Platinum‐ and CuO x ‐Decorated TiO 2 Photocatalyst for Oxidative Coupling of Methane to C 2 Hydrocarbons in a Flow Reactor

Abstract Oxidative coupling of methane (OCM) is considered one of the most promising catalytic technologies to upgrade methane. However, C 2 products (C 2 H 6 /C 2 H 4 ) from conventional methane conversion have not been produced commercially owing to competition from overoxidation and carbon accumulation at high temperatures. Herein, we report the codeposition of Pt nanoparticles and CuO x clusters on TiO 2 (PC‐50) and use of the resulting photocatalyst for OCM in a flow reactor operated at room temperature under atmospheric pressure for the first time. The optimized Cu 0.1 Pt 0.5 /PC‐50 sample showed a highest yield of C 2 product of 6.8 μmol h −1 at a space velocity of 2400 h −1 , more than twice the sum of the activity of Pt/PC‐50 (1.07 μmol h −1 ) and Cu/PC‐50 (1.9 μmol h −1 ), it might also be the highest among photocatalytic methane conversions reported so far under atmospheric pressure. A high C 2 selectivity of 60 % is also comparable to that attainable by conventional high‐temperature (>943 K) thermal catalysis. It is proposed that Pt functions as an electron acceptor to facilitate charge separation, while holes could transfer to CuO x to avoid deep dehydrogenation and the overoxidation of C 2 products.