Following recent advances in the manipulation of atoms trapped near 1D waveguides and proposals to use surface acoustic waves on piezoelectric substrates for the same purpose, the potential of two‐dimensional platforms is shown. Directional emission of atoms near photonic crystal slabs with square symmetry is used, in the ideal case, to build perfect subradiant states of 2 distant atoms, possible in 2D only for finite lattices with perfectly reflecting boundaries. These allow the design of massively parallel 1D arrays of atoms above a single crystal, useful for multi‐port output of nonclassical light, by exploiting destructive interference of guided resonance modes. Directionality of the emission is shown to be present whenever a linear iso‐frequency manifold is present in the dispersion relation of the crystal. Multi‐atom radiance properties can be predicted from a simple cross‐talk coefficient of a master equation, in good agreement with exact atom‐crystal dynamics, showing its predictive power. Departing from the ideal theoretical case, possible experimental issues in photonic crystal implementations are also discussed, and an outlook of other relevant modern platforms for 2D propagation of excitations is given. 相似文献
Periodically nanopatterned Si structures have been prepared by using a nanosphere lithography technique. The formed nanopatterned structures exhibit good anti‐reflection and enhanced optical absorption characteristics. The mean surface reflectance weighted by AM1.5 solar spectrum (300–1200 nm) is as low as 5%. By depositing Si quantum dot/SiO2 multilayers (MLs) on the nanopatterned Si substrate, the optical absorption is higher than 90%, which is significantly improved compared with the same multilayers deposited on flat Si substrate. Furthermore, the prototype n‐Si/Si quantum dot/SiO2 MLs/p‐Si heterojunction solar cells has been fabricated, and it is found that the external quantum efficiency is obviously enhanced for nanopatterned cell in a wide spectral range compared with the flat cell. The corresponding short‐circuit current density is increased from 25.5 mA cm?2 for flat cell to 29.0 mA cm?2 for nano‐patterned one. The improvement of cell performance can be attributed both to the reduced light loss and the down‐shifting effect of Si quantum dots/SiO2 MLs by forming periodically nanopatterned structures. 相似文献
CdSeS quantum dots (QDs) are firstly introduced into a NiO photocathode for photocathodic dye‐sensitized solar cells (p‐DSCs). The optimized sample exhibits a short‐circuit density (14.68 mA cm?2) and power conversion efficiency (1.02%) that are almost one order of magnitude higher than the reported value of p‐QDSCs. Steady‐state photoluminescence and time‐resolved photoluminescence measurements indicate that the photoexcited holes can be almost completely injected from CdSeS QDs into the valence band of NiO. At the same time, it can be observed from electrochemical impedance spectra measurements. 相似文献
A comprehensive review considering recent advances in self‐collimation and its applications in optical integration is covered in the current article. Self‐collimation is compared to the conventional technique of photonic bandgap engineering to control the light propagation in photonic crystal‐based structures. It is fully discussed how the self‐collimation phenomenon can be tailored to be independent of the incident angle and polarization. This adds substantial flexibility to the structure to overcome light coupling challenges and simultaneously aids in the omission of bulk and challenging elements, including polarizers and lenses from optical integrated circuits. Additionally, designed structures have the potential to be rescaled to operate in any desired frequency range thanks to the scalability rule in the field of electromagnetics. Moreover, it is shown that one can boost the coupling efficiency by applying an anti‐reflection property to the structure, which provides not only efficient index matching but also the matching between external waves with uniform amplitude and Bloch waves with periodic amplitude. 相似文献
Quantum dot‐sensitized solar cells (QDSSCs) have emerged as a promising solar architecture for next‐generation solar cells. The QDSSCs exhibit a remarkably fast electron transfer from the quantum dot (QD) donor to the TiO2 acceptor with size quantization properties of QDs that allows for the modulation of band energies to control photoresponse and photoconversion efficiency of solar cells. To understand the mechanisms that underpin this rapid charge transfer, the electronic properties of CdSe and PbSe QDs with different sizes on the TiO2 substrate are simulated using a rigorous ab initio density functional method. This method capitalizes on localized orbital basis set, which is computationally less intensive. Quite intriguingly, a remarkable set of electron bridging states between QDs and TiO2 occurring via the strong bonding between the conduction bands of QDs and TiO2 is revealed. Such bridging states account for the fast adiabatic charge transfer from the QD donor to the TiO2 acceptor, and may be a general feature for strongly coupled donor/acceptor systems. All the QDs/TiO2 systems exhibit type II band alignments, with conduction band offsets that increase with the decrease in QD size. This facilitates the charge transfer from QDs donors to TiO2 acceptors and explains the dependence of the increased charge transfer rate with the decreased QD size. 相似文献
The optical equivalent of the quantum mechanical oscillator is demonstrated in a photonic crystal cavity, owing to the balance of the background dispersion and a bichromatic potential. Consequently, several equi‐spaced resonances with large loaded Q factors are obtained within a very tiny volume. A detailed statistical analysis is carried out by exploiting the complex reflection spectra measured with Optical Coherent Tomography. The log‐normal distribution of the intrinsic Q‐factors is centered at 0.7 million. The device is made of Ga0.5In0.5P in order to suppress the two photon absorption in the Telecom spectral range considered here. This is crucial to turn the strong localization of light into ultra‐efficient parametric interactions. 相似文献
Herein a novel approach is reported to achieve tunable and high photoluminescence (PL) quantum yield (QY) from the self‐grown spherical TiO2 quantum dots (QDs) on fluorine doped TiO2 (F‐TiO2) flowers, mesoporous in nature, synthesized by a simple solvothermal process. The strong PL emission from F‐TiO2 QDs centered at ≈485 nm is associated with shallow and deep traps, and a record high PL QY of ≈5.76% is measured at room temperature. Size distribution and doping of F‐TiO2 nanocrystals (NCs) are successfully tuned by simply varying the HF concentration during synthesis. During the post‐growth rapid thermal annealing (RTA) under vacuum, the arbitrary shaped F‐TiO2 NCs transform into spherical QDs with smaller sizes and it shows dramatic enhancement (≈163 times) in the PL intensity. Electron spin resonance (ESR) and X‐ray photoelectron spectroscopy (XPS) confirm the high density of oxygen vacancy defects on the surface of TiO2 NCs. Confocal fluorescence microscopy imaging shows bright whitish emission from the F‐TiO2 QDs. Low temperature and time resolved PL studies reveal that the ultrafast radiative recombination in the TiO2 QDs results in highly efficient PL emission. A highly stable, biologically inert, and highly fluorescent TiO2 QDs/flowers without any capping agent demonstrated here is significant for emerging applications in bioimaging, energy, and environmental cleaning. 相似文献
The demonstration of high efficiency and color tunability has brought organic light‐emitting devices (OLEDs) into the lighting and display market. High efficiency is one of the key issues for their commercial applications, for which much effort has been devoted to developing novel materials and device structures. It is well known that around 80% of the generated photons are trapped in OLED structure, so that there is still the greatest scope for significant improvements in its efficiency. This has driven the research towards the integration of micro/nano patterns into device structures that benefit from their abilities in manipulating the generation and propagation of photons. Micro/nano patterns with random or periodic morphologies have demonstrated their effect on the outcoupling of the trapped photons within the device. Moreover, the emitting properties other than the light extraction could be manipulated by introducing the micro/nano patterns. This article reviews the recent progresses in improving the light extraction and manipulating the emission properties of the OLEDs through the introduction of the micro/nano patterns by various fabrication strategies. The light manipulation of the micro/nano patterns in organic photovoltaics is briefly discussed considering its similar working principle and fabrication strategies to that of the OLEDs.