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用于可调节锂离子电池负极的合金化 SiGe 纳米线的直接合成。

Direct Synthesis of Alloyed SiGe Nanowires for Performance-Tunable Lithium Ion Battery Anodes.

机构信息

Bernal Institute and Department of Chemical Sciences, University of Limerick , Limerick V94 T9PX, Ireland.

出版信息

ACS Nano. 2017 Oct 24;11(10):10088-10096. doi: 10.1021/acsnano.7b04523. Epub 2017 Sep 18.

Abstract

Here we report the formation of high capacity Li-ion battery anodes from SiGe alloy nanowire arrays that are grown directly on stainless steel current collectors, in a single-step synthesis. The direct formation of these SiGe nanowires (ranging from SiGe to SiGe) represents a simple and efficient processing route for the production of Li-ion battery anodes possessing the benefits of both Si (high capacity) and Ge (improved rate performance and capacity retention). The nanowires were characterized through SEM, TEM, XRD and ex situ HRSEM/HRTEM. Electrochemical analysis was conducted on these nanowires, in half-cell configurations, with capacities of up to 1360 mAh/g (SiGe) sustained after 250 cycles and in full cells, against a commercial cathode, where capacities up to 1364 mAh/g (SiGe) were retained after 100 cycles.

摘要

在这里,我们报告了一种由 SiGe 合金纳米线阵列形成的高容量锂离子电池阳极的形成,这些纳米线阵列直接生长在不锈钢集电器上,采用单步合成。这些 SiGe 纳米线(从 SiGe 到 SiGe)的直接形成代表了一种简单有效的生产锂离子电池阳极的方法,具有 Si(高容量)和 Ge(提高倍率性能和容量保持率)的优势。通过 SEM、TEM、XRD 和原位 HRSEM/HRTEM 对纳米线进行了表征。在半电池配置中对这些纳米线进行了电化学分析,在 250 次循环后可保持高达 1360 mAh/g(SiGe)的容量,在全电池中,与商业阴极相比,在 100 次循环后可保持高达 1364 mAh/g(SiGe)的容量。

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