Ferroelectric columnar assemblies from the bowl-to-bowl inversion of aromatic cores

• Published in: Nature communications Vol. 12; no. 1; p. 768
• Main Authors: Furukawa, Shunsuke, Wu, Jianyun, Koyama, Masaya, Hayashi, Keisuke, Hoshino, Norihisa, Takeda, Takashi, Suzuki, Yasutaka, Kawamata, Jun, Saito, Masaichi, Akutagawa, Tomoyuki
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.02.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 119/118; 140/125; 140/131; 140/58; 639/301/1005/1007; 639/301/923/3931; 639/638/541/966; Condensed matter physics; Dipoles; Ferroelectric materials; Ferroelectricity; Ferroelectrics; Humanities and Social Sciences; Inversion; Iron constituents; Materials science; multidisciplinary; Organic chemistry; Organic compounds; Science; Science (multidisciplinary); Toxicity
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-021-21019-4

Organic ferroelectrics, in which the constituent molecules retain remanent polarization, represent an important topic in condensed-matter science, and their attractive properties, which include lightness, flexibility, and non-toxicity, are of potential use in state-of-the-art ferroelectric devices. However, the mechanisms for the generation of ferroelectricity in such organic compounds remain limited to a few representative concepts, which has hitherto severely hampered progress in this area. Here, we demonstrate that a bowl-to-bowl inversion of a relatively small organic molecule with a bowl-shaped π-aromatic core generates ferroelectric dipole relaxation. The present results thus reveal an unprecedented concept to produce ferroelectricity in small organic molecules, which can be expected to strongly impact materials science. Organic ferroelectrics are of potential use in state-of-the-art ferroelectric devices but mechanistic insight in generating ferroelectricity remains limited. Here, the authors demonstrate that a bowl-to-bowl inversion of a bowl shaped organic molecule generates ferroelectric dipole relaxation, extending the concept of ferroelectricity in small organic molecules.