In this work, we integrated Ag3PO4 with Bi4Ti3O12 to form Bi4Ti3O12/Ag3PO4 heterojunction nanocomposites by an ion-exchange method. The as-prepared Bi4Ti3O12/Ag3PO4 composites were systematically characterized by means of XRD, SEM, TEM, BET, XPS, UV-vis DRS, EIS, PL spectroscopy, and photocurrent response. SEM, TEM, and XPS results demonstrate the creation of Bi4Ti3O12/Ag3PO4 heterojunction with obvious interfacial interaction between Bi4Ti3O12 and Ag3PO4. PL spectra, EIS spectra, and photocurrent responses reveal that the composites display an enhanced separation efficiency of photogenerated electron-hole pairs, which is due to the charge transfer between Bi4Ti3O12 and Ag3PO4. Rhodamine B (RhB) was chosen as the target organic pollutant to evaluate its degradation behavior over Bi4Ti3O12/Ag3PO4 composites under simulated sunlight irradiation. Compared to bare Bi4Ti3O12 and Ag3PO4 nanoparticles, the composites exhibit a significantly enhanced photocatalytic activity. The highest photocatalytic activity is observed for the 10% Bi4Ti3O12/Ag3PO4 composite with 10% Bi4Ti3O12 content, which is about 2.6 times higher than that of bare Ag3PO4. The photocatalytic mechanism involved was investigated and discussed in detail.

We report a plasmonic refractive index sensor with a wide measurement range based on periodic gold nanocubes coupled with a gold film. The theoretical sensing range is 1.0–1.8. The structure consists of two-dimensional gratings composed of periodic nanocubes that both excite local surface plasmon resonance and stimulate propagating surface plasmon resonance. The strong resonance of the multiple surface plasmons is suitable for use in refractive index sensing and effectively reduces the full width at half maximum of the resonance peak. The sensing performance of each resonant mode in the reflected spectrum is discussed in detail. The highest sensitivity and figure of merit of the proposed sensor are 1002 nm per refractive index units (RIU) and 417 RIU⁻¹, respectively. The proposed sensor will be useful for bio-chemical sensing applications such as measuring changes in the refractive index of gases or liquids.

Using P25 as the titanium source and based on a hydrothermal route, we have synthesized CaTiO₃ nanocuboids (NCs) with the width of 0.3–0.5 μm and length of 0.8–1.1 μm, and systematically investigated their growth process. Au nanoparticles (NPs) of 3–7 nm in size were assembled on the surface of CaTiO₃ NCs via a photocatalytic reduction method to achieve excellent Au@CaTiO₃ composite photocatalysts. Various techniques were used to characterize the as-prepared samples, including X-ray powder diffraction (XRD), scanning/transmission electron microscopy (SEM/TEM), diffuse reflectance spectroscopy (UV-vis DRS), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Rhodamine B (RhB) in aqueous solution was chosen as the model pollutant to assess the photocatalytic performance of the samples separately under simulated-sunlight, ultraviolet (UV) and visible-light irradiation. Under irradiation of all kinds of light sources, the Au@CaTiO₃ composites, particularly the 4.3%Au@CaTiO₃ composite, exhibit greatly enhanced photocatalytic performance when compared with bare CaTiO₃ NCs. The main roles of Au NPs in the enhanced photocatalytic mechanism of the Au@CaTiO₃ composites manifest in the following aspects: (1) Au NPs act as excellent electron sinks to capture the photoexcited electrons in CaTiO₃, thus leading to an efficient separation of photoexcited electron/hole pairs in CaTiO₃; (2) the electromagnetic field caused by localized surface plasmon resonance (LSPR) of Au NPs could facilitate the generation and separation of electron/hole pairs in CaTiO₃; and (3) the LSPR-induced electrons in Au NPs could take part in the photocatalytic reactions.