Herein, Fe-doped C₃N₄ high-performance photocatalysts, synthesized by a facile and cost effective heat stirring method, were investigated systematically using powder X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscopy (SEM) and Brunauer–Emmett–Teller (BET) surface area measurement, X-ray photoelectron (XPS), UV–Vis diffusion reflectance (DRS) and photoluminescence (PL) spectroscopy. The results showed that Fe ions incorporated into a g-C₃N₄ nanosheet in both +3 and +2 oxidation states and in interstitial configuration. Absorption edge shifted slightly toward the red light along with an increase of absorbance in the wavelength range of 430–570 nm. Specific surface area increased with the incorporation of Fe into g-C₃N₄ lattice, reaching the highest value at the sample doped with 7 mol% Fe (FeCN7). A sharp decrease in PL intensity with increasing Fe content is an indirect evidence showing that electron-hole pair recombination rate decreased. Interestingly, Fe-doped g-C₃N₄ nanosheets present a superior photocatalytic activity compared to pure g-C₃N₄ in decomposing RhB solution. FeCN7 sample exhibits the highest photocatalytic efficiency, decomposing almost completely RhB 10 ppm solution after 30 min of xenon lamp illumination with a reaction rate approximately ten times greater than that of pure g-C₃N₄ nanosheet. This is in an agreement with the BET measurement and photoluminescence result which shows that FeCN7 possesses the largest specific surface area and low electron-hole recombination rate. The mechanism of photocatalytic enhancement is mainly explained through the charge transfer processes related to Fe²⁺/Fe³⁺ impurity in g-C₃N₄ crystal lattice.

In this paper, silver (Ag) nanoclusters-loaded graphitic carbon nitride (g-C₃N₄) nanosheets are synthesized and their physical properties as well as photocatalytic activities are systematically investigated by different techniques. The existence of Ag atoms in the form of nanoclusters (NCs) rather than well-crystallized nanoparticles are evidenced by X-ray diffraction patterns, SEM images, and XPS spectra. The deposition of Ag nanoclusters on the surface of g-C₃N₄ nanosheets affect the crystal structure and slightly reduce the band gap energy of g-C₃N₄. The sharp decrease of photoluminescence intensity indicates that g-C₃N₄/Ag heterojunctions successfully prevent the recombination of photo-generated electrons and holes. The photocatalytic activities of as-synthesized photocatalysts are demonstrated through the degradation of rhodamine B (RhB) solutions under Xenon lamp irradiation. It is demonstrated that the photocatalytic activity depends strongly on the molar concentration of Ag⁺ in the starting solution. The g-C₃N₄/Ag heterojunctions prepared from 0.01 M of Ag⁺ starting solution exhibit the highest photocatalytic efficiency and allow 100% degradation of RhB after being exposed for 60 min under a Xenon lamp irradiation, which is four times faster than that of pure g-C₃N₄ nanosheets.

We report on the fabrication of desired magneto-photonic devices by a low one-photon absorption (LOPA) direct laser writing (DLW) technique on a photocurable nanocomposite consisting of magnetite ( ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ ) nanoparticles and a commercial SU-8 photoresist. The magnetic nanocomposite was synthesized by mixing ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ nanoparticles with different kinds of SU-8 photoresists. We demonstrated that the degree of dispersion of ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ nanoparticles in the nanocomposite depended on the concentration of ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ nanoparticles, the viscosity of SU-8 resist, and the mixing time. By tuning these parameters, the most homogeneous magnetic nanocomposite was obtained with a concentration of about 2 wt % of ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ nanoparticles in SU-8 2005 photoresist for the mixing time of 20 days. The LOPA-based DLW technique was employed to fabricate on demand various magneto-photonic submicrometer structures, which are similar to those obtained without ${\mathrm{Fe}}_3$ ${\mathrm{O}}_4$ nanoparticles. The magneto-photonic 2D and 3D structures with sizes as small as 150 nm were created. We demonstrated the strong magnetic field responses of the magneto-photonic nanostructures and their use as micro-actuators when immersed in a liquid solution.