Abstract

Magnetic silver-coated ferrite nanoparticles with 39.8% weight gain (relative to ferrite nanopowder coated by a silver layer) were synthesized by electroless deposition of silver on ferrite nanopowder. The mechanism of the electroless deposition was explored in terms of pretreatment, sensitization, activation, and the reduction of silver–ammonia complexes. Experiments showed that the optimal deposition conditions were a temperature of 50°C, pH value of 10 to 12, duration of 65 min with ethanol plus polyethylene glycol as additives, and ultrasonic vibration as a method of dispersing the nanoparticles. From transmission electron microscopy (TEM) images, it was observed that as-synthesized nanoparticles had a core–shell structure with a particle size of 35 nm to 90 nm and a shell thickness of 5 nm to 20 nm. X-ray diffraction (XRD) analysis confirmed that only ferrite and metallic silver were present in the product. Electrical resistance and magnetic hysteresis measurements demonstrated that the nanoparticles were both electrically conductive (volume electrical resistivity on the order of 10−4 Ω cm to 10−3 Ω cm when compressed to pressure of 2 × 10 6 Pa) and possessed ferrimagnetic properties. After a thick-film paste, obtained with the nanoparticles as the functional phase, was directly written and sintered, scanning electron microscopy (SEM) analysis and electrical resistance measurements of conductive lines in the acquired array pattern showed that an electrically conductive network with some defects and cavities was formed, with a volume electrical resistivity of 1 × 10−4 Ω cm to 1 × 10−3 Ω cm.

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