Tuning of Shells in Trilaminar Core@Shell Nanocomposites in Controlling Electromagnetic Interference through Switching of Shielding Mechanism.

Fe3O4@SiO2@PPy core-shell nanocomposites were fabricated by the coating of SiO2 on Fe3O4 through base catalyzed hydrolysis of tetraethyl orthosilicate followed by encapsulation of polypyrrole (PPy). Subsequently, these trilaminar composites have been characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller, superconducting quantum interference devices, and measurement of the total shielding efficiency in the frequency range of 2-8 GHz. Our findings showed the highest total shielding efficiency (similar to 32 dB) of Fe3O4@SiO2@PPy (Fe3O4@SiO2/ pyrrole wt/wt = 1:9) and followed reflection as the dominant shielding mechanism. Such performance was attributed to poor impedance matching between the PPy (conducting)/SiO2 (insulating) and high electrical conductivity of Fe3O4@SiO2@PPy. Alternatively, electromagnetic (EM) waves incident on the SiO2@PPy interface could also account for enhancing the total shielding efficiency of Fe3O4@SiO2@PPy because of multireflection/refraction. Our earlier work also showed excellent total shielding efficiency of Fe3O4@C@PANI nanocomposites, through absorption as the dominant shielding mechanism. These findings clearly suggest that EM interference shielding in Fe3O4@SiO2@PPy and Fe3O4@C@PANI trilaminar core@shell nanocomposites is controlled by tuning of the shells through switching of the mechanism.