Chiarello Gian Luca, Ferri Davide
Università degli Studi di Milano, Dipartimento di Chimica, Via C. Golgi 19, I-20133 Milano, Italy.
Phys Chem Chem Phys. 2015 Apr 28;17(16):10579-91. doi: 10.1039/c5cp00609k.
The sensitivity of extended X-ray absorption fine structure spectroscopy (EXAFS) for minute structural changes can be enhanced by combination with the modulated excitation approach and making use of phase sensitive analysis. A modulated EXAFS experiment of a reversible periodic Pd to PdO partial oxidation has been simulated in order to understand the effect of the phase sensitive analysis on the shape and meaning of the resulting phase-resolved EXAFS spectra. In particular, the simulation comprises either a synchronous or a delayed sinusoidal variation of the EXAFS parameters, i.e. coordination number (N), interatomic distance (R) and Debye-Waller factor (σ(2)), of first Pd-Pd, first Pd-O, and second Pd-(O)-Pd coordination shells. The effect of these variations on the resulting phase-resolved Fourier transform EXAFS spectra is discussed. The results of the simulation are validated by an in situ EXAFS experiment at the Pd K-edge over 1.6 wt% Pd/Al2O3 undergoing reversible partial oxidation in a H2vs. O2 modulation at 573 K. It is shown that phase sensitive detection (PSD) is able to separate the minor contribution at ca. 2.8 Å corresponding to the growth of the Pd-(O)-Pd shell that is otherwise hidden under the static signal of the Pd-Pd shell of reduced Pd particles. The fitting of the phase-resolved EXAFS spectra suggests that the fast H2 to O2 switch leads the partial oxidation of the Pd surface with the formation of a PdO shell covering a metallic Pd core. Therefore, the dynamics of the full system can be described with greater detail than in conventional EXAFS. The intention of this work is to provide the tools and therefore a solid guidance to qualitatively and quantitatively understand the nature of the shape of phase-resolved FT-EXAFS spectra that may prove helpful in the analysis of a wide range of functional materials.
通过与调制激发方法相结合并利用相敏分析,可以提高扩展X射线吸收精细结构光谱(EXAFS)对微小结构变化的灵敏度。为了理解相敏分析对所得相分辨EXAFS光谱的形状和意义的影响,我们模拟了可逆周期性Pd到PdO部分氧化的调制EXAFS实验。具体而言,模拟包括对第一Pd-Pd、第一Pd-O和第二Pd-(O)-Pd配位壳层的EXAFS参数(即配位数(N)、原子间距离(R)和德拜-瓦勒因子(σ(2)))进行同步或延迟正弦变化。讨论了这些变化对所得相分辨傅里叶变换EXAFS光谱的影响。通过在573K下对1.6wt% Pd/Al2O3进行H2与O2调制的原位EXAFS实验,验证了模拟结果。结果表明,相敏检测(PSD)能够分离出约2.8 Å处对应于Pd-(O)-Pd壳层生长的微小贡献,否则该贡献会隐藏在还原态Pd颗粒的Pd-Pd壳层的静态信号之下。相分辨EXAFS光谱的拟合表明,快速的H2到O2切换导致Pd表面的部分氧化,形成覆盖金属Pd核的PdO壳层。因此,与传统EXAFS相比,可以更详细地描述整个系统的动力学。这项工作的目的是提供工具,从而为定性和定量理解相分辨FT-EXAFS光谱形状的本质提供坚实的指导,这可能有助于分析各种功能材料。