{"title":"Enhanced Lithium-ion/Sodium-ion Battery Performances Using Chrysanthemum Flower-like NiO-CoO Anode: Insights into Li+/Na+ Charge Storage Mechanism","authors":"Kalidoss Kannadasan, Mani Govindasamy, Chih-Yu Kuo, Perumal Elumalai","doi":"10.1016/j.electacta.2024.145574","DOIUrl":null,"url":null,"abstract":"In the present work, a chrysanthemum flower-like nickel oxide-cobalt oxide (NiO-CoO) nanohybrid was designed hydrothermally to function as an anode for both lithium-ion and sodium-ion batteries (LIB/SIB). The crystal structure, chemical composition and surface properties of the synthesized NiO-CoO nanohybrid were analyzed using various characterization methods. The lithium and sodium-ion charge-transfer characteristics of the NiO-CoO nano hybrid electrode were evaluated through cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS). The LIB half-cell containing the NiO-CoO hybrid anode exhibited an excellent specific capacity of 739 mA h g<sup>-1</sup> at 0.1C-rate. Additionally, SIB performance was also investigated, delivering 340 mA h g<sup>-1</sup> of specific capacity at 0.1C-rate. Interestingly, a full-cell (NiO-CoO|1M LiPF<sub>6</sub>|LiCoO<sub>2</sub>) was assembled for the first time, employing the NiO-CoO nano hybrid as the anode for the LIB. Further the full cell LIB was presented for real-time applications such as powering commercial LED bulbs and a temperature sensor. The fabricated full-cell sustained illumination for over 5 hours with a green LED bulb on a single charge. The fascinating flower-like morphology of the NiO-CoO hybrid offered short diffusion path, improved electrolyte contacts and effective conversion/re-conversion reactions which in turn led to high charge storage.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"2 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2024.145574","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
In the present work, a chrysanthemum flower-like nickel oxide-cobalt oxide (NiO-CoO) nanohybrid was designed hydrothermally to function as an anode for both lithium-ion and sodium-ion batteries (LIB/SIB). The crystal structure, chemical composition and surface properties of the synthesized NiO-CoO nanohybrid were analyzed using various characterization methods. The lithium and sodium-ion charge-transfer characteristics of the NiO-CoO nano hybrid electrode were evaluated through cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS). The LIB half-cell containing the NiO-CoO hybrid anode exhibited an excellent specific capacity of 739 mA h g-1 at 0.1C-rate. Additionally, SIB performance was also investigated, delivering 340 mA h g-1 of specific capacity at 0.1C-rate. Interestingly, a full-cell (NiO-CoO|1M LiPF6|LiCoO2) was assembled for the first time, employing the NiO-CoO nano hybrid as the anode for the LIB. Further the full cell LIB was presented for real-time applications such as powering commercial LED bulbs and a temperature sensor. The fabricated full-cell sustained illumination for over 5 hours with a green LED bulb on a single charge. The fascinating flower-like morphology of the NiO-CoO hybrid offered short diffusion path, improved electrolyte contacts and effective conversion/re-conversion reactions which in turn led to high charge storage.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.