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锰掺杂的[NH][Zn(HCOO)]杂化甲酸盐框架中铁电相变和动力学效应的电子顺磁共振研究

Electron paramagnetic resonance study of ferroelectric phase transition and dynamic effects in a Mn doped [NH][Zn(HCOO)] hybrid formate framework.

作者信息

Navickas Marius, Giriūnas Laisvydas, Kalendra Vidmantas, Biktagirov Timur, Gerstmann Uwe, Schmidt Wolf Gero, Mączka Mirosław, Pöppl Andreas, Banys Jūras, Šimėnas Mantas

机构信息

Faculty of Physics, Vilnius University, Sauletekio av. 9, LT-10222 Vilnius, Lithuania.

Department of Physics, Paderborn University, Warburger 100, D-33098 Paderborn, Germany.

出版信息

Phys Chem Chem Phys. 2020 Apr 29;22(16):8513-8521. doi: 10.1039/d0cp01612h.

Abstract

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.

摘要

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。

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