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 mmol h À1 at a space velocity of 2400 h À1 , more than twice the sum of the activity of Pt/PC-50 (1.07 mmol h À1) and Cu/PC-50 (1.9 mmol h À1), 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.