Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst

Abstract In the present study, the use of a 3 wt% Fe2O3 catalyst improved the crystallisation of polysilazane PSN2. Crystallisation peaks of higher intensity were observed for Si3N4 and SiC at 1250 °C by using a 3 wt% Fe2O3 catalyst than at 1500 °C without Fe2O3. Besides, the effects of temperature...

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Main Authors: Wenshu Zhang, Shuo Wang, Honghui Ding, Xueying Zhai, De'an Yang
Format: Article
Language:English
Published: Wiley 2021-06-01
Series:Micro & Nano Letters
Online Access:https://doi.org/10.1049/mna2.12064
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spelling doaj-d1cc4801817b4a9d8f1f77003c06193f2021-07-14T13:25:19ZengWileyMicro & Nano Letters1750-04432021-06-0116739940410.1049/mna2.12064Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalystWenshu Zhang0Shuo Wang1Honghui Ding2Xueying Zhai3De'an Yang4School of Materials Science and Engineering Tianjin University Tianjin 300072 People's Republic of ChinaSchool of Materials Science and Engineering Tianjin University Tianjin 300072 People's Republic of ChinaSchool of Materials Science and Engineering Tianjin University Tianjin 300072 People's Republic of ChinaSchool of Materials Science and Engineering Tianjin University Tianjin 300072 People's Republic of ChinaSchool of Materials Science and Engineering Tianjin University Tianjin 300072 People's Republic of ChinaAbstract In the present study, the use of a 3 wt% Fe2O3 catalyst improved the crystallisation of polysilazane PSN2. Crystallisation peaks of higher intensity were observed for Si3N4 and SiC at 1250 °C by using a 3 wt% Fe2O3 catalyst than at 1500 °C without Fe2O3. Besides, the effects of temperature on the morphology of the samples were determined through scanning electron microscopy. Porous structures were observed at 1250 °C and these structures were transformed to flaky and near‐spherical nanoparticles as the temperatures were increased to 1350 and 1450 °C, respectively. Finally, the mechanism of Fe origination from Fe2O3 reduction, the production of a supersaturated liquid alloy, and the release and diffusion of N2 were proposed for Si3N4 formation.https://doi.org/10.1049/mna2.12064
collection DOAJ
language English
format Article
sources DOAJ
author Wenshu Zhang
Shuo Wang
Honghui Ding
Xueying Zhai
De'an Yang
spellingShingle Wenshu Zhang
Shuo Wang
Honghui Ding
Xueying Zhai
De'an Yang
Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
Micro & Nano Letters
author_facet Wenshu Zhang
Shuo Wang
Honghui Ding
Xueying Zhai
De'an Yang
author_sort Wenshu Zhang
title Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
title_short Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
title_full Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
title_fullStr Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
title_full_unstemmed Improved crystallisation of polysilazane‐derived Si3N4/SiC nanocomposites with Fe2O3 catalyst
title_sort improved crystallisation of polysilazane‐derived si3n4/sic nanocomposites with fe2o3 catalyst
publisher Wiley
series Micro & Nano Letters
issn 1750-0443
publishDate 2021-06-01
description Abstract In the present study, the use of a 3 wt% Fe2O3 catalyst improved the crystallisation of polysilazane PSN2. Crystallisation peaks of higher intensity were observed for Si3N4 and SiC at 1250 °C by using a 3 wt% Fe2O3 catalyst than at 1500 °C without Fe2O3. Besides, the effects of temperature on the morphology of the samples were determined through scanning electron microscopy. Porous structures were observed at 1250 °C and these structures were transformed to flaky and near‐spherical nanoparticles as the temperatures were increased to 1350 and 1450 °C, respectively. Finally, the mechanism of Fe origination from Fe2O3 reduction, the production of a supersaturated liquid alloy, and the release and diffusion of N2 were proposed for Si3N4 formation.
url https://doi.org/10.1049/mna2.12064
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