5,009 research outputs found
Recommended from our members
Manufacturing flexible light-emitting polymer displays with conductive lithographic film technology
We report on a new low-cost manufacturing process for flexible displays that has the potential to rapidly expand the market into areas that have traditionally been outside the scope of such technology. In this paper we consider the feasibility of using offset-lithography to deposit contacts for polymer light-emitting displays. We compare and contrast manufacturing criteria and present a case study detailing our initial results. It is expected that these developments will stimulate further progress in multilayer device
fabrication.
Cheap, flexible conductive interconnects have the potential to find applications in a wide variety of device structures. For the more challenging exploitation areas in multilayer devices, such as displays, it was found that the properties of conductive lithographic films were not optimal in their current form. Three parameters (conductivity, surface roughness and surface work function) were identified as critical to device fabrication. Calendering and electroless plating were investigated as methods to improve these properties. Both methods aimed to modify the surface roughness and conductivity, with the plating study also modifying the work function
Highly efficient multilayer organic pure-blue-light emitting diodes with substituted carbazoles compounds in the emitting layer
Bright blue organic light-emitting diodes (OLEDs) based on
1,4,5,8,N-pentamethylcarbazole (PMC) and on dimer of N-ethylcarbazole
(N,N'-diethyl-3,3'-bicarbazyl) (DEC) as emitting layers or as dopants in a
4,4'-bis(2,2'-diphenylvinyl)-1,1'-biphenyl (DPVBi) matrix are described. Pure
blue-light with the C.I.E. coordinates x = 0.153 y = 0.100, electroluminescence
efficiency \eta_{EL} of 0.4 cd/A, external quantum efficiency \eta_{ext.} of
0.6% and luminance L of 236 cd/m2 (at 60 mA/cm2) were obtained with PMC as an
emitter and the 2,9-dimethyl-4,7-diphenyl-1,10-phenantroline (BCP) as a
hole-blocking material in five-layer emitting devices. The highest efficiencies
\eta_{EL.} of 4.7 cd/A, and \eta_{ext} = 3.3% were obtained with a four-layer
structure and a DPVBi DEC-doped active layer (CIE coordinates x = 0.158,
y=0.169, \lambda_{peak} = 456 nm). The \eta_{ext.} value is one the highest
reported at this wavelength for blue OLEDs and is related to an internal
quantum efficiency up to 20%
Cathodic and Anodic Material Diffusion in Polymer/Semiconductor-Nanocrystal Composite Devices
In the present day, the information technologies and telecommunications sector
continually increase their demand for low cost, low power consumption, high
performance electroluminescent devices for display applications. Furthermore,
general lighting applications, such as white light and large array colour
displays, would also benefit from an increase in the overall efficiency. Several
technologies are being investigated to fulfill these needs, such as organic
light emitting diodes (OLED), polymeric light emitting diodes (PLED) and field
effect emission devices. A new and promising technology is light emitting
devices (LEDs) based on nanostructured materials. With organic LEDs (OLEDs)
already making an impact on the market in an increasingly large number of
applications, hybrid technologies based on organic/inorganic nano-composites are
a potential the next step. The incorporation of highefficiency fluorescent
semiconductor nanoparticles has been shown to have a beneficial effect on device
performance, [1] modify the colour output from the device 2 and provide a
simplified route to generation of LED type devices. [3
High-Contrast OLEDs with High-Efficiency
Peer reviewed: YesNRC publication: Ye
Synthesis and optoelectronic properties of new ethynylated pyrazine derivatives
Several diaryleneethynylpyrazine derivatives, in which the pyrazine unit is electron-deficient, have been synthesised using Sonogashira palladium-catalysed cross-coupling reactions. Compound 32, an important intermediate in the synthesis of diaryleneethynylpyrazine derivatives was made by a modified literature procedure which improved the yield. Examination of optical absorption and photoluminescence spectra of compound 37 shows that the pyrazine unit does not change the behaviour significantly compared to analogue 42, while compound 38 shows pyridine substituents have a profound effect on the photophysics of these pyrazine systems. The redox properties of representative compound 37 were studied by cyclic voltammetry, which shows that reduction of 37 to its radical anion occurs as a reversible process at high negative potentials of ca. -1.87 V. The X-ray crystal structure of 37 is also presented. Quantum mechanical calculations of the geometry and electronic structure were performed for compound 37; the known phenylene analogue 42 was calculated at the same level for comparison. The results show that the energies of both HOMO and LUMO orbitals of 37 are decreased compared to 42. The calculated value of the HOMO-LUMO gap of 37 (3.56 eV) is close to that estimated from the red edge of the longest wavelength absorption (382 nm = 3.25 eV)
- …