溶液处理αFe2O3-MoSe2复合材料在Na2SO3-KOH混合电解质中的电化学电容性能

IF 6.3 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Yang-Ming Lee , Muneer Hussain Bhat , Hwai-En Lin
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引用次数: 0

摘要

采用简单的溶液法合成了赤铁矿(αFe2O3)和花状二硒化钼(MoSe2)纳米颗粒,首先采用水热/溶剂热法制备前驱体,然后通过热处理形成具有高比表面积的纳米孔结构。将得到的αFe2O3和MoSe2粉末均匀混合,加水处理,干燥制成复合材料。处理后αFe2O3-MoSe2复合材料的形貌和晶粒尺寸基本保持不变,αFe2O3和MoSe2均保留了明显的晶相。研究了αFe2O3、MoSe2和αFe2O3-MoSe2复合材料在Na2SO3、KOH和混合电解质溶液中的电化学性能。与在Na2SO3和KOH电解质中单独使用αFe2O3或MoSe2制备的电极相比,复合电极的电容性能得到增强,在电流密度为2.5 mA·cm-2时,复合电极的比电容(Ccdc)达到236.9 F·g-1,在2000次充放电循环后,其循环稳定性为初始电容的74.7%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical capacitive performance of solution-processed αFe2O3-MoSe2 composite in Na2SO3-KOH mixed electrolyte
Hematite (αFe2O3) and flower-like molybdenum diselenide (MoSe2) nanoparticles were synthesized via a simple solution-based process involving an initial hydrothermal/solvothermal step to fabricate precursors, followed by heat treatment to form nanoporous structures with high specific surface areas. The resulting αFe2O3 and MoSe2 powders were uniformly mixed, treated with water, and dried to produce the composite material. The morphology and grain size of the αFe2O3-MoSe2 composite remained unchanged after the treatment, and the material retained distinct crystalline phases of both αFe2O3 and MoSe2. The electrochemical performance of αFe2O3, MoSe2, and the αFe2O3-MoSe2 composite was evaluated in aqueous Na2SO3, KOH, and mixed electrolyte solutions. Compared with electrodes made solely from αFe2O3 or MoSe2 in Na2SO3 and KOH electrolytes, the composite electrode exhibited enhanced capacitive performance, which achieves a specific capacitance (Ccdc) of 236.9 F·g−1 at a current density of 2.5 mA·cm−2, along with excellent cycling stability 74.7 % of its initial capacitance after 2000 charge/discharge cycles.
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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