Fabrication of a novel superaerophobic support structure for NiCo-layered double hydroxide electrocatalysts for the oxygen evolution reaction

被引:1
|
作者
Abbasi, Somayyeh [1 ]
Hao, Minghui [1 ]
Fakourihassanabadi, Mohsen [1 ]
Thorpe, Steven [2 ]
Guay, Daniel [1 ]
机构
[1] Inst Natl Rech Sci Energie Mat Tele Commun INRS EM, 1650 Lionel Boulet Blvd Varennes, Quebec City, PQ J3X 1P7, Canada
[2] Univ Toronto, Dept Mat Sci & Engn, 184 Coll St, Toronto, ON M5S 3E4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Electrolysis; Super-aerophobic; Electrocatalysts; Oxygen evolution; Layered double hydroxides; WATER ELECTROLYSIS; NICKEL FOAM; HYDROGEN EVOLUTION; NANOSHEET ARRAYS; PERFORMANCE; OXIDATION; CATALYSTS; FILM; ELECTRODEPOSITION; COMPLEX;
D O I
10.1016/j.electacta.2024.143931
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, 3D Ni substrate with superaerophobic properties were catalyzed through the deposition of NiCo layered double hydroxide (NiCo-LDH). Deposition of NiCo-LDH was achieved using a mixed solution of Ni and Co nitrate salts as precursors. Precipitation of NiCo-LDH was achieved by the application of a negative current that caused a local raise of the solution pH. NiCo-LDHs were deposited in the form of vertically aligned nanosheets that infiltrate throughout the porous structure of the superaerophobic 3D Ni substrate. Variation of the deposition current changed the composition of the NiCo-LDH. The performance and the mechanisms responsible for the OER were investigated through a series of electrochemical experiments that include electrochemical impedance spectroscopy. As exemplified by a change of the Tafel slope from ca. 60 to 40 mV/decade, the OER mechanism is modified by the deposition the NiCo-LDH. In 1 M KOH at room temperature, the best electrode has overpotential as small as 269 and 340 mV at 10 and 250 mA cm-2, respectively. Longer-term electrolysis test during 56 h at 250 mA cm-2 showed a constant overpotential of 340 mV, without any sign of degradation.
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页数:12
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