BAM Federal Institute of Materials Research and Testing, Richard-Willstatter-Strabetae 11, D-12489 Berlin, Germany.
J Am Chem Soc. 2010 Feb 3;132(4):1296-301. doi: 10.1021/ja906506j.
Although gold nanoparticles (GNP) are among the most intensely studied nanoscale materials, the actual mechanisms of GNP formation often remain unclear due to limited accessibility to in situ-derived time-resolved information about precursor conversion and particle size distribution. Overcoming such limitations, a method is presented that analyzes the formation of nanoparticles via in situ SAXS and XANES using synchrotron radiation. The method is applied to study the classical GNP synthesis route via the reduction of tetrachloroauric acid by trisodium citrate at different temperatures and reactant concentrations. A mechanism of nanoparticle formation is proposed comprising different steps of particle growth via both coalescence of nuclei and further monomer attachment. The coalescence behavior of small nuclei was identified as one essential factor in obtaining a narrow size distribution of formed particles.
虽然金纳米粒子(GNP)是研究最多的纳米材料之一,但由于难以获得关于前体转化和颗粒尺寸分布的实时信息,GNP 形成的实际机制通常仍不清楚。为了克服这些限制,提出了一种使用同步辐射通过原位 SAXS 和 XANES 分析纳米颗粒形成的方法。该方法应用于通过在不同温度和反应物浓度下用柠檬酸三钠还原四氯金酸来研究经典的 GNP 合成途径。提出了一种纳米颗粒形成的机制,包括通过核的合并和进一步单体附着来进行颗粒生长的不同步骤。小核的合并行为被确定为获得形成颗粒的窄尺寸分布的一个重要因素。