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Defect Oxygen Rich Cobalt Ferrite Nanoparticles for Practical Water Electrolysis with Sublime Activity and Durability.

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The scope of any metal oxide as catalyst for driving electrocatalytic reactions depends on its electronic structure which is correlated to its oxygen defect density. Likewise to transform a spinel… Click to show full abstract

The scope of any metal oxide as catalyst for driving electrocatalytic reactions depends on its electronic structure which is correlated to its oxygen defect density. Likewise to transform a spinel oxide such as cobalt ferrite (CoFe2O4) into a worthy pH-universal bifunctional electrocatalyst for hydrogen and oxygen evolution reactions (HER and OER), oxygen defects need to be regulated. Prepared by co-precipitation and inert calcination at 650oC, CoFe2O4 nanoparticles (NPs) require 253 and 300 mV OER overpotentials to reach current densities of 10 and 100 mA/cm2 when Ni foam (NF) is used as substrate. With cost-effective carbon fibre paper (CFP), OER overpotential increases to 372 mV at 10 mA/cm2 at pH 14. The 550oC prepared NPs need HER overpotentials of 218, 245 and 314 mV at -10 mA/cm2 in alkaline, acidic and neutral pH, respectively. The intrinsic activity is reflected from turnover frequencies (TOF) of >3 O2 s-1 and >5 H2 s-1 at 398 and 259 mV overpotentials, respectively. When coupled for overall water splitting, the extremely durable 2-electrode electrolyzer requires cell potential of only 1.63V to reach 10 mA/cm2 at pH 14. The homologous couple also splits sea water splitting at an impressively low cell voltage of 1.72 and 1.47 V at room temperature and 80°C, respectively.

Keywords: oxygen; cobalt ferrite; water; activity; cm2

Journal Title: ChemSusChem
Year Published: 2020

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