Stabilization of ultra-small [Ag2]2+ and [Agm]n+ nano-clusters through negatively charged tetrahedrons in oxyfluoride glass networks: To largely enhance the luminescence quantum yields.

Abstract

Herein, three different silver species were stably formed in SiO2-Al2O3-B2O3-Na2O-ZnF2-CaF2 glasses and were identified by their characteristic luminescence bands: violet blue luminescence (Ag+: 4d95s1 → 4d10), green white molecular fluorescence (molecule-like [Agm]n+, named ML-Ag) and orange molecular fluorescence ([Ag2]2+ pairs). Due to the relatively low aggregation degrees of [Agm]n+ and [Ag2]2+, non-radiative transitions were highly suppressed, and the PL quantum yields (QYs) of ML-Ag and [Ag2]2+ pairs reached 73.7% and 89.7%, respectively. The substitution of 0.5B2O3-0.5Na2O with SiO2 promoted the partial reduction of Ag+ to Ag0 and the subsequent aggregation of Ag+ and Ag0 to form [Agm]n+ (ML-Ag). The absence of Na2O also resulted in an increasing amount of Ag+-Ag+ pairs with closing interionic distance to form [Ag2]2+ in glass. According to the X-ray photoelectron spectra (XPS) and magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectra, a solubility strategy and a charge compensation model were proposed to describe the transformations between different silver species. The formation of ML-Ag was further controlled via the solubility of Ag+ in glass, whereas [Ag2]2+ centers could be effectively produced by lowering the total amount of other competitive charge compensators, such as Na+, or by introducing negatively charged [BO4]-, [AlO4]-, and [ZnO4]2- tetrahedrons into the glass matrix.