期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 630, 期 -, 页码 365-374出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.09.151
关键词
Potassium ion batteries; Metal-organic framework; Bismuth; Heterostructure; Carbon skeleton
In this study, a unique Bi/Bi2O3-C heterostructure was designed to enhance the performance of potassium ion battery anode materials. The heterostructure effectively promotes interfacial charge transfer, shortens ion diffusion pathway, and alleviates volume expansion, resulting in improved reversible capacity, cycle performance, and rate capability.
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/Bi2O3-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 Bi2O3 can form hetero-particles, which were uniformly embedded in a plate-like carbon skeleton, constructing a Bi/Bi2O3-C heterostructure. The carbon skeleton and the formation of numerous hetero-interfaces between Bi, Bi2O3, and carbon can effectively promote the interfacial charge transfer, shorten the K+ diffusion pathway, and alleviate the volume expansion of Bi/Bi2O3 during potassiation. Consequently, the Bi/Bi2O3-C heterostructure exhibited a high reversible capacity of 426.0 mAh g-1 at 50 mA g-1, excellent cycle performance of 251.8 mAh g-1 after 350 cycles with a capacity retention of 76.6 %, and superior rate capability of 82.7 mAh g-1 at 1 A g-1, demonstrating its promising potential for the application of PIBs anode.(c) 2022 Elsevier Inc. All rights reserved.
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