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金属原子和团簇在氧化物表面的电子相互作用和电荷转移。

Electronic interactions and charge transfers of metal atoms and clusters on oxide surfaces.

机构信息

Dipartimento di Scienza dei Materiali, Universitá di Milano-Bicocca, via Cozzi, 53-20125 Milano, Italy.

出版信息

Phys Chem Chem Phys. 2013 Feb 14;15(6):1737-57. doi: 10.1039/c2cp43731g. Epub 2013 Jan 3.

DOI:10.1039/c2cp43731g
PMID:23287900
Abstract

Understanding the interaction of small metal clusters and isolated atoms with oxide surfaces is crucial in order to rationalize the properties of heterogeneous catalysts composed of sub-nanometer metal particles dispersed on an oxide support. The interaction with the oxide surface can significantly alter the original properties of the metal deposit. In particular, the occurrence and the direction of charge transfer at the metal/oxide interface determine the chemical activity of the supported catalyst. The charge transfer depends on a number of factors like the nature of the oxide (reducible or non-reducible), the surface exposed, the presence of defects, the nature of the supported metal, etc. In this article we describe the most important conceptual aspects of the electronic metal-support interaction, a phenomenon related to the direct modification of the metal nano-particle determined by the formation of chemical bonds at the interface with the oxide. For metal nano-particles with a size of about 1 nm or below these effects become dominant although difficult to identify experimentally.

摘要

了解小分子团簇和孤立原子与氧化物表面的相互作用对于理解由分散在氧化物载体上的亚纳米金属颗粒组成的多相催化剂的性质至关重要。与氧化物表面的相互作用会显著改变金属沉积物的原始性质。特别是,金属/氧化物界面处的电荷转移的发生和方向决定了负载催化剂的化学活性。电荷转移取决于许多因素,如氧化物的性质(可还原或不可还原)、暴露的表面、缺陷的存在、负载金属的性质等。在本文中,我们描述了电子金属-载体相互作用的最重要的概念方面,这是一种与直接通过在与氧化物的界面处形成化学键来修饰金属纳米颗粒有关的现象。对于尺寸约为 1nm 或以下的金属纳米颗粒,这些效应变得占主导地位,尽管在实验上很难识别。

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