de Oliveira Jessica Fernanda Affonso, Cardoso Mateus Borba
Laboratório Nacional de Luz Síncrotron , CEP 13083-970, Caixa Postal 6192, Campinas, São Paulo, Brazil.
Langmuir. 2014 May 6;30(17):4879-86. doi: 10.1021/la403635c. Epub 2013 Dec 31.
It is well known that nanomaterials properties and applications are dependent on the size, shape, and morphology of these structures. Among nanomaterials, silver nanoparticles (AgNPs) have attracted attention since they have considerably versatile properties, such as a variable surface area to volume ratio, which is very useful for many biomedical and technological applications. Within this scenario, small nanoparticle aggregates can have their properties reduced due to the increased size and alterations in their shape/morphology. In this work, silver nanoparticles aggregation was studied through chemical reduction of silver nitrate in the presence of sodium borohydride (reducing agent) and sodium citrate (capping agent). By changing the amount of reducing agent along the reaction, unaggregated and partially aggregated samples were obtained and characterized by UV-vis, zeta potential, and SAXS techniques. pH was measured in every step of the reaction in order to correlate these results with those obtained from structural techniques. Addition of the reducing agent first causes the reduction of Ag(+) to silver nanoparticles. For higher concentrations of sodium borohydrate, the average AgNPs size is increased and NPs aggregation is observed. It was found that zeta potential and pH values have a strong influence on AgNPs formation, since reducing agent addition can induce partial removal of citrate weakly associated on the AgNPs surface and increase the ionic strength of the solution, promoting partial aggregation of the particles. This aggregation state was duly identified by coupling SAXS, zeta potential and pH measurements. In addition, the SAXS technique showed that aggregates formed along the process are elongated-like particles due to the exponential decay evidenced through SAXS curves.
众所周知,纳米材料的性质和应用取决于这些结构的尺寸、形状和形态。在纳米材料中,银纳米颗粒(AgNPs)因其具有相当广泛的性质而备受关注,例如可变的表面积与体积比,这对许多生物医学和技术应用非常有用。在这种情况下,小的纳米颗粒聚集体由于尺寸增大和形状/形态改变,其性质可能会降低。在这项工作中,通过在硼氢化钠(还原剂)和柠檬酸钠(封端剂)存在下化学还原硝酸银来研究银纳米颗粒的聚集。通过在反应过程中改变还原剂的量,获得了未聚集和部分聚集的样品,并通过紫外可见光谱、zeta电位和小角X射线散射技术对其进行了表征。在反应的每一步都测量了pH值,以便将这些结果与从结构技术获得的结果相关联。加入还原剂首先会使Ag(+)还原为银纳米颗粒。对于较高浓度的硼氢化钠,银纳米颗粒的平均尺寸会增加,并且会观察到纳米颗粒的聚集。发现zeta电位和pH值对银纳米颗粒的形成有很大影响,因为加入还原剂会导致部分与银纳米颗粒表面弱结合的柠檬酸盐被去除,并增加溶液的离子强度,从而促进颗粒的部分聚集。通过结合小角X射线散射、zeta电位和pH测量,适当地确定了这种聚集状态。此外,小角X射线散射技术表明,在该过程中形成的聚集体是细长状颗粒,这是通过小角X射线散射曲线证明的指数衰减所显示的。