Identifying and rationalizing the morphological, structural, and optical properties of β-Ag2MoO4 microcrystals, and the formation process of Ag nanoparticles on their surfaces: combining experimental data and first-principles calculations

• Main Authors: Maria T Fabbro, Carla Saliby, Larissa R Rios, Felipe A La Porta, Lourdes Gracia, Máximo S Li, Juan Andrés, Luís P S Santos, Elson Longo
• Format: Article
• Language: English
• Published: Taylor & Francis Group 2015-12-01
• Series: Science and Technology of Advanced Materials
• Subjects: theoretical calculations; morphology; electron beam irradiation; β-ag2moo4
• Online Access: http://dx.doi.org/10.1088/1468-6996/16/6/065002

We present a combined theoretical and experimental study on the morphological, structural, and optical properties of β-Ag2MoO4 microcrystals. β-Ag2MoO4 samples were prepared by a co-precipitation method. The nucleation and formation of Ag nanoparticles on β-Ag2MoO4 during electron beam irradiation were also analyzed as a function of electron beam dose. These events were directly monitored in real-time using in situ field emission scanning electron microscopy (FE-SEM). The thermodynamic equilibrium shape of the β-Ag2MoO4 crystals was built with low-index surfaces (001), (011), and (111) through a Wulff construction. This shape suggests that the (011) face is the dominating surface in the ideal morphology. A significant increase in the values of the surface energy for the (011) face versus those of the other surfaces was observed, which allowed us to find agreement between the experimental and theoretical morphologies. Our investigation of the different morphologies and structures of the β-Ag2MoO4 crystals provided insight into how the crystal morphology can be controlled so that the surface chemistry of β-Ag2MoO4 can be tuned for specific applications. The presence of structural disorder in the tetrahedral [MoO4] and octahedral [AgO6] clusters, the building blocks of β-Ag2MoO4, was used to explain the experimentally measured optical properties.