Large electrocaloric effect and energy storage performance of site-engineered lead-free Ba1-x(Bi0.5Li0.5)xTiO3ferroelectric oxides

6Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Environment-friendly solid-state cooling technology necessitates the search for energy-efficient electrocaloric (EC) materials. In this regard, the EC effect and energy storage performance have been investigated on a site-engineered lead-free Ba1-x(Bi0.5Li0.5)xTiO3 (x = 0.0, 0.10, 0.125, 0.15 and 0.175) system from the perspective of its enhanced characteristic parameters. The ferroelectric and dielectric studies reveal the tunable polarization and Curie temperature as a function of composition. The EC measurements on these samples display superior EC parameters compared to the values reported for other polycrystalline ferroelectric systems. The observed EC parameters for the x = 0.10 sample, such as the change in entropy (ΔS), adiabatic temperature change (ΔT) and EC coefficient are 2.63 J kg-1 K, 2.03 K and 0.68 K mm-1 kV, respectively. Notably, the x = 0.15 sample displays near room-temperature (307 K) EC response with ΔT ≥ 0.30 K over a broad 24 K temperature range. In addition, the energy storage performance studies elucidate that the Ba1-x(Bi0.5Li0.5)xTiO3 compound with x = 0.175 displays large energy storage efficiency (96.7%) with 144 mJ cm-3 as the storage density. The tunable EC characteristics and high energy storage efficiency demonstrated in this work illustrate the application potential of site-engineered BaTiO3 samples in efficient cooling and storage devices.

Cite

CITATION STYLE

APA

Pal, S., Biswas, P. P., Rath, M., Ramachandra Rao, M. S., Miryala, M., Murakami, M., & Murugavel, P. (2021). Large electrocaloric effect and energy storage performance of site-engineered lead-free Ba1-x(Bi0.5Li0.5)xTiO3ferroelectric oxides. Journal of Physics D: Applied Physics, 54(4). https://doi.org/10.1088/1361-6463/abbeb4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free