It has been well known that the wavelength of the light emitted from the alloy of zinc oxide and magnesium oxide (hereinafter referred to as “ZnMgO”) decreases with increasing magnesium concentration. In this research, we have found that the light emission efficiency of the alloy increases with decreasing the wavelength of the emitted light, contrary to the conventional semiconductors. This new finding is mainly because we are able to produce extremely high-quality epitaxial thin films of “ZnMgO”, which had previously been very difficult to realize; we have demonstrated a real potential of “ZnMgO” that had previously been overlooked.
Figure 1 is a schematic illustration of the cross-sectional structure of our samples. We used sapphire single crystals as substrates, and we have grown successive layers of single crystalline MgO, ZnO, and “ZnMgO” on the substrates by the molecular-beam epitaxy method. The molecular-beam epitaxy is a method to grow single crystalline epitaxial thin films by supplying vaporized elements as the source materials in the form of molecular beams on the substrates placed in ultrahigh vacuum containers. We used extremely highly pure zinc and magnesium as the source materials for “ZnMgO”. We also used oxygen radicals for the source of oxygen.
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Figure 1 Schematic illustration of the cross section of the samples
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Figure 2 shows the photoluminescence spectra obtained at 1.4 K for three samples with different magnesium concentration. The ultraviolet laser light was used for the excitation. The extremely wide emission bands from “ZnMgO” layers were observed at 335 - 365 nm. Figure 3 shows the relationship between the integrated intensity of the emission band (the area under the curves) and the concentration of magnesium in the samples. The emission intensity from “ZnMgO” layers increases with increasing magnesium concentration, indicating that the addition of magnesium into zinc oxide increases the light emission efficiency remarkably.
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Figure 2 Magnesium-concentration dependence of the photoluminescence emission spectra of “ZnMgO” at 1.4K
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Figure 3 Magnesium-concentration dependence of the photoluminescence emission intensity at 1.4K
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Figure 4 shows the relationships between the emission intensities from “ZnMgO” layers and the temperature of the samples: the intensity of emissions from the samples decreases gradually as their temperature is increased. It is well known, in general, the light emission efficiency of materials decreases with increasing temperature. The important fact shown in Figure 4 is that the degree of the decrease in emission efficiency becomes smaller with increasing magnesium concentration, although the emission intensity gradually decreases as the temperature of the sample is increased. This finding is very important since we usually use the light emission devices at room temperature (around 300 K).
We think that the same mechanism is responsible for the results shown in both Figure 3 and Figure 4. The mechanism of the very high light emission efficiency in gallium nitride system, for example, is believed to be due to the presence of an inhomogeneous concentration distribution of indium in the samples, and we believe that the same mechanism is responsible for “ZnMgO”. That is, the concentration of magnesium in the samples is fluctuating in space, and the light emission efficiency of the samples increases markedly due to the fluctuation. We believe that this significant increase in light emission efficiency is because of the exciton localization induced by the spatial fluctuation of the magnesium concentration.
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Figure 4 Temperature dependence of the photoluminescence emission intensity.
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