Published August 22, 2024 | Version v1
Journal article

Giant reversible electrocaloric effect in monolayer group-IV monochalcogenides

  • 1. School of Physics, Hunan Key Laboratory of Super Microstructure and Ultrafast Process, Hunan Key Laboratory of Nanophotonics and Devices, State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083, China

Description

Monolayer electrocaloric (EC) materials have emerged as promising candidates to achieve economic and green solid-state refrigeration, especially in micro- or nanoscale chip cooling in the post-Moore law period. In this paper, we trained a machine-learning-based deep potential (DP) model of monolayer group-IV monochalcogenides MXs (M = Ge, Sn; X = S, Se) with a database from first-principles calculations, which incorporates the accuracy of ab initio molecular dynamics and efficiency of classical method. The DP model was further applied to study the EC effect (ECE) in monolayer MXs by simulating the temperature-driven phase transitions and electric polarization dynamics under different external electric fields. The results indicate MXs featuring giant reversible isothermal entropy change (ΔS) and adiabatic temperature change (ΔT) near their order-disorder phase transition. Particularly, for E = 100 MV/m, |ΔS| = 68 J/(kg K) and |ΔT| = 75 K are obtained for GeS, which individually rival the state-of-the-art ECE figures of merit, surpassing most other ferroelectric materials, particularly the two-dimensional (2D) CuInPS and strained SrTiO3 films. Furthermore, electric field shifts of the order of 10 MV/m yield huge reversible EC strengths of ΔSE = 5.4 Jmkg1K1MV1 and ΔTE = 6 KmMV1. The origin of the giant ECE in MXs was explained through macroscopic thermodynamic ratios, phenomenological Landau theory, and microscopic phonon vibration analysis. Interestingly, the entropy change can be approximated to be proportional to the square of the polarization change (ΔP2), and the application of electric field shifts the low-frequency phonons to the higher-frequency range, with the M atom contributing more to the entropy change than the X atom. In this paper, we provide important insights for exploration and design of 2D EC materials in future practical applications.

Additional details

Identifiers

DOI
10.1103/PhysRevB.110.064103;
Crossref Funder ID
10.13039/501100001809; 10.13039/100016104; 10.13039/501100011353;

Publishing Information

Journal Title
Physical Review B
Journal Volume
110
Journal Issue
6
Journal Page Range
11 pgs.
ISSN
1550-235X

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
Subject category
S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
Descriptors DEI
ACCURACY; ATOMS; COOLING; ELECTRIC FIELDS; ENTROPY; EXPLORATION; FERROELECTRIC MATERIALS; GERMANIUM; MATERIALS; MOLECULAR DYNAMICS METHOD; NANOSTRUCTURES; PHASE TRANSFORMATIONS; PHONONS; POLARIZATION; STRAINS; THERMODYNAMICS