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Three-dimensional ordered mesoporous Co(3)O(4) enhanced by Pd for oxygen evolution reaction
Considerable efforts have been devoted recently to design and fabrication of high performance and low cost electrocatalysts for oxygen evolution reaction (OER). However, catalytic activity of current electrocatalysts is usually restricted by high onset potential and limited active sites. Herein, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278512/ https://www.ncbi.nlm.nih.gov/pubmed/28134348 http://dx.doi.org/10.1038/srep41542 |
Sumario: | Considerable efforts have been devoted recently to design and fabrication of high performance and low cost electrocatalysts for oxygen evolution reaction (OER). However, catalytic activity of current electrocatalysts is usually restricted by high onset potential and limited active sites. Herein, we fabricated three-dimensional (3D) highly ordered mesoporous Pd-Co(3)O(4) composite materials as excellent electrocatalysts for OER in alkaline solution with high activity and stability. Three-dimensional highly ordered mesoporous Co(3)O(4) material was firstly synthesized using mesoporous silica KIT-6 as hard template. Then, Pd-Co(3)O(4) nanomaterials were prepared by a simple reduction method. The as-prepared 3D mesoporous Pd-Co(3)O(4) catalysts have ordered mesoporous structure with a high surface area of 81.0 m(2) g(−1). Three-dimensional highly ordered mesoporous structure can facilitate diffusion and penetration of electrolyte and oxygen. Moreover, the catalysts can also keep catalyst particles in a well dispersed condition with more catalytic active sites. Electrochemical measurements reveal that the 3D mesoporous Pd-Co(3)O(4) catalysts exhibit superior performance in alkaline solution with low onset potential (0.415 V vs. SCE) and excellent long-duration cycling stability. |
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