NiOOH Exfoliation-Free Nickel Octahedra as Highly Active and Durable Electrocatalysts Toward the Oxygen Evolution Reaction in an Alkaline Electrolyte

被引:78
作者
Kim, Byeongyoon [1 ,2 ]
Oh, Aram [3 ]
Kabiraz, Mrinal Kanti [4 ,5 ]
Hong, Youngmin [4 ,5 ]
Joo, Jinwhan [1 ,2 ]
Baik, Hionsuck [3 ]
Choi, Sang-Il [4 ,5 ]
Lee, Kwangyeol [1 ,2 ]
机构
[1] Korea Univ, Dept Chem, Seoul 02841, South Korea
[2] Inst for Basic Sci Korea, Ctr Mol Spect & Dynam, Seoul 02841, South Korea
[3] KBSI, Seoul 02841, South Korea
[4] Kyungpook Natl Univ, Dept Chem, Daegu 41566, South Korea
[5] Kyungpook Natl Univ, Green Nano Mat Res Ctr, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
oxygen evolution reaction; electrocatalyst; nickel oxyhydroxide; heteroepitaxy; phase transformation; EFFICIENT WATER OXIDATION; FUTURE PERSPECTIVES; PHASE SEGREGATION; 1ST PRINCIPLES; CATALYSTS; OXIDE; HYDROXIDE; NI; OXYHYDROXIDE; NANOFRAME;
D O I
10.1021/acsami.7b19457
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A layered beta-NiOOH crystal with undercoordinated facets is an active and economically viable nonnoble catalyst for the oxygen evolution reaction (OER) in alkaline electrolytes. However, it is extremely difficult to enclose the beta-NiOOH crystal with undercoordinated facets because of its inevitable crystal transformation to gamma-NiOOH, resulting in the exfoliation of the catalytic surfaces. Herein, we demonstrate {111}-faceted Ni octahedra as the parent substrates whose surfaces are easily transformed to catalytically active beta-NiOOH during the alkaline OER. Electron microscopic measurements 1.2 demonstrate that the horizontally stacked beta-NiOOH on the surfaces of Ni octahedra has resistance to further oxidation to gamma-NiOOH. By contrast, significant crystal transformation and thus the exfoliation of the gamma-NiOOH sheets can be observed on the surfaces of Ni cubes and rhombic dodecahedra (RDs). Electrocatalytic measurements show that the beta-NiOOH formed on Ni octahedra exhibits highly enhanced OER durability compared to the Ni cubes, Ni RDs, and the state-of-the-art Ir/C catalysts.
引用
收藏
页码:10115 / 10122
页数:8
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