Browsing by Subject "Radiative energy transfer"

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    Nanocrystal integrated light emitting diodes based on radiative and nonradiative energy transfer for the green gap
    (IEEE, 2009) Nizamoğlu, Sedat; Sarı, Emre; Baek J.-H.; Lee I.-H.; Demir, Hilmi Volkan
    Recently the photometric conditions for ultra-efficient solid-state lighting have been discussed [1-2]. These studies show that a luminous efficacy of optical radiation at 408 lm/Wopt and a color rendering index (CRI) of 90 at a correlated color temperature (CCT) of 3000 K are achievable at the same time. For this purpose light emitting diodes (LEDs) emitting in blue, green, yellow, and red colors at 463, 530, 573, and 614 nm with relative optical power levels of 1/8, 2/8, 2/8, and 3/8, are required, respectively [1-2]. Although InxGa1-xN material system is capable to cover the whole visible by changing the In composition (x), it is technically extremely challenging to obtain efficient green/yellow light emitting diodes especially at those wavelengths (i.e., at 530 nm and 573 nm, respectively) due to reduced internal quantum efficiency [2-4]. Furthermore, by using the (Al xGa1-x)1-yInyP quaternary alloy it is also possible to cover from 650 nm to 580 nm. However, the efficiencies significantly decrease towards green. Therefore, there exists a significant gap in the green-yellow spectral regions (known as "the green gap") to make efficient light emitting diodes. To address this green gap problem, we propose and demonstrate proof-of-concept nanocrystal (NCs) hybridized green/yellow light emitting diodes that rely on both radiative energy transfer and nonradiative energy transfer (i.e., FRET-Förster resonance energy transfer) for color conversion on near-ultraviolet (near-UV) LEDs.
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    Phonon-assisted nonradiative energy transfer from colloidal quantum dots to monocrystalline bulk silicon
    (IEEE, 2012) Yeltik, Aydan; Güzeltürk, Burak; Hernandez-Martinez, Pedro L.; Demir, Volkan Demir
    Silicon is one of the most dominant materials in photovoltaics. To increase optical absorption of silicon solar cells, colloidal quantum dots (QDs) have been proposed as a good sensitizer candidate owing to their favorably high absorption cross-section and tunable emission and absorption properties. To this end, QD sensitization of silicon has previously been studied by mostly facilitating radiative energy transfer (RET) [1,2]. Although RET based sensitization has achieved a considerable increase in conversion efficiencies in silicon photovoltaics, RET is fundamentally limited due to the effective coupling problem of emitted photons to silicon. Alternatively, nonradiative energy transfer (NRET), which relies on near field dipole-dipole coupling [3], has been shown to be feasible in sensitizer-silicon hybrid systems [4-8]. Although colloidal QDs as a sensitizer have been used to facilitate NRET into silicon, the detailed mechanisms of NRET to an indirect bandgap nonluminecent material, together with the role of phonon assistance and temperature activation, have not been fully understood to date. In this study, we propose a QD-silicon nanostructure hybrid platform to study the NRET dynamics as a function of temperature for distinct separation thicknesses between the donor QDs and the acceptor silicon plane. Here, we show NRET from colloidal QDs to bulk Si using phonon assisted absorption, developing its physical model to explain temperature-dependent lifetime dynamics of NRET in these QD-Si hybrids. © 2012 IEEE.