Navickas Marius, Giriūnas Laisvydas, Kalendra Vidmantas, Biktagirov Timur, Gerstmann Uwe, Schmidt Wolf Gero, Mączka Mirosław, Pöppl Andreas, Banys Jūras, Šimėnas Mantas
Faculty of Physics, Vilnius University, Sauletekio av. 9, LT-10222 Vilnius, Lithuania.
Department of Physics, Paderborn University, Warburger 100, D-33098 Paderborn, Germany.
Phys Chem Chem Phys. 2020 Apr 29;22(16):8513-8521. doi: 10.1039/d0cp01612h.
We present an X- and Q-band continuous wave (CW) and pulse electron paramagnetic resonance (EPR) study of a manganese doped [NH4][Zn(HCOO)3] hybrid framework, which exhibits a ferroelectric structural phase transition at 190 K. The CW EPR spectra obtained at different temperatures exhibit clear changes at the phase transition temperature. This suggests a successful substitution of the Zn2+ ions by the paramagnetic Mn2+ centers, which is further confirmed by the pulse EPR and 1H ENDOR experiments. Spectral simulations of the CW EPR spectra are used to obtain the temperature dependence of the Mn2+ zero-field splitting, which indicates a gradual deformation of the MnO6 octahedra indicating a continuous character of the transition. The determined data allow us to extract the critical exponent of the order parameter (β = 0.12), which suggests a quasi two-dimensional ordering in [NH4][Zn(HCOO)3]. The experimental EPR results are supported by the density functional theory calculations of the zero-field splitting parameters. Relaxation time measurements of the Mn2+ centers indicate that the longitudinal relaxation is mainly driven by the optical phonons, which correspond to the vibrations of the metal-oxygen octahedra. The temperature behavior of the transverse relaxation indicates a dynamic process in the ordered ferroelectric phase.
我们展示了对一种锰掺杂的[NH4][Zn(HCOO)3]混合框架的X波段和Q波段连续波(CW)以及脉冲电子顺磁共振(EPR)研究,该框架在190 K时呈现铁电结构相变。在不同温度下获得的CW EPR光谱在相变温度处呈现出明显变化。这表明顺磁性的Mn2+中心成功取代了Zn2+离子,脉冲EPR和1H ENDOR实验进一步证实了这一点。对CW EPR光谱进行光谱模拟以获得Mn2+零场分裂的温度依赖性,这表明MnO6八面体逐渐变形,表明该转变具有连续特性。所确定的数据使我们能够提取序参量的临界指数(β = 0.12),这表明[NH4][Zn(HCOO)3]中存在准二维有序。零场分裂参数的密度泛函理论计算支持了实验EPR结果。Mn2+中心的弛豫时间测量表明,纵向弛豫主要由光学声子驱动,光学声子对应于金属-氧八面体的振动。横向弛豫的温度行为表明在有序铁电相中存在一个动态过程。