Mesoporous hydrogel electrodes with flexible frameworks exhibiting enhanced mass transport for the oxygen evolution reaction.

Mesoporous hydrogel electrodes with unique flexible mesopores surrounded by CoOOH nanosheets were prepared via the electrochemical deposition of hybrid cobalt hydroxide nanosheets, exhibiting high oxygen evolution reaction activity at a high current density owing to the enhanced mass transport of oxygen molecules.

Inactivation mechanism of SARS-CoV-2 by ozone in aqueous and gas phases.

The comparison of the inactivation rate of SARS-CoV-2 by ozone in water with that in gas, based on data from references and experiments, has indicated the inactivation rate of the former is remarkably higher than that of the latter. To investigate the reason for this difference, we analyzed the reaction rate using a diffusional reaction model, in which ozone is carried by micro spherical viruses to inactivate the target viruses. Using this model, we can evaluate the amount of ozone required to inactivate a virus based on the ct value. We found that inactivation in gas phase requires 1014-1015 ozone molecules per virus virion, while the inactivation in aqueous phase requires 5×1010 to 5×1011 ozone molecules. This implies that the efficiency in gas phase is 200-20,000 times lower than that in aqueous phase. This is not attributed to the lower probability of collision in gas phase than in aqueous phase. Rather, it may be due to the fact that the ozone and radicals generated by ozone react and subsequently dissipate. We proposed the diffusion of ozone into a spherical virus at a steady state and the decomposition reaction model through radicals.

Principles of Self-Repairing Ability of Tripodal Ligand-Stabilized Hybrid Cobalt Hydroxide Nanosheets for Alkaline Water Electrolysis.

Self-repairing catalysts are promising new materials for achieving long lifetime of alkaline water electrolyzers powered by renewable energy. Catalytic nanoparticles dispersed in an electrolyte were deposited on the anode to repair a catalyst layer by electrolysis. A hybrid cobalt hydroxide nanosheet modified with tris(hydroxymethyl)aminomethane on the surface (Co-ns) was used as a catalyst. Assuming a pseudo-first-order process, the rate constant of an electrochemical deposition was linearly correlated with the electrode potential during electrolysis. Thus, it is expected that the repair of the catalyst is automatically controlled by changes in the oxygen evolution reaction (OER) overpotential. The essential step of the electrochemical deposition was the anodic oxidation of Co2+ to Co3+ . Surface modification of Co-ns protects Co2+ against the autooxidation of Co2+ caused by the dissolved oxygen. The redox properties and organic modification of Co-ns make them well-suited for the self-repairing of anode catalysts.