In situ C–H activation-derived polymer@TiO2 p–n heterojunction for photocatalytic hydrogen evolution

Abstract

Semiconductor heterojunctions benefiting from efficient charge transfer and separation have been widely used in photocatalysis. Herein, heterojunctions based on polymeric and inorganic semiconductors, namely PyOT@TiO₂, have been successfully constructed via in situ C–H activation polycondensation of the pyrene unit (Py-) and 3-(2-(2-ethoxyethoxy)ethoxy)thiophene unit (-OT) in the presence of titanium dioxide (TiO₂). The combination of the polymeric semiconductor PyOT with TiO₂ not only broadens the light response of TiO₂, but also dramatically promotes the photo-generation exciton separation of PyOT. As a result, the optimized 50% PyOT@TiO₂ composite exhibited extensive visible light absorption (400–520 nm) and the highest photocatalytic hydrogen evolution rate using ascorbic acid (AA) as the sacrificial agent, which is approximately 135 and 21 times higher than those of single-components TiO₂ and PyOT, respectively. Mechanistic study by XPS, M–S plots and hydroxyl radical detection tests revealed the p–n heterojunction characteristics of PyOT@TiO₂ that contributed to the enhanced photocatalytic performance. Our work develops a promising strategy for the in situ construction of polymeric–inorganic soft–hard heterostructures via atom-economic C–H activation polymerization.