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多维协同纳米结构表现出高度稳定和超快的钠离子存储。

Multidimensional Synergistic Nanoarchitecture Exhibiting Highly Stable and Ultrafast Sodium-Ion Storage.

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070, Hubei, China.

Department of Materials Science and Engineering, University of California Los Angeles, CA, 90095-1595, USA.

出版信息

Adv Mater. 2018 May;30(18):e1707122. doi: 10.1002/adma.201707122. Epub 2018 Mar 25.

DOI:10.1002/adma.201707122
PMID:29575255
Abstract

Conversion-type anodes with multielectron reactions are beneficial for achieving a high capacity in sodium-ion batteries. Enhancing the electron/ion conductivity and structural stability are two key challenges in the development of high-performance sodium storage. Herein, a novel multidimensionally assembled nanoarchitecture is presented, which consists of V O nanoparticles embedded in amorphous carbon nanotubes that are then coassembled within a reduced graphene oxide (rGO) network, this materials is denoted V O ⊂C-NTs⊂rGO. The selective insertion and multiphase conversion mechanism of V O in sodium-ion storage is systematically demonstrated for the first time. Importantly, the naturally integrated advantages of each subunit synergistically provide a robust structure and rapid electron/ion transport, as confirmed by in situ and ex situ transmission electron microscopy experiments and kinetic analysis. Benefiting from the synergistic effects, the V O ⊂C-NTs⊂rGO anode delivers an ultralong cycle life (72.3% at 5 A g after 15 000 cycles) and an ultrahigh rate capability (165 mAh g at 20 A g , ≈30 s per charge/discharge). The synergistic design of the multidimensionally assembled nanoarchitecture produces superior advantages in energy storage.

摘要

具有多电子反应的转换型阳极有利于实现钠离子电池的高容量。提高电子/离子电导率和结构稳定性是开发高性能钠离子存储的两个关键挑战。本文提出了一种新颖的多维组装纳米结构,它由嵌入在无定形碳纳米管中的 V O 纳米颗粒组成,然后再在还原氧化石墨烯(rGO)网络中组装,这种材料被标记为 V O ⊂C-NTs⊂rGO。首次系统地证明了 V O 在钠离子存储中的选择性嵌入和多相转化机制。重要的是,每个亚单位的自然集成优势协同提供了一个坚固的结构和快速的电子/离子传输,这一点通过原位和异位透射电子显微镜实验和动力学分析得到了证实。受益于协同效应,V O ⊂C-NTs⊂rGO 阳极具有超长的循环寿命(在 5 A g 下经过 15 000 次循环后为 72.3%)和超高的倍率性能(在 20 A g 下为 165 mAh g ,≈30 s 充放电)。多维组装纳米结构的协同设计在储能方面产生了卓越的优势。

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