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Operando Investigation of the Molecular Origins of Dipole Switching in P(VDF‐TrFE‐CFE) Terpolymer for Large Adiabatic Temperature Change

Relaxor ferroelectric polymers exhibiting a giant electrocaloric effect (ECE) can potentially be used to create next‐generation solid‐state coolers. Under an electric field, poly(vinylidene fluoride‐trifluoroethylene‐chlorofluoroethylene) terpolymer goes through a large dipolar entropy change produc...

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Published in:Advanced functional materials 2024-06, Vol.34 (26), p.n/a
Main Authors: Zhu, Yuan, Wu, Hanxiang, Martin, Andrew, Beck, Paige, Allahyarov, Elshad, Wongwirat, Thumawadee, Rui, Guanchun, Zhu, Yingke, Hawthorne, Daniel, Fan, Jiacheng, Wu, Jianghan, Zhang, Siyu, Zhu, Lei, Kaur, Sumanjeet, Pei, Qibing
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container_issue 26
container_start_page
container_title Advanced functional materials
container_volume 34
creator Zhu, Yuan
Wu, Hanxiang
Martin, Andrew
Beck, Paige
Allahyarov, Elshad
Wongwirat, Thumawadee
Rui, Guanchun
Zhu, Yingke
Hawthorne, Daniel
Fan, Jiacheng
Wu, Jianghan
Zhang, Siyu
Zhu, Lei
Kaur, Sumanjeet
Pei, Qibing
description Relaxor ferroelectric polymers exhibiting a giant electrocaloric effect (ECE) can potentially be used to create next‐generation solid‐state coolers. Under an electric field, poly(vinylidene fluoride‐trifluoroethylene‐chlorofluoroethylene) terpolymer goes through a large dipolar entropy change producing a high adiabatic temperature change (ΔTECE). This work resolves the molecular origins of the large entropy change behind the electric field‐induced dipole switching. A Fourier transform infrared spectroscopy equipped with a high voltage source is used to operandoly observe the characteristic molecular vibrational modes. A short‐range trans (T) conformation of the CF2‐CH2 dyads interrupted by a gauche (G) conformation, e.g., TTTG in the terpolymer chain, undergoes a dynamic transformation that leads to a corresponding ΔTECE whenever an electric field is applied. The molecular dynamics simulation also proves that the energy barrier that the transformation from TTTGs into a long T sequence overcomes is smaller than that for all other conformations. A mixed solvent system is used to obtain T3G‐enriched terpolymer films exhibiting a 4.02 K ΔTECE at 60 MV m−1 and these films are employed to manufacture a 2‐layer‐cascaded cooling device that achieves a 6.7 K temperature lift, the highest reported value for a 2‐layer cascaded device made of fluoropolymers. The dynamic dipole switching in the relaxor ferroelectric poly(vinylidene fluoride‐trifluoroethylene‐chlorofluoroethylene) terpolymer, P(VDF‐TrFE‐CFE), under an externally applied electric field is studied with operando Fourier transform infrared spectroscopy. Short trans sequences (T3G) along the polymer chains are found to be responsible for the reversible entropy change with the field, accounting for a large electrocaloric effect.
doi_str_mv 10.1002/adfm.202314705
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A mixed solvent system is used to obtain T3G‐enriched terpolymer films exhibiting a 4.02 K ΔTECE at 60 MV m−1 and these films are employed to manufacture a 2‐layer‐cascaded cooling device that achieves a 6.7 K temperature lift, the highest reported value for a 2‐layer cascaded device made of fluoropolymers. The dynamic dipole switching in the relaxor ferroelectric poly(vinylidene fluoride‐trifluoroethylene‐chlorofluoroethylene) terpolymer, P(VDF‐TrFE‐CFE), under an externally applied electric field is studied with operando Fourier transform infrared spectroscopy. 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language eng
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source Wiley-Blackwell Read & Publish Collection
subjects Adiabatic flow
Coolers
dipole switching
Dipoles
Electric fields
electrocaloric cooling effect
Entropy
Ferroelectricity
Fluoropolymers
Fourier transforms
Molecular dynamics
operando investigation
Origins
P(VDF‐TrFE‐CFE) terpolymer
Switching
Terpolymers
Vibration mode
Vinylidene
Vinylidene fluoride
title Operando Investigation of the Molecular Origins of Dipole Switching in P(VDF‐TrFE‐CFE) Terpolymer for Large Adiabatic Temperature Change
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