Vertical ferroelectricity in two-dimensional mixed-valence tin sulfide system: Unprecedented piezoelectricity, efficient nanogenerator and facile control of morphotoropic phase transformations

Nano Energy ◽  
2021 ◽  
Vol 83 ◽  
pp. 105786
Author(s):  
Lei Li ◽  
Menghao Wu
ChemPhysChem ◽  
2004 ◽  
Vol 5 (11) ◽  
pp. 1755-1761 ◽  
Author(s):  
Jacob Overgaard ◽  
Eva Rentschler ◽  
Grigore A. Timco ◽  
Finn K. Larsen

2014 ◽  
Vol 70 (4) ◽  
pp. 351-354 ◽  
Author(s):  
Farida Hamchaoui ◽  
Véronique Alonzo ◽  
Houria Rebbah ◽  
Eric Le Fur

The title compound, hexapotassium octairon(II,III) dodecaphosphonate, exhibiting a two-dimensional structure, is a new mixed alkali/3dmetal phosphite. It crystallizes in the space groupR\overline{3}m, with two crystallographically independent Fe atoms occupying sites of \overline{3}m(Fe1) and 3m(Fe2) symmetry. The Fe2 site is fully occupied, whereas the Fe1 site presents an occupancy factor of 0.757 (3). The three independent O atoms, one of which is disordered, are situated on a mirror and all other atoms are located on special positions with 3msymmetry. Layers of formula [Fe3(HPO3)4]2−are observed in the structure, formed by linear Fe3O12trimer units, which contain face-sharing FeO6octahedra interconnected by (HPO3)2−phosphite oxoanions. The partial occupancy of the Fe1 site might be described by the formation of two [Fe(HPO3)2]−layers derived from the [Fe3(HPO3)4]2−layer when the Fe1 atom is absent. Fe2+is localized at the Fe1 and Fe2 sites of the [Fe3(HPO3)4]2−sheets, whereas Fe3+is found at the Fe2 sites of the [Fe(HPO3)2]−sheets, according to bond-valence calculations. The K+cations are located in the interlayer spaces, between the [Fe3(HPO3)4]2−layers, and between the [Fe3(HPO3)4]2−and [Fe(HPO3)2]−layers.


2014 ◽  
Vol 70 (4) ◽  
pp. 364-367 ◽  
Author(s):  
Tiantian Yao ◽  
Jing Lu ◽  
Dacheng Li ◽  
Jianmin Dou

A new tetranuclear mixed-valence cobalt complex, namely di-μ2-azido-diazidodiethanolbis{μ2-2-[(hydroxyimino)methyl]-6-methoxyphenolato}bis{μ3-6-methoxy-2-[(oxidoimino)methyl]phenolato}dicobalt(II)dicobalt(III) ethanol disolvate, [CoII2CoIII2(C8H7NO3)2(C8H8NO3)2(N3)4(C2H5OH)2]·2C2H5OH, has been synthesized by the reaction of Co(OAc)2·4H2O (OAc is acetate) with 3-methoxysalicylaldoxime (H2mosao) in an ethanol solution. In the complex, the four Co cations all display distorted octahedral coordination environments and they are bridged by two κ2,κ1,κ1;μ3-mosao2−ligands, two κ2,κ2;μ2-Hmosao−ligands and two μ2-N3−anions to form a tetranuclear [Co4N4O4] cluster. Adjacent clusters are connected through weak C—H...N and C—H...O interactions, resulting in a two-dimensional supramolecular network parallel to theacplane. The magnetic properties of the complex have also been studied.


2014 ◽  
Vol 140 (8) ◽  
pp. 084505 ◽  
Author(s):  
Karla M. Slenkamp ◽  
Michael S. Lynch ◽  
Benjamin E. Van Kuiken ◽  
Jennifer F. Brookes ◽  
Caitlin C. Bannan ◽  
...  

2012 ◽  
Vol 134 (14) ◽  
pp. 6401-6408 ◽  
Author(s):  
Yang Li ◽  
Jie Xiao ◽  
Tatyana E. Shubina ◽  
Min Chen ◽  
Ziliang Shi ◽  
...  

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