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氧空位在锐钛矿 TiO2(101)表面的亚表面迁移。

(Sub)surface mobility of oxygen vacancies at the TiO2 anatase (101) surface.

机构信息

Institute of Applied Physics, Vienna University of Technology, Vienna, Austria.

出版信息

Phys Rev Lett. 2012 Sep 28;109(13):136103. doi: 10.1103/PhysRevLett.109.136103.

Abstract

Anatase is a metastable polymorph of TiO2. In contrast to the more widely studied TiO2 rutile, O vacancies (V(O)'s) are not stable at the anatase (101) surface. Low-temperature STM shows that surface V(O)'s, created by electron bombardment at 105 K, start migrating to subsurface sites at temperatures ≥200 K. After an initial decrease of the V(O) density, a temperature-dependent dynamic equilibrium is established where V(O)'s move to subsurface sites and back again, as seen in time-lapse STM images. We estimate that activation energies for subsurface migration lie between 0.6 and 1.2 eV; in comparison, density functional theory calculations predict a barrier of ca. 0.75 eV. The wide scatter of the experimental values might be attributed to inhomogeneously distributed subsurface defects in the reduced sample.

摘要

锐钛矿是 TiO2 的一种亚稳态多晶型物。与更为广泛研究的 TiO2 金红石相比,氧空位(V(O)'s)在锐钛矿(101)表面不稳定。低温 STM 表明,在 105 K 下通过电子轰击产生的表面 V(O)'s 在温度≥200 K 时开始迁移到次表面位置。在 V(O)'s 密度最初下降后,建立了一个温度相关的动态平衡,其中 V(O)'s 迁移到次表面位置并再次返回,如延时 STM 图像所示。我们估计,亚表面迁移的激活能在 0.6 和 1.2 eV 之间;相比之下,密度泛函理论计算预测的势垒约为 0.75 eV。实验值的广泛分散可能归因于还原样品中分布不均匀的亚表面缺陷。

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