Light Absorption and Scattering Properties of Ag@TiO₂ Nanosphere Dimer for Photocatalytic Water Purification

Finding high-performance and low-cost materials is essential for high-quality photocatalytic water purification to expand the spectral response and improve light utilization. In this paper, we used relatively inexpensive materials such as Ag and TiO₂. The influence of particle spacing, core radius, shell thickness, environmental refractive index, and incident light direction angle on the light absorption and scattering properties, local electric field enhancement, and photothermal effect of the Ag@TiO₂ core-shell nanosphere dimer is investigated by using the finite element method and the finite difference time domain. The formation mechanism of multipole resonance mode of the dimer is revealed by means of the multipole decomposition theory and the internal current distribution of the particles. The results show that light absorption and scattering of the dimer can be tuned within the visible light range by changing the particle spacing, core radius, and shell thickness. With the azimuth angle of incident light increases, the longitudinal local surface plasmon resonance (L-LSPR) mode will transform into the transverse local surface plasmon resonance (T-LSPR) mode, and the L-LSPR mode makes the dimer have better local electric field enhancement. Strong light absorption can easily cause a sharp increase in the temperature around the dimer, accelerating the rate of catalytic oxidation reactions and the elimination of bacteria and viruses in water. Strong light scattering causes a significant enhancement of the electric field between the particles, making the generation of hydroxyl and other active oxides more efficient and convenient. This work establishes a theoretical basis for designing efficient water purification photocatalysts.