Autor: |
Lukas Ahrens, Yvonne J. Hofstetter, Baris Celik, Julian F. Butscher, Frank Rominger, Jan Freudenberg, Yana Vaynzof, Uwe H. F. Bunz |
Jazyk: |
angličtina |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
Organic Materials, Vol 03, Iss 02, Pp 168-173 (2021) |
Druh dokumentu: |
article |
ISSN: |
2625-1825 |
DOI: |
10.1055/s-0041-1726459 |
Popis: |
Abstract Two covalently linked triisopropylsilyl-ethynylated phenazinothiadiazoles were prepared through condensation of a spirocyclic and a bicyclic tetraketone with a 5,6-diaminobenzothiadiazole. The spirobisindene- and the ethanoanthracene-based linkers render the electron acceptors amorphous in thin films. The optoelectronic properties of the non-conjugated dimers are indistinguishable from that of the crystalline monomer. Bulk heterojunction solar cells were prepared with power conversion efficiencies peaking at 1.6%. The choice of linker neither influenced optical and electrochemical properties nor device performance. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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