Mączka Mirosław, Zaręba Jan K, Gągor Anna, Fedoruk-Piskorska Katarzyna, Stefańska Dagmara, Drozdowski Dawid, Ptak Maciej, Sieradzki Adam
W. Trzebiatowski Institute of Low Temperature and Structural Research of the Polish Academy of Sciences, Okólna 2, 50-422 Wroclaw, Poland.
Institute of Advanced Materials, Faculty of Chemistry, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław, Poland.
ACS Appl Mater Interfaces. 2024 Nov 6;16(44):60564-60575. doi: 10.1021/acsami.4c14244. Epub 2024 Oct 24.
Two-dimensional lead halide perovskites represent a fascinating class of hybrid semiconductors for solar cell, light-emitting, nonlinear optical (NLO), and ferroelectric applications. A notable subset within this category is luminescent ferroelectrics, which have garnered considerable attention for their potential in integrated photoelectronic devices. In this study, we employed an organic amine halogenation strategy (also referred to as halogen engineering), which is renowned for its efficacy in inducing polar order through crystal engineering. Consequently, we synthesized a layered Ruddlesden-Popper (RP) lead chloride comprising 3-chloropropylammonium cations (CPA), with the chemical formula CPAPbCl. This compound features as many as four temperature-dependent crystal phases, with phase transitions observed at = 353.1 K (343.9 K), = 211.7 K (208.6 K), and = 182.0 K (178.2 K) in the heating (cooling) cycles. Employing a multitechnique approach─including thermal analysis, X-ray diffraction, dielectric and pyroelectric current measurements, Raman spectroscopy, and second-harmonic generation (SHG) studies─we determined the mechanisms of the structural phase transitions. Our findings demonstrate polar order of phase (space group 2), phase (space group 2), and phase (space group 2), while also confirming the centrosymmetric nature of phase (space group ). X-ray diffraction data revealed that the to PT is of a ferroelectric nature, devoid of ferroelastic strain, a conclusion further supported by pyroelectric measurements. CPAPbCl features negative linear thermal expansion and broadband emission, which transitions to white light above 180 K. Remarkably, CPAPbCl also demonstrates high-temperature SHG on-off switching with a high contrast ratio of 300:1 along with good switching stability, as evidenced by SHG cycling studies at heating/cooling rates ranging from 5 to 50 K/min. This SHG study also sets new standards for the field of SHG switching by providing a method to quantify the thermal responsiveness of SHG-switchable materials using the (time requirement) parameter. Overall, our findings show that the halogenation strategy has led to the discovery of a rare example of an RP perovskite exhibiting coexistence of white-light emission, SHG thermal bistability, ferroelectricity, and negative linear thermal expansion.
二维卤化铅钙钛矿是一类用于太阳能电池、发光、非线性光学(NLO)和铁电应用的迷人的混合半导体。这一类别中的一个显著子集是发光铁电体,因其在集成光电器件中的潜力而备受关注。在本研究中,我们采用了一种有机胺卤化策略(也称为卤化工程),该策略以其通过晶体工程诱导极性有序的功效而闻名。因此,我们合成了一种包含3-氯丙基铵阳离子(CPA)的层状Ruddlesden-Popper(RP)氯化铅,化学式为CPAPbCl。该化合物具有多达四个温度依赖的晶相,在加热(冷却)循环中,在 = 353.1 K(343.9 K)、 = 211.7 K(208.6 K)和 = 182.0 K(178.2 K)处观察到相变。采用包括热分析、X射线衍射、介电和热释电电流测量、拉曼光谱和二次谐波产生(SHG)研究在内的多技术方法,我们确定了结构相变的机制。我们的研究结果表明了相 (空间群2)、相 (空间群2)和相 (空间群2)的极性有序,同时也证实了相 (空间群 )的中心对称性质。X射线衍射数据表明从 到 的相变具有铁电性质,没有铁弹性应变,热释电测量进一步支持了这一结论。CPAPbCl具有负线性热膨胀和宽带发射,在180 K以上转变为白光。值得注意的是,CPAPbCl还展示了高温SHG开-关切换,对比度高达300:1,并且具有良好的切换稳定性,加热/冷却速率在5至50 K/min范围内的SHG循环研究证明了这一点。这项SHG研究还通过提供一种使用 (时间要求)参数量化SHG可切换材料热响应性的方法,为SHG切换领域设定了新的标准。总体而言,我们 的研究结果表明,卤化策略导致发现了一个罕见的RP钙钛矿例子,该例子表现出白光发射、SHG热双稳性、铁电性和负线性热膨胀的共存。