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有机分子铁电体中不常见的长程有序、非共格结构调制。

Unusual Long-Range Ordering Incommensurate Structural Modulations in an Organic Molecular Ferroelectric.

机构信息

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou, Fujian 350002, China.

College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, China.

出版信息

J Am Chem Soc. 2017 Nov 8;139(44):15900-15906. doi: 10.1021/jacs.7b08950. Epub 2017 Oct 24.

Abstract

The incommensurate (IC) behaviors of ferroelectrics have been widely investigated in inorganic oxides as an exciting branch for aperiodic materials, whereas it still remains a great challenge to achieve such intriguing effects in organic systems. Here, we present that successive ordering of dynamic dipoles in an organic molecular ferroelectric, N-isopropylbenzylaminium trichloroacetate (1), enables unusual incommensurately modulated structures between its paraelectric phase and ferroelectric phase. In particular, 1 exhibits three distinct IC states coupling with a long-range ordering modulation. That is, the incommensurately modulated lattice is ∼7 times as large as its periodic prototype, and the IC structure is well solved using a (3 + 1)D superspace group with the modulated wavevector q = (0, 0, 0.1589). To the best of our knowledge, 1 is the first organic ferroelectric showing such a long-range ordering IC structural modulation. In addition, structural analyses reveal that slowing down dynamic motions of anionic moieties accounts for its modulation behaviors, which also results in dramatic reorientation of dipolar moments and concrete ferroelectric polarization of 1 (∼0.65 μC/cm). The combination of unique IC structural modulations and ferroelectricity makes 1 a potential candidate for the assembly of an artificially modulated lattice, which will allow for a deep understanding of the underlying chemistry and physics of aperiodic materials.

摘要

铁电体的非调谐(IC)行为已在无机氧化物中得到广泛研究,作为非周期性材料的一个令人兴奋的分支,而在有机体系中实现这种有趣的效应仍然是一个巨大的挑战。在这里,我们提出,在有机分子铁电体 N-异丙基苯甲胺三氯乙酸酯(1)中,动态偶极子的连续有序化能够在其顺电相和铁电相之间产生不寻常的非调谐调制结构。特别是,1 表现出三种不同的与长程有序调制耦合的非调谐 IC 态。也就是说,非调谐调制的晶格比其周期性原型大约 7 倍,并且使用调制波矢 q =(0,0,0.1589)的(3 + 1)D 超空间群可以很好地解决非调谐结构。据我们所知,1 是第一个表现出这种长程有序 IC 结构调制的有机铁电体。此外,结构分析表明,减慢阴离子部分的动态运动是其调制行为的原因,这也导致了偶极矩的剧烈重新取向和 1 的具体铁电极化(约 0.65 μC/cm)。独特的 IC 结构调制和铁电性的结合使 1 成为组装人工调制晶格的潜在候选材料,这将使人们能够深入了解非周期性材料的基础化学和物理。

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