In this work, we report the enhanced catalytic reduction of 4-nitrophenol driven by Fe₃O₄-Au magnetic nanocomposite interface engineering. A facile solvothermal method is employed for Fe₃O₄ hollow microspheres and Fe₃O₄-Au magnetic nanocomposite synthesis via a seed deposition process. Complementary structural, chemical composition and valence state studies validate that the as-obtained samples are formed in a pure magnetite phase. A series of characterizations including conventional scanning/transmission electron microscopy (SEM/TEM), Mössbauer spectroscopy, magnetic testing and elemental mapping is conducted to unveil the structural and physical characteristics of the developed Fe₃O₄-Au magnetic nanocomposites. By adjusting the quantity of Au seeds coating on the polyethyleneimine-dithiocarbamates (PEI-DTC)-modified surfaces of Fe₃O₄ hollow microspheres, the correlation between the amount of Au seeds and the catalytic ability of Fe₃O₄-Au magnetic nanocomposites for 4-nitrophenol (4-NP) is investigated systematically. Importantly, bearing remarkable recyclable features, our developed Fe₃O₄-Au magnetic nanocomposites can be readily separated with a magnet. Such Fe₃O₄-Au magnetic nanocomposites shine the light on highly efficient catalysts for 4-NP reduction at the mass production level.

The nanocaps array of TiO₂/Ag bilayer with different Ag thicknesses and co-sputtering TiO₂-Ag monolayer with different TiO₂ contents were fabricated on a two-dimensional colloidal array substrate for the investigation of Surface enhanced Raman scattering (SERS) properties. For the TiO₂/Ag bilayer, when the Ag thickness increased, SERS intensity decreased. Meanwhile, a significant enhancement was observed when the sublayer Ag was 10 nm compared to the pure Ag monolayer, which was ascribed to the metal-semiconductor synergistic effect that electromagnetic mechanism (EM) provided by roughness surface and charge-transfer (CT) enhancement mechanism from TiO₂-Ag composite components. In comparison to the TiO₂/Ag bilayer, the co-sputtered TiO₂-Ag monolayer decreased the aggregation of Ag particles and led to the formation of small Ag particles, which showed that TiO₂ could effectively inhibit the aggregation and growth of Ag nanoparticles.

Many studies have shown that it is important to consider the harmful effects of phenolic hormones on the human body. Traditional UV detection has many limitations, so there is a need to develop new detection methods. We demonstrated a simple and rapid surface-enhanced resonance Raman scattering (SERRS) based detection method of trace amounts of phenolic estrogen. As a result of the coupling reaction, there is the formation of strong SERRS activity of azo compound. Therefore, the detection limits are as low as 0.2 × 10⁻⁴ for estrone (E1), estriol (E3), and bisphenol A (BPA). This method is universal because each SERRS fingerprint of the azo dyes a specific hormone. The use of this method is applicable for the testing of phenolic hormones through coupling reactions, and the investigation of other phenolic molecules. Therefore, this new method can be used for efficient detection.

Hexagonal Ag nanoparticle arrays are exclusively grown on top of the interstices of Au nanobowl arrays.