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Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors

[Image: see text] The aim of this study was the preparation of different amorphous silicon–carbon hybrid thin-layer materials according to the liquid phase deposition (LPD) process using single-source precursors. In our study, 2-methyl-2-silyltrisilane (methylisotetrasilane; 2), 1,1,1-trimethyl-2,2-...

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Autores principales: Sauermoser, Aileen, Lainer, Thomas, Knoechl, Andreas, Goni, Freskida, Fischer, Roland C., Fitzek, Harald, Dienstleder, Martina, Prietl, Christine, Kelterer, Anne-Marie, Bandl, Christine, Jakopic, Georg, Kothleitner, Gerald, Haas, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523434/
https://www.ncbi.nlm.nih.gov/pubmed/37700615
http://dx.doi.org/10.1021/acs.inorgchem.3c01846
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author Sauermoser, Aileen
Lainer, Thomas
Knoechl, Andreas
Goni, Freskida
Fischer, Roland C.
Fitzek, Harald
Dienstleder, Martina
Prietl, Christine
Kelterer, Anne-Marie
Bandl, Christine
Jakopic, Georg
Kothleitner, Gerald
Haas, Michael
author_facet Sauermoser, Aileen
Lainer, Thomas
Knoechl, Andreas
Goni, Freskida
Fischer, Roland C.
Fitzek, Harald
Dienstleder, Martina
Prietl, Christine
Kelterer, Anne-Marie
Bandl, Christine
Jakopic, Georg
Kothleitner, Gerald
Haas, Michael
author_sort Sauermoser, Aileen
collection PubMed
description [Image: see text] The aim of this study was the preparation of different amorphous silicon–carbon hybrid thin-layer materials according to the liquid phase deposition (LPD) process using single-source precursors. In our study, 2-methyl-2-silyltrisilane (methylisotetrasilane; 2), 1,1,1-trimethyl-2,2-disilyltrisilane (trimethylsilylisotetrasilane; 3), 2-phenyl-2-silyltrisilane (phenylisotetrasilane; 4), and 1,1,2,2,4,4,5,5-octamethyl-3,3,6,6-tetrasilylcyclohexasilane (cyclohexasilane; 5) were utilized as precursor materials and compared with the parent compound 2,2-disilyltrisilane (neopentasilane; 1). Compounds 2–5 were successfully oligomerized at λ = 365 nm with catalytic amounts of the neopentasilane oligomer (NPO). These oligomeric mixtures (NPO and 6–9) were used for the preparation of thin-layer materials. Optimum solution and spin coating conditions were investigated, and amorphous silicon–carbon films were obtained. All thin-layer materials were characterized via UV/vis spectroscopy, light microscopy, spectroscopic ellipsometry, XPS, SEM, and SEM/EDX. Our results show that the carbon content and especially the bandgap can be easily tuned using these single-source precursors via LPD.
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spelling pubmed-105234342023-09-28 Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors Sauermoser, Aileen Lainer, Thomas Knoechl, Andreas Goni, Freskida Fischer, Roland C. Fitzek, Harald Dienstleder, Martina Prietl, Christine Kelterer, Anne-Marie Bandl, Christine Jakopic, Georg Kothleitner, Gerald Haas, Michael Inorg Chem [Image: see text] The aim of this study was the preparation of different amorphous silicon–carbon hybrid thin-layer materials according to the liquid phase deposition (LPD) process using single-source precursors. In our study, 2-methyl-2-silyltrisilane (methylisotetrasilane; 2), 1,1,1-trimethyl-2,2-disilyltrisilane (trimethylsilylisotetrasilane; 3), 2-phenyl-2-silyltrisilane (phenylisotetrasilane; 4), and 1,1,2,2,4,4,5,5-octamethyl-3,3,6,6-tetrasilylcyclohexasilane (cyclohexasilane; 5) were utilized as precursor materials and compared with the parent compound 2,2-disilyltrisilane (neopentasilane; 1). Compounds 2–5 were successfully oligomerized at λ = 365 nm with catalytic amounts of the neopentasilane oligomer (NPO). These oligomeric mixtures (NPO and 6–9) were used for the preparation of thin-layer materials. Optimum solution and spin coating conditions were investigated, and amorphous silicon–carbon films were obtained. All thin-layer materials were characterized via UV/vis spectroscopy, light microscopy, spectroscopic ellipsometry, XPS, SEM, and SEM/EDX. Our results show that the carbon content and especially the bandgap can be easily tuned using these single-source precursors via LPD. American Chemical Society 2023-09-13 /pmc/articles/PMC10523434/ /pubmed/37700615 http://dx.doi.org/10.1021/acs.inorgchem.3c01846 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Sauermoser, Aileen
Lainer, Thomas
Knoechl, Andreas
Goni, Freskida
Fischer, Roland C.
Fitzek, Harald
Dienstleder, Martina
Prietl, Christine
Kelterer, Anne-Marie
Bandl, Christine
Jakopic, Georg
Kothleitner, Gerald
Haas, Michael
Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title_full Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title_fullStr Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title_full_unstemmed Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title_short Fabrication of Amorphous Silicon–Carbon Hybrid Films Using Single-Source Precursors
title_sort fabrication of amorphous silicon–carbon hybrid films using single-source precursors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523434/
https://www.ncbi.nlm.nih.gov/pubmed/37700615
http://dx.doi.org/10.1021/acs.inorgchem.3c01846
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