Harishchandra S. Nishad, Sagar M. Mane, Jaewoong Lee and Pravin S. Walke
{"title":"Iron oxide@CoFe-LDH nanocomposites for highly stable aqueous hybrid supercapacitors†","authors":"Harishchandra S. Nishad, Sagar M. Mane, Jaewoong Lee and Pravin S. Walke","doi":"10.1039/D5LF00004A","DOIUrl":null,"url":null,"abstract":"<p >CoFe-LDH (layered double hydroxide) nanomaterials are widely explored as battery-type electrode materials owing to their excellent redox activity, layered structure, and fast ion diffusion. However, their practical application is often hindered by poor cyclic stability. The nanocomposite of CoFe-LDH with iron oxide has great potential to overcome this limitation. The layered structure of CoFe-LDH facilitates a fast ion diffusion and realizes synergistic activities of multiple metal elements, while iron oxide prevents the self-restacking and aggregation of CoFe-LDH layers, which ultimately enhance their structural stability and electrochemical performance. In this work, we prepared an Fe<small><sub>16</sub></small>O<small><sub>20</sub></small>/CoFe-LDH (FO@CoFe-LDH) nanocomposite <em>via</em> a single-step hydrothermal method. As composition tuning was a major concern to regulate the electrochemical performance, two samples with different compositions were prepared by tuning the mole ratios of Co and Fe. Electrochemical investigations of FO@CoFe-LDH1 (3 : 1 ratio of Co : Fe) demonstrated a specific capacity of 84 C g<small><sup>−1</sup></small> at 1 A g<small><sup>−1</sup></small>, while FO@CoFe-LDH2 (3 : 2 ratio of Co : Fe) was limited to 25 C g<small><sup>−1</sup></small> at 1 A g<small><sup>−1</sup></small> in a 6 M KOH electrolyte solution. Furthermore, an aqueous hybrid supercapacitor (AHS) fabricated using FO@CoFe-LDH1 as the positive electrode and activated carbon (AC) as the negative electrode exhibited remarkable cyclic stability, retaining 99.9% after 4000 cycles. This study demonstrates the potential of FO@CoFe-LDH1 nanocomposites as battery-type electrodes for AHS devices, paving the way for durable energy storage devices.</p>","PeriodicalId":101138,"journal":{"name":"RSC Applied Interfaces","volume":" 3","pages":" 808-821"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/lf/d5lf00004a?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Applied Interfaces","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/lf/d5lf00004a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
CoFe-LDH (layered double hydroxide) nanomaterials are widely explored as battery-type electrode materials owing to their excellent redox activity, layered structure, and fast ion diffusion. However, their practical application is often hindered by poor cyclic stability. The nanocomposite of CoFe-LDH with iron oxide has great potential to overcome this limitation. The layered structure of CoFe-LDH facilitates a fast ion diffusion and realizes synergistic activities of multiple metal elements, while iron oxide prevents the self-restacking and aggregation of CoFe-LDH layers, which ultimately enhance their structural stability and electrochemical performance. In this work, we prepared an Fe16O20/CoFe-LDH (FO@CoFe-LDH) nanocomposite via a single-step hydrothermal method. As composition tuning was a major concern to regulate the electrochemical performance, two samples with different compositions were prepared by tuning the mole ratios of Co and Fe. Electrochemical investigations of FO@CoFe-LDH1 (3 : 1 ratio of Co : Fe) demonstrated a specific capacity of 84 C g−1 at 1 A g−1, while FO@CoFe-LDH2 (3 : 2 ratio of Co : Fe) was limited to 25 C g−1 at 1 A g−1 in a 6 M KOH electrolyte solution. Furthermore, an aqueous hybrid supercapacitor (AHS) fabricated using FO@CoFe-LDH1 as the positive electrode and activated carbon (AC) as the negative electrode exhibited remarkable cyclic stability, retaining 99.9% after 4000 cycles. This study demonstrates the potential of FO@CoFe-LDH1 nanocomposites as battery-type electrodes for AHS devices, paving the way for durable energy storage devices.
CoFe-LDH(层状双氢氧化物)纳米材料因其优异的氧化还原活性、层状结构和快速的离子扩散而被广泛用作电池型电极材料。然而,它们的实际应用往往受到循环稳定性差的阻碍。钴-乳酸脱氢酶与氧化铁的纳米复合材料有很大的潜力克服这一限制。fe - ldh的层状结构促进了离子的快速扩散,实现了多种金属元素的协同作用,而氧化铁则阻止了fe - ldh层的自堆积和聚集,最终提高了fe - ldh层的结构稳定性和电化学性能。本文采用单步水热法制备了Fe16O20/CoFe-LDH (FO@CoFe-LDH)纳米复合材料。通过调整Co和Fe的摩尔比,制备了两种不同组成的样品。电化学研究表明,FO@CoFe-LDH1 (1:1 Co: Fe)在1 a g−1时的比容量为84 C g−1,而FO@CoFe-LDH2 (3:2 Co: Fe)在6 M KOH电解质溶液中,在1 a g−1时的比容量限制为25 C g−1。此外,以FO@CoFe-LDH1为正极,活性炭(AC)为负极制备的水性杂化超级电容器(AHS)在4000次循环后仍保持99.9%的循环稳定性。这项研究证明了FO@CoFe-LDH1纳米复合材料作为AHS设备的电池型电极的潜力,为耐用储能设备铺平了道路。