Tailored Band Gaps in Sulfur- and Nitrogen-Containing Porous Donor-Acceptor Polymers
Creators
- 1. Department of Organic Chemistry, Charles University, Prague 2, Czech Republic.
- 2. Department of Functional Materials, Technical University Berlin, Berlin, Germany.
- 3. Heyrovsky Institute for Physical Chemistry, Academy of Science Czech Republic, Prague 8, Czech Republic.
- 4. Leibniz-Institut fuer Polymerforschung Dresden e.V., Dresden, Germany.
- 5. Technical University Bergakademie Freiberg, Freiberg, Germany.
- 6. Department of Physical and Macromolecular Chemistry, Charles University, Prague 2, Czech Republic.
- 7. Institute of Organic Chemistry and Biochemistry of the CAS, Prague 6, Czech Republic.
Description
This is the pre-peer reviewed version of the following article: Schwarz, D.; Kochergin, Y. S.; Acharja, A.; Ichangi, A.; Opanasenko, M. V.; Čejka, J.; Lappan, U.; Arki, P.; He, J.; Schmidt, J.; Nachtigall, P.; Thomas, A.; Bojdys,* M. J. Chem. – Eur. J. 2017, DOI: 10.1002/chem.201703332.
Donor-acceptor dyads hold the key to tuning of electrochemical properties and enhanced mobility of charge carriers, yet their incorporation into a heterogeneous polymer network proves difficulty due to the fundamentally different chemistry of the donor- and acceptor-subunits. We present a family of sulphur and nitrogen containing porous polymers (SNPs) that are obtained via Sonogashira-Hagihara cross-coupling and that combine electron-withdrawing triazine (C3N3) and electron donating, sulphur-containing linkers. Choice of building blocks and synthetic conditions determines the optical band gap (from 1.67 to 2.58 eV) and nanoscale ordering of these microporous materials with BET surface areas of up to 545 m2 g-1 and CO2 capacities up to 1.56 mmol g-1. Our results highlight the advantages of the modular design of SNPs, and we report one of the highest photocatalytic hydrogen evolution rates for a cross-linked polymer without Pt co-catalyst (194 µmol h-1 g-1).
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