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利用电子或光子辅助氧化反应对银进行表面图案化处理。

Surface patterning of silver using an electron- or photon-assisted oxidation reaction.

机构信息

Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 11, 81377 Munich, Germany.

出版信息

Chemphyschem. 2010 May 17;11(7):1525-32. doi: 10.1002/cphc.200900740.

Abstract

We have investigated a recently developed method of patterning Ag surfaces. The method uses an electron beam to irradiate Ag surfaces during NO(2) dosing at 300 K and leads to sharp oxide patterns on otherwise metallic surfaces. Investigations were performed on an Ag(111) single crystal and on an Ag foil with LEEM (low-energy electron microscopy), LEED (low-energy electron diffraction), MEM (mirror electron microscopy), and XPEEM (X-ray photo-emission electron microscopy). The oxidation reaction, which is based on the electron-induced desorption of NO molecules, proceeds in steps, from a layer of O atoms adsorbed on the metallic Ag via an intermediate phase to an amorphous Ag(2)O film. Our measurements evidence a high cross section for electron-induced NO desorption with 30-40 eV electrons, indicating that only a few electrons per adsorbing NO(2) molecule are required to initiate the process. The intermediate phase, which forms a partially ordered quadratic structure, contains oxygen species in an oxide-like environment, coexisting with an adsorbate covered metallic Ag(111) surface. While the intermediate phase dissolves within hours under UHV conditions, fully developed oxide patches, consisting of several layers of thick, amorphous Ag(2)O, are kinetically stable. The oxidation method also works with 40 eV (and 700 eV) photons instead of electrons. In preliminary experiments local patterns could also be created with photons, suggesting that mask techniques can be applied for the process.

摘要

我们研究了一种最近开发的 Ag 表面图案化方法。该方法在 300 K 时用电子束辐照 Ag 表面,并在其他金属表面上导致 sharp 氧化物图案。在 Ag(111)单晶和 Ag 箔上进行了 LEEM(低能电子显微镜)、LEED(低能电子衍射)、MEM(镜电子显微镜)和 XPEEM(X 射线光电子发射电子显微镜)的研究。基于电子诱导的 NO 分子脱附的氧化反应是分步进行的,从吸附在金属 Ag 上的 O 原子层开始,经过中间相到非晶态 Ag(2)O 薄膜。我们的测量结果表明,电子诱导的 NO 脱附具有 30-40 eV 电子的高截面,这表明每个吸附的 NO(2)分子只需要几个电子就能启动该过程。中间相形成部分有序的二次结构,其中包含处于类似氧化物环境中的氧物种,与吸附覆盖的金属 Ag(111)表面共存。虽然在 UHV 条件下中间相在数小时内溶解,但完全发展的氧化物斑块由几层厚的非晶态 Ag(2)O 组成,具有动力学稳定性。该氧化方法也可以用 40 eV(和 700 eV)光子代替电子进行。在初步实验中,也可以用光子产生局部图案,这表明掩模技术可以应用于该过程。

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