Department of Materials and Interfaces , Weizmann Institute of Science , Rehovot 76100 , Israel.
Acc Chem Res. 2018 May 15;51(5):1238-1248. doi: 10.1021/acs.accounts.8b00054. Epub 2018 Apr 20.
Crystals are physical arrays delineated by polar surfaces and often contain imperfections of a polar nature. Understanding the structure of such defects on the molecular level is of topical importance since they strongly affect the macroscopic properties of materials. Moreover, polar imperfections in crystals can be created intentionally and specifically designed by doping nonpolar crystals with "tailor-made" additives as dopants, since their incorporation generally takes place in a polar mode. Insertion of dopants also induces a polar deformation of neighboring host molecules, resulting in the creation of polar domains within the crystals. The contribution of the distorted host molecules to the polarity of such domains should be substantial, particularly in crystals composed of molecules with large dipole moments, such as the zwitterionic amino acids, which possess dipole moments as high as ∼14 D. Polar materials are pyroelectric, i.e., they generate surface charge as a result of temperature change. With the application of recent very sensitive instruments for measuring electric currents, coupled with theoretical computations, it has become possible to determine the structure of polar imperfections, including surfaces, at a molecular level. The detection of pyroelectricity requires attachment of electrodes, which might induce various artifacts and modify the surface of the crystal. Therefore, a new method for contactless pyroelectric measurement using X-ray photoelectron spectroscopy was developed and compared to the traditional periodic temperature change technique. Here we describe the molecular-level determination of the structure of imperfections of different natures in molecular crystals and how they affect the macroscopic properties of the crystals, with the following specific examples: (i) Experimental support for the nonclassical crystal growth mechanism as provided by the detection of pyroelectricity from near-surface solvated polar layers present at different faces of nonpolar amino acid crystals. (ii) Enantiomeric disorder in dl-alanine crystals disclosed by detection of anomalously strong pyroelectricity along their nonpolar directions. The presence of such disorder, which is not revealed by accurate diffraction techniques, explains the riddle of their needlelike morphology. (iii) The design of mixed polar crystals of l-asparagine·HO/l-aspartic acid with controlled degrees of polarity, as determined by pyroelectricity and X-ray diffraction, and their use in mechanistic studies of electrofreezing of supercooled water. (iv) Pyroelectricity coupled with dispersion-corrected density functional theory calculations and molecular dynamics simulations as an analytical method for the molecular-level determination of the structure of polar domains created by doping of α-glycine crystals with different l-amino acids at concentrations below 0.5%. (v) Selective insertion of minute amounts of alcohols within the bulk of α-glycine crystals, elucidating their role as inducers of the metastable β-glycine polymorph. In conclusion, the various examples demonstrate that although these imperfections are present in minute amounts, they can be detected by the sensitive pyroelectric measurement, and by combining them with theoretical computations one can elucidate their diverse emerging functionalities.
晶体是由极性表面界定的物理排列,通常包含具有极性性质的缺陷。了解这些缺陷在分子水平上的结构具有重要的现实意义,因为它们强烈影响材料的宏观性质。此外,可以通过掺杂非极性晶体来有意且专门地创建晶体中的极性缺陷,将“定制”添加剂作为掺杂剂,因为掺杂剂的掺入通常以极性模式发生。掺杂剂的插入也会导致相邻主体分子的极性变形,从而在晶体内部产生极性畴。这种畴的扭曲主体分子对极性的贡献应该是相当大的,特别是在由具有大偶极矩的分子组成的晶体中,例如带有高达约 14 D 的偶极矩的两性离子氨基酸。极性材料是热释电的,也就是说,它们会由于温度变化而产生表面电荷。随着最近用于测量电流的非常灵敏仪器的应用,以及理论计算的结合,已经可以在分子水平上确定包括表面在内的极性缺陷的结构。热释电的检测需要连接电极,这可能会引起各种伪影并改变晶体的表面。因此,开发了一种使用 X 射线光电子能谱的非接触式热释电测量新方法,并与传统的周期性温度变化技术进行了比较。在这里,我们描述了在分子晶体中不同性质的缺陷的结构在分子水平上的确定,以及它们如何影响晶体的宏观性质,并给出了以下具体示例:(i)通过检测非极性氨基酸晶体不同面上存在的近表面溶剂化极性层的热释电性,为非经典晶体生长机制提供实验支持。(ii)通过检测 dl-丙氨酸晶体沿非极性方向的异常强热释电性,揭示出其对映体无序性。这种无序性无法通过精确的衍射技术揭示出来,它解释了它们针状形态的谜团。(iii)通过热释电和 X 射线衍射确定了 l-天冬酰胺·HO/l-天冬氨酸混合极性晶体的控制极性度的设计,并将其用于超冷水的电冻结机制研究。(iv)通过热释电与修正后的密度泛函理论计算和分子动力学模拟相结合,作为通过掺杂不同浓度低于 0.5%的 l-氨基酸来确定α-甘氨酸晶体中创建的极性畴的结构的分析方法。(v)在α-甘氨酸晶体的体相中选择性地插入少量醇,阐明其作为亚稳定β-甘氨酸多晶型的诱导物的作用。总之,这些不同的例子表明,尽管这些缺陷的含量很少,但可以通过灵敏的热释电测量来检测到,并且通过将它们与理论计算相结合,可以阐明它们的各种新兴功能。