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单根硅纳米线负极的超快电化学嵌锂

Ultrafast electrochemical lithiation of individual Si nanowire anodes.

机构信息

Center for Integrated Nanotechnologies, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States.

出版信息

Nano Lett. 2011 Jun 8;11(6):2251-8. doi: 10.1021/nl200412p. Epub 2011 May 12.

DOI:10.1021/nl200412p
PMID:21563798
Abstract

Using advanced in situ transmission electron microscopy, we show that the addition of a carbon coating combined with heavy doping leads to record-high charging rates in silicon nanowires. The carbon coating and phosphorus doping each resulted in a 2 to 3 orders of magnitude increase in electrical conductivity of the nanowires that, in turn, resulted in a 1 order of magnitude increase in charging rate. In addition, electrochemical solid-state amorphization (ESA) and inverse ESA were directly observed and characterized during a two-step phase transformation process during lithiation: crystalline silicon (Si) transforming to amorphous lithium-silicon (Li(x)Si) which transforms to crystalline Li(15)Si(4) (capacity 3579 mAh·g(-1)). The ultrafast charging rate is attributed to the nanoscale diffusion length and the improved electron and ion transport. These results provide important insight in how to use Si as a high energy density and high power density anode in lithium ion batteries for electrical vehicle and other electronic power source applications.

摘要

利用先进的原位透射电子显微镜,我们发现,碳涂层的添加与重掺杂相结合,使得硅纳米线的充电速率达到了创纪录的水平。碳涂层和磷掺杂都使纳米线的电导率提高了 2 到 3 个数量级,进而使充电速率提高了 1 个数量级。此外,在锂化过程中的两步相变过程中,直接观察到并描述了电化学固态非晶化(ESA)和逆 ESA:晶体硅(Si)转变为非晶态锂硅(Li(x)Si),然后再转变为晶体 Li(15)Si(4)(容量为 3579 mAh·g(-1))。超快的充电速率归因于纳米级的扩散长度以及电子和离子传输的改善。这些结果为如何将硅用作锂离子电池中的高能量密度和高功率密度阳极提供了重要的见解,适用于电动汽车和其他电子电源应用。

相似文献

1
Ultrafast electrochemical lithiation of individual Si nanowire anodes.单根硅纳米线负极的超快电化学嵌锂
Nano Lett. 2011 Jun 8;11(6):2251-8. doi: 10.1021/nl200412p. Epub 2011 May 12.
2
Nanostructured hybrid silicon/carbon nanotube heterostructures: reversible high-capacity lithium-ion anodes.纳米结构杂化硅/碳纳米管异质结构:可逆高容量锂离子负极。
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3
In situ X-ray diffraction studies of (de)lithiation mechanism in silicon nanowire anodes.原位 X 射线衍射研究硅纳米线阳极的(脱)锂机制。
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Demonstration of an electrochemical liquid cell for operando transmission electron microscopy observation of the lithiation/delithiation behavior of Si nanowire battery anodes.用于原位透射电子显微镜观察硅纳米线电池负极的嵌锂/脱锂行为的电化学液池的演示。
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Tailoring lithiation behavior by interface and bandgap engineering at the nanoscale.通过纳米尺度的界面和能带工程定制锂化行为。
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Self-limiting lithiation in silicon nanowires.硅纳米线中的自限性锂化。
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Crystalline-amorphous core-shell silicon nanowires for high capacity and high current battery electrodes.用于高容量和高电流电池电极的晶态-非晶态核壳结构硅纳米线
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In situ TEM investigation of congruent phase transition and structural evolution of nanostructured silicon/carbon anode for lithium ion batteries.原位透射电子显微镜研究锂离子电池纳米硅/碳复合负极的一致相转变和结构演变。
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Graphene encapsulated and SiC reinforced silicon nanowires as an anode material for lithium ion batteries.石墨烯封装和碳化硅增强的硅纳米线作为锂离子电池的阳极材料。
Nanoscale. 2013 Sep 21;5(18):8689-94. doi: 10.1039/c3nr02788k.

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