Stable Water Oxidation Catalysts Based on in-situ Electrochemical Transition of Nickel Phosphate

β-Ni(OH) 2 has been synthesized using Ni 3 (PO 4 ) 2 nanowires as precursors by in-situ electrochemical method. X-ray diffraction and selected area electron diffraction displayed that as-prepared Ni 3 (PO 4 ) 2 nanowires were transformed into β-Ni(OH) 2 with superlattice structure after activation....

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Veröffentlicht in:Catalysis letters 2022-08, Vol.152 (8), p.2333-2341
Hauptverfasser: Chen, Jiaye, Jayabal, Subramaniam, Geng, Dongsheng, Hu, Xun
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container_title Catalysis letters
container_volume 152
creator Chen, Jiaye
Jayabal, Subramaniam
Geng, Dongsheng
Hu, Xun
description β-Ni(OH) 2 has been synthesized using Ni 3 (PO 4 ) 2 nanowires as precursors by in-situ electrochemical method. X-ray diffraction and selected area electron diffraction displayed that as-prepared Ni 3 (PO 4 ) 2 nanowires were transformed into β-Ni(OH) 2 with superlattice structure after activation. It has been found that extremely small size is crucial for the complete conversion of Ni 3 (PO 4 ) 2 and the formation of the superlattice structure. The resulting catalysts by in-situ conversion showed high activity and stability toward oxygen evolution reaction (OER) with an overpotential of 310 mV to reach the current density of 10 mA cm −2 and a long-term stability of 110 h. The large amount of NiOOH in the superlattice structure not only increases the OER activity of β-Ni(OH) 2 , but also improves the oxidation potential of nickel, thereby decreasing the dissolution. This work proves the feasibility of in-situ electrochemical synthesis for high-performance and stable hydroxide catalysts towards OER. Graphic Abstract
doi_str_mv 10.1007/s10562-021-03816-0
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X-ray diffraction and selected area electron diffraction displayed that as-prepared Ni 3 (PO 4 ) 2 nanowires were transformed into β-Ni(OH) 2 with superlattice structure after activation. It has been found that extremely small size is crucial for the complete conversion of Ni 3 (PO 4 ) 2 and the formation of the superlattice structure. The resulting catalysts by in-situ conversion showed high activity and stability toward oxygen evolution reaction (OER) with an overpotential of 310 mV to reach the current density of 10 mA cm −2 and a long-term stability of 110 h. The large amount of NiOOH in the superlattice structure not only increases the OER activity of β-Ni(OH) 2 , but also improves the oxidation potential of nickel, thereby decreasing the dissolution. This work proves the feasibility of in-situ electrochemical synthesis for high-performance and stable hydroxide catalysts towards OER. 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X-ray diffraction and selected area electron diffraction displayed that as-prepared Ni 3 (PO 4 ) 2 nanowires were transformed into β-Ni(OH) 2 with superlattice structure after activation. It has been found that extremely small size is crucial for the complete conversion of Ni 3 (PO 4 ) 2 and the formation of the superlattice structure. The resulting catalysts by in-situ conversion showed high activity and stability toward oxygen evolution reaction (OER) with an overpotential of 310 mV to reach the current density of 10 mA cm −2 and a long-term stability of 110 h. The large amount of NiOOH in the superlattice structure not only increases the OER activity of β-Ni(OH) 2 , but also improves the oxidation potential of nickel, thereby decreasing the dissolution. This work proves the feasibility of in-situ electrochemical synthesis for high-performance and stable hydroxide catalysts towards OER. 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subjects Alternative energy sources
Catalysis
Catalysts
Chemical synthesis
Chemistry
Chemistry and Materials Science
Conversion
Diffraction
Electric properties
Electron diffraction
Hydrogen
Hydroxides
Industrial Chemistry/Chemical Engineering
Microscopy
Nanowires
Nickel
Nickel compounds
Nitrates
Organometallic Chemistry
Oxidation
Oxidation-reduction reaction
Oxygen evolution reactions
Phosphates
Physical Chemistry
Spectrum analysis
Stability
Superlattices
Voltammetry
X-rays
title Stable Water Oxidation Catalysts Based on in-situ Electrochemical Transition of Nickel Phosphate
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