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从超高真空到近大气压条件下AuPd(100)上的CO氧化:相邻钯原子的关键作用。

CO oxidation over AuPd(100) from ultrahigh vacuum to near-atmospheric pressures: the critical role of contiguous Pd atoms.

作者信息

Gao Feng, Wang Yilin, Goodman D Wayne

机构信息

Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, USA.

出版信息

J Am Chem Soc. 2009 Apr 29;131(16):5734-5. doi: 10.1021/ja9008437.

Abstract

It is demonstrated that gas-phase CO pressure higher than approximately 0.1 Torr is required to segregate a sufficient amount of Pd to the surface of a well-annealed AuPd(100) sample to form contiguous Pd sites. These contiguous sites are critical in dissociating O(2) for low-temperature CO oxidation, where CO chemisorbed on Au sites clearly participates in the reaction at temperatures below approximately 400 K. Measured reaction kinetics demonstrates that the higher reaction rate is achieved on a surface with higher coverages of contiguous Pd sites.

摘要

结果表明,对于充分退火的AuPd(100)样品,要使足够量的Pd偏析到其表面以形成连续的Pd位点,气相CO压力需高于约0.1托。这些连续位点对于低温CO氧化中O(2)的解离至关重要,在约400 K以下的温度下,吸附在Au位点上的CO显然参与了反应。测得的反应动力学表明,在具有更高连续Pd位点覆盖率的表面上能实现更高的反应速率。

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