Nanoscale probing of bandgap states on oxide particles using electron energy-loss spectroscopy

被引:10
作者
Liu, Qianlang [1 ]
March, Katia [2 ]
Crozier, Peter A. [1 ]
机构
[1] Arizona State Univ, Sch Engn Matter Transport & Energy, Tempe, AZ 85287 USA
[2] Univ Paris Sud, Lab Phys Solides, Batiment 510, F-91405 Orsay, France
关键词
Bandgap states; Surface states; Dielectric property; Electronic structure; Nanoparticle; OPTICAL-PROPERTIES; RADIATION-DAMAGE; SURFACE-STATES; TIO2; MGO; INTERFACE; SPECIMENS; SPECTRA;
D O I
10.1016/j.ultramic.2016.06.010
中图分类号
TH742 [显微镜];
学科分类号
摘要
Surface and near-surface electronic states were probed with nanometer spatial resolution in MgO and TiO2 anatase nanoparticles using ultra-high energy resolution electron energy-loss spectroscopy (EELS) coupled to a scanning transmission electron microscope (STEM). This combination allows the surface electronic structure determined with spectroscopy to be correlated with nanoparticle size, morphology, facet etc. By acquiring the spectra in aloof beam mode, radiation damage to the surface can be significantly reduced while maintaining the nanometer spatial resolution. MgO and TiO2 showed very different bandgap features associated with the surface/sub-surface layer of the nanoparticles. Spectral simulations based on dielectric theory and density of states models showed that a plateau feature found in the pre-bandgap region in the spectra from (100) surfaces of 60 nm MgO nanocubes is consistent with a thin hydroxide surface layer. The spectroscopy shows that this hydroxide species gives rise to a broad filled surface state at 1.1 eV above the MgO valence band. At the surfaces of TiO2 nanoparticles, pronounced peaks were observed in the bandgap region, which could not be well fitted to defect states. In this case, the high refractive index and large particle size may make Cherenkov or guided light modes the likely causes of the peaks. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 11
页数:10
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