{"title":"Design of free-standing porous carbon nanofibers anodes for lithium/sodium/potassium storage batteries","authors":"Jingjing Xie, Yiran Zhu, Yida Wang, Yunyong Hu, Kuo Cao, Sihan Zeng, Juntao Si, Chunhua Chen","doi":"10.1016/j.jpowsour.2025.236893","DOIUrl":null,"url":null,"abstract":"<div><div>Porous carbon nanofibers (PCNFs) are promising anode materials for alkali metal-ion batteries due to their 3D conductive network structure, large specific surface area and active storage sites for low-valance metal ions. However, the effects of PCNFs with different pore structures on the electrochemical performances and energy storage mechanism are still unknown. Herein, mesoporous F127-PCNF and macroporous SiO<sub>2</sub>-etched-PCNF are prepared by electrospinning method as independent anodes for lithium-ion batteries (LIBs), sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs), respectively. The experimental results and DFT calculations indicate that intercalation is the main energy storage mechanism in LIBs. The enlarged interlayer spacing of SiO<sub>2</sub>-etched-PCNF is more conducive to intercalation/deintercalation of Li<sup>+</sup>, and it can deliver a reversible capacity of 716 mAh g<sup>−1</sup> after 200 cycles at 0.1 A g<sup>−1</sup>, which is clearly higher than that of F127-PCNF (568 mAh g<sup>−1</sup>). In contrast, the adsorption mechanism is dominant in SIBs and PIBs. The higher specific surface area and abundant defect sites of F127-PCNF achieve efficient adsorption of Na<sup>+</sup>/K<sup>+</sup>, resulting in superior cycling and rate performance compared to SiO<sub>2</sub>-etched-PCNF. This comparative study provides a reference for the understanding of different energy storage mechanisms and furnishes guidelines for the effective development of PCNFs-based anode materials.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"641 ","pages":"Article 236893"},"PeriodicalIF":7.9000,"publicationDate":"2025-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Power Sources","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378775325007293","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Porous carbon nanofibers (PCNFs) are promising anode materials for alkali metal-ion batteries due to their 3D conductive network structure, large specific surface area and active storage sites for low-valance metal ions. However, the effects of PCNFs with different pore structures on the electrochemical performances and energy storage mechanism are still unknown. Herein, mesoporous F127-PCNF and macroporous SiO2-etched-PCNF are prepared by electrospinning method as independent anodes for lithium-ion batteries (LIBs), sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs), respectively. The experimental results and DFT calculations indicate that intercalation is the main energy storage mechanism in LIBs. The enlarged interlayer spacing of SiO2-etched-PCNF is more conducive to intercalation/deintercalation of Li+, and it can deliver a reversible capacity of 716 mAh g−1 after 200 cycles at 0.1 A g−1, which is clearly higher than that of F127-PCNF (568 mAh g−1). In contrast, the adsorption mechanism is dominant in SIBs and PIBs. The higher specific surface area and abundant defect sites of F127-PCNF achieve efficient adsorption of Na+/K+, resulting in superior cycling and rate performance compared to SiO2-etched-PCNF. This comparative study provides a reference for the understanding of different energy storage mechanisms and furnishes guidelines for the effective development of PCNFs-based anode materials.
多孔碳纳米纤维(PCNFs)具有三维导电网络结构、较大的比表面积和低价金属离子的活性存储位点,是碱金属离子电池极具发展前景的负极材料。然而,不同孔隙结构的PCNFs对其电化学性能和储能机理的影响尚不清楚。本文采用静电纺丝法制备了介孔F127-PCNF和大孔sio2 -蚀刻pcnf,分别作为锂离子电池(LIBs)、钠离子电池(SIBs)和钾离子电池(PIBs)的独立阳极。实验结果和DFT计算表明,插层是锂离子电池的主要储能机制。增大的层间距有利于Li+的插/脱插,在0.1 a g−1下循环200次后可提供716 mAh g−1的可逆容量,明显高于F127-PCNF (568 mAh g−1)。相比之下,SIBs和PIBs的吸附机制占主导地位。F127-PCNF具有较高的比表面积和丰富的缺陷位点,实现了对Na+/K+的高效吸附,与sio2蚀刻的pcnf相比,具有更好的循环性能和速率性能。这一对比研究为理解不同的储能机制提供了参考,并为pcnfs基负极材料的有效开发提供了指导。
期刊介绍:
The Journal of Power Sources is a publication catering to researchers and technologists interested in various aspects of the science, technology, and applications of electrochemical power sources. It covers original research and reviews on primary and secondary batteries, fuel cells, supercapacitors, and photo-electrochemical cells.
Topics considered include the research, development and applications of nanomaterials and novel componentry for these devices. Examples of applications of these electrochemical power sources include:
• Portable electronics
• Electric and Hybrid Electric Vehicles
• Uninterruptible Power Supply (UPS) systems
• Storage of renewable energy
• Satellites and deep space probes
• Boats and ships, drones and aircrafts
• Wearable energy storage systems