Suppr超能文献

用于超级电容器应用的低维高熵氧化物 (FeCoCrMnNi)O。

Low-dimensional high entropy oxide (FeCoCrMnNi)O for supercapacitor applications.

机构信息

College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China.

Mineral Development Section for International Relation, Department of Mines and Ministry of Natural Resources and Environmental, Nay Pyi Taw 15011, Myanmar.

出版信息

Dalton Trans. 2023 Jul 4;52(26):9005-9016. doi: 10.1039/d3dt00909b.

Abstract

Previous studies have found that high entropy oxides can be used as electrode materials for supercapacitors. However, there is still the problem of their low energy density. We tried to increase the energy density while increasing the specific capacitance of high entropy oxides from the potential window. Transition metal elements Fe, Co, Cr, Mn and Ni were selected for their electrochemical activity, and high entropy oxides were prepared by a sol-gel method under different calcination temperatures. The calcination temperature affects the structural morphology and crystallinity of the high entropy oxides and thus also affects the electrochemical performance. The spinel-phase (FeCoCrMnNi)O with a high specific surface area of 63.1 m g was prepared at a low calcination temperature of 450 °C. The specific capacitance is 332.2 F g at a current density of 0.3 A g in 1 M KOH electrolyte with a wide potential window of (-1, 0.6). An improved energy density of 103.8 W h kg is reached the designed microstructure of the high entropy oxide electrode.

摘要

先前的研究发现,高熵氧化物可用作超级电容器的电极材料。然而,它们的能量密度仍然较低。我们试图从电势窗口增加高熵氧化物的比电容,同时提高其能量密度。选择电化学活性较高的过渡金属元素 Fe、Co、Cr、Mn 和 Ni,通过溶胶-凝胶法在不同的煅烧温度下制备高熵氧化物。煅烧温度会影响高熵氧化物的结构形态和结晶度,从而影响电化学性能。在 450°C 的低温下制备出具有高比表面积 63.1 m²/g 的尖晶石相 (FeCoCrMnNi)O。在 1 M KOH 电解质中,电流密度为 0.3 A/g 时,比电容为 332.2 F/g,具有较宽的电势窗口(-1,0.6)。通过设计高熵氧化物电极的微观结构,实现了能量密度的提高,达到了 103.8 W h kg 的水平。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验