X射线光电子能谱
材料科学
分析化学(期刊)
四方晶系
纳米颗粒
镨
结构精修
高分辨率透射电子显微镜
兴奋剂
晶格常数
粒径
透射电子显微镜
结晶学
晶体结构
纳米技术
衍射
化学
化学工程
物理化学
色谱法
冶金
光学
物理
光电子学
工程类
作者
F.F.H. Aragón,Ismael González,J. A. H. Coaquira,Pilar Hidalgo,Hermi F. Brito,José D. Ardisson,W. A. A. Macedo,P.C. Morais
标识
DOI:10.1021/acs.jpcc.5b00761
摘要
In the present study, we report on the successful synthesis of Pr-doped SnO2 (SnO2:Pr) nanoparticles using a polymeric precursor method while setting the Pr-content in the range from 0 to 10.0 mol %. The as-prepared samples were characterized in regard to their structural, morphological and surface properties. X-ray diffraction (XRD) patterns recorded from all samples revealed the tetragonal rutile-type structure with a systematic average size reduction (in the range from 11 to 4 nm) while enhancing the residual strain (in the range of 0.186 to 0.480%) as the Pr-content was increased. From the Rietveld refinement analysis we found that the lattice parameters (a, c, u, and V) showed a linear behavior, indicating a solid solution regimen for the Pr-doping. Transmission electron micrographs provided mean particle sizes of 8.7 ± 0.5 nm, for 2.5 mol % Pr-content, and 5.2 ± 0.5 nm,for 10.0 mol % Pr-content, which are in very good agreement with values obtained from the XRD data analysis: 7.4 ± 1.0 nm and 4.0 ± 1.0 nm, respectively. From X-ray photoelectron spectroscopy (XPS) measurements [O]/[Sn] = 1.44 ratio has been estimated at the surface of the undoped SnO2 nanoparticles, which is below the expected value for bulk compound ([O]/[Sn] = 2), suggesting that the system is strongly nonstoichiometric at the nanoparticle surface. Actually, we found the [O]/[Sn] ratio value increasing monotonically as the Pr-content was increased, which was interpreted as due to the elimination of the surface chemisorbed oxygen and/or oxygen-related vacancies. Moreover, a redshift of the Sn(3d) XPS peaks has been determined as the Pr-content was increased, evidencing the change of the oxidation state of tin ions from Sn4+ to Sn2+. Our analyzes of the Pr(3d) XPS peaks indicated the preference of the Pr-ions for the Pr3+ oxidation state, although small amounts of the Pr4+-ions could not be completely ruled out, particularly for the lower Pr-doping samples.
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