Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12202/3975
Title: An In-Situ View of the Electrostriction Effect in Gd-Doped Ceria Using Quick Extended Absorption Fine Structure with Modulation Excitation
Authors: Lerner, Alyssa
Keywords: Cerium compounds
Chemical reactions
Gadolinium
Issue Date: 27-Apr-2015
Publisher: Stern College for Women
Abstract: As more applications are found for electromechanical materials, studying their properties becomes increasingly relevant. The presence of an external electric field can lead to a mechanical response, which is useful for a wide variety of applications, from actuators for precise scientific instruments and home electronics to transducers for audio speakers and sonars. These materials are currently limited in their voltage requirements and physical dimensions, and the next generation of electromechanical solid materials will have an increased magnitude of electromechanical response. As more effective materials, they will require lower operating voltage and be physically smaller. While properties such as pyroelectricity and piezoelectricity were traditionally attributed to certain crystal structures, it has been found that materials can form polar quasiamorphous phases as thin films, with random networks of local bonding units that can create local dipole moments. This was first demonstrated for barium zirconate (BaZrO3) and strontium titanate (SrTiO3). A similar local dipole mechanism was then observed when both gadolinium-doped ceria thin films (Ce0.8Gd0.2O1.9) and oxygen-deficient ceria thin films (CeO2-x) exhibited chemical strain effects. Upon further investigation, Ce0.8Gd0.2O1.9 was revealed to have an unusually large electrostriction effect, exceeding that of conventionally used materials. The aliovalent Gd3+ dopant creates oxygen vacancies in the material, and these vacancies are thought to be responsible for the films’ exceptional electromechanical properties, for which local dipoles are required.
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URI: https://hdl.handle.net/20.500.12202/3975
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Appears in Collections:S. Daniel Abraham Honors Student Theses

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