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Operando Spectrokinetic Investigations of Low Temperature Water-Gas Shift Catalysts: SSITKA- DRIFTS-MS

机译:低温水气移催化剂的手术分频器研究:Ssitka-漂移-sms

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The reactivity and the role of formate species on ceria-based water-gas shift (WGS, CO + H2O →CO2 + H2) catalysts and the corresponding reaction mechanisms have been much debated. Many of the conflicting conclusions are due to the fact that different materials and experimental conditions were used. In addition, a major source of discrepancy probably resides in the fact that the surface reactivity of adsorbates is often investigated using non-chemical-steady-state methods, leading to erroneous conclusions. In the present work, it is shown that a combination of spectroscopic and kinetic data obtained at the chemical steady-state allows quantification of the concentration of reaction intermediates and excludes the role of the formate species that are visible by DRIFT for a range of catalyst based on Au or Pt supported on reducible oxides.
机译:甲酸盐物种对基于二氧化铈的水 - 气体移位(WGS,CO + H2O→CO 2 + H 2)催化剂的反应性和作用,以及相应的反应机制已经存在了很大竞争。许多相互矛盾的结论是由于使用不同的材料和实验条件。此外,主要的差异来源可能存在于通常使用非化学稳态方法研究吸附物的表面反应性,从而导致错误的结论。在本作的工作中,显示在化学稳态上获得的光谱和动力学数据的组合允许定量反应中间体的浓度,并排除甲酸种类的作用,其通过漂移基于一系列催化剂可见在Au或Pt上支持可还原氧化物。

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