Defect emission photoluminescence peak tuning by encapsulation of Au-NPs on ZnO mesoporous nanosponges

We synthesized Au nanoparticles (Au-NPs) encapsulated zinc oxide (ZnO:Au) nanosponges by the fraternization of ZnO nanoflowers with HCl (0-30 mM) concentrated colloidal Au-NPs at room temperature. The crystallite size (D) of mesoporous ZnO:Au decreased from 44 nm to 22 nm and the strain (tau) increased from 2.5 x 10(-3) to 4.7 x 10(-3) as the HCl concentration of colloidal Au-NPs increased from 0 mM to 30 mM. For elemental composition of ZnO:Au nanosponges, the STM-mapping confirmed the Au-NPs encapsulation on nanostructured ZnO. The bandgap, E-g, and the Urbach energy, E-u, of ZnO:Au decreased from 3.26 to 2.96 eV, and from 0.335 to 0.318 eV, as the colloidal Au-NPs increased from 0 mM to 30 mM, respectively. The structural and microstructure analysis showed the sponge like morphology along with wurtzite hexagonal structure of ZnO, which tuned the PL emission for the sensor selectivity. The visible emission of ZnO:Au nanosponges was greatly tuned from 600 nm to 500 nm with respect to the HCl diluted colloidal Au-NPs. The excellent photoluminescence (PL) performance of nanostructured ZnO:Au was attributed to the surface-plasmon-mediated sequential transfer of defect energy from ZnO to Au and electron transfer from excited Au to ZnO.

Automated summary

Au nanoparticles encapsulated zinc oxide nanosponges were synthesized by grafting colloidal Au nanoparticles with ZnO nanoflowers at room temperature. The size of the nanosponges decreased and the strain increased with the concentration of colloidal Au nanoparticles. STM mapping and structural analysis confirmed the encapsulation of Au nanoparticles on ZnO. The visible emission and photoluminescence properties were also affected by the concentration of colloidal Au nanoparticles.