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Highly efficient oxygen evolution and stable water splitting by coupling NiFe LDH with metal phosphides
- Source :
- Science China Materials. 64:1662-1670
- Publication Year :
- 2021
- Publisher :
- Springer Science and Business Media LLC, 2021.
-
Abstract
- It is a great challenge to develop highly active oxygen evolution reaction (OER) electrocatalysts with superior durability. In this study, a NiFe layered double hydroxide-decorated phosphide (NiFe LDH@CoP/NiP3) was constructed to display satisfactory OER activity and good stability for water splitting in alkaline media. At an overpotential of 300 mV, NiFe LDH@CoP/NiP3 achieved a current density of 82 mA cm−2 for the OER, which was 9.1 and 2.3 times that of CoP/NiP3 and NiFe LDH, respectively. Moreover, the reconstruction behavior, during which oxyhydroxides formed, was studied by a combination of X-ray photoelectron spectroscopy, Raman spectroscopy, and scanning electron microscopy. A synergistic effect between NiFe LDH and CoP/NiP3 was also observed for the hydrogen evolution reaction. Furthermore, when NiFe LDH@CoP/NiP3 acted as both the cathode and anode for overall water splitting, a high current density of 100 mA cm−2 was maintained for more than 275 h. In addition, under Xe light irradiation, a solar to hydrogen efficiency of 9.89% was achieved for solar-driven water splitting. This work presents the coupling of different active compositions, and can provide a reference for designing bifunctional electrocatalysts.
- Subjects :
- Materials science
Hydrogen
Phosphide
Oxygen evolution
Layered double hydroxides
chemistry.chemical_element
02 engineering and technology
engineering.material
Overpotential
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Cathode
0104 chemical sciences
law.invention
Anode
chemistry.chemical_compound
chemistry
Chemical engineering
law
engineering
Water splitting
General Materials Science
0210 nano-technology
Subjects
Details
- ISSN :
- 21994501 and 20958226
- Volume :
- 64
- Database :
- OpenAIRE
- Journal :
- Science China Materials
- Accession number :
- edsair.doi...........23b0040b923c46dfc18aea12c04417c0