Structure-property relationships for covalent triazine-based frameworks: The effect of spacer length on photocatalytic hydrogen evolution from water

被引:148
作者
Meier, Christian B. [1 ]
Sprick, Reiner Sebastian [1 ]
Monti, Adriano [2 ]
Guiglion, Pierre [2 ]
Lee, Jet-Sing M. [1 ]
Zwijnenburg, Martijn A. [2 ]
Cooper, Andrew I. [1 ]
机构
[1] Univ Liverpool, Dept Chem & Mat Innovat Factory, Crown St, Liverpool L69 72D, Merseyside, England
[2] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England
基金
英国工程与自然科学研究理事会;
关键词
Photocatalysis; Hydrogen evolution from water; Covalent triazine-based framework (CTF); GRAPHITIC CARBON NITRIDE; POROUS CONJUGATED POLYMERS; ORGANIC SOLAR-CELLS; VISIBLE-LIGHT; RESIDUAL PALLADIUM; GENERATION; PHOTOREDUCTION; TRIETHYLAMINE; PERFORMANCE; CATALYSIS;
D O I
10.1016/j.polymer.2017.04.017
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
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 CfF-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. (C) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:283 / 290
页数:8
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