4.8 Article

Operando Reconstruction toward Dual-Cation-Defects Co-Containing NiFe Oxyhydroxide for Ultralow Energy Consumption Industrial Water Splitting Electrolyzer

Journal

ADVANCED ENERGY MATERIALS
Volume 13, Issue 10, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202203595

Keywords

dual-cation-defects; high-current-density; NiFe catalysts; operando electrocatalysis

Ask authors/readers for more resources

Guided by density functional theory, the interaction of cation vacancies and dopants can manipulate d band centers, thus achieving near-optimal binding energies of the oxygenated intermediates and ultralow potentials. This principle is implemented experimentally by catalysis operando variations synthesis, where Mo leaching from high-entropy Co, Mo co-doped NiFe hydroxide precursors forms Co dopant and cation vacancy coexistent NiFe oxyhydroxide. Operando electrochemical spectroscopy reveals that dual-cation-defects promote the easier oxidation transition of metal sites, contributing to a low overpotential of 255 mV at 100 mA cm(-2). Furthermore, dual-regulated NiFe oxyhydroxide electrodes operate stably at 8 A in practical industrial electrolyzers with an ultralow energy consumption of approximately 4.6 kWh m(-3) H-2, verifying the feasibility of lab-constructed novel catalysts towards industrialization.
Nickel-iron oxygen evolution catalysts have been under the spotlight as substitutes for precious metals, however, they rarely operate efficiently in practical industrial electrolyzers due to their moderate activity. Guided by density functional theory, the interaction of cation vacancies and dopants can manipulate d band centers, thus gaining near-optimal binding energies of the oxygenated intermediates and ultralow potentials. This principle is implemented experimentally by catalysis operando variations synthesis, more specifically, in situ Mo leaching from high-entropy Co, Mo co-doped NiFe hydroxide precursors form Co dopant and cation vacancy coexistent NiFe oxyhydroxide. Operando electrochemical spectroscopy uncovers that dual-cation-defects promote the readier oxidation transition of metal sites, thus contributing to a low overpotential of 255 mV at 100 mA cm(-2). Furthermore, dual-regulated NiFe oxyhydroxide electrodes operate stably at 8 A in practical industrial electrolyzers with ultralow energy consumption of approximate to 4.6 kWh m(-3) H-2, verifying the feasibility of lab-constructed novel catalysts towards industrialization.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available