Kim Kyungmo, Li Yang, Ok Kang Min
Department of Chemistry, Sogang University, Seoul 04107, Republic of Korea.
J Am Chem Soc. 2025 Jan 22;147(3):2880-2888. doi: 10.1021/jacs.4c16985. Epub 2025 Jan 8.
Two-dimensional (2D) organic-inorganic hybrid metal halides (OIMHs), characterized by noncentrosymmetric structures arising from the incorporation of chiral organic molecules that break inversion symmetry, have attracted significant attention. Particularly, chiral-polar 2D OIMHs offer a unique platform for multifunctional applications, as the coexistence of chirality and polarity enables the simultaneous manifestation of distinct properties such as nonlinear optical (NLO) effects, circular dichroism (CD), and ferroelectricity. In this study, we report the first synthesis of hafnium (Hf)-based chiral 2D OIMHs, achieved through the strategic incorporation of -substituents on the benzene ring of chiral organic components. By tuning the substituents, we successfully modulate the polarity of the crystal structures, resulting in both chiral-nonpolar and chiral-polar systems. Our analysis of structural and optical properties, supported by density functional theory calculations, demonstrates that the polarity of these materials can be systematically tuned, enabling adjustable band gaps and CD in the UV range (200-280 nm). Notably, halogen substitution at the -position of the benzene ring in the organic layer produces tunable optical band gaps ranging from 4.33 to 4.48 eV, the widest reported to date for chiral-polar 2D OIMHs. Furthermore, these materials exhibit enhanced NLO properties, including a remarkable 3.3-fold increase in second-harmonic generation intensity in chiral-polar compounds compared to their chiral-nonpolar counterparts. These findings position Hf-based chiral 2D OIMHs as promising candidates for UV-region applications, such as UV NLO devices and self-driven circularly polarized light detectors, offering new opportunities for designing multifunctional optoelectronic materials by harnessing the interplay between chirality and polarity.
二维(2D)有机-无机杂化金属卤化物(OIMHs)因其引入了打破反演对称性的手性有机分子而具有非中心对称结构,备受关注。特别是,手性-极性二维OIMHs为多功能应用提供了一个独特的平台,因为手性和极性的共存使得诸如非线性光学(NLO)效应、圆二色性(CD)和铁电性等不同性质能够同时表现出来。在本研究中,我们报告了基于铪(Hf)的手性二维OIMHs的首次合成,这是通过在手性有机组分的苯环上有策略地引入取代基实现的。通过调整取代基,我们成功地调节了晶体结构的极性,从而得到了手性-非极性和手性-极性体系。我们在密度泛函理论计算的支持下对结构和光学性质进行的分析表明,这些材料的极性可以系统地调节,从而在紫外范围(200-280nm)实现可调的带隙和CD。值得注意的是,在有机层苯环的α位进行卤素取代会产生4.33至4.48eV的可调光学带隙,这是迄今为止报道的手性-极性二维OIMHs中最宽的。此外,这些材料表现出增强的NLO性质,与手性-非极性对应物相比,手性-极性化合物的二次谐波产生强度显著增加了3.3倍。这些发现使基于Hf的手性二维OIMHs成为紫外区域应用(如紫外NLO器件和自驱动圆偏振光探测器)的有前途的候选材料,通过利用手性和极性之间的相互作用为设计多功能光电子材料提供了新的机会。