Synthesis of ZrN–SiO2 core–shell particles by a sol–gel process and use as particle‐based structured coloring material
ZrN–SiO2 core–shell particles were prepared, where the ZrN core nanoparticles and SiO2 shell were designed to exhibit localized surface plasmon resonances (LSPRs) and structural coloring. The heating of ZrO2 nanoparticles with Mg3N2 under a nitrogen gas flow produced ZrN nanoparticles with a diamete...
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Veröffentlicht in: | Journal of the American Ceramic Society 2024-10, Vol.107 (10), p.6885-6895 |
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Sprache: | eng |
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Zusammenfassung: | ZrN–SiO2 core–shell particles were prepared, where the ZrN core nanoparticles and SiO2 shell were designed to exhibit localized surface plasmon resonances (LSPRs) and structural coloring. The heating of ZrO2 nanoparticles with Mg3N2 under a nitrogen gas flow produced ZrN nanoparticles with a diameter in the range of 10–20 nm. The dispersion of ZrN nanoparticles in water exhibited an absorption maximum at approximately 700 nm owing to LSPRs. An SiO2 shell was formed on the ZrN nanoparticles using a sol–gel process. Scanning transmission electron microscopy confirmed the formation of ZrN–SiO2 core–shell particles containing ZrN particles with a diameter of approximately 10 nm. The SiO2 shell thickness was controlled by varying the reaction time to form SiO2. The use of particles as a structural component of a structural color material owing to the high uniformity of the size of obtained core–shell particles was investigated. The obtained ZrN–SiO2 core–shell particles were arrayed on a glass substrate using a layer‐by‐layer method. The particle‐stacked film of the ZrN–SiO2 core–shell particles exhibited the maximum reflection depending on the particle size of the SiO2 shell.
ZrN–SiO2 core–shell particles were synthesized, with 10–20 nm ZrN nanoparticle cores designed for localized surface plasmon resonances (LSPRs) and SiO2 shells for structural coloring. ZrN nanoparticles, exhibiting an absorption peak at 700 nm due to LSPRs, were coated with SiO2 through a sol–gel process, which allowed control of shell thickness by adjusting the reaction time. The particle‐stacked films demonstrated light reflection characteristics dependent on the SiO2 shell thickness. |
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ISSN: | 0002-7820 1551-2916 |
DOI: | 10.1111/jace.19981 |