Mesoporous nickel-iron binary oxide nanorods for efficient electrocatalytic water oxidation
The design and fabrication of low-cost, high-effidency, and stable oxygen-evolving catalysts are essential for promoting the overall efficiency of water electrolysis. In this study, mesoporous Ni1-xFexOy (0 〈 x 〈 1, 1 〈y 〈 1.5) nanorods were synthesized by the facile thermal decomposition of Ni-Fe-b...
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Published in: | Nano research Vol. 10; no. 6; pp. 2096 - 2105 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Beijing
Tsinghua University Press
01-06-2017
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | The design and fabrication of low-cost, high-effidency, and stable oxygen-evolving catalysts are essential for promoting the overall efficiency of water electrolysis. In this study, mesoporous Ni1-xFexOy (0 〈 x 〈 1, 1 〈y 〈 1.5) nanorods were synthesized by the facile thermal decomposition of Ni-Fe-based coordination polymers. These polymers passed their nanorod-like morphology to oxides, which served as active catalysts for oxygen evolution reaction (OER). Increasing the Fe-doping amount to 33 at.% decreased the particle size and charge-transfer resistance and increased the surface area, resulting in a reduced overpotential (-302 mV) at 10 mA/cm^2 and a reduced Tafel slope (-42 mV/dec), which were accompanied by a far improved OER activity compared with those of commercial RuO2 and IrO2 electrocatalysts. At Fe-doping concentrations higher than 33 at.%, the trend of the electrocatalytic parameters started to reverse. The shift in the dopant concentration of Fe was further reflected in the structural transformation from a NiO (〈33 at.% Fe) rock-salt structure to a biphasic NiO/NiFe204 (33 at.% Fe) heterostructure, a NiFe204 (66 at.% Fe) spinel structure, and eventually to α-fe203 (100 at.% Fe). The efficient water-oxidation activity is ascribed to the highly mesoporous one-dimensional nanostructure, large surface area, and optimal amounts of the dopant Fe. The merits of abundance in the Earth, scalable synthesis, and highly efficient electrocatalytic activity make mesoporous Ni-Fe binary oxides promising oxygen-evolving catalysts for water splitting. |
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Bibliography: | 11-5974/O4 water splitting,oxygen evolving,electrocatalytic,Ni-Fe binary oxide,nanorods The design and fabrication of low-cost, high-effidency, and stable oxygen-evolving catalysts are essential for promoting the overall efficiency of water electrolysis. In this study, mesoporous Ni1-xFexOy (0 〈 x 〈 1, 1 〈y 〈 1.5) nanorods were synthesized by the facile thermal decomposition of Ni-Fe-based coordination polymers. These polymers passed their nanorod-like morphology to oxides, which served as active catalysts for oxygen evolution reaction (OER). Increasing the Fe-doping amount to 33 at.% decreased the particle size and charge-transfer resistance and increased the surface area, resulting in a reduced overpotential (-302 mV) at 10 mA/cm^2 and a reduced Tafel slope (-42 mV/dec), which were accompanied by a far improved OER activity compared with those of commercial RuO2 and IrO2 electrocatalysts. At Fe-doping concentrations higher than 33 at.%, the trend of the electrocatalytic parameters started to reverse. The shift in the dopant concentration of Fe was further reflected in the structural transformation from a NiO (〈33 at.% Fe) rock-salt structure to a biphasic NiO/NiFe204 (33 at.% Fe) heterostructure, a NiFe204 (66 at.% Fe) spinel structure, and eventually to α-fe203 (100 at.% Fe). The efficient water-oxidation activity is ascribed to the highly mesoporous one-dimensional nanostructure, large surface area, and optimal amounts of the dopant Fe. The merits of abundance in the Earth, scalable synthesis, and highly efficient electrocatalytic activity make mesoporous Ni-Fe binary oxides promising oxygen-evolving catalysts for water splitting. |
ISSN: | 1998-0124 1998-0000 |
DOI: | 10.1007/s12274-016-1398-x |