Enhancing Short‐Range Interactions to Broaden the Temperature Range for Coexistence of Antiferroelectricity and Ferroelasticity

Author:

Cai Zhuoer1,Zhang Yinan1,He Xiaofan1,Chen Jian1,Hua Xiu‐Ni2,Shi Ping‐Ping3,Sun Baiwang1ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering Southeast University Nanjing 211189 P. R. China

2. School of Environmental Science Nanjing Xiaozhuang University Nanjing 211171 P. R. China

3. School of Chemical and Environmental Engineering Anhui Polytechnic University Wuhu 241000 P. R. China

Abstract

AbstractAntiferroelectric (AFE) materials, characterized by double electric hysteresis loops, can be transformed to the ferroelectric (FE) phase under an external electric field, making them promising candidates for electronic energy storage and solid‐state refrigeration. Additionally, the field‐induced strain in AFE materials is contingent upon the direction of the electric field, rendering it with a switching characteristic. Although AFE materials have made progress in the field of energy storage and negative electrocaloric effect, the coexistence of AFE and ferroelasticity is still rarely reported. Here, two isomorphic organic‐inorganic hybrid perovskites, HDAEPbCl4 and HDAEPbBr4 (HDAE is [2‐(hydroxydimethylammonio)ethan‐1‐aminium]), exhibiting FE‐AFE‐PE (PE is paraelectric) phase transitions, are presented. Remarkably, the temperature range where AFE and ferroelasticity coexist is significantly broadened from 59.9 K to 115.1 K by strengthening short‐range forces via halogen substitution. This discovery extends the family of FE, AFE, and ferroelastic materials, contributing to the development of multifunctional materials and advancing multifunctional material development.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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