Spinel of Nickel-Cobalt Oxide with Rod-Like Architecture as Electrocatalyst for Oxygen Evolution Reaction

被引:13
|
作者
Dymerska, Anna [1 ]
Kukulka, Wojciech [1 ]
Biegun, Marcin [1 ]
Mijowska, Ewa [1 ]
机构
[1] West Pomeranian Univ Technol, Dept Nanomat Physicochem, Piastow Ave 45, PL-70311 Szczecin, Poland
关键词
spinel; electrocatalyst; oxygen evolution reaction; thermal treatment; TRANSITION-METAL OXIDES; EFFICIENT ELECTROCATALYSTS; BIFUNCTIONAL ELECTROCATALYSTS; MESOPOROUS NICO2O4; NANOWIRE ARRAYS; REDUCTION; GRAPHENE; FOAM; MORPHOLOGY; NANOSHEETS;
D O I
10.3390/ma13183918
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 renewable energy technologies require electrocatalysts for reactions, such as the oxygen and/or hydrogen evolution reaction (OER/HER). They are complex electrochemical reactions that take place through the direct transfer of electrons. However, mostly they have high over-potentials and slow kinetics, that is why they require electrocatalysts to lower the over-potential of the reactions and enhance the reaction rate. The commercially used catalysts (e.g., ruthenium nanoparticles-Ru, iridium nanoparticles-Ir, and their oxides: RuO2, IrO2, platinum-Pt) contain metals that have poor stability, and are not economically worthwhile for widespread application. Here, we propose the spinel structure of nickel-cobalt oxide (NiCo2O4) fabricated to serve as electrocatalyst for OER. These structures were obtained by a facile two-step method: (1) One-pot solvothermal reaction and subsequently (2) pyrolysis or carbonization, respectively. This material exhibits novel rod-like morphology formed by tiny spheres. The presence of transition metal particles such as Co and Ni due to their conductivity and electron configurations provides a great number of active sites, which brings superior electrochemical performance in oxygen evolution and good stability in long-term tests. Therefore, it is believed that we propose interesting low-cost material that can act as a super stable catalyst in OER.
引用
收藏
页码:1 / 12
页数:12
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