Interface Engineering of Heterogeneous CeO2–CoO Nanofibers with Rich Oxygen Vacancies for Enhanced Electrocatalytic Oxygen Evolution Performance

析氧 过电位 材料科学 电催化剂 催化作用 化学工程 煅烧 纳米纤维 氧化物 电解质 静电纺丝 电化学 分解水 纳米技术 无机化学 电极 化学 光催化 冶金 复合材料 工程类 物理化学 生物化学 聚合物
作者
Weimo Li,Lusi Zhao,Ce Wang,Xiaofeng Lu,Wei Chen
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (39): 46998-47009 被引量:80
标识
DOI:10.1021/acsami.1c11101
摘要

The development of highly efficient and cheap electrocatalysts for the oxygen evolution reaction (OER) is highly desirable in typical water-splitting electrolyzers to achieve renewable energy production, yet it still remains a huge challenge. Herein, we have presented a simple procedure to construct a new nanofibrous hybrid structure with the interface connecting the surface of CeO2 and CoO as a high-performance electrocatalyst toward the OER through an electrospinning–calcination–reduction process. The resultant CeO2–CoO nanofibers exhibit excellent electrocatalytic properties with a small overpotential of 296 mV at 10 mA cm–2 for the OER, which is superior to many previously reported nonprecious metal-based and commercial RuO2 catalysts. Furthermore, the prepared CeO2–CoO nanofibers display remarkable long-term stability, which can be maintained for 130 h with nearly no attenuation of OER activity in an alkaline electrolyte. A combined experimental and theoretical investigation reveals that the excellent OER properties of CeO2-CoO nanofibers are due to the unique interfacial architecture between CeO2 and CoO, where abundant oxygen vacancies can be generated due to the incomplete matching of atomic positions of two parts, leading to the formation of many low-coordinated Co sites with high OER catalytic activity. This research provides a practical and promising opportunity for the application of heterostructured nonprecious metal oxide catalysts for high-efficiency electrochemical water oxidation.
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