Aneta Ciupa

Perovskite metal formate framework of [NH2-CH(+)-NH2]Mn(HCOO)3]: phase transition, magnetic, dielectric, and phonon properties.

We report the synthesis, crystal structure, and thermal, dielectric, phonon, and magnetic properties of [NH2-CH(+)-NH2][Mn(HCOO)3] (FMDMn). The anionic framework of [(Mn(HCOO)3(-)] is counterbalanced by formamidinium (FMD(+)) cations located in the cavities of the framework. These cations form extensive N-H···O hydrogen bonding with the framework. The divalent manganese ions have octahedral geometry and are bridged by the formate in an anti-anti mode of coordination. We have found that FMDMn undergoes a structural phase transition around 335 K. According to the X-ray diffraction, the compound shows R3̅c symmetry at 355 K and C2/c symmetry at 295 and 110 K. The FMD(+) cations are dynamically disordered in the high-temperature phase, and the disorder leads to very large bandwidths of Raman and IR bands corresponding to vibrations of the NH2 groups. Temperature-dependent studies show that the phase transition in FMDMn is associated with ordering of the FMD(+) cations. Detailed analysis shows, however, that these cations still exhibit some reorientational motions down to about 200 K. The ordering of the FMD(+) cations is associated with significant distortion of the anionic framework. On the basis of the magnetic data, FMDMn is a weak ferromagnet with the critical temperature Tc = 8.0 K.

Structural, magnetic and dielectric properties of two novel mixed-valence iron(II)–iron(III) metal formate frameworks

Two novel mixed-valence iron(II)–iron(III) formate frameworks templated by ethylammonium and diethylammonium cations have been prepared and characterized by DSC, X-ray diffraction and spectroscopic methods. We also report dielectric and magnetic properties of the obtained samples. Both MOFs crystallize in the P1c structure and exhibit magnetic order at 39 K. The analogue with diethylammonium cations undergoes a structural phase transition near 240 K into a triclinic phase. This transition has an order–disorder character and it is associated with pronounced dielectric anomaly. This compound is therefore the second discovered mixed-valence metal formate exhibiting multiferroic properties.

Electron paramagnetic resonance of a copper doped [(CH3)(2)NH2][Zn(HCOO)(3)] hybrid perovskite framework

We report a continuous-wave (CW) and pulse electron paramagnetic resonance (EPR) as well as pulse electron nuclear double resonance (ENDOR) study of Cu2+ doped [(CH3)2NH2][Zn(HCOO)3] hybrid perovskite which exhibits a structural phase transition. The multifrequency (X, Q and W-band) CW EPR measurements allow the temperature evolution of the Cu2+ ion local environment to be studied. The spectrum of the ordered (low-temperature) phase reveals an axially distorted octahedral Cu2+ site confirming the successful replacement of the Zn2+ ions and formation of the CuO6 octahedra. The CW EPR spectrum of the disordered (high-temperature) phase shows an additional broad line which gradually diminishes on cooling. The EPR linewidth of the axially symmetric Cu2+ ion site exhibits an anomaly at the phase transition point and Arrhenius-type behavior in the disordered phase. The temperature dependent Cu2+ spin Hamiltonian parameters change abruptly at the phase transition point indicating a strong first-order character of the transition. The X-band pulse ENDOR spectrum of the ordered phase reveals several protons in the vicinity of the Cu2+ center.

On the origin of ferroelectric structural phases in perovskite-like metal–organic formate

Metal–organic frameworks (MOFs), formed of metal centers coupled by organic molecules, exhibit inherent porosity and crystallinity. Although these systems have been examined for many potential applications, their multiferroic properties remain poorly understood. One of the approaches to get an insight into the ferroic features of these materials is the study of frameworks templated by protonated organic molecules possessing rotational and conformational freedom. The embedded organic cation with an internal electric dipole moment may be ordered on cooling, leading to the appearance of ferroelectric-like properties. Herein, we report a study of two structural phase transitions in one such material, the methylhydrazinium zinc formate [CH3NH2NH2][Zn(HCOO)3] framework (MHyZn), using various experimental techniques. High-temperature (HT) improper ferroelectric phase transition and low-temperature (LT) biferroic phase transition in MHyZn single crystals have been investigated in a broad temperature range using X-ray diffraction, longitudinal ultrasonic velocity and attenuation measurements, pyrocurrent measurements, and broadband dielectric spectroscopy. In addition, noncentrosymmetric to centrosymmetric structural transformation was confirmed for the HT phase transition with the use of temperature-resolved second harmonic generation on powder samples, while polarizing microscopy observation of a large deformation of ferroelastic-like domains attested to the noncontinuous character of the crystallographic system transformation (trigonal to triclinic) in the LT biferroic phase transition. Finally, we proved that the spontaneous electric polarization occurs due to freezing of motion around the 2- and 3-axes of the methylhydrazinium cation.