期刊
CHINESE JOURNAL OF STRUCTURAL CHEMISTRY
卷 41, 期 1, 页码 2201019-2201024出版社
CHINESE JOURNAL STRUCTURAL CHEMISTRY
DOI: 10.14102/j.cnki.0254-5861.2021-0037
关键词
oxygen evolution reaction; NiSe2; CoSe2; hetero-structure; electrocatalysis
资金
- National Natural Science Foundation of China [21972124]
- Priority Academic Program Development of Jiangsu Higher Education Institution
- Six Talent Peaks Project of Jiangsu Province [XCL-070-2018]
In this study, a novel NiSe2-CoSe2 catalyst system consisting of nanorods and nanoparticles was introduced for efficient oxygen evolution reaction (OER) in alkaline electrolyte. The catalyst exhibited high catalytic performance, stability, and kinetics, attributed to the high valence states of Ni and Co and the strong synergetic coupling effect between the nanorods and nanoparticles.
Hetero-structure induced high performance catalyst for oxygen evolution reaction (OER) in the water splitting reaction has received increased attention. Herein, we demonstrated a novel catalyst system of NiSe2-CoSe2 consisting of nanorods and nanoparticles for the efficient OER in the alkaline electrolyte. This catalyst system can be easily fabricated via a low-temperature selenization of the solvothermal synthesized NiCo(OH)(x) precursor and the unique morphology of hybrid nanorods and nanoparticles was found by the electron microscopy analysis. The high valence state of the metal species was indicated by X-ray photoelectron spectroscopy study and a strong electronic effect was found in the NiSe2-CoSe2 catalyst system compared to their counterparts. As a result, NiSe2-CoSe2 exhibited high catalytic performance with a low overpotential of 250 mV to reach 10 mA.cm(-2) for OER in the alkaline solution. Furthermore, high catalytic stability and catalytic kinetics were also observed. The superior performance can be attributed to the high valence states of Ni and Co and their strong synergetic coupling effect between the nanorods and nanoparticles, which could accelerate the charge transfer and offer abundant electrocatalytic active sites. The current work offers an efficient hetero-structure catalyst system for OER, and the results are helpful for the catalysis understanding.
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