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PNNL-13501 - Pacific Northwest National Laboratory

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Spontaneous Formation of Cu2O Nano-Corrals<br />

In addition to Cu2O quantum dots, we have also<br />

developed a process for growth of Cu2O nano-corrals on<br />

SrTiO3 substrates. These were grown by first depositing a<br />

layer of copper metal on a SrTiO3 substrate, then<br />

subsequently annealing the Cu/SrTiO3 in oxygen plasma<br />

at elevated temperatures. The resulting surface exhibited<br />

corrals with diameters ranging from approximately 50 nm<br />

to 80 nm, as shown in Figure 3. The chemical state of<br />

copper was examined by x-ray photoelectron<br />

spectroscopy. Results confirmed that copper at the<br />

surface was copper (I) instead of copper (II), suggesting<br />

these corrals consisted of Cu2O instead of a CuO phase.<br />

The importance of this finding is that these nanoscale ring<br />

structures can exhibit artificial magnetic and conducting<br />

properties, as was predicted by Laudauer et al. (1985) and<br />

Figure 3. An atomic force microscopy image of Cu 2O nanocorrals<br />

formed on a SrTiO 3 substrate surface<br />

recently confirmed by Lorke et al. (2000) on InAs. The<br />

driving force for the formation of these nano-corrals is<br />

currently unclear. We speculate that they are due to stress<br />

relaxation and subsequent dislocation formation at the<br />

Cu2O/SrTiO3 interface.<br />

Photoluminescence Behavior of Cu2O Quantum Dots<br />

One potential application of the Cu2O/SrTiO3 quantumdot<br />

system is photocatalysis. It is important to<br />

characterize the optical properties of this system. We<br />

conducted photoluminescence measurements on<br />

Cu2O/SrTiO3. Results are shown in Figure 4. The<br />

photoluminescence spectrum shows a broad distribution<br />

Figure 4. Photoluminescence spectrum of Cu 2O quantum<br />

dots showing typical luminescence behavior from quantum<br />

dots. The spectrum was taken at 18 K to eliminate photon<br />

scattering effects.<br />

with a peak centered around 480 nm. The breadth of the<br />

spectrum is due to the size distribution of quantum dots,<br />

as has been demonstrated in other quantum dots systems<br />

(Bimberg et al. 1999). The fact that these Cu2O quantum<br />

dots exhibit photoluminescence under above-gap<br />

irradiation suggests that the defect density of this system<br />

is low. It would otherwise show no photoluminescence<br />

because of scattering and recombinations mediated by<br />

defects.<br />

References<br />

Bimberg D, M Grundmann, and N Ledentsov. 1999.<br />

Quantum dot heterostructure. John Wiley & Sons, New<br />

York.<br />

Laudauer R et al. 1985. Phys. Lett. 96A, 365.<br />

Lorke A, RJ Luyken, AO Govorov, and JP Kotthaus.<br />

2000. “Spectroscopy of nanoscopic semiconductor<br />

rings.” Phys. Rev. Lett. 84, 2223.<br />

Presentation<br />

Liang Y, D McCready, S Lea, S Chambers, and S Gan.<br />

November 2000. “A novel stable quantum dot system for<br />

electron-hole pair separation: self-assembled Cu2O<br />

quantum dots on SrTiO3(001).” Material Research<br />

Society Meeting, Boston.<br />

Micro/Nano Technology 355

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