基于水溶液的碳异构岩盐复合阴极开发合成方法及其局限性

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Venkata Sai Avvaru , Mateusz Zuba , Beth L. Armstrong , Shilong Wang , Dong-Min Kim , Isik Su Buyuker , Carrie Siu , Brett A Helms , Ozgenur Kahvecioglu , Haegyeom Kim
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引用次数: 0

摘要

无序的岩盐阴极具有高比容量和高能量密度,但其低电子传导性是一个巨大的挑战。在此,我们首次探索了一种基于水溶液的合成路线,该路线涉及控制 Li1.2Mn0.6Ti0.2O1.8F0.2 (LMTOF)的表面电荷,使其被几层还原氧化石墨烯(rGO)锚定。带负电荷的 rGO 和带正电荷的 LMTOF 颗粒之间的静电吸引实现了 LMTOF 颗粒表面均匀的 rGO 包裹。虽然与原始 LMTOF 相比,rGO-LMTOF 复合材料的初始比容量增加了 58%,但该复合材料在循环过程中出现了严重的容量衰减。从电感耦合等离子体分析和 X 射线衍射分析中可以看出,在水介质中的合成过程导致了 Li+/H+ 交换和 TM 溶解。因此,这项工作表明需要寻找合成碳-有序岩盐阴极复合材料的替代介质或条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aqueous solution-based synthesis approach for carbon-disordered rocksalt composite cathode development and its limitations
Disordered rocksalt cathodes exhibit high specific capacities and high energy density; however, their low electronic conductivity poses a great challenge. Herein, we explored an aqueous-solution-based synthesis route that involves controlling the surface charges of Li1.2Mn0.6Ti0.2O1.8F0.2 (LMTOF) to be anchored by a few-layer reduced graphene oxide (rGO) for the first time. The uniform rGO wrapping on the surface of the LMTOF particles is achieved by electrostatic attraction between the negatively charged rGO and positively charged LMTOF particles. Although the initial specific capacity of rGO-LMTOF composite increased by 58 % compared to the pristine LMTOF, the composite experienced a severe capacity fade over cycling. The synthesis process in an aqueous medium resulted in Li+/H+ exchange and TM dissolution as evidenced from inductively coupled plasmon analysis and X-ray diffraction analysis. Therefore, this work suggests the search for alternative media or conditions for the synthesis of carbon-disordered rock salt cathode composite.
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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