Abstract

Electronic metal-support interactions (EMSI) in catalysis are commonly rationalized in terms of an electron transfer between support material and supported metal catalyst particles. This general perspective, however, cannot fully explain experimentally observed EMSI for metallic nanoparticulate catalysts, because the strong charge screening of metals should locally confine effects of direct electronic interaction with the support to the catalyst-support interface (CSI), which, apart from the perimeter, is largely inaccessible for catalysis reactants. The concept of capacitive EMSI is proposed here for catalyst particles at the nanometer scale, where electronic equilibration results in a long-range charging of the catalytically active outer surface (CAOS) bypassing the expected strong metallic charge screening, which is confirmed and quantified by electrostatic and density functional theory simulations revealing a strong dependence on the coverage of the support surface with catalyst particles. This long-range charge transfer leads to a shift of the local work function at the CAOS. In order to describe the catalytic consequences, an amendment of $d$-band theory in terms of `$d$-band + work function' is proposed. Furthermore, the charging of remote catalytic sites at the CAOS scales with the relative dielectric constant of the surrounding medium, and it is concluded that EMSI can have surprisingly strong influence especially in the presence of a strongly polarizable dielectric.

Highlights

  • Nanoscopic metal catalyst particles supported on metal oxides or carbon materials constitute the majority of heterogeneous catalysts and electrocatalysts used in the chemical industry and studied in catalysis research [1,2]

  • The concept of capacitive Electronic metal-support interactions (EMSI) is proposed here for catalyst particles at the nanometer scale, where electronic equilibration results in a long-range charging of the catalytically active outer surface (CAOS) bypassing the expected strong metallic charge screening, which is confirmed and quantified by electrostatic and density functional theory simulations revealing a strong dependence on the coverage of the support surface with catalyst particles

  • The charging of remote catalytic sites at the CAOS scales with the relative dielectric constant of the surrounding medium, and it is concluded that EMSI can have surprisingly strong influence especially in the presence of a strongly polarizable dielectric

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Summary

Introduction

Nanoscopic metal catalyst particles supported on metal oxides or carbon materials constitute the majority of heterogeneous catalysts and electrocatalysts used in the chemical industry and studied in catalysis research [1,2]. E.g., on structural or compositional modifications, this ‘carrier effect’ has been explained by an electron transfer between support material and metal catalyst particles [4,5]. Such ‘electronic metal-support interactions’ (EMSI) [6] can be rationalized in terms of an electron transfer for metal adatoms and small subnanometer sized metal clusters [7,8,9,10,11] due to the formation of polar chemical bonds with more or less ionic character between the support surface atoms and the metal cluster ‘adsorbate.’ Substantial charge transfer of the order of 0.1–1 |e|/atom can be observed when metal adatoms or sub-nm clusters interact directly with the support surface [12], especially with oxide support defects or with surface cations of transition metal

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