Structure-property relationships for covalent triazine-based frameworks: The effect of spacer length on photocatalytic hydrogen evolution from water. (22nd September 2017)

• Record Type: Journal Article
• Authors: Meier, Christian B.; Sprick, Reiner Sebastian; Monti, Adriano; Guiglion, Pierre; Lee, Jet-Sing M.; Zwijnenburg, Martijn A.; Cooper, Andrew I.
• Is Part Of: Polymer. Volume 126(2017)
• Page Start: 283
• Page End: 290
• Publication Date: 2017-09-22
• Subjects: Photocatalysis -- Hydrogen evolution from water -- Covalent triazine-based framework (CTF); Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; 547.7
• DOI: 10.1016/j.polymer.2017.04.017
• Languages: English
• ISSNs: 0032-3861

Abstract

Abstract: Covalent triazine-based frameworks (CTFs) are a subclass of conjugated microporous polymers (CMPs) that can be used as organic photocatalysts for photocatalytic hydrogen evolution from water. Seven materials with varied spacer units from phenylene to quarterphenylene were synthesized, either by trifluoromethanesulfonic acid (TfOH) catalysis from nitriles or by Suzuki-Miyaura polycondensation. The photocatalytic performance under visible light of all materials was systematically studied in the presence of a hole-scavenger, showing that both synthesis routes produce CTFs with similar hydrogen evolution rates (HER), but different optical properties. The highest hydrogen evolution rate in the cyclotrimerized series was found for CTF-2 with an apparent quantum yield of 1.6% at 420 nm in a mixture of water and triethanolamine with a platinum co-catalyst. Based on (TD-)DFT calculations, the highest performance was expected for CTF-1 and this discrepancy is explained by a trade-off between increased light absorption and decreased thermodynamic driving force. Graphical abstract: Highlights: Two methods were used to synthesize covalent triazine-based frameworks (CTFs) with varied phenylene spacer lengths. Impact of phenylene linker length on photocatalytic performance was studied. A trade-off between driving-force for scavenger oxidation and light absorption was found, supported by (TD-)DFT calculations. Residual palladium from the synthesis seems to act as a co-catalyst.