scholarly journals Phase transition and switchable dielectric behaviours in an organic–inorganic hybrid compound: (3-nitroanilinium) 2 (18-crown-6) 2 (H 2 PO 4 ) 2 (H 3 PO 4 ) 3 (H 2 O)

2018 ◽  
Vol 5 (10) ◽  
pp. 180738 ◽  
Author(s):  
Yang Liu ◽  
Chun-li Zhu ◽  
Xiao-yuan Zheng ◽  
Liu-lei Qin ◽  
Shuang-xi Yang ◽  
...  

An organic–inorganic hybrid compound with an extensive three-dimensional (3D) crystal structure, (3-nitroanilinium) 2 (18-crown-6) 2 (H 2 PO 4 ) 2 (H 3 PO 4 ) 3 (H 2 O) ( 1 ), was synthesized under slow evaporation conditions. Differential scanning calorimetry measurements indicated that 1 underwent a reversible phase transition at ca 231 K with a hysteresis width of 10 K. Variable-temperature X-ray single-crystal diffraction revealed that the phase transition of 1 can be ascribed to coupling of pendulum-like motions of its nitro group with proton transfer in O–H···O hydrogen bonds of the 3D framework. The temperature dependence of its dielectric permittivity demonstrated a step-like change in the range of 150–280 K with remarkable dielectric anisotropy, making 1 a promising switchable dielectric material. Potential energy calculations further supported the possibility of dynamic motion of the cationic nitro group. Overall, our findings may inspire the development of other switchable dielectric phase transition materials by introducing inorganic anions into organic–inorganic hybrid systems.

2019 ◽  
Vol 270 ◽  
pp. 226-230 ◽  
Author(s):  
Yanhuan Hao ◽  
Shuyao Wen ◽  
Jiaojiao Yao ◽  
Zhenhong Wei ◽  
Xiuxiu Zhang ◽  
...  

2021 ◽  
Author(s):  
Yao Liu ◽  
Yu-Kong Li ◽  
Ting-Ting Ying ◽  
Yu-Hui Tan ◽  
Yun Zhi Tang ◽  
...  

Organic-inorganic hybrid metal halides with dielectric properties have attracted widespread attention due to their applications in the field of optoelectronics. Here, we successfully synthesized a novel dielectric material (C8H18BrN)2SnBr6 (1),...


2011 ◽  
Vol 7 (2) ◽  
pp. 1348-1358 ◽  
Author(s):  
W. Wamani ◽  
N. Hannachi ◽  
T. Mhiri ◽  
M. Belhouchet

Organic–inorganic hybrid sample NH3(C6H4)2NH3HgCl4 was characterized by differential scanning calorimetry (DSC), TGA analysis and electrical impedance spectroscopy. DSC studies indicated the presence of a one-phase transition at 391 K. As for the ac conductivity of the compound NH3(C6H4)2NH3HgCl4, it has been measured in the temperature range of 358 - 413K and the frequency range of 209 Hz–5 MHz. Concerning the Z’ and Z’’ versus frequency plots, they were well-fitted to an equivalent circuit model. The equivalent circuit is composed of a series of combination of two parallel (R//CPE) circuits. Besides, the frequency dependence of the conductivity was interpreted in terms of Jonscher's law σ(ω) = σdc +A ωn.  As regards the conductivity, it follows the Arrhenius relation. The variation of the value of the conductivity with temperatures confirmed the availability of the phase transition at 391K detected by DSC and electrical measurements.


2019 ◽  
Vol 6 (7) ◽  
pp. 1761-1766 ◽  
Author(s):  
Tao Yang ◽  
Bing Teng ◽  
Shiguo Han ◽  
Maofan Li ◽  
Zhiyun Xu ◽  
...  

We presented a new inorganic–organic hybrid compound, which exhibits phase transition and dielectric anisotropy properties.


2020 ◽  
Vol 282 ◽  
pp. 121104 ◽  
Author(s):  
Jiang ZhenTao ◽  
Hao Yanhuan ◽  
Wang Hui ◽  
Zhang Xiuxiu ◽  
Yao Jiaojiao ◽  
...  

Author(s):  
Tamara J. Bednarchuk ◽  
Wolfgang Hornfeck ◽  
Vasyl Kinzhybalo ◽  
Zhengyang Zhou ◽  
Michal Dušek ◽  
...  

The organic–inorganic hybrid compound 4-aminopyridinium tetraaquabis(sulfato)iron(III), (C5H7N2)[FeIII(H2O)4(SO4)2] (4apFeS), was obtained by slow evaporation of the solvent at room temperature and characterized by single-crystal X-ray diffraction in the temperature range from 290 to 80 K. Differential scanning calorimetry revealed that the title compound undergoes a sequence of three reversible phase transitions, which has been verified by variable-temperature X-ray diffraction analysis during cooling–heating cycles over the temperature ranges 290–100–290 K. In the room-temperature phase (I), space group C2/c, oxygen atoms from the closest Fe-atom environment (octahedral) were disordered over two equivalent positions around a twofold axis. Two intermediate phases (II), (III) were solved and refined as incommensurately modulated structures, employing the superspace formalism applied to single-crystal X-ray diffraction data. Both structures can be described in the (3+1)-dimensional monoclinic X2/c(α,0,γ)0s superspace group (where X is ½, ½, 0, ½) with modulation wavevectors q = (0.2943, 0, 0.5640) and q = (0.3366, 0, 0.5544) for phases (II) and (III), respectively. The completely ordered low-temperature phase (IV) was refined with the twinning model in the triclinic P{\overline 1} space group, revealing the existence of two domains. The dynamics of the disordered anionic substructure in the 4apFeS crystal seems to play an essential role in the phase transition mechanisms. The discrete organic moieties were found to be fully ordered even at room temperature.


2010 ◽  
Vol 66 (3) ◽  
pp. 387-395 ◽  
Author(s):  
Heng-Yun Ye ◽  
Li-Zhuang Chen ◽  
Ren-Gen Xiong

Pyridinium-3-carboxylic acid perchlorate was synthesized and separated as crystals. Differential scanning calorimetry (DSC) measurements show that this compound undergoes a reversible phase transition at ∼ 135 K with a wide hysteresis of 15 K. Dielectric measurements confirm the transition at ∼ 127 K. Measurement of the unit-cell parameters versus temperature shows that the values of the c axis and β angle change abruptly and remarkably at 129 (2) K, indicating that the system undergoes a first-order transition at T c = 129 K. The crystal structures determined at 103 and 298 K are all monoclinic in P21/c, showing that the phase transition is isosymmetric. The crystal contains one-dimensional hydrogen-bonded chains of the pyridinium-3-carboxylic acid cations, which are further linked to perchlorate anions by hydrogen bonds to form well separated infinite planar layers. The most distinct differences between the structures of the higher-temperature phase and the lower-temperature phase are the change of the distance between the adjacent pyridinium ring planes within the hydrogen-bonded chains and the relative displacement between the hydrogen-bonded layers. Structural analysis shows that the driving force of the transition is the reorientation of the pyridinium-3-carboxylic acid cations. The degree of order of the perchlorate anions may be a secondary order parameter.


Polyhedron ◽  
2015 ◽  
Vol 85 ◽  
pp. 41-47 ◽  
Author(s):  
M. Amine Fersi ◽  
I. Chaabane ◽  
M. Gargouri ◽  
Alain Bulou

2020 ◽  
Vol 49 (21) ◽  
pp. 7252-7257 ◽  
Author(s):  
Xiuli You ◽  
Jiaojiao Yao ◽  
Zhenhong Wei

Two discrete tin based organic–inorganic hybrid compounds [(FMBA)2SnX6] (X = Cl and Br) showed reversible phase transition and dielectric anomaly above 400 K which were originated from the order-disorder of a fluorine-substituted organic amine.


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