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介孔CoO@CdS纳米棒作为高性能锂离子电池的阳极,具有改善的锂存储容量和循环寿命。

Mesoporous CoO@CdS nanorods as anode for high-performance lithium ion batteries with improved lithium storage capacity and cycle life.

作者信息

Waleed Hamza, Rasheed Haroon Ur, Faiz Faisal, Zafar Amina, Javed Saqib, Liu Yanguo, Karim Shafqat, Sun Hongyu, Faiz Yasir, Hussain Shafqat, Khalid Atia, Yu Yanlong, Nisar Amjad, Ahmad Mashkoor

机构信息

Nanomaterials Research Group, Physics Division, PINSTECH Islamabad 44000 Pakistan

Department of Physics, Faculty of Basic & Applied Sciences, IIU Islamabad 44000 Pakistan.

出版信息

RSC Adv. 2024 Apr 15;14(17):11900-11907. doi: 10.1039/d4ra01028k. eCollection 2024 Apr 10.

DOI:10.1039/d4ra01028k
PMID:38623285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11017193/
Abstract

Transition metal oxides based anodes are facing crucial problems of capacity fading at long cycles and high rates due to electrode degradations. In this prospective, an effective strategy is employed to develop advanced electrode materials for lithium-ion batteries (LIBs). In the present work, a mesoporous CoO@CdS hybrid sructure is developed and investigated as anode for LiBs. The hybrid structure owning porous nature and large specific surface area, provides an opportunity to boost the lithium storage capabilities of CoO nanorods. The CoO@CdS electrode delivers an initial discharge capacity of 1292 mA h g at 0.1C and a very stable reversible capacity of 760 mA h g over 200 cycles with a capacity retention rate of 92.7%. In addition, the electrode exhibits excellent cyclic stability even after 800 cycles and good rate performance as compared to previously reported electrodes. Moreover, density functional theory (DFT) and electrochemical impedance spectroscopy (EIS) confirm the enhanced kinetics of the CoO@CdS electrode. The efficient performance of the electrode may be due to the increased surface reactivity, abundant active sites/interfaces for rapid Li ion diffusion and the synergy between CoO and CdS NPs. This work demonstrates that CoO@CdS hybrid structures have great potential for high performance batteries.

摘要

基于过渡金属氧化物的负极由于电极退化,在长循环和高倍率下面临容量衰减的关键问题。在此前景下,采用一种有效策略来开发用于锂离子电池(LIBs)的先进电极材料。在当前工作中,开发并研究了一种介孔CoO@CdS混合结构作为锂离子电池的负极。这种具有多孔性质和大比表面积的混合结构,为提高CoO纳米棒的锂存储能力提供了契机。CoO@CdS电极在0.1C下的初始放电容量为1292 mA h g,在200次循环中具有760 mA h g的非常稳定的可逆容量,容量保持率为92.7%。此外,与先前报道的电极相比,该电极即使在800次循环后仍表现出优异的循环稳定性和良好的倍率性能。而且,密度泛函理论(DFT)和电化学阻抗谱(EIS)证实了CoO@CdS电极动力学的增强。该电极的高效性能可能归因于表面反应性的提高、用于快速锂离子扩散的丰富活性位点/界面以及CoO和CdS纳米颗粒之间的协同作用。这项工作表明CoO@CdS混合结构在高性能电池方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/a2f8f0180a14/d4ra01028k-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/e969703845dc/d4ra01028k-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/9835ec3df6ea/d4ra01028k-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/718bcf0bedf9/d4ra01028k-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/a2f8f0180a14/d4ra01028k-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/e969703845dc/d4ra01028k-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/9835ec3df6ea/d4ra01028k-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/718bcf0bedf9/d4ra01028k-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2c/11017193/a2f8f0180a14/d4ra01028k-f4.jpg

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本文引用的文献

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