纳米颗粒
材料科学
化学物理
纳米材料
X射线光电子能谱
电子转移
纳米技术
成核
氧化物
Atom(片上系统)
物理化学
化学工程
化学
嵌入式系统
工程类
有机化学
冶金
计算机科学
作者
Yaroslava Lykhach,Sergey M. Kozlov,Tomáš Škála,Andrii Tovt,Vitalii Stetsovych,Nataliya Tsud,Filip Dvořák,Viktor Johánek,Armin Neitzel,Josef Mysliveček,Stefano Fabris,Vladimı́r Matolín,Konstantin M. Neyman,Jörg Libuda
出处
期刊:Nature Materials
[Springer Nature]
日期:2015-12-14
卷期号:15 (3): 284-288
被引量:627
摘要
The electronic interaction between deposited metal nanoparticles and their support material can influence their functionality. Here, a quantification of the charge transfer between platinum nanoparticles and a ceria support is presented. Electronic interactions between metal nanoparticles and oxide supports control the functionality of nanomaterials, for example, the stability, the activity and the selectivity of catalysts1,2,3,4,5. Such interactions involve electron transfer across the metal/support interface. In this work we quantify this charge transfer on a well-defined platinum/ceria catalyst at particle sizes relevant for heterogeneous catalysis. Combining synchrotron-radiation photoelectron spectroscopy, scanning tunnelling microscopy and density functional calculations we show that the charge transfer per Pt atom is largest for Pt particles of around 50 atoms. Here, approximately one electron is transferred per ten Pt atoms from the nanoparticle to the support. For larger particles, the charge transfer reaches its intrinsic limit set by the support. For smaller particles, charge transfer is partially suppressed by nucleation at defects. These mechanistic and quantitative insights into charge transfer will help to make better use of particle size effects and electronic metal–support interactions in metal/oxide nanomaterials.
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