4.7 Article

Positron Annihilation Lifetime Spectroscopy Insight on Free Volume Conversion of Nanostructured MgAl2O4 Ceramics

期刊

NANOMATERIALS
卷 11, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/nano11123373

关键词

nanostructured ceramics; positron annihilation; positronium decay; positron trapping; free-volume defects; nanopores

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This study demonstrates the use of positron annihilation lifetime spectroscopy (PALS) method for investigating free volume changes in functional ceramic materials, using nanostructured MgAl2O4 spinel as a case study. The analysis shows that technological modifications can lead to volume shrinking and decrease in defect-related voids in ceramics with well-developed porosity. The approach presented here can be applied to a wide range of functional nanomaterials with pronounced porosity.
Herein we demonstrate the specifics of using the positron annihilation lifetime spectroscopy (PALS) method for the study of free volume changes in functional ceramic materials. Choosing technological modification of nanostructured MgAl2O4 spinel as an example, we show that for ceramics with well-developed porosity positron annihilation is revealed through two channels: positron trapping channel and ortho-positronium decay. Positron trapping in free-volume defects is described by the second component of spectra and ortho-positronium decay process by single or multiple components, depending on how well porosity is developed and on the experimental configuration. When using proposed positron annihilation lifetime spectroscopy approaches, three components are the most suitable fit in the case of MgAl2O4 ceramics. In the analysis of the second component, it is shown that technological modification (increasing sintering temperature) leads to volume shrinking and decreases the number of defect-related voids. This process is also accompanied by the decrease of the size of nanopores (described by the third component), while the overall number of nanopores is not affected. The approach to the analysis of positron annihilation lifetime spectra presented here can be applied to a wide range of functional nanomaterials with pronounced porosity.

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