Ce–Metal–Organic Framework-Derived CeO2–GO: An Efficient Electrocatalyst for Oxygen Evolution Reaction

塔菲尔方程 电催化剂 析氧 过电位 线性扫描伏安法 介电谱 循环伏安法 计时安培法 材料科学 X射线光电子能谱 化学工程 氧化物 无机化学 化学 电化学 物理化学 冶金 电极 工程类
作者
P.C. Nagajyothi,K. Pavani,R. Ramaraghavulu,Jaesool Shim
出处
期刊:Inorganics (Basel) [Multidisciplinary Digital Publishing Institute]
卷期号:11 (4): 161-161 被引量:5
标识
DOI:10.3390/inorganics11040161
摘要

The oxygen evolution reaction (OER) is a crucial half-reaction in water splitting. However, this reaction is kinetically sluggish owing to the four-electron (4 e−) transfer process. Therefore, the development of low-cost, stable, highly efficient, and earth-abundant electrocatalysts for the OER is highly desirable. Metal oxides derived from metal–organic frameworks (MOFs) are among the most efficient electrocatalysts for the OER. Herein, Ce–MOF-derived CeO2/graphene oxide (GO) composites were successfully prepared using a facile method. The composites with 0, 25, 50, and 100 mg GO were named CeO2, CeO2–GO-1, CeO2–GO-2, and CeO2–GO-3, respectively. The physicochemical characteristics of the electrocatalysts were assessed using several analytical techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) analysis. The TEM results revealed that the CeO2 had a sheet-like morphology and that a GO layer was noticeable in the synthesized CeO2–GO-3 composite. The characterization results confirmed the formation of impurity-free CeO2–GO composites. The OER activity and stability were measured using cyclic voltammetry (CV), linear sweep voltammetry (LSV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). The CeO2–GO-3 electrocatalyst has a smaller Tafel slope (176 mV·dec−1) and lower overpotential (240 mV) than the other electrocatalysts. In addition, it exhibited high cyclic stability for up to 10 h. Therefore, the inexpensive CeO2–GO-3 electrocatalyst is a promising OER candidate.
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