{"title":"From NiCo-glycerate to tri-metallic selenide: engineering yolk–shell MnNiCoSe spheres with nanosheet arrays for hybrid supercapacitors†","authors":"Majid Shirvani and Davoud Nasr Esfahani","doi":"10.1039/D5QM00321K","DOIUrl":null,"url":null,"abstract":"<p >The progress of the supercapacitor industry heavily depends on the development and synthesis of novel electrode materials with specific architectures. Transition metal selenides have recently gained recognition as promising materials for energy storage devices due to their high theoretical capacitance and excellent electronic conductivity. This has spurred extensive research on mono- and di-selenide active materials. However, reports on tri-metallic selenides are scarce, and their charge storage mechanisms remain unclear. In this study, uniform NiCo-glycerate precursors were employed as sacrificial templates in combination with a selenization process to synthesize tri-metallic MnNiCoSe yolk–shell spheres encased in nanosheets through a straightforward self-templating method. The resulting MnNiCoSe electrode material demonstrates exceptional electrochemical performance, attributed to its numerous redox-active sites, large surface area with mesoporous pathways, high electrical conductivity, and the synergistic interaction of manganese, nickel, and cobalt elements. The MnNiCoSe electrode material exhibits a high specific capacity of 263.67 mA h g<small><sup>−1</sup></small> at 1 A g<small><sup>−1</sup></small>, retains 76.63% of its capacity at 20 A g<small><sup>−1</sup></small>, and maintains 84.28% of its capacity after 10 000 GCD cycles. Moreover, the hybrid supercapacitor device, assembled using NiF@MnNiCoSe as the positive electrode and NiF@AC as the negative electrode, achieves an impressive energy density of 53.32 W h kg<small><sup>−1</sup></small> at a power density of 1031.39 W kg<small><sup>−1</sup></small>.</p>","PeriodicalId":86,"journal":{"name":"Materials Chemistry Frontiers","volume":" 14","pages":" 2200-2212"},"PeriodicalIF":6.4000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Chemistry Frontiers","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qm/d5qm00321k","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The progress of the supercapacitor industry heavily depends on the development and synthesis of novel electrode materials with specific architectures. Transition metal selenides have recently gained recognition as promising materials for energy storage devices due to their high theoretical capacitance and excellent electronic conductivity. This has spurred extensive research on mono- and di-selenide active materials. However, reports on tri-metallic selenides are scarce, and their charge storage mechanisms remain unclear. In this study, uniform NiCo-glycerate precursors were employed as sacrificial templates in combination with a selenization process to synthesize tri-metallic MnNiCoSe yolk–shell spheres encased in nanosheets through a straightforward self-templating method. The resulting MnNiCoSe electrode material demonstrates exceptional electrochemical performance, attributed to its numerous redox-active sites, large surface area with mesoporous pathways, high electrical conductivity, and the synergistic interaction of manganese, nickel, and cobalt elements. The MnNiCoSe electrode material exhibits a high specific capacity of 263.67 mA h g−1 at 1 A g−1, retains 76.63% of its capacity at 20 A g−1, and maintains 84.28% of its capacity after 10 000 GCD cycles. Moreover, the hybrid supercapacitor device, assembled using NiF@MnNiCoSe as the positive electrode and NiF@AC as the negative electrode, achieves an impressive energy density of 53.32 W h kg−1 at a power density of 1031.39 W kg−1.
超级电容器工业的进步在很大程度上取决于具有特定结构的新型电极材料的开发和合成。过渡金属硒化物由于其较高的理论电容和优异的电子导电性,近年来被认为是一种有前途的储能材料。这激发了对单硒化物和二硒化物活性材料的广泛研究。然而,关于三金属硒化物的报道很少,其电荷储存机制尚不清楚。在本研究中,采用均匀的nico -甘油前体作为牺牲模板,结合硒化工艺,通过简单的自模板方法合成了包裹在纳米片中的三金属MnNiCoSe蛋黄壳球。所得到的MnNiCoSe电极材料表现出优异的电化学性能,归因于其众多的氧化还原活性位点,具有介孔通路的大表面积,高导电性以及锰,镍和钴元素的协同相互作用。MnNiCoSe电极材料在1 a g−1条件下具有263.67 mA h g−1的高比容量,在20 a g−1条件下保持76.63%的容量,在10000次GCD循环后保持84.28%的容量。此外,以NiF@MnNiCoSe为正极,NiF@AC为负极组装的混合超级电容器器件,在1031.39 W kg - 1的功率密度下,获得了令人瞩目的53.32 W h kg - 1的能量密度。
期刊介绍:
Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome.
This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.