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一种基于金属有机框架衍生的方法来制备原位碳包覆的Bi/BiO异质结构作为钾离子电池的高性能阳极。

A metal-organic framework derived approach to fabricate in-situ carbon encapsulated Bi/BiO heterostructures as high-performance anodes for potassium ion batteries.

作者信息

Zhang Peng, Wei Yi, Zhou Shujie, Soomro Razium Ali, Jiang Mingchi, Xu Bin

机构信息

State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029, China; Beijing Advanced Innovation Centre for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

J Colloid Interface Sci. 2023 Jan 15;630(Pt A):365-374. doi: 10.1016/j.jcis.2022.09.151. Epub 2022 Oct 13.

Abstract

Bismuth-based materials are regarded as promising anode materials for potassium ion batteries (PIBs) due to their high theoretical capacity and low working potential. However, the large volume expansion and sluggish kinetics during cycling are major limitations to their practical application. Herein, a unique Bi/BiO-C heterostructure was designed through a simple Bi-metal-organic framework (MOF) modulation-pyrolysis process. X-ray photoelectron spectroscopy, transmission electron microscopy, and X-ray diffraction revealed that the Bi and BiO can form hetero-particles, which were uniformly embedded in a plate-like carbon skeleton, constructing a Bi/BiO-C heterostructure. The carbon skeleton and the formation of numerous hetero-interfaces between Bi, BiO, and carbon can effectively promote the interfacial charge transfer, shorten the K diffusion pathway, and alleviate the volume expansion of Bi/BiO during potassiation. Consequently, the Bi/BiO-C heterostructure exhibited a high reversible capacity of 426.0 mAh g at 50 mA g, excellent cycle performance of 251.8 mAh g after 350 cycles with a capacity retention of 76.6 %, and superior rate capability of 82.7 mAh g at 1 A g, demonstrating its promising potential for the application of PIBs anode.

摘要

铋基材料因其高理论容量和低工作电位而被视为钾离子电池(PIBs)有前景的负极材料。然而,循环过程中的大体积膨胀和缓慢动力学是其实际应用的主要限制。在此,通过简单的铋金属有机框架(MOF)调制-热解过程设计了一种独特的Bi/BiO-C异质结构。X射线光电子能谱、透射电子显微镜和X射线衍射表明,Bi和BiO可以形成异质颗粒,这些颗粒均匀地嵌入板状碳骨架中,构建了Bi/BiO-C异质结构。碳骨架以及Bi、BiO和碳之间大量异质界面的形成可以有效促进界面电荷转移,缩短钾扩散路径,并减轻铋化过程中Bi/BiO的体积膨胀。因此,Bi/BiO-C异质结构在50 mA g下表现出426.0 mAh g的高可逆容量,350次循环后具有251.8 mAh g的优异循环性能,容量保持率为76.6%,在1 A g下具有82.7 mAh g的优异倍率性能,证明了其在PIBs负极应用中的广阔潜力。

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