吸附剂的非热等离子活化:铂上的 CO

JACS Au Pub Date : 2024-07-12 DOI:10.1021/jacsau.4c00309
Minseok Kim, Sohag Biswas, Isabel Barraza Alvarez, Phillip Christopher, Bryan M. Wong, Lorenzo Mangolini
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摘要

非热等离子体为电驱动异相催化过程提供了一种独特的方法。尽管社会各界对此兴趣浓厚,但对这些过程的基本活化途径仍然知之甚少。在这里,我们研究了在氩非反应气氛中持续暴露于非热等离子体如何影响铂纳米颗粒对一氧化碳(CO)的解吸。温度编程解吸测量结果表明,等离子体将一氧化碳与铂表面的有效结合能(BE)降低了 ∼ 0.3 eV,结合能的降低与等离子体密度成线性关系。我们发现,与配位良好的位点(台阶)相比,配位不足的位点(台阶和边缘)的一氧化碳有效结合能降低幅度最大。密度泛函理论计算表明,这是由于催化剂表面的等离子体诱导充电和电场优先影响了欠配位位点。这项研究提供了等离子体诱导非热活化吸附剂-催化剂耦合的直接实验证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nonthermal Plasma Activation of Adsorbates: The Case of CO on Pt
Nonthermal plasmas provide a unique approach to electrically driven heterogeneous catalytic processes. Despite much interest from the community, fundamental activation pathways in these processes remain poorly understood. Here, we investigate how exposure to a nonthermal plasma sustained in an argon nonreactive atmosphere affects the desorption of carbon monoxide (CO) from platinum nanoparticles. Temperature-programmed desorption measurements indicate that the plasma reduces the effective binding energy (BE) of CO to Pt surfaces by as much as ∼0.3 eV, with the reduction in the BE scaling linearly with the plasma density. We find that the effective CO BE is most strongly reduced for under-coordinated sites (steps and edges) compared to well-coordinated sites (terraces). Density functional theory calculations suggest that this is due to plasma-induced charging and electric fields at the catalyst surface, which preferentially affect under-coordinated sites. This study provides direct experimental evidence of plasma-induced nonthermal activation of the adsorbate-catalyst couple.
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