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Title: Why is the electrocaloric effect so small in ferroelectrics?

Journal Article · · APL Materials
DOI:https://doi.org/10.1063/1.4950788· OSTI ID:1356630
ORCiD logo [1];  [2]
  1. Argonne National Lab. (ANL), Argonne, IL (United States). Materials Science Division; Univ. of Costa Rica, San Jose (Costa Rica)
  2. Argonne National Lab. (ANL), Argonne, IL (United States); Univ. of Chicago, IL (United States). James Franck Inst.

Ferroelectrics are attractive candidate materials for environmentally friendly solid state refrigeration free of greenhouse gases. Their thermal response upon variations of external electric fields is largest in the vicinity of their phase transitions, which may occur near room temperature. The magnitude of the effect, however, is too small for useful cooling applications even when they are driven close to dielectric breakdown. Insight from microscopic theory is therefore needed to characterize materials and provide guiding principles to search for new ones with enhanced electrocaloric performance. Here, we derive from well-known microscopic models of ferroelectricity meaningful figures of merit for a wide class of ferroelectric materials. Such figures of merit provide insight into the relation between the strength of the effect and the characteristic interactions of ferroelectrics such as dipolar forces. We find that the long range nature of these interactions results in a small effect. A strategy is proposed to make it larger by shortening the correlation lengths of fluctuations of polarization. In addition, we bring into question other widely used but empirical figures of merit and facilitate understanding of the recently observed secondary broad peak in the electrocalorics of relaxor ferroelectrics.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Contributing Organization:
Univ. of Costa Rica, San Jose (Costa Rica); Univ. of Chicago, IL (United States)
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1356630
Journal Information:
APL Materials, Vol. 4, Issue 6; ISSN 2166-532X
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 22 works
Citation information provided by
Web of Science

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Cited By (10)

Giant electrocaloric effect at the antiferroelectric-to-ferroelectric phase boundary in Pb(Zr x Ti 1– x )O 3 journal July 2019
Self-heating of relaxor and ferroelectric ceramics during electrocaloric field cycling journal July 2019
Electrocaloric effect in the two spin-1/2 XXZ Heisenberg edge-shared tetrahedra and spin-1/2 XXZ Heisenberg octahedron with Dzyaloshinskii–Moriya interaction journal July 2019
Strongly enhanced electrocaloric effects in doped BaTiO 3 with reduced grain size journal November 2018
Atomic-scale measurement of polar entropy journal September 2019
Ferrielectricity in the metal-organic ferroelectric tris-sarcosine calcium chloride journal March 2017
Electrocaloric effects in the lead-free Ba ( Zr , Ti ) O 3 relaxor ferroelectric from atomistic simulations journal July 2017
BiFeO 3 -BaTiO 3 : A new generation of lead-free electroceramics journal December 2018
Electrocaloric effect in the two spin-1/2 XXZ Heisenberg edge-shared tetrahedra and spin-1/2 XXZ Heisenberg octahedron with Dzyaloshinskii-Moriya interaction text January 2019
A scaling law for distinct electrocaloric cooling performance in low-dimensional organic, relaxor and anti-ferroelectrics journal September 2017