Boita Jocenir, Castegnaro Marcus Vinicius, Alves Maria do Carmo Martins, Morais Jonder
Laboratório de Espectroscopia de Elétrons (LEe-), Instituto de Física, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Bento Gonçalves 9500, CEP-91501-970, Porto Alegre, Rio Grande do Sul - RS 15051, Brazil.
Instituto de Química, Universidde Federal do Rio Grande do Sul (UFRGS), Av. Bento Gaonçalves 9500, CEP-91501-970, Porto Alegre, Rio Grande do Sul - RS 15003, Brazil.
J Synchrotron Radiat. 2015 May;22(3):736-44. doi: 10.1107/S1600577515003434. Epub 2015 Apr 8.
In situ time-resolved X-ray absorption spectroscopy (XAS) measurements collected at the Pt L3-edge during the synthesis of Pt nanoparticles (NPs) in aqueous solution are reported. A specially designed dispenser-reactor apparatus allowed for monitoring changes in the XAS spectra from the earliest moments of Pt ions in solution until the formation of metallic nanoparticles with a mean diameter of 4.9 ± 1.1 nm. By monitoring the changes in the local chemical environment of the Pt atoms in real time, it was possible to observe that the NPs formation kinetics involved two stages: a reduction-nucleation burst followed by a slow growth and stabilization of NPs. Subsequently, the synthesized Pt NPs were supported on activated carbon and characterized by synchrotron-radiation-excited X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS). The supported Pt NPs remained in the metallic chemical state and with a reduced size, presenting slight lattice parameter contraction in comparison with the bulk Pt values.
报道了在水溶液中合成铂纳米颗粒(NP)过程中,于铂L3边缘进行的原位时间分辨X射线吸收光谱(XAS)测量。一种专门设计的分配器-反应器装置能够监测从溶液中铂离子最初时刻到形成平均直径为4.9±1.1 nm的金属纳米颗粒期间XAS光谱的变化。通过实时监测铂原子局部化学环境的变化,有可能观察到纳米颗粒的形成动力学涉及两个阶段:先是还原-成核爆发,随后是纳米颗粒的缓慢生长和稳定。随后,将合成的铂纳米颗粒负载在活性炭上,并通过同步辐射激发的X射线光电子能谱(XPS)、X射线衍射(XRD)和扩展X射线吸收精细结构(EXAFS)进行表征。负载的铂纳米颗粒保持金属化学状态且尺寸减小,与块状铂值相比呈现出轻微的晶格参数收缩。