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在 Ag(110) 上添加行核生成之前的 O(2) 离解:原子力扫描隧道显微镜观察。

O(2) dissociation before the onset of added row nucleation on Ag(110): an atomistic scanning tunnelling microscopy view.

机构信息

Dipartimento di Fisica, Università degli Studi di Genova, Genova, Italy.

出版信息

J Phys Condens Matter. 2010 Aug 4;22(30):304015. doi: 10.1088/0953-8984/22/30/304015. Epub 2010 Jul 13.

Abstract

We present here a scanning tunnelling microscopy (STM) study on O(2) adsorption at Ag(110) at T = 175 K, i.e. in the temperature range between the onset of O(2) dissociation and the formation of the added row reconstruction. In agreement with previous studies at lower surface coverage, we observe several structures forming upon O(2) dissociation, including Ag-O complexes randomly distributed on the surface. We suggest that the presence of the latter structures, characterized by a large cross section for low energy electrons, can account for the marked decrease of the surface electron reflectivity and for the corresponding increase of the diffuse elastic intensity previously reported in a HREELS investigation of the same system.

摘要

我们在此呈现了一项在 T = 175 K 下对 Ag(110)上 O(2)吸附的扫描隧道显微镜 (STM)研究,即在 O(2)离解开始和添加行重构形成之间的温度范围内。与之前在较低表面覆盖度下的研究一致,我们观察到在 O(2)离解后形成了几种结构,包括随机分布在表面上的 Ag-O 复合物。我们认为,后者结构的存在,其特征是对低能电子的大横截面,可以解释表面电子反射率的显著降低,以及在对相同系统的高分辨能量损失电子谱 (HREELS)研究中报告的相应的漫反射弹性强度的增加。

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