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通过 XANES 和 EXAFS 确定水煤气变换反应中 Pt 和 Au 上的 CO、H2O 和 H2 的覆盖度。

Determination of CO, H2O and H2 coverage by XANES and EXAFS on Pt and Au during water gas shift reaction.

机构信息

Chemical Sciences and Engineering Division, Argonne National Lab, Argonne, IL 60439-4837, USA.

出版信息

Phys Chem Chem Phys. 2010 Jun 7;12(21):5678-93. doi: 10.1039/c000240m. Epub 2010 May 4.

Abstract

The turn-over-rate (TOR) for the water gas shift (WGS) reaction at 200 degrees C, 7% CO, 9% CO(2), 22% H(2)O, 37% H(2) and balance Ar, of 1.4 nm Au/Al(2)O(3) is approximately 20 times higher than that of 1.6 nm Pt/Al(2)O(3). Operando EXAFS experiments at both the Au and Pt L(3) edges reveal that under reaction conditions, the catalysts are fully metallic. In the absence of adsorbates, the metal-metal bond distances of Pt and Au catalysts are 0.07 A and 0.13 A smaller than those of bulk Pt and Au foils, respectively. Adsorption of H(2) or CO on the Pt catalysts leads to significantly longer Pt-Pt bond distances; while there is little change in Au-Au bond distance with adsorbates. Adsorption of CO, H(2) and H(2)O leads to changes in the XANES spectra that can be used to determine the surface coverage of each adsorbate under reaction conditions. During WGS, the coverage of CO, H(2)O, and H(2) are obtained by the linear combination fitting of the difference XANES, or DeltaXANES, spectra. Pt catalysts adsorb CO, H(2), and H(2)O more strongly than the Au, in agreement with the lower CO reaction order and higher reaction temperatures.

摘要

在 200°C、7%CO、9%CO2、22%H2O、37%H2 和平衡 Ar 条件下,水煤气变换(WGS)反应的周转率(TOR)对于 1.4nm Au/Al2O3 是 1.6nm Pt/Al2O3 的约 20 倍。在 Au 和 Pt L(3)边缘的 operando EXAFS 实验表明,在反应条件下,催化剂是完全金属的。在没有吸附物的情况下,Pt 和 Au 催化剂的金属-金属键距离分别比体相 Pt 和 Au 箔的小 0.07Å 和 0.13Å。在 Pt 催化剂上吸附 H2 或 CO 会导致 Pt-Pt 键距离显著变长;而在吸附物存在下,Au-Au 键距离几乎没有变化。CO、H2 和 H2O 的吸附会导致 XANES 光谱发生变化,可用于确定反应条件下每种吸附物的表面覆盖率。在 WGS 过程中,通过对差分 XANES(DeltaXANES)光谱进行线性组合拟合,获得 CO、H2O 和 H2 的覆盖率。Pt 催化剂比 Au 催化剂更强烈地吸附 CO、H2 和 H2O,这与较低的 CO 反应级数和较高的反应温度一致。

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