Sol-Gel Synthesized High Entropy Metal Oxides as High-Performance Catalysts for Electrochemical Water Oxidation

催化作用 循环伏安法 傅里叶变换红外光谱 氧化物 电化学 材料科学 甲醇 无机化学 扫描电子显微镜 分析化学(期刊) 化学工程 电极 化学 物理化学 冶金 有机化学 工程类 复合材料
作者
Muhammad Asim,Akbar Hussain,Safia Khan,Javeria Arshad,Tehmeena Maryum Butt,Amina Hana,Mehwish Munawar,Farhat Saira,Malika Rani,Arshad Mahmood,Naveed Kausar Janjua
出处
期刊:Molecules [Multidisciplinary Digital Publishing Institute]
卷期号:27 (18): 5951-5951 被引量:35
标识
DOI:10.3390/molecules27185951
摘要

Hexanary high-entropy oxides (HEOs) were synthesized through the mechanochemical sol-gel method for electrocatalytic water oxidation reaction (WOR). As-synthesized catalysts were subjected to characterization, including X-ray diffraction (XRD), Fourier transforms infrared (FTIR) analysis, and scanning electron microscopy (SEM). All the oxide systems exhibited sharp diffraction peaks in XRD patterns indicating the defined crystal structure. Strong absorption between 400–700 cm−1 in FTIR indicated the formation of metal-oxide bonds in all HEO systems. WOR was investigated via cyclic voltammetry using HEOs as electrode platforms, 1M KOH as the basic medium, and 1M methanol (CH3OH) as the facilitator. Voltammetric profiles for both equiatomic (EHEOs) and non-equiatomic (NEHEOs) were investigated, and NEHEOs exhibited the maximum current output for WOR. Moreover, methanol addition improved the current profiles, thus leading to the electrode utility in direct methanol fuel cells as a sequential increase in methanol concentration from 1M to 2M enhanced the OER current density from 61.4 to 94.3 mA cm−2 using NEHEO. The NEHEOs comprising a greater percentage of Al, ([Al0.35(Mg, Fe, Cu, Ni, Co)0.65]3O4) displayed high WOR catalytic performance with the maximum diffusion coefficient, D° (10.90 cm2 s−1) and heterogeneous rate constant, k° (7.98 cm s−1) values. These primary findings from the EC processes for WOR provide the foundation for their applications in high-energy devices. Conclusively, HEOs are proven as novel and efficient catalytic platforms for electrochemical water oxidation.
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