{"title":"Tailoring the electrochemical performance of rods-like Co-MOF: Fe-derived Co3O4: Fe electrodes for supercapacitor applications","authors":"","doi":"10.1016/j.fuel.2024.133574","DOIUrl":null,"url":null,"abstract":"<div><div>With the increasing global demand for energy, there is a critical need for efficient and sustainable energy storage solutions. Supercapacitors (SCs) have emerged as promising candidates due to their high-power density, long cycle life, and environmental friendliness. This study explores the development of iron-doped cobalt metal–organic frameworks (Co-MOFs: Fe) and their derived oxides supported on Ni foam as high-performance supercapacitor electrodes. The impact of conversion temperature on electrochemical properties of Co-MOFs: Fe derived Co<sub>3</sub>O<sub>4</sub>: Fe was evaluated. The results disclosed that the conversion at 500 °C significantly enhances the surface area, specific capacitance, and charge transfer efficiency of the electrodes. It exhibited the highest specific capacity of ∼ 2135.08 F g<sup>−1</sup> at a current density of 1 A/g, along with excellent cycling stability of 87 %. Subsequently, an asymmetric supercapacitor was constructed with the MOF-derived Co<sub>3</sub>O<sub>4</sub>: Fe at 500 °C as anode and activated carbon as cathode materials. The device exhibited a specific capacitance of 233.98 F g<sup>−1</sup> at 1 A/g with an energy density of ∼ 51.99 Wh/kg, power density of 500.14 W/kg, and a significant capacity retention of ∼ 89 % over 10,000 cycles. These findings validate the potential of Co-MOF: Fe derived Fe-doped Co<sub>3</sub>O<sub>4</sub> as potential materials for practical energy storage applications.</div></div>","PeriodicalId":325,"journal":{"name":"Fuel","volume":null,"pages":null},"PeriodicalIF":6.7000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0016236124027236","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
With the increasing global demand for energy, there is a critical need for efficient and sustainable energy storage solutions. Supercapacitors (SCs) have emerged as promising candidates due to their high-power density, long cycle life, and environmental friendliness. This study explores the development of iron-doped cobalt metal–organic frameworks (Co-MOFs: Fe) and their derived oxides supported on Ni foam as high-performance supercapacitor electrodes. The impact of conversion temperature on electrochemical properties of Co-MOFs: Fe derived Co3O4: Fe was evaluated. The results disclosed that the conversion at 500 °C significantly enhances the surface area, specific capacitance, and charge transfer efficiency of the electrodes. It exhibited the highest specific capacity of ∼ 2135.08 F g−1 at a current density of 1 A/g, along with excellent cycling stability of 87 %. Subsequently, an asymmetric supercapacitor was constructed with the MOF-derived Co3O4: Fe at 500 °C as anode and activated carbon as cathode materials. The device exhibited a specific capacitance of 233.98 F g−1 at 1 A/g with an energy density of ∼ 51.99 Wh/kg, power density of 500.14 W/kg, and a significant capacity retention of ∼ 89 % over 10,000 cycles. These findings validate the potential of Co-MOF: Fe derived Fe-doped Co3O4 as potential materials for practical energy storage applications.
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.