Journal
NANO RESEARCH
Volume 15, Issue 6, Pages 4942-4949Publisher
TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-4024-5
Keywords
oxygen evolution reaction (OER); V doping; binder-free catalyst; large active surface
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Funding
- Natural Science Foundation of Hubei Province, China [2019CFB569, 2020CFB430]
- Science and Technology Foundation for Creative Research Group of Hubei Normal University, China [2019CZ08]
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This study proposes a versatile multiscale manipulating strategy to construct a V-NiFe2O4@Ni2P/NF heterostructure with superior activity and stability. The in-situ generated Ni2P phase induced by selective phosphorylation of the NiFe-precursor exhibits excellent catalytic activity. In addition, metal V doping stimulates the activity by modulating the electronic structure. The binder-free catalyst, built with a large active surface and robust scaffold, demonstrates outstanding OER activity and long-term stability.
Water electrolysis is severely impeded by the kinetically sluggish oxygen evolution reaction (OER) due to its inherent multistep four-electron transfer mechanism. However, designing advanced OER electrocatalysts with abundant active sites, robust stability, and low cost remains a huge challenge. Herein, a facile and versatile multiscale manipulating strategy was proposed to construct a novel V-NiFe2O4@Ni2P heterostructure self-supported on Ni foam (V-NiFe2O4@Ni2P/NF). In such unique architecture, the intrinsic OER catalytic activity was greatly boosted by the in-situ generated heterogeneous Ni2P phase induced by precisely selective phosphorylation of the NiFe-precursor, while the synchronous metal V doping stimulated the activity via modulating the electronic configuration, thus synergistically promoting its OER kinetics. In addition, the binder-free catalyst built from three-dimensional (3D) nanosheet arrays (NSs) can offer a large active surface for efficient charge/mass transfer and a robust scaffold for the integrated structure. The as-prepared flexible electrode exhibited superior OER activity with an ultra-low overpotential of 230 mV at 50 mA.cm(-2) and outstanding long-term stability for 40 h. This discovery is expected to provide an opportunity to explore efficient and stable commercial materials for scalable, efficient, and robust electrochemical hydrogen (H-2) production.
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