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Recent Progress on NiFe-Based Electrocatalysts for the Oxygen Evolution Reaction
- Source :
- Small (Weinheim an der Bergstrasse, Germany). 16(51)
- Publication Year :
- 2020
-
Abstract
- The seriousness of the energy crisis and the environmental impact of global anthropogenic activities have led to an urgent need to develop efficient and green fuels. Hydrogen, as a promising alternative resource that is produced in an environmentally friendly and sustainable manner by a water splitting reaction, has attracted extensive attention in recent years. However, the large-scale application of water splitting devices is hindered predominantly by the sluggish oxygen evolution reaction (OER) at the anode. Therefore, the design and exploration of high-performing OER electrocatalysts is a critical objective. Considering their low prices, abundant reserves, and intrinsic activities, NiFe-based bimetal compounds are widely studied as excellent OER electrocatalysts. Moreover, recent progress on NiFe-based OER electrocatalysts in alkaline environments is comprehensively and systematically introduced through various catalyst families including NiFe-layered hydroxides, metal-organic frameworks, NiFe-based (oxy)hydroxides, NiFe-based oxides, NiFe alloys, and NiFe-based nonoxides. This review briefly introduces the advanced NiFe-based OER materials and their corresponding reaction mechanisms. Finally, the challenges inherent to and possible strategies for producing extraordinary NiFe-based electrocatalysts are discussed.
- Subjects :
- Materials science
Oxygen evolution
Nanotechnology
02 engineering and technology
General Chemistry
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Environmentally friendly
0104 chemical sciences
Catalysis
Biomaterials
Water splitting
General Materials Science
0210 nano-technology
Biotechnology
Subjects
Details
- ISSN :
- 16136829
- Volume :
- 16
- Issue :
- 51
- Database :
- OpenAIRE
- Journal :
- Small (Weinheim an der Bergstrasse, Germany)
- Accession number :
- edsair.doi.dedup.....91fdb3bd7d02671658ed5d44e71d3c94