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利用碱离子散射谱、X 射线光电子能谱和热脱附谱研究 Zn/Pt(111) 双金属表面的合金形成和化学吸附。

Alloy formation and chemisorption at Zn/Pt(111) bimetallic surfaces using alkali ISS, XPD, and TPD.

机构信息

Department of Chemical and Materials Engineering, Tunghai University , Taichung 40704, Taiwan.

出版信息

J Phys Chem A. 2013 Nov 21;117(46):11684-94. doi: 10.1021/jp4006668. Epub 2013 May 22.

Abstract

Alloy formation and chemisorption at bimetallic surfaces formed by vapor-depositing Zn on a Pt(111) single crystal were investigated primarily by using X-ray photoelectron diffraction (XPD), X-ray photoelectron spectroscopy (XPS), low-energy alkali ion scattering spectroscopy (ALISS), low electron energy diffraction (LEED), and temperature programmed desorption (TPD). A wide range of conditions were investigated to explore whether deposition and annealing of Zn films could produce well-defined, ordered alloy surfaces, similar to those encountered for Sn/Pt(111) surface alloys. These attempts were unsuccessful, although weak, diffuse (2 × 2) spots were observed under special conditions. The particular PtZn bimetallic alloy created by annealing one monolayer of Zn on Pt(111) at 600 K, which has a Zn composition in the surface layer of about 5 at. %, was investigated in detail by using XPD and ALISS. Only a diffuse (1 × 1) pattern was observed from this surface by LEED, suggesting that no long-range, ordered alloy structure was formed. Zn atoms were substitutionally incorporated into the Pt(111) crystal to form a near-surface alloy in which Zn atoms were found to reside primarily in the topmost and second layers. The alloyed Zn atoms in the topmost layer are coplanar with the Pt atoms in the surface layer, without any "buckling" of Zn, that is, displacement in the vertical direction. This result is expected because of the similar size of Pt and Zn, based on previous studies of bimetallic Pt alloys. Zn atoms desorb upon heating rather than diffusing deep into the bulk of the Pt crystal. Temperature programmed desorption (TPD) measurements show that both CO and NO have lower desorption energies on the PtZn alloy surface compared to that on the clean Pt(111) surface.

摘要

通过气相沉积在 Pt(111)单晶上沉积 Zn 来形成双金属表面,主要通过 X 射线光电子衍射 (XPD)、X 射线光电子能谱 (XPS)、低能碱离子散射光谱 (ALISS)、低能电子衍射 (LEED) 和程序升温脱附 (TPD) 来研究其合金形成和化学吸附。研究了广泛的条件,以探索沉积和退火 Zn 薄膜是否可以产生明确、有序的合金表面,类似于在 Sn/Pt(111)表面合金中遇到的情况。尽管在特殊条件下观察到了较弱的弥散 (2 × 2) 斑点,但这些尝试均未成功。在 600 K 下退火单层 Zn 在 Pt(111)上形成的特殊 PtZn 双金属合金,其表面层中的 Zn 组成约为 5 at.%,通过 XPD 和 ALISS 进行了详细研究。通过 LEED 从该表面仅观察到弥散的 (1 × 1) 图案,表明没有形成长程、有序的合金结构。Zn 原子被置换到 Pt(111)晶体中形成近表面合金,其中 Zn 原子主要位于最顶层和第二层。最顶层中的合金化 Zn 原子与表面层中的 Pt 原子共面,没有任何 Zn 的“翘曲”,即垂直方向的位移。根据先前对双金属 Pt 合金的研究,由于 Pt 和 Zn 的尺寸相似,因此预计会出现这种结果。Zn 原子在加热时会解吸而不是扩散到 Pt 晶体的深处。程序升温脱附 (TPD) 测量表明,与清洁的 Pt(111)表面相比,CO 和 NO 在 PtZn 合金表面的脱附能更低。

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