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具有增强锂存储性能的高振实密度铁掺杂氢氧化镍

High-Tap-Density Fe-Doped Nickel Hydroxide with Enhanced Lithium Storage Performance.

作者信息

Li Yanwei, Huang Renshu, Pan Guanlin, Yao Jinhuan, Zou Zhengguang

机构信息

Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering and College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China.

出版信息

ACS Omega. 2019 Apr 29;4(4):7759-7765. doi: 10.1021/acsomega.9b00579. eCollection 2019 Apr 30.

Abstract

Nickel hydroxide has attracted much attention as an anode material for lithium-ion batteries (LIBs) due to its high specific capacity, low cost, and easy preparation. However, the poor cycling stability greatly hampers its application. Herein, Fe-doped nickel hydroxide powders with a high tap density (2.16 g cm) are synthesized by a simple chemical co-precipitation method. Compared to undoped nickel hydroxide, this Fe-doped nickel hydroxide exhibits better lithium storage activity, enhanced cycling stability and rate capability, and improved electrochemical reaction kinetics. As an anode material for LIBs, the Fe-doped nickel hydroxide delivers a specific discharge capacity of 1080 mA h g at 200 mA g after 30 cycles, which is almost twice that (519 mA h g) of undoped nickel hydroxide; at a high current density of 2000 mA g, Fe-doped nickel hydroxide shows a specific capacity of 661 mA h g, significantly higher than that (182 mA h g) of undoped nickel hydroxide. Kinetic analysis reveals that Fe doping decreases the electrochemical reaction resistance and improves the lithium ion diffusivity in a nickel hydroxide electrode.

摘要

氢氧化镍因其高比容量、低成本和易于制备等优点,作为锂离子电池(LIBs)的负极材料受到了广泛关注。然而,其较差的循环稳定性极大地阻碍了它的应用。在此,通过一种简单的化学共沉淀法合成了具有高振实密度(2.16 g/cm³)的铁掺杂氢氧化镍粉末。与未掺杂的氢氧化镍相比,这种铁掺杂氢氧化镍表现出更好的储锂活性、增强的循环稳定性和倍率性能,以及改善的电化学反应动力学。作为LIBs的负极材料,铁掺杂氢氧化镍在200 mA/g的电流密度下循环30次后,比放电容量为1080 mA h/g,几乎是未掺杂氢氧化镍(519 mA h/g)的两倍;在2000 mA/g的高电流密度下,铁掺杂氢氧化镍的比容量为661 mA h/g,显著高于未掺杂氢氧化镍(182 mA h/g)。动力学分析表明,铁掺杂降低了电化学反应电阻,提高了氢氧化镍电极中锂离子的扩散率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2d7/6648726/8b5f55b50d2d/ao-2019-00579j_0007.jpg

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