3D Carbon Materials for Efficient Oxygen and Hydrogen Electrocatalysis
Sustainable energy production at an acceptable cost is key for its widespread application. At present, noble metals and metal oxides are the most widely used for electrocatalysis, but they suffer from low selectivity, poor durability, and scarcity. Because of this, metal‐free carbons have become the...
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Veröffentlicht in: | Advanced energy materials 2020-03, Vol.10 (11), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Sustainable energy production at an acceptable cost is key for its widespread application. At present, noble metals and metal oxides are the most widely used for electrocatalysis, but they suffer from low selectivity, poor durability, and scarcity. Because of this, metal‐free carbons have become the subject of great interest as promising alternative electrocatalysts for energy conversion and storage devices, and remarkable progress has been accomplished in the advance of metal‐free carbons as electrocatalysts for renewable energy technologies. Particularly interesting are 3D porous carbon architectures, which exhibit outstanding features for electrocatalysis applications, including broad range of active sites, interconnected porosity, high conductivity, and mechanical stability. This review summarizes the latest advances in 3D porous carbon structures for oxygen and hydrogen electrocatalysis. The structure–performance relationship of these materials is consequently rationalized and perspectives on creating more efficient 3D carbon electrocatalysts are suggested.
Metal‐free carbon‐based materials with a 3D porous architecture are earmarked to be the platform for the next generation of electrocatalysts in energy conversion and storage technologies. This review highlights the latest findings in 3D porous carbon nanostructured materials, main challenges, and future directions for further development of these exciting materials into highly performing oxygen and hydrogen electrocatalysts. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.201902494 |