Direct Quantification of Cu Vacancies and Spatial Localization of Surface Plasmon Resonances in Copper Phosphide Nanocrystals

被引:16
作者
Bertoni, Giovanni [1 ,2 ]
Ramasse, Quentin [3 ,4 ,5 ]
Brescia, Rosaria [6 ]
De Trizio, Luca [2 ]
De Donato, Francesco [2 ]
Manna, Liberato [2 ]
机构
[1] CNR, Ist Nanosci, Via Campi 213-A, I-41125 Modena, Italy
[2] Ist Italiano Tecnol, Dept Nanochem, Via Morego 30, I-16163 Genoa, Italy
[3] SciTech Daresbury, SuperSTEM, Sci & Innovat Campus,Keckwick Lane, Daresbury WA4 4AD, England
[4] Univ Leeds, Sch Chem & Proc Engn, Leeds LS2 9JT, W Yorkshire, England
[5] Univ Leeds, Sch Phys, Leeds LS2 9JT, W Yorkshire, England
[6] Ist Italiano Tecnol, Electron Microscopy Facil, Via Morego 30, I-16163 Genoa, Italy
来源
ACS MATERIALS LETTERS | 2019年 / 1卷 / 06期
基金
英国工程与自然科学研究理事会;
关键词
EXCITATIONS; CRYSTAL; LOSSES;
D O I
10.1021/acsmaterialslett.9b00412
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Copper chalcogenides and pnictogenides often behave as heavily doped p-type semiconductors, because of the presence of a high density of Cu vacancies, with corresponding hole carriers in the valence band. If the free-carrier concentration is high enough, localized surface plasmon resonances can be sustained in nanocrystals of these materials, with frequencies that are typically observed in the infrared region of the spectrum (<1 eV), differently from the typical resonances featured in the visible range by metallic nanoparticles. Here, we demonstrate that Cu vacancies in hexagonal Cu3-xP nanocrystals can be directly quantified by scanning transmission electron microscopy (STEM) analysis. We also report, for the first time, the spatial localization of the plasmon resonances in individual Cu3-xP nanocrystals by means of STEM energy loss spectroscopy (EELS), which is an achievement that, to date, had been possible only on nanoparticles of noble metals. Two plasmon modes can be seen from STEM-EELS, which are in agreement with the resonances calculated from the vacancy concentration obtained from the STEM analysis.
引用
收藏
页码:665 / 670
页数:11
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