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可控氮掺杂CuCoO@C薄膜作为超稳定钠离子电池的自支撑阳极

Controllable N-Doped CuCo O @C Film as a Self-Supported Anode for Ultrastable Sodium-Ion Batteries.

作者信息

Wang Xiaojun, Cao Kangzhe, Wang Yijing, Jiao Lifang

机构信息

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Nankai University, Tianjin, 300071, China.

Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin, 300071, China.

出版信息

Small. 2017 Aug;13(29). doi: 10.1002/smll.201700873. Epub 2017 Jun 1.

Abstract

Rational synthesis of flexible electrodes is crucial to rapid growth of functional materials for energy-storage systems. Herein, a controllable fabrication is reported for the self-supported structure of CuCo O nanodots (≈3 nm) delicately inserted into N-doped carbon nanofibers (named as 3-CCO@C); this composite is first used as binder-free anode for sodium-ion batteries (SIBs). Benefiting from the synergetic effect of ultrasmall CuCo O nanoparticles and a tailored N-doped carbon matrix, the 3-CCO@C composite exhibits high cycling stability (capacity of 314 mA h g at 1000 mA g after 1000 cycles) and high rate capability (296 mA h g , even at 5000 mA g ). Significantly, the Na storage mechanism is systematically explored, demonstrating that the irreversible reaction of CuCo O , which decomposes to Cu and Co, happens in the first discharge process, and then a reversible reaction between metallic Cu/Co and CuO/Co O occurrs during the following cycles. This result is conducive to a mechanistic study of highly promising bimetallic-oxide anodes for rechargeable SIBs.

摘要

柔性电极的合理合成对于储能系统功能材料的快速发展至关重要。在此,报道了一种可控制备方法,用于将尺寸约为3纳米的CuCoO纳米点精细地插入到氮掺杂碳纳米纤维中形成自支撑结构(命名为3-CCO@C);这种复合材料首次用作钠离子电池(SIBs)的无粘结剂阳极。得益于超小CuCoO纳米颗粒与定制的氮掺杂碳基体的协同效应,3-CCO@C复合材料表现出高循环稳定性(在1000 mA g下循环1000次后容量为314 mA h g)和高倍率性能(即使在5000 mA g时也有296 mA h g)。值得注意的是,系统地探究了钠存储机制,表明在首次放电过程中发生了CuCoO分解为Cu和Co的不可逆反应,随后在后续循环中金属Cu/Co与CuO/CoO之间发生可逆反应。这一结果有助于对用于可充电SIBs的极具前景的双金属氧化物阳极进行机理研究。

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