Sulfide oxidation tuning in 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b]d ithiophene based dual acceptor copolymers for highly efficient photocatalytic hydrogen evolution

Polymeric photocatalysts for hydrogen evolution by water splitting have drawn tremendous research interest in recent years. However, the relatively low photocatalytic hydrogen evolution efficiency still needs to be overcome for further development. Recently, a growing body of literature has shown that the sulfone group can act as an electron-output site owing to its strong electron-withdrawing ability. Therefore, this study reports a sulfide oxidation tuning approach in 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b ']dithiophene (BDTT) for constructing a series of sulfone-based dual acceptor(1-2) (A(1)-A(2))-type copolymers with different numbers of sulfonyl groups and demonstrates that the A(1)-A(2)-type copolymer possesses the potential to supersede the D-A-type copolymer and A-A-type homopolymer. Moreover, the resulting polymer, PBDTTS-1SO displayed high photocatalytic activities of 97.1 mmol h(-1) g(-1) and 473 mu mol h(-1) (6 mg) under visible-light illumination and an apparent quantum yield exceeding 18% at a wavelength of 500 nm, which seems to be the highest value recorded among the reported polymer photocatalysts to date. This study presents an alternative material design strategy to boost photocatalytic efficiency.