The oxygen evolution reaction (OER) is hindered by slow kinetics due to its four-electron process, limiting overall efficiency. The rational design of metal-organic framework (MOF)-based nanomaterials is crucial for enhancing the oxygen production rate. Using a straightforward strategy, we synthesized cobalt-iron layered double hydroxide (CoFe-LDH) hollow polyhedra loaded with CeO2, with zeolite imidazolate framework-67 (ZIF-67) serving as the precursor. The CoFe-LDH/CeO2 composite demonstrates outstanding OER performance, including a lower overpotential (315 mV) at 10 mA cm-2, a smaller Tafel slope (49.53 mV dec-1), and remarkable stability. The high OER activity of CoFe-LDH/CeO2 is attributed to the electron transition of CeO2 within the CoFe-LDH carrier layer, which enhances electron interactions with the CoFe-LDH hollow polyhedra and promotes the catalytic reaction. Leveraging the excellent catalytic properties of CoFe-LDH/CeO2, this study offers a promising approach for developing green, cost-effective, and efficient electrocatalysts.
Keywords: CeO(2); Co-Fe layered double hydroxides; Hollow polyhedral; Oxygen evolution reaction; ZIF-67.
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