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Improved Performance of Si Nanowire Lithium Ion Battery Anodes By Au Catalyst Nanodot Formation on TiN

机译:通过Au催化剂纳米粒子形成在锡催化剂纳米液体形成改进了Si纳米线锂离子电池阳极性能的提高

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While silicon (Si) is considered to be an excellent candidate for next-generation lithium ion battery (LIB) anodes due to its abundance and high gravimetric capacity, Si suffers from large volume expansion as a result of lithiation. Nanowires (NWs) allow for radial expansion and strain release. Due to this volume expansion, the formation of bulk-like Si structures during the NWs growth process significantly degrades battery performance. Here we report suppression of bulk-like Si formation by interfacial energy contrast between the NWs nucleation catalysts (spontaneously formed gold (Au) nanodots) and titanium nitride (TiN) films. The TiN film promoted a narrow distribution of Si NWs' diameters and a direct electrical connection to the stainless steel current collector. The characteristics of the solid electrolyte interphase and lithiation/charge transfer mechanisms in Si NWs were also investigated using electrochemical impedance spectroscopy (EIS). The EIS data suggest that the impedance to lithium diffusion within the NWs is approximately 40% smaller in the NWs grown on TiN than the NWs grown directly on stainless steel. LIB anodes fabricated with the Au-catalyzed Si NWs on TiN films displayed enhanced specific gravimetric capacities (>30%) under diverse charge/discharge rates and significantly improved capacity retention over 500 cycles.
机译:虽然硅(Si)被认为是下一代锂离子电池(Lib)阳极的优异候选者,但由于其丰度和高重量容量,Si由于锂化而遭受大的体积膨胀。纳米线(NWS)允许径向膨胀和应变释放。由于该体积膨胀,在NWS生长过程中形成散装的Si结构显着降低了电池性能。在这里,我们通过NWS成核催化剂(自发形成的金(Au)纳米蛋白)和氮化钛(TiN)膜之间的界面能量对比度报告抑制块状的Si形成。锡膜促进了Si NWS直径的窄分布和与不锈钢集电器的直接电连接。还使用电化学阻抗光谱(EIS)研究了Si NWS中固体电解质界相和锂化/电荷转移机制的特征。 EIS数据表明,在NWS内的锂扩散的阻抗在锡中生长的NW在锡中生长的NW大约为40%,而不是直接在不锈钢上生长的NW。用锡膜上的Au催化的SiNW制造的LIB阳极在不同的充电/放电速率下显示出增强的特异性重量容量(> 30%),并显着提高了500次循环的容量潴留。

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