首页 | 本学科首页   官方微博 | 高级检索  
     


Novel MoSe2–Ni(OH)2 nanocomposite as an electrocatalyst for high efficient hydrogen evolution reaction
Affiliation:1. Departamento Físico Química, Facultad Ciencias Químicas, Universidad de Concepción, Concepción, Chile;2. Millenium Nuclei on Catalytic Processes Towards Sustainable Chemistry (CSC), Chile;3. Clean Technologies Laboratory, Engineering Faculty, Universidad Católica de la Santísima Concepción, Concepción, Chile;4. Advanced Ceramics and Nanotechnology Laboratory, Department of Materials Engineering, University of Concepcion, Concepcion, Chile;5. Technological Development Unit (UDT), University of Concepcion, Coronel Industrial Park, Coronel, Chile
Abstract:Nowadays, there is a great demand for low-cost and highly active electrocatalyst for the production of clean renewable energy. However, most of the electrocatalysts are noble metal-based which are very costly and unstable. To counter this, electrochemical water splitting in energy storage systems is been widely applied, using non-noble metal-based nanostructured electrocatalysts. In this work, a novel noble metal-free MoSe2–Ni(OH)2 nanocomposite electrocatalyst is synthesized using a multi-step hydrothermal technique for efficient hydrogen evolution reaction (HER). The morphology, structural, chemical composition, and functional features of the synthesized nanomaterials were characterized using different techniques that include scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction analysis (XRD), X-ray photoelectron spectroscopy (XPS), and Raman analysis. The new developed MoSe2–Ni(OH)2 nanocomposite combines a high active surface area with a high chemical stability, generating a novel material with a synergistic effect that enhances water splitting process performance. Thus, an outstanding low Tafel slope of 54 mV dec−1 is accomplished in the hydrogen evolution reaction.
Keywords:Electrocatalysis  Hydrogen evolution  Nanoflowers  Water splitting
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号