Anchoring Single‐Atomic Metal Sites in Metalloporphyrin‐Based Covalent Organic Frameworks for Enhanced Photocatalytic Hydrogen Evolution

A photoactive covalent organic framework (COF) was built from metalloporphyrin and bipyridine monomers and single-atomic Pt sites were subsequently installed. Integrating photosensitizing metalloporphyrin and substrate-activating Pt(bpy) moieties in a single solid facilitates multielectron transfer and accelerates photocatalytic hydrogen evolution with a maximum production rate of 80.4 mmol h