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Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials

Nanocrystalline tungsten nitride (WN(x)) aggregates and nanosheets are synthesized with a new alkylamine-based synthesis strategy for potential applications in nanoelectronics and catalysis. These applications preferentially require crystalline materials with controlled morphology, which has been ra...

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Autores principales: Wenzel, Olivia, Rein, Viktor, Hugenschmidt, Milena, Schilling, Frank, Feldmann, Claus, Gerthsen, Dagmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038014/
https://www.ncbi.nlm.nih.gov/pubmed/35480759
http://dx.doi.org/10.1039/d1ra04448f
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author Wenzel, Olivia
Rein, Viktor
Hugenschmidt, Milena
Schilling, Frank
Feldmann, Claus
Gerthsen, Dagmar
author_facet Wenzel, Olivia
Rein, Viktor
Hugenschmidt, Milena
Schilling, Frank
Feldmann, Claus
Gerthsen, Dagmar
author_sort Wenzel, Olivia
collection PubMed
description Nanocrystalline tungsten nitride (WN(x)) aggregates and nanosheets are synthesized with a new alkylamine-based synthesis strategy for potential applications in nanoelectronics and catalysis. These applications preferentially require crystalline materials with controlled morphology, which has been rarely demonstrated for WN(x) nanomaterials in the past. In the synthesis approach presented in this work, the morphology of nanoscale WN(x) is controlled by long-chained amines that form lyotropic or lamellar phases depending on the surfactant concentration. The structural and chemical properties of the WN(x) nanomaterials are studied in detail using different electron microscopic techniques in combination with electron spectroscopic analyses. Material synthesis and sample preparation for transmission electron microscopy (TEM) were performed in an argon atmosphere (Schlenk line and glovebox). The samples were inserted into the electron microscope via an air-tight TEM transfer holder to protect the material from hydrolysis and oxidation. From the lyotropic phase nanocrystalline WN(x) aggregates were obtained, which consist of 2.4 ± 0.8 nm small crystallites of the cubic WN(x) phase with a composition of WN(0.7). The lamellar phase with a higher surfactant concentration yields WN(x) nanosheets with lateral dimensions up to 500 nm and a mean thickness of 2.1 ± 1.1 nm. The nanosheets are N rich with a composition WN(1.7–3.7) and occur in the hexagonal crystal structure. The nanosheets are often stacked on top of one another with frequent rotations of 4–6° around the hexagonal c axis, thereby forming commensurate interface structures between nanosheets. High stacking-fault densities and signs of nanotwins can be repeatedly observed in WN(x) nanosheets.
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spelling pubmed-90380142022-04-26 Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials Wenzel, Olivia Rein, Viktor Hugenschmidt, Milena Schilling, Frank Feldmann, Claus Gerthsen, Dagmar RSC Adv Chemistry Nanocrystalline tungsten nitride (WN(x)) aggregates and nanosheets are synthesized with a new alkylamine-based synthesis strategy for potential applications in nanoelectronics and catalysis. These applications preferentially require crystalline materials with controlled morphology, which has been rarely demonstrated for WN(x) nanomaterials in the past. In the synthesis approach presented in this work, the morphology of nanoscale WN(x) is controlled by long-chained amines that form lyotropic or lamellar phases depending on the surfactant concentration. The structural and chemical properties of the WN(x) nanomaterials are studied in detail using different electron microscopic techniques in combination with electron spectroscopic analyses. Material synthesis and sample preparation for transmission electron microscopy (TEM) were performed in an argon atmosphere (Schlenk line and glovebox). The samples were inserted into the electron microscope via an air-tight TEM transfer holder to protect the material from hydrolysis and oxidation. From the lyotropic phase nanocrystalline WN(x) aggregates were obtained, which consist of 2.4 ± 0.8 nm small crystallites of the cubic WN(x) phase with a composition of WN(0.7). The lamellar phase with a higher surfactant concentration yields WN(x) nanosheets with lateral dimensions up to 500 nm and a mean thickness of 2.1 ± 1.1 nm. The nanosheets are N rich with a composition WN(1.7–3.7) and occur in the hexagonal crystal structure. The nanosheets are often stacked on top of one another with frequent rotations of 4–6° around the hexagonal c axis, thereby forming commensurate interface structures between nanosheets. High stacking-fault densities and signs of nanotwins can be repeatedly observed in WN(x) nanosheets. The Royal Society of Chemistry 2021-08-20 /pmc/articles/PMC9038014/ /pubmed/35480759 http://dx.doi.org/10.1039/d1ra04448f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wenzel, Olivia
Rein, Viktor
Hugenschmidt, Milena
Schilling, Frank
Feldmann, Claus
Gerthsen, Dagmar
Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title_full Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title_fullStr Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title_full_unstemmed Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title_short Impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
title_sort impact of synthesis conditions on the morphology and crystal structure of tungsten nitride nanomaterials
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038014/
https://www.ncbi.nlm.nih.gov/pubmed/35480759
http://dx.doi.org/10.1039/d1ra04448f
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