Increasing the Sensitivity to Short-Lived Species in a Modulated Excitation Experiment

被引:21
|
作者
Marchionni, Valentina [1 ,2 ]
Ferri, Davide [1 ]
Krocher, Oliver [1 ,3 ]
Wokaun, Alexander [1 ,2 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[3] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
IN-SITU; METHANE OXIDATION; SOLID CATALYSTS; CO OXIDATION; SPECTROSCOPY; DIFFRACTION; NANOPARTICLES; MECHANISMS; RESOLUTION; EVOLUTION;
D O I
10.1021/acs.analchem.6b04939
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The combination of spectroscopic and diffraction methods to study chemical transformations is fundamental for the understanding of reaction mechanisms. The identification of short-lived species, likely active species, is often hindered by the contribution of spectator species not directly involved in the reaction. The present study considers two different approaches to obtain increased sensitivity to transient species for experiments obeying the modulated excitation paradigm and exploiting phase sensitive detection (PSD). First, the variation of the frequency of the external stimulation (omega) during the experiment is considered. We demonstrate using the Fourier analysis that the increase of omega, i.e., the decrease of the modulation period T, enhances the sensitivity to short-lived species. The second alternative is the use of a single stimulation frequency (omega) during the measurement and the variation of the demodulation frequency (n omega) during data analysis. The absolute intensity of the phase-resolved signals is reduced by increasing n. However, species with slow kinetics are more attenuated than species with fast kinetics. Thus, transient species possessing fast kinetics are enhanced relative to other components and can be, in principle, discerned with improved sensitivity in the phase-resolved data obtained with n > 1. Experimental results in the field of heterogeneous catalysis are provided that support our findings.
引用
收藏
页码:5802 / 5810
页数:9
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