A photoluminescent covalent triazine framework: CO2 adsorption, light-driven hydrogen evolution and sensing of nitroaromatics

Abstract

A highly photoluminescent (PL) porous covalent triazine-based framework (PCTF-8) is synthesized from tetra(4-cyanophenyl)ethylene by using trifluoromethanesulfonic acid as the catalyst at room temperature. Due to triazine units in the framework, the PCTF-8 exhibits excellent thermal stability (>400 °C). The Brunauer-Emmett-Teller (BET) specific surface area of PCTF-8 is 625 m2 g-1 which is lower than the one obtained from the synthesis under Lewis acid conditions (ZnCl2). At 1 bar and 273 K, the PCTF-8 adsorbs a significant amount of CO2 (56 cm3 g-1) and CH4 (17 cm3 g-1) which is highly comparable to nanoporous 1,3,5-triazine frameworks (NOP-1-6, 29-56 cm3 g-1). This nitrogen rich framework exhibits good ideal selectivity (61:1 (85% N2:15% CO2) at 273 K, 1 bar). Thus, it can be used as a promising candidate for potential applications in post-combustion CO2 capture and sequestration technologies. In addition, photoluminescence properties as well as the sensing behaviour towards nitroaromatics have been demonstrated. The fluorescence emission intensity of PCTF-8 is quenched by ca. 71% in the presence of 2,4,6-trinitrophenol (TNP). From time-resolved studies, a static quenching behaviour was found. This high photoluminescence property is used for hydrogen evolving organic photocatalysis from water in the presence of a sacrificial electron donor and a cocatalyst.