Management of Triplet States in Modified Mononuclear Ruthenium(II) Complexes for Enhanced Photocatalysis

Abstract Controlling the interplay between relaxation and charge/energy transfer processes in the excited states of photocatalysts is crucial for the performance of artificial photosynthesis. Metal‐to‐ligand charge‐transfer triplet states ( 3 MLCT*) of ruthenium(II) complexes are broadly implemented for photocatalysis, but an effective means of managing the triplets for enhanced photocatalysis has been lacking. Herein, We proposed a strategy to considerably prolong the triplet excited‐state lifetime by decorating a ruthenium(II) phosphine complex (RuP‐1) with pendent polyaromatic hydrocarbons (PAHs). Systematic studies demonstrate that in RuP‐4 decorated with anthracene, sub‐picosecond electron transfer from anthracene to 3 MLCT* leads to a charge‐separated state that can mediate the formation of the intra‐ligand triplet state ( 3 IL) of anthracene, resulting in an exceptionally long excited‐state up to several milliseconds. This triplet management strategy enables impressive photocatalytic reduction of CO 2 to CO with a turnover number (TON) of 404, an optimized quantum yield of 43 % and 100 % selectivity, which is the highest reported performance for mononuclear photocatalysts without additional photosensitizers. RuP‐4 also catalyzes photochemical hydrogen generation under argon. This work opens up an avenue for regulating the excited‐state charge/energy flow for the development of long‐lived 3 IL multi‐functional mononuclear photocatalysts to boost artificial photosynthesis.