NiFe layered double hydroxide (NiFe LDH) derived oxyhydroxides are promising electrocatalysts for the alkaline oxygen evolution reaction (OER). However, NiFe LDH with a stable metal-oxygen-metal (M-O-M) structure suffers from inadequate NiFe interaction, leading to undesirable activity and stability. Herein, we develop a NiFe hydroxide-organic framework (NiFe HOF) via modification of NiFe LDH with an organic linker to break the structural constraint of M-O-M and thus boost the OER. NiFe HOF with reconfigurable metal sites facilitates structural reengineering under the OER condition to form abundant NiFe interaction and prolonged M-O bonds, stimulating lattice oxygen mechanism. Therefore, NiFe HOF shows a distinctly decreased overpotential at 50 mA cm-2, which is 68 mV lower than that of NiFe LDH. The anion exchange membrane electrolyzer using NiFe HOF as anode electrode displays ultralong stability exceeding 1050 h at 1 A cm-2 with a low attenuation of 0.16 mV h-1.
Keywords: Lattice oxygen; Metal hydroxide−organic framework; NiFe interaction; NiFe layered double hydroxide; Oxygen evolution reaction.