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Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface

Organic-inorganic material hybridization at the solid-state level is indispensable for the integration of IoT applications, but still remains a challenging issue. Existing bonding strategies in the field of electronic packaging tend to employ vacuum or ultrahigh temperature; however, these can cause...

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Autores principales: Yang, Tilo H., Kao, C. Robert, Shigetou, Akitsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345999/
https://www.ncbi.nlm.nih.gov/pubmed/30679603
http://dx.doi.org/10.1038/s41598-018-37052-1
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author Yang, Tilo H.
Kao, C. Robert
Shigetou, Akitsu
author_facet Yang, Tilo H.
Kao, C. Robert
Shigetou, Akitsu
author_sort Yang, Tilo H.
collection PubMed
description Organic-inorganic material hybridization at the solid-state level is indispensable for the integration of IoT applications, but still remains a challenging issue. Existing bonding strategies in the field of electronic packaging tend to employ vacuum or ultrahigh temperature; however, these can cause process complications and material deterioration. Here we report an easy-to-tune method to achieve hybrid bonding at the solid-state level and under the ambient atmosphere. Vacuum-ultraviolet (VUV)-induced reorganization with ethanol was used to develop hydroxyl-carrying alkyl chains through coordinatively-bonded carboxylate onto aluminum, whereas numerous hydroxyl-carrying alkyls were created on polyimide. The triggering of dehydration through these hydroxyls by merely heating at 150 °C for a few minutes produced robust organic-inorganic reticulated complexes within the aluminum/polyimide interface. The as-bonded aluminum/polyimide interface possessed an superior fracture energy of (2.40 ± 0.36) × 10(3) (J/m(2)) compared with aluminum and polyimide matrices themselves, which was mainly attributed to crack deflection due to the nano-grains of inorganic-organic reticulated complexes. The interfacial adhesion was successfully kept after humidity test, which was contributed by those anti-hydrolytic carboxylates. To the best of our knowledge, for the first time organic-inorganic bonding at the solid-state level was achieved using the ethanol-assisted VUV (E-VUV) process, a strategy which should be applicable to a diversity of plastics and metals with native oxides.
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spelling pubmed-63459992019-01-29 Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface Yang, Tilo H. Kao, C. Robert Shigetou, Akitsu Sci Rep Article Organic-inorganic material hybridization at the solid-state level is indispensable for the integration of IoT applications, but still remains a challenging issue. Existing bonding strategies in the field of electronic packaging tend to employ vacuum or ultrahigh temperature; however, these can cause process complications and material deterioration. Here we report an easy-to-tune method to achieve hybrid bonding at the solid-state level and under the ambient atmosphere. Vacuum-ultraviolet (VUV)-induced reorganization with ethanol was used to develop hydroxyl-carrying alkyl chains through coordinatively-bonded carboxylate onto aluminum, whereas numerous hydroxyl-carrying alkyls were created on polyimide. The triggering of dehydration through these hydroxyls by merely heating at 150 °C for a few minutes produced robust organic-inorganic reticulated complexes within the aluminum/polyimide interface. The as-bonded aluminum/polyimide interface possessed an superior fracture energy of (2.40 ± 0.36) × 10(3) (J/m(2)) compared with aluminum and polyimide matrices themselves, which was mainly attributed to crack deflection due to the nano-grains of inorganic-organic reticulated complexes. The interfacial adhesion was successfully kept after humidity test, which was contributed by those anti-hydrolytic carboxylates. To the best of our knowledge, for the first time organic-inorganic bonding at the solid-state level was achieved using the ethanol-assisted VUV (E-VUV) process, a strategy which should be applicable to a diversity of plastics and metals with native oxides. Nature Publishing Group UK 2019-01-24 /pmc/articles/PMC6345999/ /pubmed/30679603 http://dx.doi.org/10.1038/s41598-018-37052-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yang, Tilo H.
Kao, C. Robert
Shigetou, Akitsu
Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title_full Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title_fullStr Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title_full_unstemmed Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title_short Organic-Inorganic Solid-State Hybridization with High-Strength and Anti-Hydrolysis Interface
title_sort organic-inorganic solid-state hybridization with high-strength and anti-hydrolysis interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345999/
https://www.ncbi.nlm.nih.gov/pubmed/30679603
http://dx.doi.org/10.1038/s41598-018-37052-1
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