Jeffrey Joseph John Jeya Kamaraj, Lawrence Daniel Stephen Tamil, Senthil Pandian Muthu and Ramasamy Perumalsamy
{"title":"用于高性能不对称超级电容器的阳离子增强型 CoMoSe2@Ti3C2 混合电极框架†","authors":"Jeffrey Joseph John Jeya Kamaraj, Lawrence Daniel Stephen Tamil, Senthil Pandian Muthu and Ramasamy Perumalsamy","doi":"10.1039/D4NJ04065A","DOIUrl":null,"url":null,"abstract":"<p >The increasing global energy demands, rapid consumption of fossil fuels, and rising environmental crisis are all crucial challenges requiring immediate attention. Maximizing supercapacitor performance necessitates superior electrochemical performance and outstanding stability in the electrode materials. Altering the structural and electrochemical characteristics of transition metal selenides by substituting cations and subsequently hybridizing them with MXenes is a potential strategy for designing efficient supercapacitors. Herein, facile solvothermal technique was employed to synthesize cation-substituted CoMoSe<small><sub>2</sub></small> nanoparticles, which were subsequently hybridized with Ti<small><sub>3</sub></small>C<small><sub>2</sub></small> before being employed as a supercapacitor electrode. This novel attempt to substitute molybdenum (Mo) in the CoSe<small><sub>2</sub></small> lattice and the subsequent hybridization resulted in a supercapacitor electrode that exhibited enhanced electrochemical properties owing to its improved charge transfer kinetics, multivalences, and enhanced active sites. The outstanding faradaic redox characteristics of the fabricated electrodes show remarkable pseudocapacitive behaviour within a potential range between −0.2 and 0.45 V. The developed electrodes in a standard three-electrode setup show a specific capacitance of 520 F g<small><sup>−1</sup></small> at a current density of 1 A g<small><sup>−1</sup></small>, which is greater than that of pure CoMoSe<small><sub>2</sub></small> and mono-metal selenide CoSe<small><sub>2</sub></small>. Over 5000 cycles at 5 A g<small><sup>−1</sup></small>, the optimal CoMoSe<small><sub>2</sub></small>@Ti<small><sub>3</sub></small>C<small><sub>2</sub></small> electrode maintains 97.43% of its initial specific capacitance. Furthermore, the designed asymmetric supercapacitor device (ASC) exhibited exceptional performance and stability with an energy density of 73.7 W h kg<small><sup>−1</sup></small> at 740 W kg<small><sup>−1</sup></small> power density and 93.3% retention after 15 000 cycles. This work thus demonstrates that metal selenides are a suitable material for supercapacitors. Furthermore, the cation substitution and MXene hybridization could potentially be employed as performance-enhancing strategies.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 44","pages":" 18683-18694"},"PeriodicalIF":2.7000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cation-boosted CoMoSe2@Ti3C2 hybrid electrode framework for high-performance asymmetric supercapacitors†\",\"authors\":\"Jeffrey Joseph John Jeya Kamaraj, Lawrence Daniel Stephen Tamil, Senthil Pandian Muthu and Ramasamy Perumalsamy\",\"doi\":\"10.1039/D4NJ04065A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The increasing global energy demands, rapid consumption of fossil fuels, and rising environmental crisis are all crucial challenges requiring immediate attention. Maximizing supercapacitor performance necessitates superior electrochemical performance and outstanding stability in the electrode materials. Altering the structural and electrochemical characteristics of transition metal selenides by substituting cations and subsequently hybridizing them with MXenes is a potential strategy for designing efficient supercapacitors. Herein, facile solvothermal technique was employed to synthesize cation-substituted CoMoSe<small><sub>2</sub></small> nanoparticles, which were subsequently hybridized with Ti<small><sub>3</sub></small>C<small><sub>2</sub></small> before being employed as a supercapacitor electrode. This novel attempt to substitute molybdenum (Mo) in the CoSe<small><sub>2</sub></small> lattice and the subsequent hybridization resulted in a supercapacitor electrode that exhibited enhanced electrochemical properties owing to its improved charge transfer kinetics, multivalences, and enhanced active sites. The outstanding faradaic redox characteristics of the fabricated electrodes show remarkable pseudocapacitive behaviour within a potential range between −0.2 and 0.45 V. The developed electrodes in a standard three-electrode setup show a specific capacitance of 520 F g<small><sup>−1</sup></small> at a current density of 1 A g<small><sup>−1</sup></small>, which is greater than that of pure CoMoSe<small><sub>2</sub></small> and mono-metal selenide CoSe<small><sub>2</sub></small>. Over 5000 cycles at 5 A g<small><sup>−1</sup></small>, the optimal CoMoSe<small><sub>2</sub></small>@Ti<small><sub>3</sub></small>C<small><sub>2</sub></small> electrode maintains 97.43% of its initial specific capacitance. Furthermore, the designed asymmetric supercapacitor device (ASC) exhibited exceptional performance and stability with an energy density of 73.7 W h kg<small><sup>−1</sup></small> at 740 W kg<small><sup>−1</sup></small> power density and 93.3% retention after 15 000 cycles. This work thus demonstrates that metal selenides are a suitable material for supercapacitors. 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引用次数: 0
摘要
全球日益增长的能源需求、化石燃料的快速消耗以及不断加剧的环境危机都是亟待解决的重大挑战。要最大限度地提高超级电容器的性能,电极材料必须具有卓越的电化学性能和出色的稳定性。通过取代阳离子改变过渡金属硒化物的结构和电化学特性,然后将其与二氧化二烯杂化,是设计高效超级电容器的一种潜在策略。本文采用简便的溶热技术合成了阳离子取代的 CoMoSe2 纳米粒子,并在将其用作超级电容器电极之前与 Ti3C2 进行了杂化。这种在 CoSe2 晶格中替代钼(Mo)的新尝试以及随后的杂化,使得超级电容器电极的电化学性质得到了增强,这得益于其电荷转移动力学的改善、多价性和活性位点的增强。在标准三电极设置中,所开发的电极在电流密度为 1 A g-1 时的比电容为 520 F g-1,高于纯 CoMoSe2 和单金属硒 CoSe2。在 5 A g-1 条件下循环 5000 次后,最佳 CoMoSe2@Ti3C2 电极的比电容仍能保持 97.43% 的初始比电容。此外,所设计的非对称超级电容器装置(ASC)表现出卓越的性能和稳定性,在功率密度为 740 W kg-1 时,能量密度为 73.7 W h kg-1,在 15000 次循环后,能量密度保持率为 93.3%。因此,这项工作证明金属硒化物是超级电容器的合适材料。此外,阳离子置换和 MXene 杂化有可能被用作提高性能的策略。
Cation-boosted CoMoSe2@Ti3C2 hybrid electrode framework for high-performance asymmetric supercapacitors†
The increasing global energy demands, rapid consumption of fossil fuels, and rising environmental crisis are all crucial challenges requiring immediate attention. Maximizing supercapacitor performance necessitates superior electrochemical performance and outstanding stability in the electrode materials. Altering the structural and electrochemical characteristics of transition metal selenides by substituting cations and subsequently hybridizing them with MXenes is a potential strategy for designing efficient supercapacitors. Herein, facile solvothermal technique was employed to synthesize cation-substituted CoMoSe2 nanoparticles, which were subsequently hybridized with Ti3C2 before being employed as a supercapacitor electrode. This novel attempt to substitute molybdenum (Mo) in the CoSe2 lattice and the subsequent hybridization resulted in a supercapacitor electrode that exhibited enhanced electrochemical properties owing to its improved charge transfer kinetics, multivalences, and enhanced active sites. The outstanding faradaic redox characteristics of the fabricated electrodes show remarkable pseudocapacitive behaviour within a potential range between −0.2 and 0.45 V. The developed electrodes in a standard three-electrode setup show a specific capacitance of 520 F g−1 at a current density of 1 A g−1, which is greater than that of pure CoMoSe2 and mono-metal selenide CoSe2. Over 5000 cycles at 5 A g−1, the optimal CoMoSe2@Ti3C2 electrode maintains 97.43% of its initial specific capacitance. Furthermore, the designed asymmetric supercapacitor device (ASC) exhibited exceptional performance and stability with an energy density of 73.7 W h kg−1 at 740 W kg−1 power density and 93.3% retention after 15 000 cycles. This work thus demonstrates that metal selenides are a suitable material for supercapacitors. Furthermore, the cation substitution and MXene hybridization could potentially be employed as performance-enhancing strategies.