Molecular hydrogen (H) generation through water splitting with minimum energy loss has become practically possible due to the recent evolution of high-performance electrocatalysts. In this study, we fabricated, evaluated, and presented such a high-performance catalyst which is the NiSe nanoassemblies that can efficiently catalyze water splitting in neutral and alkaline media. A hierarchical nanoassembly of NiSe was fabricated by functionalizing the surface-cleaned Ni foam using NaHSe solution as the Se source with the assistance of microwave irradiation (300 W) for 3 min followed by 5 h of aging at room temperature (RT). The fabricated NiSe nanoassemblies were subjected to catalyze water electrolysis in neutral and alkaline media. For a defined current density of 50 mA cm, the NiSe nanoassemblies required very low overpotentials for the oxygen evolution reaction (OER), viz., 232, 244, and 321 mV at pH 14.5, 14.0, and 13.0 respectively. The associated lower Tafel slope values (33, 30, and 40 mV dec) indicate the faster OER kinetics on NiSe surfaces in alkaline media. Similarly, in the hydrogen evolution reaction (HER), for a defined current density of 50 mA cm, the NiSe nanoassemblies required low overpotentials of 211, 206, and 220 mV at pH 14.5, 14.0, and 13.0 respectively. The Tafel slopes for HER at pH 14.5, 14.0, and 13.0 are 165, 156, and 128 mV dec, respectively. A comparative study on both OER and HER was carried out with the state-of-the-art RuO and Pt under identical experimental conditions, the results of which revealed that our NiSe is a far better high-performance catalyst for water splitting. Besides, the efficiency of NiSe nanoassemblies in catalyzing water splitting in neutral solution was carried out, and the results are better than many previous reports. With these amazing advantages in fabrication method and in catalyzing water splitting at various pH, the NiSe nanoassemblies can be an efficient, cheaper, nonprecious, and high-performance electrode for water electrolysis with low overpotentials.
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http://dx.doi.org/10.1021/acsami.6b15980 | DOI Listing |
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