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碘掺杂红磷纳米颗粒的锂离子电池负极的溶液合成。

Solution Synthesis of Iodine-Doped Red Phosphorus Nanoparticles for Lithium-Ion Battery Anodes.

机构信息

Department of Chemical Engineering, National Tsing Hua University , 101, Section 2, Kuang-Fu Road, Hsinchu, Taiwan 30013, ROC.

出版信息

Nano Lett. 2017 Feb 8;17(2):1240-1247. doi: 10.1021/acs.nanolett.6b05081. Epub 2017 Jan 24.

Abstract

Red phosphorus (RP) is a promising anode material for lithium-ion batteries due to its earth abundance and a high theoretical capacity of 2596 mA h g. Although RP-based anodes for lithium-ion batteries have been reported, they were all in the form of carbon-P composites, including P-graphene, P-graphite, P-carbon nanotubes (CNTs), and P-carbon black, to improve P's extremely low conductivity and large volume change during cycling process. Here, we report the large-scale synthesis of red phosphorus nanoparticles (RPNPs) with sizes ranging from 100 to 200 nm by reacting PI with ethylene glycol in the presence of cetyltrimethylammonium bromide (CTAB) in ambient environment. Unlike the insulator behavior of commercial RP (conductivity of <10 S m), the conductivity of RPNPs is between 2.62 × 10 and 1.81 × 10 S m, which is close to that of semiconductor germanium (1.02 × 10 S m), and 2 orders of magnitude higher than silicon (5.35 × 10 S m). Around 3-5 wt % of iodine-doping was found in RPNPs, which was speculated as the key to significantly improve the conductivity of RPNPs. The significantly improved conductivity of RPNPs and their uniform colloidal nanostructures enable them to be used solely as active materials for LIBs anodes. The RPNPs electrodes exhibit a high specific capacity of 1700 mA h g (0.2 C after 100 cycles, 1 C = 2000 mA g), long cycling life (∼900 mA h g after 500 cycles at 1 C), and outstanding rate capability (175 mA h g at the charge current density of 120 A g, 60 C). Moreover, as a proof-of-concept example, pouch-type full cells using RPNPs anodes and Li(NiCoMn)O (NCM-532) cathodes were assembled to show their practical uses.

摘要

红磷(RP)是一种很有前途的锂离子电池阳极材料,因为它在地壳中含量丰富,理论比容量高达 2596 mA h g。尽管已经有报道称 RP 基锂离子电池阳极,但它们都是以碳-P 复合材料的形式存在的,包括 P-石墨烯、P-石墨、P-碳纳米管(CNTs)和 P-炭黑,以提高 P 在循环过程中极低的导电性和巨大的体积变化。在这里,我们报告了在环境条件下,通过在 PI 与乙二醇反应中引入十六烷基三甲基溴化铵(CTAB),大规模合成尺寸在 100 到 200nm 之间的红磷纳米颗粒(RPNPs)。与商业 RP 的绝缘体行为(<10 S m 的电导率)不同,RPNPs 的电导率在 2.62×10 和 1.81×10 S m 之间,接近于半导体锗(1.02×10 S m),比硅(5.35×10 S m)高 2 个数量级。在 RPNPs 中发现了约 3-5wt%的碘掺杂,这被认为是显著提高 RPNPs 电导率的关键。RPNPs 显著提高的电导率及其均匀的胶体纳米结构使其能够单独用作 LIBs 阳极的活性材料。RPNPs 电极表现出高比容量 1700 mA h g(100 次循环后 0.2C,1C=2000 mA g),长循环寿命(在 1C 下 500 次循环后约 900 mA h g)和出色的倍率性能(在 120 A g 的充电电流密度下 175 mA h g,60 C)。此外,作为一个概念验证示例,组装了使用 RPNPs 阳极和 Li(NiCoMn)O(NCM-532)阴极的袋式全电池,以展示它们的实际用途。

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