期刊
SMALL
卷 -, 期 -, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202301609
关键词
NiFe-based (oxy)hydroxide; oxygen evolution reaction; superaerophobic; superhydrophilicity; ultrafine nanosheet arrays
Ultrafine Mo modified NiFeOxHy (oxy)hydroxide nanosheet arrays were successfully synthesized using molybdates as unique precursors and an electrochemical activation process. The optimized catalyst exhibited excellent performance for the oxygen evolution reaction (OER) with small overpotential and long-term stability.
NiFe-based (oxy)hydroxides are the benchmark catalysts for the oxygen evolution reaction (OER) in alkaline medium, however, it is still challenging to control their structures and compositions. Herein, molybdates (NiFe(MoO4)(x)) are applied as unique precursors to synthesize ultrafine Mo modified NiFeOxHy (oxy)hydroxide nanosheet arrays. The electrochemical activation process enables the molybdate ions (MoO42-) in the precursors gradually dissolve, and at the same time, hydroxide ions (OH-) in the electrolyte diffuse into the precursor and react with Ni2+ and Fe3+ ions in confined space to produce ultrafine NiFeOxHy (oxy)hydroxides nanosheets (<10 nm), which are densely arranged into microporous arrays and maintain the rod-like morphology of the precursor. Such dense ultrafine nanosheet arrays produce rich edge planes on the surface of NiFeOxHy (oxy)hydroxides to expose more active sites. More importantly, the capillary phenomenon of microporous structures and hydrophilic hydroxyl groups induce the superhydrophilicity and the rough surface produces the superaerophobic characteristic for bubbles. With these advantages, the optimized catalyst exhibits excellent performance for OER, with a small overpotential of 182 mV at 10 mA cm(-2) and long-term stability (200 h) at 200 mA cm(-2). Theoretical calculations show that the modification of Mo enhances the electron delocalization and optimizes the adsorption of intermediates.
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