A high-temperature double perovskite molecule-based antiferroelectric with excellent anti-breakdown capacity for energy storage

© 2023. The Author(s)..

Halide double perovskites have recently emerged as an environmentally green candidate toward electronic and optoelectronic applications owing to their non-toxicity and versatile physical merits, whereas study on high-temperature antiferroelectric (AFE) with excellent anti-breakdown property remains a huge blank in this booming family. Herein, we present the first high-temperature AFE of the lead-free halide double perovskites, (CHMA)2CsAgBiBr7 (1, where CHMA+ is cyclohexylmethylammonium), by incorporating a flexible organic spacer cation. The typical double P-E hysteresis loops and J-E curves reveal its concrete high-temperature AFE behaviors, giving large polarizations of ~4.2 μC/cm2 and a high Curie temperature of 378 K. Such merits are on the highest level of molecular AFE materials. Particularly, the dynamic motional ordering of CHMA+ cation contributes to the formation of antipolar alignment and high electric breakdown field strength up to ~205 kV/cm with fatigue endurance over 104 cycles, almost outperforming the vast majority of molecule counterparts. This is the first demonstration of high-temperature AFE properties in the halide double perovskites, which will promote the exploration of new "green" candidates for anti-breakdown energy storage capacitor.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:14

Enthalten in:

Nature communications - 14(2023), 1 vom: 27. Apr., Seite 2420

Sprache:

Englisch

Beteiligte Personen:

Liu, Yi [VerfasserIn]
Ma, Yu [VerfasserIn]
Zeng, Xi [VerfasserIn]
Xu, Haojie [VerfasserIn]
Guo, Wuqian [VerfasserIn]
Wang, Beibei [VerfasserIn]
Hua, Lina [VerfasserIn]
Tang, Liwei [VerfasserIn]
Luo, Junhua [VerfasserIn]
Sun, Zhihua [VerfasserIn]

Links:

Volltext

Themen:

Journal Article

Anmerkungen:

Date Completed 30.04.2023

Date Revised 01.05.2023

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1038/s41467-023-38007-5

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM356095452