Abstract

Enhanced thermal, chemical, and mechanical properties of different metal nanoparticle morphologies integrated with metal oxides have been reported in multiple instances. The chemical and material robustness of metal nanoparticles incorporated surficially and into the bulk of distinct as well as spontaneously formed morphologies of metal oxides through solution-based and microwave-based approaches are investigated in this study. These composites were tested for their chemical and material robustness by exposing films formed on quartz substrates to high temperatures (800 °C) in an air ambient as well as to extreme conditions of pH, often encountered in harsh environment applications such as sensing and catalysis. The changes in the optical properties and crystallinity have been studied using in situ absorption and ex situ X-ray diffraction analyses and electron microscopy. The trends observed with respect to the changes in the plasmonic absorbance were validated theoretically and found to be in reasonable agreement with the experimental data. Confirmations of the phenomena occurring in different morphologies and architectures were thereby corroborated through careful interpretations from experiments and predictions from theoretical models. We, therefore, report a simple solution-based process for achieving engineered harsh environment-compatible nanocomposites through studies specifically tailored for such applications such as catalysis, sensing, energy storage, and enhanced luminescence.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.