Literature DB >> 28727178

Tailored Band Gaps in Sulfur- and Nitrogen-Containing Porous Donor-Acceptor Polymers.

Dana Schwarz1, Yaroslav S Kochergin1, Amitava Acharjya2, Arun Ichangi1,3, Maksym V Opanasenko4, Jiří Čejka4, Uwe Lappan5, Pal Arki6, Junjie He7, Johannes Schmidt2, Petr Nachtigall7, Arne Thomas2, Ján Tarábek3, Michael J Bojdys1,3.   

Abstract

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 owing to the fundamentally different chemistry of the donor and acceptor subunits. A family of sulfur- and nitrogen-containing porous polymers (SNPs) are obtained via Sonogashira-Hagihara cross-coupling and combine electron-withdrawing triazine (C3 N3 ) and electron-donating, sulfur-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 one of the highest photocatalytic hydrogen evolution rates for a cross-linked polymer without Pt co-catalyst is attained (194 μmol h-1  g-1 ).
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  conjugated microporous polymers; donor-acceptor dyads; photocatalysis; sulfur; triazine

Year:  2017        PMID: 28727178     DOI: 10.1002/chem.201703332

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  A π-Conjugated, Covalent Phosphinine Framework.

Authors:  Jieyang Huang; Ján Tarábek; Ranjit Kulkarni; Cui Wang; Martin Dračínský; Glen J Smales; Yu Tian; Shijie Ren; Brian R Pauw; Ute Resch-Genger; Michael J Bojdys
Journal:  Chemistry       Date:  2019-08-13       Impact factor: 5.236

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.