Carbazole‐Based Thin Microporous Polymer Films for Photocatalytic Hydrogen Evolution

V Veit Dippold (Technische Universität Berlin Department of Chemistry/ Functional Materials Hardenbergstr. 40 10623 Berlin Germany) H Hüseyin Küçükkeçeci (Technische Universität Berlin Department of Chemistry/ Functional Materials Hardenbergstr. 40 10623 Berlin Germany) E Eugenia Bosler (Department of Micro and Precision Devices Technische Universität Berlin Pascalstraße 8‐9 10587 Berlin Germany) J Johannes Schmidt (Department of Chemistry, Technische Universität Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany) S Samrat Ghosh (Department of Molecular Engineering, Kyoto University) G Gregor Michl (Department of Chemistry/Functional Materials Technische Universität Berlin Hardenbergstr. 40 10623 Berlin Germany) I Islam E. Khalil (Department of Chemistry, Functional Materials) L Lisa Gerland (Research Unit Molecular Biophysics Leibniz‐Forschungsinstitut für Molekulare Pharmakologie Robert‐Roessle‐Str. 10 13125 Berlin Germany) A Adam Lange D Dirk Oberschmidt (Department of Micro and Precision Devices Technische Universität Berlin Pascalstraße 8‐9 10587 Berlin Germany) A Arne Thomas (Functional Materials, Department of Chemistry, Technische Universität Berlin, Hardenbergstraße 40, Berlin 10623, Germany)

Abstract

AbstractPhotocatalytic hydrogen evolution is a direct pathway to store solar energy in chemicals. Conjugated microporous polymers (CMPs) are porous organic photocatalysts, that are typically applied in powder form in heterogenous catalytic reactions. However, the use of powder photocatalysts in dispersion poses some major challenges when it comes to practical applications in larger scales. In this manuscript, the photocatalytic performance of a carbazole‐based porous organic polymer (C‐POP) film produced by electro polymerizing 1,2,3,5‐Tetrakis(carbazol‐9‐yl)‐4,6‐dicyanobenzene (4CzIPN) is investigated, well‐known for its intriguing photocatalytic properties. The thickness of the intrinsic microporous film is tuneable by the amount of cyclic voltammetry cycles but it is shown that the hydrogen production is not dependent on film thickness. It can therefore be concluded that catalysis is mainly occuring on the outer surface of the films, questioning whether high surface areas are always required for efficient photocatalysis. A microstructured film offers the advantage that, with a reduced amount of polymer material, a constant or even increased external surface area of the film can be achieved. The approach presented here is therefore advantageous for achieving high hydrogen production per unit area with minimal amounts of polymer, as very thin layers are already sufficient for high activity.

Article Details

Volume / Issue Vol. 37, Issue 38
Published September 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

V

Veit Dippold

Technische Universität Berlin Department of Chemistry/ Functional Materials Hardenbergstr. 40 10623 Berlin Germany

H

Hüseyin Küçükkeçeci

Technische Universität Berlin Department of Chemistry/ Functional Materials Hardenbergstr. 40 10623 Berlin Germany

E

Eugenia Bosler

Department of Micro and Precision Devices Technische Universität Berlin Pascalstraße 8‐9 10587 Berlin Germany

J

Johannes Schmidt

Department of Chemistry, Technische Universität Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany

S

Samrat Ghosh

Department of Molecular Engineering, Kyoto University

G

Gregor Michl

Department of Chemistry/Functional Materials Technische Universität Berlin Hardenbergstr. 40 10623 Berlin Germany

I

Islam E. Khalil

Department of Chemistry, Functional Materials

L

Lisa Gerland

Research Unit Molecular Biophysics Leibniz‐Forschungsinstitut für Molekulare Pharmakologie Robert‐Roessle‐Str. 10 13125 Berlin Germany

A

Adam Lange

D

Dirk Oberschmidt

Department of Micro and Precision Devices Technische Universität Berlin Pascalstraße 8‐9 10587 Berlin Germany

A

Arne Thomas

Functional Materials, Department of Chemistry, Technische Universität Berlin, Hardenbergstraße 40, Berlin 10623, Germany