Revealing Complexity of Nanoparticle Synthesis in Solution by in Situ Hard X-ray Spectroscopy-Today and Beyond

被引:41
作者
Koziej, Dorota [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Mat, Lab Multifunct Mat, HCI F505,Vladimir Prelog Weg 5, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
PAIR DISTRIBUTION FUNCTION; FINE-STRUCTURE SPECTROSCOPY; ABSORPTION SPECTROSCOPY; ELECTRONIC-STRUCTURE; EMISSION-SPECTROSCOPY; STRUCTURAL-ANALYSIS; PD NANOPARTICLES; ATOMIC-STRUCTURE; QUANTUM DOTS; GROWTH;
D O I
10.1021/acs.chemmater.6b00486
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Over the past few decades, material scientists have developed a wide variety of approaches to deliberately introduce chemical and structural inhomogeneities into nanoparticles, achieving for example intentional doping, concentration gradients, and multicomponent structures. This perspective presents a sense of how modern hard X-ray spectroscopic methods, far from merely providing new tools, are extending the way we study and understand such complex nanoparticles. Particularly, the possibility to select with high resolution the incident and emission hard X-ray energies offers unprecedented site selectivity, and rapid data acquisition helps to uncover the complex chemical world behind the state-of-the-art synthetic methods like hot-injection, Brust-Schiffrin, super-critical-flow, and nonaqueous synthesis. Therefore, today the in situ spectroscopic studies provide a new view into the genesis of heterogeneity in colloidal nanoparticles.
引用
收藏
页码:2478 / 2490
页数:13
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