Nickel selenide nanostructures as an electrocatalyst for hydrogen evolution reaction
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Date
2018
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Publisher
Elsevier Ltd
Abstract
Electrochemical water splitting has gained momentum for the development of alternative energy sources. Herein, we report the synthesis of two different nickel selenide nanostructures of different morphology and composition employing hydrothermal method. NiSe<inf>2</inf> nanosheets were obtained by the anion-exchange reaction of Ni(OH)<inf>2</inf> with Se ions for 15 h. On the other hand, NiSe nanoflakes were synthesized by the direct selenization of nickel surface with the reaction time of 2 h. Tested as an electrocatalyst for hydrogen evolution reaction, NiSe<inf>2</inf> nanosheets and NiSe nanoflakes can afford a geometric current density of 10 mA cm?2 at an overpotential of 198 mV and 217 mV respectively. The measured Tafel slope values of NiSe nanoflakes are 28.6 mV dec?1, which is three times lower as compared with NiSe<inf>2</inf> nanosheets (72.1 mV dec?1). These results indicates the HER kinetics of NiSe nanoflakes are at par with the state-of-the-art Pt/C catalyst and also complimented with the short synthesis time of 2 h. Further, both nickel selenides exhibit ultra-long term stability for 30 h as evident from constant current chronopotentiometry and electrochemical impedance spectroscopy results. © 2018 Hydrogen Energy Publications LLC
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Keywords
Electrocatalysts, Electrochemical impedance spectroscopy, Hydrothermal synthesis, Nanosheets, Selenium compounds, Surface reactions, Alternative energy source, Chronopotentiometry, Hydrogen Energy, Hydrogen evolution reactions, Hydrothermal methods, Morphology and composition, Selenides, Tafel slope values, Nickel compounds
Citation
International Journal of Hydrogen Energy, 2018, 43, 43, pp. 19851-19863
