Department of Materials Science and Engineering, Texas A&M University, College Station, TX 77843, USA; Electrochemical Materials Science (ECMS) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi 630006, Tamil Nadu, India.
Department of Mechanical Engineering, Texas A&M University, College Station, TX 77843, USA.
J Colloid Interface Sci. 2017 Jul 15;498:248-262. doi: 10.1016/j.jcis.2017.03.058. Epub 2017 Mar 16.
Three morphologies of silver nanoparticles (Ag NPs) such as nanocubes, aggregated anisotropic Ag NPs, and nanospheres were prepared using polystyrene sulfonate (PSS) and citrate as stabilizing agents utilizing a simple wet-chemical and microwave heating route respectively. Ag nanocubes were prepared within one min through microwave heating whereas anisotropic Ag NPs and spherical Ag NPs via 5 and 30min of normal stirring at room temperature (RT) respectively. The shape effect of three different morphologies of Ag NPs were examined in catalysis reaction and in surface enhanced Raman scattering (SERS) studies. For catalysis experiments, reduction of various nitroaromatics was done taking excess NaBH in presence of those morphologically different Ag NPs as catalyst and the corresponding catalytic activity is ordered as: Ag nanospheres>aggregated anisotropic Ag NPs>Ag nanocubes. The highest catalytic rate of ∼1.34×10min was observed with citrate capped Ag nanospheres. SERS study was done taking methylene blue (MB) as the Raman probe where a highest enhancement factor (EF) of ∼1.05×10 was observed with Ag nanospheres and the order of EF values is as follows: Ag nanospheres>Ag nanocubes>aggregated anisotropic Ag NPs. The highest catalytic and SERS activity of citrate stabilized spherical Ag NPs are attributed due to the fast electron transfer in catalysis and creation of more number of surface active 'hot spots' in SERS studies. In future, the overall process we highlighted here might found potential application for the preparation of other varieties of nanomaterials applicable to catalysis reaction and in SERS-based trace analysis of various biologically important molecules and fine chemicals.
采用聚苯乙烯磺酸钠(PSS)和柠檬酸钠分别作为稳定剂,通过简单的湿化学法和微波加热法制备了三种形貌的银纳米粒子(Ag NPs),分别为纳米立方体、聚集各向异性的 Ag NPs 和纳米球。通过微波加热在 1 分钟内制备了 Ag 纳米立方体,而通过室温(RT)下 5 分钟和 30 分钟的常规搅拌分别制备了各向异性 Ag NPs 和球形 Ag NPs。在催化反应和表面增强拉曼散射(SERS)研究中研究了三种不同形貌的 Ag NPs 的形状效应。在催化实验中,在过量 NaBH 存在下,用这些形貌不同的 Ag NPs 作为催化剂还原各种硝基芳烃,相应的催化活性顺序为:Ag 纳米球>聚集各向异性 Ag NPs>Ag 纳米立方体。用柠檬酸稳定的 Ag 纳米球观察到最高的催化速率约为 1.34×10min。用亚甲基蓝(MB)作为拉曼探针进行 SERS 研究,用 Ag 纳米球观察到最高的增强因子(EF)约为 1.05×10,EF 值的顺序如下:Ag 纳米球>Ag 纳米立方体>聚集各向异性 Ag NPs。柠檬酸稳定的球形 Ag NPs 具有最高的催化和 SERS 活性归因于在催化过程中快速的电子转移和在 SERS 研究中产生更多的表面活性“热点”。在未来,我们在这里强调的整个过程可能会发现适用于制备其他种类的纳米材料的潜在应用,这些纳米材料可应用于催化反应和基于 SERS 的各种生物重要分子和精细化学品的痕量分析。