Abstract

In this context, we report the acoustic shock wave processing on amorphous Carbon quantum dots (a-CQD) such that its degree of graphitization and magnetic properties are analyzed. Analytical techniques such as the Raman spectrometer, high resonation–transmission electron microscopy (HR-TEM) and vibrating sample magnetometer (VSM) are utilized to understand the structural, morphological and magnetic properties changes under shocked conditions. The Raman spectroscopic data reveal that the ID/IG ratio is slightly reduced under shocked conditions and the observed values are 0.78, 0.77 and 0.75 for the respective 0, 150 and 300 shocked conditions. The formation of ultra-short-range graphitic nanostructures is confirmed by HR-TEM results at the 300-shocked condition. The most convincing and supporting results for the enhancement of the degree of graphitization are found by the outcome of the magnetic properties such that the saturation magnetization (Ms) is found to be linearly reduced with respect to the number of shock pulses and the observed values are 0.869, 0.757 and 0.710 emu/g for the 0, 150 and 300 shocked conditions, respectively. The electrical resistance of the a-CQD is found to be linearly reduced with respect to the number of shock pulses due to the reduction of sp3 carbon networks. The formation of crystalline graphitic nanostructures in amorphous CQD is explained on the basis of the hot-spot nucleation mechanism. Based on the obtained Raman, HR-TEM and VSM results, during the shocked conditions, slight enhancement of the graphitization is observed; however, from the structural stability point of view, the Carbon dots have high shock resistance than that of the amorphous carbon nanoparticles, multi-wall carbon nanotubes, and reduced graphene oxide nanoparticles. Hence, the title quantum dots can be strongly considered for the applications of device fabrication.

Full Text
Paper version not known

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.