Tabish Aftab, Osbel Almora, J. Ferré‐Borrull, L. Marsal
{"title":"基于阳极氧化铝模板的三维纳米结构电极,用于制造稳定的伪电容器","authors":"Tabish Aftab, Osbel Almora, J. Ferré‐Borrull, L. Marsal","doi":"10.1002/pssr.202400144","DOIUrl":null,"url":null,"abstract":"This study investigates the preparation of nickel nanostructured electrodes for the enhancement of supercapacitor (SC) performance. The nanostructured electrodes were synthesized using nanoporous anodic aluminium oxide (NAA) as a template via the pulsed electrodeposition method. Structural properties were examined using field‐emission scanning electron microscopy (FESEM), while electrochemical characterization was conducted through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results reveal that Ni nanorod arrays can be obtained embedded in the NAA matrix and with electrical contact with the aluminium substrate. On average, the rods are spaced 90 nm apart, with a diameter of 70 nm and a length of 2 µm. The Ni@NAA electrode exhibit an enlarged active area and exceptional electrochemical performance, demonstrating remarkable stability over 5000 cycles of CV at a scan rate of 50 mV·s‐1. Specific capacitance values exceeding 100 mF·cm‐2 and maximum charging times of less than 10 minutes are reported, highlighting its suitability for high‐power energy devices requiring pseudo‐supercapacitance. The study underscores the significance of nanostructured electrodes in advancing energy storage technologies and presents promising prospects for practical applications.This article is protected by copyright. All rights reserved.","PeriodicalId":20059,"journal":{"name":"physica status solidi (RRL) – Rapid Research Letters","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"3D Nanostructured Electrodes based on Anodic Alumina Templates for Stable Pseudo‐capacitors\",\"authors\":\"Tabish Aftab, Osbel Almora, J. Ferré‐Borrull, L. Marsal\",\"doi\":\"10.1002/pssr.202400144\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study investigates the preparation of nickel nanostructured electrodes for the enhancement of supercapacitor (SC) performance. The nanostructured electrodes were synthesized using nanoporous anodic aluminium oxide (NAA) as a template via the pulsed electrodeposition method. Structural properties were examined using field‐emission scanning electron microscopy (FESEM), while electrochemical characterization was conducted through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results reveal that Ni nanorod arrays can be obtained embedded in the NAA matrix and with electrical contact with the aluminium substrate. On average, the rods are spaced 90 nm apart, with a diameter of 70 nm and a length of 2 µm. The Ni@NAA electrode exhibit an enlarged active area and exceptional electrochemical performance, demonstrating remarkable stability over 5000 cycles of CV at a scan rate of 50 mV·s‐1. Specific capacitance values exceeding 100 mF·cm‐2 and maximum charging times of less than 10 minutes are reported, highlighting its suitability for high‐power energy devices requiring pseudo‐supercapacitance. The study underscores the significance of nanostructured electrodes in advancing energy storage technologies and presents promising prospects for practical applications.This article is protected by copyright. All rights reserved.\",\"PeriodicalId\":20059,\"journal\":{\"name\":\"physica status solidi (RRL) – Rapid Research Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"physica status solidi (RRL) – Rapid Research Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/pssr.202400144\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"physica status solidi (RRL) – Rapid Research Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/pssr.202400144","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
3D Nanostructured Electrodes based on Anodic Alumina Templates for Stable Pseudo‐capacitors
This study investigates the preparation of nickel nanostructured electrodes for the enhancement of supercapacitor (SC) performance. The nanostructured electrodes were synthesized using nanoporous anodic aluminium oxide (NAA) as a template via the pulsed electrodeposition method. Structural properties were examined using field‐emission scanning electron microscopy (FESEM), while electrochemical characterization was conducted through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results reveal that Ni nanorod arrays can be obtained embedded in the NAA matrix and with electrical contact with the aluminium substrate. On average, the rods are spaced 90 nm apart, with a diameter of 70 nm and a length of 2 µm. The Ni@NAA electrode exhibit an enlarged active area and exceptional electrochemical performance, demonstrating remarkable stability over 5000 cycles of CV at a scan rate of 50 mV·s‐1. Specific capacitance values exceeding 100 mF·cm‐2 and maximum charging times of less than 10 minutes are reported, highlighting its suitability for high‐power energy devices requiring pseudo‐supercapacitance. The study underscores the significance of nanostructured electrodes in advancing energy storage technologies and presents promising prospects for practical applications.This article is protected by copyright. All rights reserved.