Physical vapour deposition of cyanine salts and their first application in organic electronic devices

被引:7
|
作者
Gesevicius, Donatas [1 ,2 ]
Neels, Antonia [3 ]
Duchene, Leo [4 ]
Hack, Erwin [5 ]
Heier, Jakob [1 ]
Nuesch, Frank [1 ,6 ]
机构
[1] Empa, Lab Funct Polymers, Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, Dubendorf, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, ISIC, Stn 6, CH-1015 Lausanne, Switzerland
[3] Empa, Ctr Xray Analyt, Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, Dubendorf, Switzerland
[4] Empa, Lab Mat Energy Convers, Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, Dubendorf, Switzerland
[5] Empa, Lab Transport Nanoscale Interfaces, Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, Dubendorf, Switzerland
[6] Ecole Polytech Fed Lausanne, Inst Mat, Stn 6, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
LIGHT-EMITTING DEVICES; ENERGY; VAPORIZATION; PERFORMANCE; EFFICIENT; EXCHANGE;
D O I
10.1039/c8tc05286g
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A symmetrical trimethine indocyanine dye chromophore was modified with the bistriflylimide anion to study the changes in Coulomb interactions, thermal stability and the volatility of the organic salt. The bulky bistriflylimide anion minimizes electrostatic interactions and increases the vapour pressure of the compound resulting in an increased volatility of the organic salt. First examples of entirely vacuum-processed bulk heterojunction organic photovoltaic devices show the proof of concept. We give evidence that the well dispersed negative charge of the bistriflylimide introduces quasi gas phase conditions to the cyanine chromophore. This overcomes the existing restriction of thin film formation via spincasting in cyanine dye based organic electronics and expands the thin film fabrication process choices towards physical vapour deposition.
引用
收藏
页码:414 / 423
页数:10
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