Microscopic Origins of the Large Piezoelectricity of Leadfree (Ba,Ca)(Zr,Ti)O3

Abstract

In light of directives around the world to eliminate toxic materials in various technologies, finding lead-free materials with high piezoelectric responses constitutes an important current scientific goal. As such, the recent discovery of a large electromechanical conversion near room temperature in (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 compounds has directed attention to understanding its origin. Here, we report the development of a large-scale atomistic scheme providing a microscopic insight into this technologically promising material. We find that its high piezoelectricity originates from the existence of large fluctuations of polarization in the orthorhombic state arising from the combination of a flat free-energy landscape, a fragmented local structure, and the narrow temperature window around room temperature at which this orthorhombic phase is the equilibrium state. In addition to deepening the current knowledge on piezoelectricity, these findings have the potential to guide the design of other lead-free materials with large electromechanical responses.

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Document Details

Document Type
Technical Report
Publication Date
Jun 20, 2017
Accession Number
AD1061434

Entities

People

  • Alireza Akbarzadeh
  • Igor Kornev
  • Jorge IƱiguez
  • L. Bellaiche
  • Raymond Walter
  • Sergei Prokhorenko
  • Sergey Prosandeev
  • Yousra Nahas

Organizations

  • University of Arkansas

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Coefficients
  • Crystals
  • Curie Temperature
  • Density Functional Theory
  • Domain Walls
  • Dynamics
  • Electric Fields
  • Free Energy
  • Materials
  • Molecular Dynamics
  • Phase Diagrams
  • Phase Transformations
  • Physical Properties
  • Simulations
  • Solid Solutions
  • Transition Temperature
  • Transitions

Readers

  • Economics
  • Materials Science and Engineering.

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene