Pyrene‐ and Bipyridine‐based Covalent Triazine Framework as Versatile Platform for Photocatalytic Solar Fuels Production**

Author:

Fávaro Marcelo Alves12,Yang Jin3,Ditz Daniel2,Küçükkeçeci Hüseyin3,Alkhurisi Mohammed H.4,Bergwinkl Sebastian5,Thomas Arne3ORCID,Quadrelli Elsje Alessandra1ORCID,Palkovits Regina26ORCID,Canivet Jérôme1ORCID,Wisser Florian M.47ORCID

Affiliation:

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

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

3. Fakultät II Institut für Chemie Technische Universität Berlin Hardenbergstraße 40 10623 Berlin Germany

4. Institute of Inorganic Chemistry University of Regensburg Universitätsstraße 31 93053 Regensburg Germany

5. Institute of Physical and Theoretical Chemistry University of Regensburg Universitätsstraße 31 93053 Regensburg Germany

6. Max-Planck-Institute for Chemical Energy Conversion Stiftstraße 34–36 45470 Mülheim an der Ruhr Germany

7. Erlangen Center for Interface Research and Catalysis Friedrich-Alexander-Universität Erlangen-Nürnberg Egerlandstraße 3 91058 Erlangen Germany

Abstract

AbstractThe ability to molecularly engineer materials is a powerful tool toward increasingly performing heterogeneous catalysts. Porous organic polymers stand out as photocatalysts due to their high chemical stability, outstanding optoelectronic properties and their easy and tunable syntheses. In photocatalysis, the insertion of photosensitizing π‐extended molecules into molecularly well‐defined donor‐acceptor junctions is supposed to increase the catalytic activity, but yet remain experimentally underdeveloped. This study presents a pyrene‐based Covalent Triazine Framework (CTF) synthesized through a polycondensation approach, which was designed to contain a molecularly‐defined pyrene‐triazine‐bipyridine donor‐acceptor‐acceptor triad as the repetition unit of the CTF. The CTF is an efficient photocatalyst for hydrogen evolution from water reaching a significant production rate of 61.5 mmolH2/h/gcat. Moreover, the same CTF can easily be used as porous macroligand for an organometallic Rh complex to efficiently catalyze the carbon dioxide photoreduction into formic acid under visible light.

Funder

Deutsche Bundesstiftung Umwelt

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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