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通过聚乙烯吡咯烷酮(PVP)控制合成法制备的(CoFeNiMnCr)O的粒径对其结构及析氧反应催化剂的影响。

The effect of particle size on structural and catalysts for oxygen evolution reaction of (CoFeNiMnCr)O prepared by controlled synthesis with polyvinylpyrrolidone (PVP).

作者信息

Alves Ricardo F, Raimundo Rafael A, Lima Bruno A S G, Loureiro Francisco J A, Fagg Duncan P, Macedo Daniel A, Gomes Uilame U, Morales Marco A

机构信息

Federal University of Rio Grande do Norte, Department of Materials Science and Engineering, 59078-970 Natal, RN, Brazil.

Federal University of Paraíba, Department of Materials Science and Engineering, 58051-900 João Pessoa, PB, Brazil; TEMA - Centre for Mechanical Technology and Automation, Department of Mechanical Engineering, University of Aveiro, 3810-193 Aveiro, Portugal.

出版信息

J Colloid Interface Sci. 2025 Feb 15;680(Pt A):818-831. doi: 10.1016/j.jcis.2024.11.068. Epub 2024 Nov 12.

Abstract

In this study, high-entropy spinel oxides (CoNiMnFeCr)O were synthesized using a PVP-assisted sol-gel method, marking the first report of this approach for producing high-entropy oxides. This method provides new insights into morphology customization through precise temperature control during calcination. Samples were calcined at 800, 900, and 1000 °C, and structural, optical, and electrochemical characterizations were performed to evaluate the impact of synthesis conditions on the oxygen evolution reaction (OER) performance. X-ray diffraction (XRD) confirmed the formation of a single-phase spinel structure with face-centered cubic symmetry. UV-Vis spectroscopy revealed a band gap shift associated with calcination temperature, indicating subtle changes in electronic structure that can influence catalytic behavior. The S-HEO 800 sample exhibited the highest catalytic activity, achieving an overpotential of 316 mV at 10 mA cm. Electrochemical tests showed excellent short-term durability, with the electrodes maintaining stable performance for 24 h at 10 mA cm. Field emission gun scanning electron microscopy (FEGSEM) analysis revealed that particle size increased with calcination temperature, ranging from 96 nm (S-HEO 800) to 475 nm (S-HEO 1000). X-ray photoelectron spectroscopy (XPS) showed a higher concentration of Cr, Cr, and Ni ions on the surface of S-HEO 800, correlating with its superior OER performance. Additionally, Raman and FT-IR spectra confirmed the formation of the spinel phase and provided insights into metal-oxygen bonding. Electrochemical impedance spectroscopy (EIS) results indicated that S-HEO 800 exhibited the lowest charge transfer resistance (R), further supporting its enhanced catalytic behavior. These findings demonstrate the potential of the PVP-assisted sol-gel method to produce customized high-entropy oxides with tunable morphology, making them promising candidates for energy conversion applications, particularly in water electrolysis.

摘要

在本研究中,采用聚乙烯吡咯烷酮辅助溶胶-凝胶法合成了高熵尖晶石氧化物(CoNiMnFeCr)O,这是该方法用于制备高熵氧化物的首次报道。该方法通过煅烧过程中的精确温度控制,为形态定制提供了新的见解。样品在800、900和1000℃下煅烧,并进行结构、光学和电化学表征,以评估合成条件对析氧反应(OER)性能的影响。X射线衍射(XRD)证实形成了具有面心立方对称性的单相尖晶石结构。紫外-可见光谱显示带隙随煅烧温度发生位移,表明电子结构发生了细微变化,这可能会影响催化行为。S-HEO 800样品表现出最高的催化活性,在10 mA cm下过电位为316 mV。电化学测试显示出优异的短期耐久性,电极在10 mA cm下保持稳定性能24小时。场发射枪扫描电子显微镜(FEGSEM)分析表明,粒径随煅烧温度升高而增大,范围从96 nm(S-HEO 800)到475 nm(S-HEO 1000)。X射线光电子能谱(XPS)显示S-HEO 800表面Cr、Cr和Ni离子浓度较高,与其优异的OER性能相关。此外,拉曼光谱和傅里叶变换红外光谱证实了尖晶石相的形成,并提供了有关金属-氧键的见解。电化学阻抗谱(EIS)结果表明,S-HEO 800表现出最低的电荷转移电阻(R),进一步支持了其增强的催化行为。这些发现证明了聚乙烯吡咯烷酮辅助溶胶-凝胶法在制备具有可调形态的定制高熵氧化物方面的潜力,使其成为能量转换应用,特别是水电解领域有前景的候选材料。

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