 4 O 12 . Optimal dielectric properties (Ɛ r = 5238 and tan δ = 0.009 at 1 kHz) and an enhanced nonlinearity coefficient (∼4.22) were simultaneously obtained for the Ca 0.5 Cd 0.5 Cu 3 Ti 4 O 12 thin film. This study demonstrates that the extrinsic mechanism is the main origin of the high dielectric constant values in Ca 1–x Cd x Cu 3 Ti 4 O 12 films. The resulting films are suitable for applications in capacitors.

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