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通过 Kirkendall 扩散效应制备包含核壳结构 Sn@void@SnO/SnO₂和空心 SnO/SnO₂以及 SnO₂纳米球的纳米纤维及其电化学性能。

Nanofibers Comprising Yolk-Shell Sn@void@SnO/SnO₂ and Hollow SnO/SnO₂ and SnO₂ Nanospheres via the Kirkendall Diffusion Effect and Their Electrochemical Properties.

机构信息

Department of Materials Science and Engineering, Korea University, Anam-Dong, Seongbuk-Gu, Seoul, 136-713, Republic of Korea.

出版信息

Small. 2015 Sep;11(36):4673-81. doi: 10.1002/smll.201500940. Epub 2015 Jun 8.

Abstract

Nanofibers with a unique structure comprising Sn@void@SnO/SnO2 yolk-shell nanospheres and hollow SnO/SnO2 and SnO2 nanospheres are prepared by applying the nanoscale Kirkendall diffusion process in conventional electrospinning process. Under a reducing atmosphere, post-treatment of tin 2-ethylhexanoate-polyvinylpyrrolidone electrospun nanofibers produce carbon nanofibers with embedded spherical Sn nanopowders. The Sn nanopowders are linearly aligned along the carbon nanofiber axis without aggregation of the nanopowders. Under an air atmosphere, oxidation of the Sn-C composite nanofibers produce nanofibers comprising Sn@void@SnO/SnO2 yolk-shell nanospheres and hollow SnO/SnO2 and SnO2 nanospheres, depending on the post-treatment temperature. The mean sizes of the hollow nanospheres embedded within tin oxide nanofibers post-treated at 500 °C and 600 °C are 146 and 117 nm, respectively. For the 250th cycle, the discharge capacities of the nanofibers prepared by the nanoscale Kirkendall diffusion process post-treated at 400 °C, 500 °C, and 600 °C at a high current density of 2 A g(-1) are 663, 630, and 567 mA h g(-1), respectively. The corresponding capacity retentions are 77%, 84%, and 78%, as calculated from the second cycle. The nanofibers prepared by applying the nanoscale Kirkendall diffusion process exhibit superior electrochemical properties compared with those of the porous-structured SnO2 nanofibers prepared by the conventional post-treatment process.

摘要

采用纳米尺度的 Kirkendall 扩散过程在传统静电纺丝过程中制备了具有独特结构的纳米纤维,该结构由 Sn@void@SnO/SnO2 核壳纳米球和空心 SnO/SnO2 和 SnO2 纳米球组成。在还原气氛下,对锡辛酸-聚乙烯吡咯烷酮电纺纳米纤维进行后处理,生成嵌入球形 Sn 纳米粉末的碳纳米纤维。Sn 纳米粉末沿碳纳米纤维轴线性排列,纳米粉末没有聚集。在空气气氛下,Sn-C 复合纳米纤维的氧化生成了包含 Sn@void@SnO/SnO2 核壳纳米球和空心 SnO/SnO2 和 SnO2 纳米球的纳米纤维,这取决于后处理温度。在 500°C 和 600°C 下后处理的氧化锡纳米纤维中嵌入的空心纳米球的平均尺寸分别为 146nm 和 117nm。在 250 次循环中,在 2A g-1 的高电流密度下,在 400°C、500°C 和 600°C 下经纳米尺度 Kirkendall 扩散过程处理制备的纳米纤维的放电容量分别为 663、630 和 567mA h g-1,相应的容量保持率分别为 77%、84%和 78%,这是从第二次循环计算得出的。与通过传统后处理过程制备的多孔结构的 SnO2 纳米纤维相比,采用纳米尺度 Kirkendall 扩散过程制备的纳米纤维表现出优异的电化学性能。

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