Bartual-Murgui Carlos, Rubio-Giménez Víctor, Meneses-Sánchez Manuel, Valverde-Muñoz Francisco Javier, Tatay Sergio, Martí-Gastaldo Carlos, Muñoz M Carmen, Real José Antonio
Instituto de Ciencia Molecular (ICMol), Universitat de València, C/Catedrático José Beltrán Martínez 2, 46980 Paterna, Spain.
Departamento de Física Aplicada, Universitat Politècnica de València. Camino de Vera s/n, E-46022, Valencia, Spain.
ACS Appl Mater Interfaces. 2020 Jul 1;12(26):29461-29472. doi: 10.1021/acsami.0c05733. Epub 2020 Jun 18.
Integration of the ON-OFF cooperative spin crossover (SCO) properties of Fe coordination polymers as components of electronic and/or spintronic devices is currently an area of great interest for potential applications. This requires the selection and growth of thin films of the appropriate material onto selected substrates. In this context, two new series of cooperative SCO two-dimensional Fe coordination polymers of the Hofmann-type formulated {Fe(Pym)[M(CN)]·HO} and {Fe(Isoq)[M(CN)]} (Pym = pyrimidine, Isoq = isoquinoline; M = Ni, Pd, Pt) have been synthesized, characterized, and the corresponding Pt derivatives selected for fabrication of thin films by liquid-phase epitaxy (LPE). At ambient pressure, variable-temperature single-crystal X-ray diffraction, magnetic, and calorimetric studies of the Pt and Pd microcrystalline materials of both series display strong cooperative thermal induced SCO properties. In contrast, this property is only observed for higher pressures in the Ni derivatives. The SCO behavior of the {Fe(L)[Pt(CN)]} thin films (L = Pym, Isoq) were monitored by magnetization measurements in a SQUID magnetometer and compared with the homologous samples of the previously reported isostructural {Fe(Py)[Pt(CN)]} (Py = pyridine). Application of the theory of regular solutions to the SCO of the three derivatives allowed us to evaluate the effect on the characteristic SCO temperatures and the hysteresis, as well as the associated thermodynamic parameters when moving from microcrystalline bulk solids to nanometric thin films.
将铁配位聚合物的开-关协同自旋交叉(SCO)特性集成到电子和/或自旋电子器件中作为其组件,目前是具有潜在应用价值的一个备受关注的领域。这需要在选定的衬底上选择并生长合适材料的薄膜。在此背景下,已经合成并表征了两个新系列的霍夫曼型协同SCO二维铁配位聚合物,其化学式为{Fe(Pym)[M(CN)]·HO}和{Fe(Isoq)[M(CN)]}(Pym = 嘧啶,Isoq = 异喹啉;M = Ni、Pd、Pt),并选择了相应的Pt衍生物通过液相外延(LPE)制备薄膜。在常压下,对这两个系列的Pt和Pd微晶材料进行变温单晶X射线衍射、磁性和量热研究,结果显示出强烈的协同热诱导SCO特性。相比之下,这种特性仅在Ni衍生物的较高压力下才观察到。通过在超导量子干涉仪磁力计中进行磁化测量,监测了{Fe(L)[Pt(CN)]}薄膜(L = Pym、Isoq)的SCO行为,并与先前报道的同构{Fe(Py)[Pt(CN)]}(Py = 吡啶)的同源样品进行了比较。将正规溶液理论应用于这三种衍生物的SCO,使我们能够评估从微晶块状固体转变为纳米薄膜时对特征SCO温度和磁滞的影响,以及相关的热力学参数。