We report the successful fabrication of a compact deep ultraviolet emission device via a marriage of AlGaN quantum wells and graphene nanoneedle field electron emitters. The device demonstrated a 20-mW deep ultraviolet output power and an approximately 4% power efficiency. The performance of this device may lead toward the realization of an environmentally friendly, convenient and practical deep ultraviolet light source.
We report the successful fabrication of a novel type of blackbody material based on a graphene nanostructure. We demonstrate that the graphene nanostructure not only shows a low reflectance comparable to that of a carbon nanotube array but also shows an extremely high heat resistance at temperatures greater than 2500 K. The graphene nanostructure, which has an emissivity higher than 0.99 over a wide range of wavelengths, behaves as a standard blackbody material; therefore, the radiation spectrum and the temperature can be precisely measured in a simple manner. Here, the spectral emissivities of tungsten and tantalum are experimentally obtained using this ideal blackbody material and are compared to previously reported spectra. We clearly demonstrate the existence of a temperature-independent fixed point of emissivity at a certain wavelength. Both the spectral emissivity as a function of temperature and the cross-over point in the emissivity spectrum are well described by the complex dielectric function based on the Lorentz-Drude model with the phonon-scattering effect.
Fluorescence lifetimes of organic thin films alternately deposited with diamine derivative (TPD) and aluminium quinoline (Alq3) were measured. The alternating deposition structure was shown to enhance the emission from Alq3 in spite of imperfect film structures. Energy transfer from TPD to Alq3 was evidenced by the correlation between lifetime and period number. It was found to be a competitive process with the TPD radiation process, and its rate of TPD radiation was estimated to be 1.2×1010 s-1. The authors suggested that the presence of the region mixed with TPD and Alq3 at the TPD/Alq3 interface plays an important role in the electroluminescence (EL) process. The Alq3 exciton confinement was clarified experimentally since the component of the faster fluorescence lifetime of Alq3 increased in the short-wavelength region. In addition, the authors proposed a possible EL model based on the suppression of the thermal inactivation of Alq3 excitons during their diffusion.
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