Photo-mediated Seedless Synthesis of Silver Nanoparticles Using CW-Laser and Sunlight Irradiation F. Félix-Domínguez 1 , R. C. Carrillo-Torres 2 , J. A. González 1 , J. Hernández-Paredes 2 , R. Sánchez- Zeferino 2 , M. E. Álvarez-Ramos 2 . 1. Doctorado en Nanotecnología, Departamento de Física, Universidad de Sonora, Hermosillo, Sonora, México. 2. Departamento de Física, Universidad de Sonora, Hermosillo, Sonora, México. Noble metal nanoparticles, such as silver nanoparticles (AgNPs), have found technological applications due to their localized surface plasmon resonance (LSPR). In this context, a great quantity of synthetic methods for the preparation of AgNPs have been developed, including photo-chemical synthesis [1]. The photo-chemical synthesis is an advantageous technique because it is simple and environmentally friendly [2]. In this work, synthesis of AgNPs was performed via direct photo-reduction process of the silver nitrate and sodium citrate solutions without the previous addition of silver seeds. Silver nanoparticles were synthesized in aqueous solution using a mixture of silver nitrate (5 mM) as metallic precursor and sodium citrate (3 mM) as reducing agent. 300 μL of reaction mixture was placed in a polystyrene cuvette and was irradiated with laser light (λ = 488 nm, 130 mW) from an Ar ion CW- Laser (Melles-Griot, USA) or direct sunlight (near noon) varying irradiation time from 5 to 60 minutes. Both synthesis took place at ~20 °C. Scanning Transmission Electron Microscopy (STEM) analysis was carried out with a field emission microscope JEOL JSM-7800F, operated at 30 kV. The synthesis is achieved by photo-oxidation of sodium citrate to acetone-1,3-dicarboxylate, reducing ionic silver to Ag 0 in the process. Furthermore, acetone-1,3-dicarboxylate can be chemisorbed on the nanoparticle surface controlling their growth and also stabilizing the nanostructures in the solution [3]. Therefore, the only residual product is CO2, which makes of this synthetic route a clean technique. In all cases laser synthesized AgNPs showed high size polydispersity. The size of the NPs ranges from a few nanometers (~10 nm) up to more than 100 nm, forming large aggregates with irregular morphology (Figure 1). Moreover, it can be seen that as the irradiation time elapses there is a decrease in the number of the smaller NPs. It is worth to mention that the agglomeration of NPs hampered to obtain the size distribution curve. Sunlight mediated AgNPs showed better size distribution and morphologies than that obtained by laser irradiation. The size of the nanoparticles increased with the increase of the irradiation time (Figure 2 a-c). It is proposed that the improvement in size and morphology is achieved thanks to the uniform illumination over the reaction cuvette when using sunlight. It is important to note that the laser beam passes through a small volume of reaction mixture causing a localized reaction in the sample. Sunlight mediated synthesis overcomes the later, so we can assume that all the solution receives the same quantity of light in every point at the same time, inducing a uniform nucleation and growth of the nanoparticles in the solution. In order to study the effect of silver/citrate ratio on the size and morphology of the NPs, we performed an experiment using a lower silver nitrate concentration (0.1 mM) keeping constant the sodium citrate concentration. This solution was exposed to 60 minutes of sunlight. Figure 2d shows the obtained nanoparticles. In this case, it is possible to observe small uniform spheroidal nanoparticles and large plate- 1902 doi:10.1017/S1431927617010170 Microsc. Microanal. 23 (Suppl 1), 2017 © Microscopy Society of America 2017 https://doi.org/10.1017/S1431927617010170 Downloaded from https://www.cambridge.org/core. IP address: 54.234.194.95, on 29 Nov 2021 at 13:17:48, subject to the Cambridge Core terms of use, available at https://www.cambridge.org/core/terms.