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寻找光催化的最佳点——基于联吡啶的共价有机框架的案例研究

Finding the Sweet Spot of Photocatalysis─A Case Study Using Bipyridine-Based CTFs.

作者信息

Alves Fávaro Marcelo, Ditz Daniel, Yang Jin, Bergwinkl Sebastian, Ghosh Ashta C, Stammler Michael, Lorentz Chantal, Roeser Jérôme, Quadrelli Elsje Alessandra, Thomas Arne, Palkovits Regina, Canivet Jérôme, Wisser Florian M

机构信息

Université de Lyon, Université Claude Bernard Lyon 1, CNRS, IRCELYON - UMR 5256, 2 Avenue Albert Einstein, 69626 Villeurbanne Cedex, France.

Institut für Technische und Makromolekulare Chemie, RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany.

出版信息

ACS Appl Mater Interfaces. 2022 Mar 30;14(12):14182-14192. doi: 10.1021/acsami.1c24713. Epub 2022 Mar 16.

Abstract

Covalent triazine frameworks (CTFs) are a class of porous organic polymers that continuously attract growing interest because of their outstanding chemical and physical properties. However, the control of extended porous organic framework structures at the molecular scale for a precise adjustment of their properties has hardly been achieved so far. Here, we present a series of bipyridine-based CTFs synthesized through polycondensation, in which the sequence of specific building blocks is well controlled. The reported synthetic strategy allows us to tailor the physicochemical features of the CTF materials, including the nitrogen content, the apparent specific surface area, and optoelectronic properties. Based on a comprehensive analytical investigation, we demonstrate a direct correlation of the CTF bipyridine content with the material features such as the specific surface area, band gap, charge separation, and surface wettability with water. The entirety of these parameters dictates the catalytic activity as demonstrated for the photocatalytic hydrogen evolution reaction (HER). The material with the optimal balance between optoelectronic properties and highest hydrophilicity enables HER production rates of up to 7.2 mmol/(h·g) under visible light irradiation and in the presence of a platinum cocatalyst.

摘要

共价三嗪框架(CTFs)是一类多孔有机聚合物,因其出色的化学和物理性质而不断吸引着越来越多的关注。然而,到目前为止,几乎尚未实现从分子尺度上控制扩展的多孔有机框架结构以精确调节其性质。在此,我们展示了一系列通过缩聚反应合成的基于联吡啶的CTFs,其中特定结构单元的顺序得到了很好的控制。所报道的合成策略使我们能够定制CTF材料的物理化学特性,包括氮含量、表观比表面积和光电性质。基于全面的分析研究,我们证明了CTF联吡啶含量与诸如比表面积、带隙、电荷分离以及与水的表面润湿性等材料特性之间的直接关联。正如光催化析氢反应(HER)所证明的那样,所有这些参数决定了催化活性。在可见光照射和铂助催化剂存在的情况下,具有最佳光电性质和最高亲水性平衡的材料能够实现高达7.2 mmol/(h·g)的HER产率。

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