Cobalt-Modified Covalent Organic Framework as a Robust Water Oxidation Electrocatalyst

The development of stable, efficient oxygen evolution reaction (OER) catalyst capable of oxidizing water is one of the premier challenges in the conversion of solar energy to electrical energy, because of its poor kinetics. Herein, a bipyridine-containing covalent organic framework (TpBpy) is utilized as an OER catalyst by way of engineering active Co­(II) ions into its porous framework. The as-obtained Co-TpBpy retains a highly accessible surface area (450 m²/g) with exceptional stability, even after 1000 cycles and 24 h of OER activity in phosphate buffer under neutral pH conditions with an overpotential of 400 mV at a current density of 1 mA/cm². The unusual catalytic stability of Co-TpBpy arises from the synergetic effect of the inherent porosity and presence of coordinating units in the COF skeleton

A Distinctive PdCl₂‑Mediated Transformation of Fe-Based Metallogels into Metal–Organic Frameworks

Simple, efficient conversion of viable Fe³⁺-based metallogels into Fe-metal–organic frameworks (MOFs) has been achieved by PdCl₂-mediated gel degradation. The metallogels and the resulting MOFs have been characterized, and a probable mechanism for the event has been elucidated