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Quantitative super-resolution imaging uncovers reactivity patterns on single nanocatalysts
被引:0
|作者:
Xiaochun Zhou
Nesha May Andoy
Guokun Liu
Eric Choudhary
Kyu-Sung Han
Hao Shen
Peng Chen
机构:
[1] Cornell University,Department of Chemistry and Chemical Biology
关键词:
D O I:
10.1038/nnano.2012.18
中图分类号:
学科分类号:
摘要:
Metal nanoparticles are used as catalysts in a variety of important chemical reactions1,2, and can have a range of different shapes3,4,5,6,7,8, with facets and sites that differ in catalytic reactivity1,2,9. To develop better catalysts it is necessary to determine where catalysis occurs on such nanoparticles and what structures are more reactive. Surface science experiments or theory can be used to predict the reactivity of surfaces with a known structure1,2,10, and the reactivity of nanocatalysts can often be rationalized from a knowledge of their well-defined surface facets3,4,5. Here, we show that a knowledge of the surface facets of a gold nanorod catalyst is insufficient to predict its reactivity, and we must also consider defects on the surface of the nanorod. We use super-resolution fluorescence microscopy to quantify the catalysis of the nanorods at a temporal resolution of a single catalytic reaction and a spatial resolution of ∼40 nm. We find that within the same surface facets on the sides of a single nanorod, the reactivity is not constant and exhibits a gradient from the centre of the nanorod towards its two ends. Furthermore, the ratio of the reactivity at the ends of the nanorod to the reactivity at the sides varies significantly from nanorod to nanorod, even though they all have the same surface facets.
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页码:237 / 241
页数:4
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