Powder electrocatalysts for oxygen evolution reactions usually need adhesives for electrocatalytic performance tests, leading to the increase of resistance, reduction of catalyst loading, and easy stripping of the catalyst under long-time or high current operation. In this study, Ce-doped CoFe layered double hydroxides were uniformly grown on nickel foam by a one-step hydrothermal route. A nanostructured self-supported electrode Ce-CoFe-LDH/NF without adhesive was obtained directly, which has a regular nanoneedle morphology with a length of ∼1.2 μm and tip width of ∼20 nm. Adopting Ce 3+ ions with a large radius to partially displace Fe 3+ ions with a small radius produced lattice distortion and more defects in the host layer of CoFe-LDH, whereby possessing the great potential to enhance catalytic behaviors. Once used as an electrocatalyst for the oxygen evolution reaction, Ce-CoFe-LDH/NF shows an outstanding electrocatalytic performance, including an optimized overpotential of 225 mV at 10 mA cm -2 , a decreased Tafel slope of 34.34 mV dec -1 , and a low charge transfer impedance of 2.4 Ω in 1 M KOH electrolyte. Moreover, the overpotential of the working electrode increased by only 0.04 V after 24 hours and was maintained at a current density of 50 mA cm -2 . These results demonstrate a low-cost strategy compared to using noble metal OER electrocatalysts. Thus, this study highlights a ready universal approach to fabricate high-performance supported catalysts for energy-related applications.
Keyphrases
- metal organic framework
- reduced graphene oxide
- highly efficient
- quantum dots
- signaling pathway
- low cost
- ionic liquid
- visible light
- lps induced
- energy transfer
- room temperature
- oxidative stress
- pi k akt
- nuclear factor
- photodynamic therapy
- magnetic resonance
- gold nanoparticles
- carbon nanotubes
- immune response
- carbon dioxide
- cell proliferation
- municipal solid waste
- aqueous solution
- transition metal