Organic single-component ferroelectrics, as an important kind of metal-free ferroelectrics, are highly desirable for their easy processing, mechanical flexibility, and biocompatibility. However, although nearly 50 years have passed since the...
Polarization in ferroelectrics is
generally switched by an applied
external electric field. Light is highly attractive as a noncontact
and noninvasive means, but optically controlled ferroelectric polarization
has been mainly realized in some inorganic ferroelectrics, and rarely
found in molecular ferroelectrics, which have superiorities of easy
processing, light weight, mechanical flexibility, and good biocompatibility.
In this work, we reported an organic ferroelectric salicylideneaniline
derivative N-3,5-di-tert-butylsalicylidene-2-aminoaniline
(1), which shows optically controlled polarization switching. 1 not only exhibits a light-induced phase transition of photoisomerization
between enol and trans-keto molecular configurations
but also presents a temperature-triggered phase transition at around
364 K related to the order–disorder transition of a tert-butyl group in the structure. P–E (polarization–electric field) hysteresis loops
and box-in-box ferroelectric domain reversal confirm its ferroelectricity.
Upon photoirradiation, the ferroelectric domains show obvious variations
and demonstrate reversible polarization switching under UV and visible
light, originating from the photoinduced structural isomerization.
This finding sheds light on the development of molecular ferroelectrics
with noncontact and remote control of polarization switching by light
for potential application in next-generation optically controlled
ferroelectric devices.
[(S)-3-Aminopyrrolidinium I]2Bi2/3I4 is a novel chiral two-dimensional perovskite-like lead-free bismuth(iii) iodide hybrid showing a high phase transition temperature and a narrow bandgap.
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