O sub(2) adsorption dependent photoluminescence emission from metal oxide nanoparticles

• Published in: Physical chemistry chemical physics : PCCP Vol. 16; no. 43; pp. 23922 - 23929
• Main Authors: Gheisi, Amir R, Neygandhi, Chris, Sternig, Andreas K, Carrasco, Esther, Marbach, Hubertus, Thomele, Daniel, Diwald, Oliver
• Format: Journal Article
• Language: English
• Published: 01.10.2014
• Subjects: Adsorption; Magnesium oxide; Metal oxides; Nanoparticles; Optical properties; Photoluminescence; Surface chemistry; Zinc oxide
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c4cp03080j

Optical properties of metal oxide nanoparticles are subject to synthesis related defects and impurities. Using photoluminescence spectroscopy and UV diffuse reflectance in conjunction with Auger electron spectroscopic surface analysis we investigated the effect of surface composition and oxygen adsorption on the photoluminescence properties of vapor phase grown ZnO and MgO nanoparticles. On hydroxylated MgO nanoparticles as a reference system, intense photoluminescence features exclusively originate from surface excitons, the radiative deactivation of which results in collisional quenching in an O sub(2) atmosphere. Conversely, on as-prepared ZnO nanoparticles a broad yellow emission feature centered at h nu sub(Em) = 2.1 eV exhibits an O sub(2) induced intensity increase. Attributed to oxygen interstitials as recombination centers this enhancement effect originates from adsorbate-induced band bending, which is pertinent to the photoluminescence active region of the nanoparticles. Annealing induced trends in the optical properties of the two prototypical metal oxide nanoparticle systems, ZnO and MgO, are explained by changes in the surface composition and underline that particle surface and interface changes that result from handling and processing of nanoparticles critically affect luminescence.