Abstract

• A Ru-doped flower-like Ni 2 P/NiO heterostructure nanosheets catalyst was prepared. • Ru-Ni 2 P/NiO/NF HNSs catalyst exhibits top-level HER activity (12 mV@10 mA cm −2 ). • XPS and DFT results reveal the electronic reconfiguration. • Superb activity originates from synergistic effect of dopants and heterostructure. Developing efficient alkaline hydrogen evolution reaction (HER) electrocatalysts remain a critical challenge for the realization of large-scale hydrogen production from water splitting, while the high energy barrier of the Volmer-step considerably impedes the catalytic activity in water-alkali electrolyzers. Herein, a novel Ru-doped hierarchical flower-like Ni 2 P/NiO heterostructure nanosheets vertically aligned on Ni foam substrates (Ru-Ni 2 P/NiO/NF HNSs) electrocatalyst is synthesized by a top-down strategy to achieve a top-level performance of HER in alkaline media. Benefitting from electronic reconfiguration, hierarchical flower-like nanosheet structure, and abundant heterogeneous interfaces, the as-obtained Ru-Ni 2 P/NiO/NF HNSs require an ultralow onset overpotential of 0 mV, a minimum overpotential of 12 mV and 112 mV to afford 10 mA cm −2 and 1000 mA cm −2 , respectively, and a Tafel slope of 22.6 mV decade −1 . Further X-ray photoelectron spectroscopy analysis combined with density functional theory calculations reveal the charge density redistribution, where electron accumulation on Ru favors the optimization of H 2 O absorption energies and the reduced energy barrier of the Volmer step, whereas the coupling effect of Ni 2 P/NiO heterogeneous interfaces is responsible for accelerating the Tafel step activity, synergistically resulting in accelerating alkaline HER kinetics. These findings reveal the significance of the rational combination of noble metal doping and heterostructure engineering toward the rational design and preparing of highly efficient electrocatalysts for the HER and beyond.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.