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Quantum efficiency relative

The internal quantum efficiency of a LED is governed by the relative radiative and nonradiative recombination rates. The total recombination rate,... [Pg.114]

The first detailed investigation of the reaction kinetics was reported in 1984 (68). The reaction of bis(pentachlorophenyl) oxalate [1173-75-7] (PCPO) and hydrogen peroxide cataly2ed by sodium saUcylate in chlorobenzene produced chemiluminescence from diphenylamine (DPA) as a simple time—intensity profile from which a chemiluminescence decay rate constant could be determined. These studies demonstrated a first-order dependence for both PCPO and hydrogen peroxide and a zero-order dependence on the fluorescer in accord with an earher study (9). Furthermore, the chemiluminescence quantum efficiencies Qc) are dependent on the ease of oxidation of the fluorescer, an unstable, short-hved intermediate (r = 0.5 /is) serves as the chemical activator, and such a short-hved species "is not consistent with attempts to identify a relatively stable dioxetane as the intermediate" (68). [Pg.266]

It is well-known that para substituents on the phenyl groups of H2TPP have no influence on the tautomerism rates in the ground state (see Section III,A,1). In the case of PHB, there seems to be only a small substituent effect on <1>phb (the quantum efficiency for hole burning) through modification of the relative energy of Ti (93CM366). [Pg.28]

Fluorescent small molecules are used as dopants in either electron- or hole-transporting binders. These emitters are selected for their high photoluminescent quantum efficiency and for the color of their emission. Typical examples include perylene and its derivatives 44], quinacridones [45, penlaphenylcyclopenlcne [46], dicyanomethylene pyrans [47, 48], and rubrene [3(3, 49]. The emissive dopant is chosen to have a lower excited state energy than the host, such that if an exciton forms on a host molecule it will spontaneously transfer to the dopant. Relatively small concentrations of dopant are used, typically in the order of 1%, in order to avoid concentration quenching of their luminescence. [Pg.535]

Interesting results have also been obtained with light-induced oscillations of silicon in contact with ammonium fluoride solutions. The quantum efficiency was found to oscillate complementarity with the PMC signal. The calculated surface recombination rate also oscillated comple-mentarily with the charge transfer rate.27,28 The explanation was a periodically oscillating silicon oxide surface layer. Because of a periodically changing space charge layer, the situation turned out to be nevertheless relatively complicated. [Pg.487]

Figure 9. Quantum efficiency of a Rockwell 2Kx2K HAWAII array. The atmospheric windows of I, H, and K are shown. Note the relatively constant QE across the 1-2.5 p,m wavelength region, with peak QE of 84% in the K-band (centered at 2.2 /um). Eigure courtesy of J. Garnett, Rockwell Scientific. Figure 9. Quantum efficiency of a Rockwell 2Kx2K HAWAII array. The atmospheric windows of I, H, and K are shown. Note the relatively constant QE across the 1-2.5 p,m wavelength region, with peak QE of 84% in the K-band (centered at 2.2 /um). Eigure courtesy of J. Garnett, Rockwell Scientific.
The quantum efficiency of fluorescence of a molecule is decided by the relative rates of fluorescence, internal conversion and intersystem crossing to the triplet state. Up to the present time it has proved impossible to predict these relative rates. Thus, whilst it is now possible to calculate theoretically the wavelengths of maximum absorption and of maximum fluorescence of an organic molecule, it remains impossible to predict which molecular structures will be strong fluorescers. Design of new FBAs still relies on semi-empirical knowledge plus the instinct of the research chemist. [Pg.302]

A fluorophore in the proximity of the NP senses the altered EM-field and its fluorescence properties are consequently modified. There are (at least) two enhancement effects an increase in the excitation of the fluorophore and an increase in its quantum efficiency (QE). The increased excitation of the fluorophore is directly proportional to the to the square of the strength of the E-field and is a function of the wavelength and relative position of the NP. The maximum enhancement of this type is achieved if /.res equals the peak absorption wavelength of the dye. [Pg.210]

The luminance reaches 100 cd/m2 at 2.5 V with EL efficiency of 2.5 cd/ A. The corresponding external quantum efficiency is about 2% ph/el. At —10 V bias, the photosensitivity at 430 nm is around 90 mA/W, corresponding to a quantum yield of 20% el/ph [135], The carrier collection efficiency at zero bias was relatively low in the order of 10-3 ph/el. The photosensitivity showed a field dependence with activation energy of 10 2 eV [135], This value is consistent with the trap distribution measured in the PPV-based conjugated polymers [136,137],... [Pg.19]

There is no reason why the same principle cannot be applied for light-emitting polymers as host materials to pave a way to high-efficiency solution-processible LEDs. In fact, polymer-based electrophosphorescent LEDs (PPLEDs) based on polymer fluorescent hosts and lanthanide organic complexes have been reported only a year after the phosphorescent OLED was reported [8]. In spite of a relatively limited research activity in PPLEDs, as compared with phosphorescent OLEDs, it is hoped that 100% internal quantum efficiency can also be achieved for polymer LEDs. In this chapter, we will give a brief description of the photophysics beyond the operation of electrophosphorescent devices, followed by the examples of the materials, devices, and processes, experimentally studied in the field till the beginning of 2005. [Pg.414]

One of the major limitations in semiconductor photocatalysis is the relatively low value of the overall quantum efficiency mainly due to the high rate of recombination of photoinduced electron-hole pairs at or near the surface. Some success in enhancing the efficiency of photocatalysts... [Pg.441]


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