Subpicosecond time-resolved Raman spectroscopy has been used to measure the lifetime of the LO phonon mode in GaN for photoexcited electron-hole pair density ranging from 1016to2×1019cm−3. The lifetime has been found to decrease from 2.5ps, at low density, to 0.35ps, at the highest density. The experimental findings should help resolve the recent controversy over the lifetime of LO phonon mode in GaN.
Defect radiation has been always considered as the most important loss for an emitter based on band gap emission. Here, we propose a novel approach which goes against this conventional wisdom. Based on the resonance effect between the surface plasmon of metal nanoparticles and defect emission, it is possible to convert the useless defect radiation to the useful excitonic emission with a giant enhancement factor. Through the transfer of the energetic electrons excited by surface plasmon from metal nanoparticles to the conduction band of the emitter, the band gap emission can be greatly enhanced, while the defect emission can be suppressed to noise level.
Decay of the longitudinal-optical (LO) phonons in wurtzite GaN has been studied by subpicosecond time-resolved Raman spectroscopy. Our experimental results show that among the various possible decay channels, the LO phonons in wurtzite GaN decay primarily into a large wave-vector TO and a large wave-vector LA or TA phonon. These experimental results are consistent with the recent theoretical calculations of the phonon dispersion curves for wurtzite GaN.
We demonstrate an unconventional and revolutionary method for selective inactivation
of micro-organisms by using near-infrared femtosecond laser pulses. We show
that if the wavelength and pulse width of the excitation femtosecond laser are
appropriately selected, there exists a window in power density that enables us to achieve
selective inactivation of target viruses and bacteria without causing cytotoxicity in
mammalian cells. This strategy targets the mechanical (vibrational) properties
of micro-organisms, and thus its antimicrobial efficacy is likely unaffected by
genetic mutation in the micro-organisms. Such a method may be effective against a
wide variety of drug resistant micro-organisms and has broad implications in
disinfection as well as in the development of novel treatments for viral and bacterial
pathogens.
We report experimental results on the inactivation of encephalomyocarditis virus, M13 bacteriophage, and Salmonella typhimurium by a visible femtosecond laser. Our results suggest that inactivation of virus and bacterium by a visible femtosecond laser involves completely different mechanisms. Inactivation of viruses by a visible femtosecond laser involves the breaking of hydrogen∕hydrophobic bonds or the separation of the weak protein links in the protein shell of a viral particle. In contrast, inactivation of bacteria is related to the damage of their DNAs due to irradiation of a visible femtosecond laser. Possible mechanisms for the inactivation of viruses and bacteria are discussed.
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