An Alkaline-Stable, Metal Hydroxide Mimicking Metal-Organic Framework for Efficient Electrocatalytic Oxygen Evolution

Postsynthetic ion exchange of [Co-2(mu-Cl)(2)(btta)] (MAF-X27-Cl, H(2)bbta =1H,5H-benzo (1,2-d:4,5-d')bistriazole) possessing open metal sites on its pore surface yields a material [Co-2(mu-OH)(2)(bbta)] (MAF-X27-OH) functionalized by both open metal sites and hydroxide ligands, giving drastically improved electrocatalytic activities for the oxygen evolution reaction (an overpotential of 292 mV at 10.0 mA cm(-2) in 1.0 M KOH solution). Isotope tracing experiments further confirm that the hydroxide ligands are involved in the OER process to provide a low-energy intraframework coupling pathway.