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Boron-Incorporated Cobalt-Nickel Oxide Nanosheets for Electrochemical Oxygen Evolution Reaction
被引:2
|作者:
Wang, Yue
[1
]
Kumar, Ashwani
[1
]
Budiyanto, Eko
[1
]
Cheraparambil, Haritha
[1
]
Weidenthaler, Claudia
[1
]
Tueysuez, Harun
[1
]
机构:
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim An Der Ruhr, Germany
关键词:
water electrolysis;
oxygen evolution reaction;
green hydrogen;
CoNi oxide catalyst;
Fe impurity;
WATER OXIDATION;
METAL-OXIDES;
ELECTROCATALYSTS;
CATALYSTS;
NANOPARTICLES;
OXYHYDROXIDE;
TEMPERATURE;
HYDROXIDE;
DEFECTS;
COOOH;
D O I:
10.1021/acsaem.3c03136
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The composition and crystal structure are crucial parameters for the activity and stability of the electrocatalysts. Herein, we synthesize a series of Co x Ni-B oxide nanosheets with low degree of crystallinity for alkaline media oxygen evolution reaction (OER). The sample with an optimized ratio Co8Ni-B oxide shows the best OER performance, achieving a current density of 10 mA/cm2 at an overpotential of 312 mV and a Tafel slope of 47 mV/dec in the 1 M KOH electrolyte. This sample is stable in the purified Fe-free KOH electrolyte and strongly activated in the nonpurified commercial electrolyte due to the Fe impurity uptake. The high surface area and partially crystalline structure caused by boron incorporation and low-temperature treatment provide more accessible active sites with retaining good stability against leaching during the OER. In situ electrochemical Raman spectroscopy investigation reveals the formation of OER active Co and Ni oxyhydroxides in Co8Ni-B oxides under a potential bias. The Ni substitution in Co oxides modulates the electronic structure of Co, and the OER activity of the electrocatalyst can be enhanced by Fe uptake from the KOH electrolyte.
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页码:3145 / 3156
页数:12
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