Ultrafast time-resolved photoluminescence spectroscopy following one-and two-photon excitations of ZnO powder is used to gain unprecedented insight into the surprisingly high external quantum efficiency of its "green" defect emission band. The role of exciton diffusion, the effects of reabsorption, and the spatial distributions of radiative and nonradiative traps are comparatively elucidated for the ultraviolet excitonic and "green" defect emission bands in both unannealed nanometer-sized ZnO powders and annealed micrometersized ZnO:Zn powders. We find that the primary mechanism limiting quantum efficiency is surface recombination because of the high density of nonradiative surface traps in these powders. It is found that unannealed ZnO has a high density of bulk nonradiative traps as well, but the annealing process reduces the density of these bulk traps while simultaneously creating a high density of green-emitting defects near the particle surface. The data are discussed in the context of a simple rate equation model that accounts for the quantum efficiencies of both emission bands. The results indicate how defect engineering could improve the efficiency of ultraviolet-excited ZnO:Zn-based white light phosphors.

A series of continuous-wave spectroscopic measurements elucidates the mechanism responsible for the technologically important green emission from deep-level traps in ZnO:Zn powders. Analysis of low-temperature photoluminescence (PL) and PL excitation spectra for bound excitons compared to the temperature-dependent behavior of the green emission reveals a deep correlation between green PL and specific donor-bound excitons. Direct excitation of these bound excitons produces highly efficient green emission from near-surface defects. When normalized by the measured external quantum efficiency, the integrated PL for both excitonic and green emission features grows identically with excitation intensity, confirming the strong connection between green emission and excitons. The implications of these findings are used to circumscribe operational characteristics of doped ZnO-based white light phosphors whose quantum efficiency is almost twice as large when the bound excitons are directly excited.

The effect of laser excitation power density on the efficiency of intrinsic defect emission in ZnO powders was characterized by varying the laser irradiance over three orders of magnitude and monitoring changes in the samples' photoluminescence. The external quantum efficiency of the visible wavelength, broadband defect photoluminescence was found to depend not only on laser irradiance but also on temperature and prior annealing conditions. This material system is potentially useful as an ultraviolet-photoexcited, white light phosphor under low-power excitation ͑Ͻ0.2 W / cm 2 ͒ at room temperature and below.

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We report the mode locking of a diode pumped Nd:YVO 4 crystal laser by using a transmission type single walled carbon nanotube saturable absorber. The laser operated at 1064 nm pumped by a fiber coupled laser diode with the cavity length of 1826 mm, generated a pulse width of 14 ps at a repetition rate of 82 MHz. The output power of 120 mW was obtained at the absorbed pumping power of 1400 mW.