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嵌入主体中的合金化:金属钛铌酸盐作为可充电碱离子电池的阳极

Alloying in an Intercalation Host: Metal Titanium Niobates as Anodes for Rechargeable Alkali-Ion Batteries.

作者信息

Das Suman, Swain Diptikanta, Araujo Rafael B, Shi Songxin, Ahuja Rajeev, Row Tayur N Guru, Bhattacharyya Aninda J

机构信息

Solid State and Structural Chemistry Unit, Indian Institute of Science, Bengaluru-, 560012, India.

Condensed Matter Theory Group, Department of Physics and Astronomy, Uppsala University, Box 516, 75120, Uppsala, Sweden.

出版信息

Chem Asian J. 2018 Feb 2;13(3):299-310. doi: 10.1002/asia.201701602. Epub 2018 Jan 11.

Abstract

We discuss here a unique flexible non-carbonaceous layered host, namely, metal titanium niobates (M-Ti-niobate, M: Al , Pb , Sb , Ba , Mg ), which can synergistically store both lithium ions and sodium ions via a simultaneous intercalation and alloying mechanisms. M-Ti-niobate is formed by ion exchange of the K ions, which are specifically located inside galleries between the layers formed by edge and corner sharing TiO and NbO octahedral units in the sol-gel synthesized potassium titanium niobate (KTiNbO ). Drastic volume changes (approximately 300-400 %) typically associated with an alloying mechanism of storage are completely tackled chemically by the unique chemical composition and structure of the M-Ti-niobates. The free space between the adjustable Ti/Nb octahedral layers easily accommodates the volume changes. Due to the presence of an optimum amount of multivalent alloying metal ions (50-75 % of total K ) in the M-Ti-niobate, an efficient alloying reaction takes place directly with ions and completely eliminates any form of mechanical degradation of the electroactive particles. The M-Ti-niobate can be cycled over a wide voltage range (as low as 0.01 V) and displays remarkably stable Li and Na ion cyclability (>2 Li /Na per formula unit) for widely varying current densities over few hundreds to thousands of successive cycles. The simultaneous intercalation and alloying storage mechanisms is also studied within the density functional theory (DFT) framework. DFT expectedly shows a very small variation in the volume of Al-titanium niobate following lithium alloying. Moreover, the theoretical investigations also conclusively support the occurrence of the alloying process of Li ions with the Al ions along with the intercalation process during discharge. The M-Ti-niobates studied here demonstrate a paradigm shift in chemical design of electrodes and will pave the way for the development of a multitude of improved electrodes for different battery chemistries.

摘要

我们在此讨论一种独特的柔性非碳质层状主体,即金属钛铌酸盐(M - 钛铌酸盐,M:Al、Pb、Sb、Ba、Mg),它可通过同时的嵌入和合金化机制协同存储锂离子和钠离子。M - 钛铌酸盐是通过K离子的离子交换形成的,这些K离子特别位于溶胶 - 凝胶合成的钛酸钾铌(KTiNbO)中由边缘和角落共享的TiO和NbO八面体单元形成的层间通道内。通常与存储合金化机制相关的大幅体积变化(约300 - 400%)通过M - 钛铌酸盐独特的化学成分和结构在化学上得到了完全解决。可调节的Ti/Nb八面体层之间的自由空间很容易容纳体积变化。由于M - 钛铌酸盐中存在适量的多价合金化金属离子(占总K的50 - 75%),与离子直接发生高效的合金化反应,完全消除了电活性颗粒的任何形式的机械降解。M - 钛铌酸盐可在很宽的电压范围内(低至0.01 V)循环,并且在数百到数千次连续循环中,对于广泛变化的电流密度,显示出非常稳定的Li和Na离子循环性能(每个化学式单元>2 Li/Na)。同时的嵌入和合金化存储机制也在密度泛函理论(DFT)框架内进行了研究。DFT预期显示锂合金化后铝钛铌酸盐的体积变化非常小。此外,理论研究还确凿地支持了放电过程中锂离子与铝离子的合金化过程以及嵌入过程的发生。这里研究的M - 钛铌酸盐展示了电极化学设计的范式转变,并将为开发多种用于不同电池化学体系的改进电极铺平道路。

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