Carbonized wood fiber-supported S, N-codoped carbon layer-coated multinary metal sulfide nanoarchitecture for efficient oxygen evolution reaction at ampere-level current density.

Multinary metal sulfides (MMSs) are highly suitable candidates for the application of electrocatalysis as they offer numerous parameters for optimizing the electronic structure and catalytic sites. Herein, a stable nanoarchitecture consisting of MMSs ((NiCoCrMnFe)S) nanoparticles embedded in S, N-codoped carbon (SNC) layers derived from metal organic framework (MOF) and supported on carbonized wood fibers (CWF) was fabricated by directly carbonization. Benefiting from this carbon-coated configuration, along with the synergistic effects within multinary metal systems, (NiCoCrMnFe)S@SNC/CWF delivers an exceptionally low overpotential of 260 mV at a high current density of 1000 mA cm, a small Tafel slope of 48.

Synergistic engineering of P, N-codoped carbon-confined bimetallic cobalt/nickel phosphides with tailored electronic structures for boosting urea electro-oxidation.

Bimetallic phosphides exhibit superior electrocatalytic activities and synergistic effects that make them ideal electrocatalysts for the urea oxidation reaction (UOR). Herein, P, N-codoped carbon-encapsulated cobalt/nickel phosphides derived from NiCo-MOF-74 (NiCoP@PNC) and anchored on P-doped carbonized wood fiber (PCWF) for UOR were prepared through synchronous carbonization and phosphorization. By benefiting from the synergistic effect of structural and electronic modulation, NiCoP@PNC/PCWF exhibits excellent UOR electrocatalytic performance under alkaline conditions, achieving a current density of 50 mA cm with a potential of only 1.