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在单一成分分子晶体中实现高于室温的铁电性。

Above-room-temperature ferroelectricity in a single-component molecular crystal.

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8562, Japan.

出版信息

Nature. 2010 Feb 11;463(7282):789-92. doi: 10.1038/nature08731.

DOI:10.1038/nature08731
PMID:20148035
Abstract

Ferroelectrics are electro-active materials that can store and switch their polarity (ferroelectricity), sense temperature changes (pyroelectricity), interchange electric and mechanical functions (piezoelectricity), and manipulate light (through optical nonlinearities and the electro-optic effect): all of these functions have practical applications. Topological switching of pi-conjugation in organic molecules, such as the keto-enol transformation, has long been anticipated as a means of realizing these phenomena in molecular assemblies and crystals. Croconic acid, an ingredient of black dyes, was recently found to have a hydrogen-bonded polar structure in a crystalline state. Here we demonstrate that application of an electric field can coherently align the molecular polarities in crystalline croconic acid, as indicated by an increase of optical second harmonic generation, and produce a well-defined polarization hysteresis at room temperature. To make this simple pentagonal molecule ferroelectric, we switched the pi-bond topology using synchronized proton transfer instead of rigid-body rotation. Of the organic ferroelectrics, this molecular crystal exhibits the highest spontaneous polarization ( approximately 20 muC cm(-2)) in spite of its small molecular size, which is in accord with first-principles electronic-structure calculations. Such high polarization, which persists up to 400 K, may find application in active capacitor and nonlinear optics elements in future organic electronics.

摘要

铁电体是一种能够存储和切换其极性(铁电性)、感知温度变化(热释电性)、交换电能和机械能(压电性)以及操纵光(通过光学非线性和电光效应)的电活性材料:所有这些功能都具有实际应用价值。在有机分子中,如酮-烯醇转化,π共轭的拓扑转变一直被认为是在分子组装体和晶体中实现这些现象的一种手段。最近发现,黑染料的成分之一克罗酸在晶体状态下具有氢键极性结构。在这里,我们证明了在结晶克罗酸中施加电场可以使分子极性产生相干排列,这表现为光学二次谐波产生的增加,并在室温下产生明确的极化滞后。为了使这个简单的五边形分子具有铁电性,我们使用同步质子转移而不是刚体旋转来切换π键拓扑。在有机铁电体中,尽管分子尺寸较小,但这种分子晶体表现出最高的自发极化(约 20 μC cm(-2)),这与第一性原理电子结构计算相符。如此高的极化强度可持续到 400 K,这可能会在未来的有机电子学中应用于有源电容器和非线性光学元件。

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