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Synthesis and assessment of new cyclopenta-2,4-dienone derivatives for energy storage applications

机译:用于储能的新型环戊2,4-二烯酮衍生物的合成和评估

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摘要

A series of tetraphenylcyclopenta-2,4-dienones with various substituents including hydrogen, thiophene and methoxy groups were prepared to compare their suitability as materials for forming alkali metal-based (Li or Na) solvated electron solutions (SESs) for potential use as anode materials for flow Li-Air (or Na) batteries at ambient temperature condition. The materials are amorphous, not luminescent and have moderate E-g,E- (opt) in range 1.84-1.91 eV. They also possess good thermal stability (stable above 200 degrees C), exhibit quasi-reversible reduction and oxidation reactions. It was also found that the type of substituent can influence the ability of the cyclopentadienones to form SES with alkali metals, where the derivatives with hydrogen or methoxy units were found to form SESs with lithium, but the thienyl derivative did not. Parallel studies also indicated that our big IT-systems were thermodynamically more favorably to solvate the electrons than small and simple aromatic or polar aprotic solvent molecules such as benzene, toluene, xylene, tetrahydrofuran, solvate acetone, etc. (C) 2014 Elsevier B.V. All rights reserved.
机译:制备了一系列具有各种取代基(包括氢,噻吩和甲氧基)的四苯基环戊-2,4-二烯酮,以比较它们作为形成碱金属基(Li或Na)溶剂化电子溶液(SES)的材料的适用性,以用作阳极环境温度条件下的锂-空气(或钠)流通电池材料。该材料是非晶态的,不发光,并且具有在1.84-1.91eV范围内的适度的E-g,E-(opt)。它们还具有良好的热稳定性(在200摄氏度以上稳定),表现出准可逆的还原和氧化反应。还发现取代基的类型可以影响环戊二烯酮与碱金属形成SES的能力,其中发现具有氢或甲氧基单元的衍生物与锂形成SES,而噻吩基衍生物则没有。并行研究还表明,与小而简单的芳香族或极性非质子传递溶剂分子(例如苯,甲苯,二甲苯,四氢呋喃,溶剂化丙酮等)相比,我们的大型IT系统在热力学上更有利于溶剂化电子。(C)2014 Elsevier BV All版权所有。

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