Molecule-Driven Unusual Incommensurate Modulation in a 2D Hybrid Perovskite Ferroelectric

IF 16.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Lijun Xu,Hongfei Ma,Ji Qi,Hang Li,Chengshu Zhang,Huang Ye,Haiqing Zhong,Yuan Yu,Chengmin Ji,Zhenyue Wu,Lina Li,Xiaobin Fu,Junliang Sun,Junhua Luo
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Abstract

Incommensurate modulation has been extensively investigated in inorganic oxides, representing an emerging frontier in aperiodic materials that enables the discovery of novel quantum phenomena and the manipulation of physical properties, whereas it remains largely unexplored in hybrid perovskites (HPs). Here, we present the driving of successive dynamic rotation of the interlayer dipoles in a two-dimensional HP ferroelectric (DFBZ)2(FA)Pb2I7 (DFBZ is 2,5-difluorobenzylammonium, FA is formamidinium), which enables an unusual incommensurate modulated structure between the paraelectric and ferroelectric phases. Specifically, (DFBZ)2(FA)Pb2I7 exhibits an incommensurate modulated state over a broad temperature range of 313–370 K, and transforms to commensurate modulation at 400–474 K. The incommensurate superstructure at 330 K is ∼6 times larger than its periodic prototype, and its structure can be solved using a (3 + 1)D superspace group with a modulation wavevector of q = (1, 0, 0.1578). The inorganic layers feature a pronounced undulation, while the interlayer organic cations are trapped in distinct rotational states. To the best of our knowledge, (DFBZ)2(FA)Pb2I7 is the first HP ferroelectric that exhibits such a long-range ordered incommensurate modulation. Moreover, its large spontaneous polarization (9.4 μC cm–2) and the near-room temperature ferroelectric-to-incommensurate phase transition result in a giant pyroelectric coefficient of 7.41 μC cm–2 K–1. This unusual incommensurate modulation in HP ferroelectrics offers new insights into the understanding of aperiodic materials and ferroelectric mechanisms.

Abstract Image

二维杂化钙钛矿铁电体中分子驱动的异常不相称调制
无机氧化物中的不相称调制已被广泛研究,代表了非周期材料的新兴前沿,能够发现新的量子现象和物理性质的操纵,而它在混合钙钛矿(HPs)中仍未被广泛探索。在这里,我们提出了驱动二维HP铁电(DFBZ)2(FA)Pb2I7 (DFBZ为2,5-二氟双酶铵,FA为甲酰胺)层间偶极子的连续动态旋转,这使得在准电相和铁电相之间形成了不寻常的不相称调制结构。具体来说,(DFBZ)2(FA)Pb2I7在313-370 K的宽温度范围内呈现出不相称调制状态,并在400-474 K时转变为相称调制。330 K下的不适应超结构比其周期原型大约6倍,其结构可以用调制波矢量q =(1,0,0.1578)的(3 + 1)D超空间群来求解。无机层具有明显的波动,而层间有机阳离子被困在不同的旋转状态。据我们所知,(DFBZ)2(FA)Pb2I7是第一个表现出这种远距离有序不相称调制的高压铁电体。此外,它的自发极化(9.4 μC cm-2)和近室温铁电-不相称相变导致其热释电系数高达7.41 μC cm-2 K-1。高压铁电体中这种不寻常的不相称调制为理解非周期材料和铁电机制提供了新的见解。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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