A Lewis acid-free and phenolate-based magnesium electrolyte for rechargeable magnesium batteries

2015 ◽  
Vol 51 (28) ◽  
pp. 6214-6217 ◽  
Author(s):  
Baofei Pan ◽  
Junjie Zhang ◽  
Jinhua Huang ◽  
John T. Vaughey ◽  
Lu Zhang ◽  
...  

Development of a strong Lewis acid-free and phenolate-based electrolyte for rechargeable magnesium-ion batteries.

2019 ◽  
Vol 34 (01n03) ◽  
pp. 2040012
Author(s):  
Zekun Wang ◽  
Jianfeng Huang ◽  
Jiayin Li

In this work, we reported a Chevrel phase [Formula: see text], which was synthesized by a molten salt approach, and its electrochemical performance as a cathode material for rechargeable magnesium batteries. The phase composition and micromorphology of the product were measured and analyzed by X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Chevrel phase sulfide delivered an excellent specific capacity of 91 mAh g[Formula: see text] at a current density of 0.2 C after 70 cycles. Its excellent reversible capacity, rate performance and cycle stability demonstrate the feasibility of the Chevrel phase [Formula: see text] materials for future rechargeable magnesium batteries.


2017 ◽  
Vol 5 (22) ◽  
pp. 10815-10820 ◽  
Author(s):  
Zhirong Zhao-Karger ◽  
Maria Elisa Gil Bardaji ◽  
Olaf Fuhr ◽  
Maximilian Fichtner

Easily synthesized fluorinated magnesium alkoxyborates with non-corrosive and chemically stable features show high electrochemical performance as magnesium ion conducting salts.


Author(s):  
Changliang Du ◽  
Waqar Younas ◽  
Zhitao Wang ◽  
Xinyu Yang ◽  
Erchao Meng ◽  
...  

Copper selenide has been considered as a much more promising conversion-type cathode material for rechargeable magnesium batteries than copper sulfide because of its better conductivity. However, the magnesium ion diffusion...


2017 ◽  
Vol 29 (7) ◽  
pp. 3174-3180 ◽  
Author(s):  
Sung-Jin Kang ◽  
Sung-Chul Lim ◽  
Hyeonji Kim ◽  
Jongwook W. Heo ◽  
Sunwook Hwang ◽  
...  

2016 ◽  
Vol 128 (11) ◽  
pp. 3768-3772 ◽  
Author(s):  
Hongmin Zhao ◽  
Jian Zhou ◽  
Puru Jena

2004 ◽  
Vol 82 (10) ◽  
pp. 1452-1461 ◽  
Author(s):  
Pascal Mongrain ◽  
Jasmin Douville ◽  
Jonathan Gagnon ◽  
Marc Drouin ◽  
Andreas Decken ◽  
...  

The strong Lewis acid tungsten oxo complex of calix[4]arene can be obtained in both hydrated and non-hydrated forms. This complex coordinates a water molecule inside the cavity via strong O···W interactions with relatively short distances of 2.284(4) and 2.329(2) Å for the tungsten oxo complex of calix[4]arene··H2O·aniline (1), and the tungsten oxo complex of calix[4]arene·H2O·toluene (2·toluene), respectively. The strong interactions are also deduced by the relatively high H2O elimination temperature observed by TGA and DSC (above 200 °C). The coordinated water molecule inside the calix[4]arene cavity is characterized by a strong IR absorption at 3616 cm–1, and a narrow resonance at ~1.2 ppm (the chemical shifts of the uncoordinated water are 1.55 and 1.60 ppm in C6D6 and CDCl3, respectively). This water molecule gives rise to H-bonds with aniline in 1. The tungsten oxo complex of 5,11,17,23-tetrabromocalix[4]arene (4), also binds H2O as the characteristic signatures are observed. The successful removal of H2O in 2, is performed under mild conditions using bis(tetrahydrofuran)-uranyl nitrate as a competitive Lewis acid. When this reaction is performed in acetonitrile, butyronitrile or tert-butylnitrile, the corresponding tungsten oxo complexes of calix[4]arene·acetonitrile (3), ·butyronitrile (5), and ·tert-butylnitrile (6) are obtained. The use of uranyl as a H2O abstractor is unprecedented. The X-ray structure of 3 consists of a tungsten oxo complex of calix[4]arene coordinated by an acetonitrile molecule (d(W···N = 2.412(2) Å). The tetra-5,11,17,23-choromethyl-25,26,27,28-tetrahydroxycalix[4]arene reacts with M(O)Cl4 (M = Mo, W) in a 1:1 stoichiometry, via a tetra Friedel–Crafts addition of benzene or toluene, followed by a lower-rim complexation of the metal oxide, to form "flower-shaped" calix[4]arenes. This "one pot" double functionalization is unprecedented.Key words: calix[4]arene, tungsten, molybdenum, X-ray, host–guest, Friedel–Crafts, Lewis acid, uranyl, DSC, TGA.


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