Zeolitic Imidazolate Framework‐Derived Ru/RuO ₂ –Co ₃ O ₄ Catalyst for Methanol Oxidation Reaction in Alkaline Media

Abstract The present study explores the possibility of a hybrid nanostructure of ruthenium (Ru) and cobalt oxide (Co 3 O 4 ) for effective methanol oxidation reaction (MOR) in alkaline media. The spherical Ru/RuO 2 nanoparticle, uniformly dispersed in zeolitic Co 3 O 4 derived from its ZIF‐67 precursor, showed significant activity in MOR process. The duly characterized material exhibited a maximum current density of 131 mAcm −2 with an onset potential of ∼1.07 V vs RHE (reversible hydrogen electrode). Under the electrocatalytic condition, the material exhibited stability up to 500 cycles of 12 h without substantial loss in current density. A comparative study showed that incorporation of Ru/RuO 2 into zeolitic spinel Co 3 O 4 altered the activity in the MOR process. The catalyst had a good methanol (CH 3 OH) concentration tolerance up to 2.5 M in alkaline media. A diffusion‐controlled MOR process was indicated by the linear dependency of the current density against the square root of the scan rate. It was predicted that the temperature influenced the MOR process, and the apparent activation energy, E a(app) , calculated from the Arrhenius plot, was 27.45 kJmol −1 . The mechanism of the MOR was studied by using the density functional theory (DFT) calculation, and it was supported experimentally through the FTIR (Fourier transform infrared) and Raman analysis. DFT suggested for the engagement of both cobalt (Co) and Ruthenium (Ru) in the catalytic cycle. FTIR study showed that Ru nanoparticles get poisoned through CO (carbon monoxide) adsorption after 100 cycles and retard the activity after 12 h. On the other hand, the Raman study predicted that the Co 3 O 4 surface gets hydroxylated, forming ─CoOOH (cobalt oxyhydroxide) species that participated in the deprotonation of CH 3 OH with the assistance of Ru/RuO 2 nanoparticles.