scholarly journals Luminescent copper(i) complexes with bisphosphane and halogen-substituted 2,2′-bipyridine ligands

2018 ◽  
Vol 47 (40) ◽  
pp. 14263-14276 ◽  
Author(s):  
Sarah Keller ◽  
Alessandro Prescimone ◽  
Henk Bolink ◽  
Michele Sessolo ◽  
Giulia Longo ◽  
...  

Light-emitting electrochemical cells with Cu(i) emitters with halo-substituted 2,2′-bipyridine ligands display orange electroluminescence and short turn-on times.

2007 ◽  
Vol 17 (11) ◽  
pp. 1807-1813 ◽  
Author(s):  
J.-H. Shin ◽  
N. D. Robinson ◽  
S. Xiao ◽  
L. Edman

1997 ◽  
Vol 488 ◽  
Author(s):  
F. P. Wenzl ◽  
S. Tasch ◽  
J. Gao ◽  
L. Holzer ◽  
U. Scherf ◽  
...  

AbstractWe report the application of the blue light emitting conjugated polymer m-LPPP (methyl substituted laddertype poly(paraphenylene) ) in light emitting electrochemical cells. The active layer of the LEC consists of a blend of m-LPPP with the ionically conductive polymer PEO and LiCF3SO3 as ionic salt. Investigations of different concentrations of PEO and salt showed that the best LECs made of m-LPPP up to now where realised with an active layer consisting of a blend of m-LPPP:PEO:salt in the range of 20:10:3. In this case we are able to realise LECs with response times in the range of 30 μs. The I/U characteristics show low turn on voltages both for current and electroluminescence, but only in the case of ITO biased as a cathode. The initial electroluminescence spectra are quite the same as those for LEDs made of m-LPPP but turn into green after some time of operation.


2008 ◽  
Vol 20 (2) ◽  
pp. 388-396 ◽  
Author(s):  
Eli Zysman-Colman ◽  
Jason D. Slinker ◽  
Jeffrey B. Parker ◽  
George G. Malliaras ◽  
Stefan Bernhard

2013 ◽  
Vol 1567 ◽  
Author(s):  
Takeo Akatsuka ◽  
Stephan van Reenen ◽  
Enrico Bandiello ◽  
Henk J. Bolink

ABSTRACTLight-Emitting Electrochemical Cells (LECs) consist of solution processable ionic light-emitting materials and use air stable electrodes. Their operational mechanism relies on both ionic and electronic conduction. The dynamic behavior is primarily determined by the ionic conductivity. Here, we demonstrate that with increasing temperature the LECs turn-on faster yet without decreasing the efficiency. This is due to the activation energy of ionic transport and the temperature independent photoluminescence quantum yields.


2019 ◽  
Vol 11 (43) ◽  
pp. 40372-40381 ◽  
Author(s):  
Isabelle Gerz ◽  
E. Mattias Lindh ◽  
Pall Thordarson ◽  
Ludvig Edman ◽  
Jolla Kullgren ◽  
...  

Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1937
Author(s):  
Tatiana G. Liashenko ◽  
Anatoly P. Pushkarev ◽  
Arnas Naujokaitis ◽  
Vidas Pakštas ◽  
Marius Franckevičius ◽  
...  

Inexpensive perovskite light-emitting devices fabricated by a simple wet chemical approach have recently demonstrated very prospective characteristics such as narrowband emission, low turn-on bias, high brightness, and high external quantum efficiency of electroluminescence, and have presented a good alternative to well-established technology of epitaxially grown III-V semiconducting alloys. Engineering of highly efficient perovskite light-emitting devices emitting green, red, and near-infrared light has been demonstrated in numerous reports and has faced no major fundamental limitations. On the contrary, the devices emitting blue light, in particular, based on 3D mixed-halide perovskites, suffer from electric field-induced phase separation (segregation). This crystal lattice defect-mediated phenomenon results in an undesirable color change of electroluminescence. Here we report a novel approach towards the suppression of the segregation in single-layer perovskite light-emitting electrochemical cells. Co-crystallization of direct band gap CsPb(Cl,Br)3 and indirect band gap Cs4Pb(Cl,Br)6 phases in the presence of poly(ethylene oxide) during a thin film deposition affords passivation of surface defect states and an increase in the density of photoexcited charge carriers in CsPb(Cl,Br)3 grains. Furthermore, the hexahalide phase prevents the dissociation of the emissive grains in the strong electric field during the device operation. Entirely resistant to 5.7 × 106 V·m−1 electric field-driven segregation light-emitting electrochemical cell exhibits stable emission at wavelength 479 nm with maximum external quantum efficiency 0.7%, maximum brightness 47 cd·m−2, and turn-on bias of 2.5 V.


2010 ◽  
Vol 22 (4) ◽  
pp. 1288-1290 ◽  
Author(s):  
Rubén D. Costa ◽  
Antonio Pertegás ◽  
Enrique Ortí ◽  
Henk J. Bolink

1999 ◽  
Vol 102 (1-3) ◽  
pp. 1138-1139 ◽  
Author(s):  
F.P. Wenzl ◽  
L. Holzer ◽  
S. Tasch ◽  
U. Scherf ◽  
K. Müllen ◽  
...  

2008 ◽  
Author(s):  
Henk Bolink ◽  
Rubén D. Costa ◽  
Enrique Orti ◽  
Michele Sessolo ◽  
Stefan Graber ◽  
...  

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