Johnnys da Silva Hortêncio, Rafael A Raimundo, Allan J M Araújo, André Luiz Menezes de Oliveira, Daniel A Macedo, Sherlan Guimarães Lemos, Fausthon Fred da Silva
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引用次数: 0
Abstract
The development of high-performance electrocatalysts for oxygen evolution reaction (OER) is still a challenge to produce green hydrogen. Thus, herein, a new bifunctional metal-organic frameworks (MOF)-derived CuCo2O4 is obtained, applied as OER electrocatalyst and electrode for supercapacitors. All physicochemical and morphological characterization indicates the formation of a pure spinel structure CuCo2O4 crystalline phase and coral reef-like morphology. X-ray photoelectron spectroscopy data showed major presence of Co3+ and Cu+ ions on the surface and high concentration of oxygen vacancies. OER electrocatalytic assays conducted in alkaline medium (1.0 M KOH) show a reduced overpotential (η) of 317 mV at 10 mA cm-2 and Tafel slope of only 49 mV dec-1, besides excellent electrochemical stability up to 12 h. The material is also studied for supercapacitors applications via cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) analysis. CuCo2O4 material presents specific capacity near 75 C g-1, at least ≈2.8 times higher than pristine CuO and Co3O4 at 1 A g-1. This results indicate the MOFs-derived CuCo2O4 as a promising bifunctional material for energy conversion and storage.
开发高性能的析氧反应电催化剂仍然是实现绿色氢生产的一个挑战。因此,本文获得了一种新的双功能金属-有机框架(MOF)衍生的CuCo2O4,用于超级电容器的OER电催化剂和电极。所有物化、形态表征均表明形成了纯尖晶石结构的CuCo2O4晶相和珊瑚礁状形态。x射线光电子能谱数据显示,表面主要存在Co3+和Cu+离子,并存在高浓度的氧空位。在碱性介质(1.0 M KOH)中进行的OER电催化实验表明,在10 mA cm-2下,过电位(η)降低了317 mV, Tafel斜率仅为49 mV dec1,并且在12 h内具有优异的电化学稳定性。通过循环伏安法(CV)和恒流充放电(GCD)分析,还研究了该材料在超级电容器中的应用。CuCo2O4材料的比容量在75℃g-1附近,比原始CuO和Co3O4材料在1℃g-1时的比容量至少高出约2.8倍。这些结果表明mofs衍生的CuCo2O4是一种很有前途的能量转换和存储双功能材料。
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