In this work, a N-doped CsTi2NbO7@g-C3N4 (NTCN) heterojunction nanocomposite was synthesized by a simple one-step calcination method. The as-prepared samples were characterized by means of X-ray diffraction patterns, scanning electron microscopy, high-angle annular dark-field scanning transmission electron microscopy, and Fourier transformed infrared spectroscopy. The results showed that g-C3N4 was formed both on the surface and within the interlayers of CsTi2NbO7, in which CsTi2NbO7 was in situ doped by nitrogen atoms to form N–CsTi2NbO7. The NTCN composite displayed higher electrocatalytic activity toward the detection of nitrite than pure CsTi2NbO7 and g-C3N4. The main reasons could be attributed to the synergistic effects of morphology engineering, N-doping, and layered heterojunction. The NTCN-based electrochemical sensor expressed a good linear relationship range from 0.0999 to 3.15 mmol/L with a detection limit of 2.63 × 10−5 mol/L. The good recovery, stability, and reproducibility of this biosensor showed the potential application in environmental monitoring.

Integration of the III–V material systems on Si is an enabling technology for achieving high efficiency heterojunction Si-based photovoltaic devices. Gallium phosphide (GaP) offers numerous potential electrical, optical, and material advantages over amorphous silicon (a-Si) for the realization of several heterojunction solar cell designs. In this paper, details are given for the growth, fabrication, and characterization of different n-GaP/n-Si heterojunction solar cells to explore the effect of GaP as a carrier-selective contact. The cell performance is promising with high Si bulk lifetime (∼2.2 ms at the injection level of 1015 cm−3) and an open-circuit voltage of 618 mV and an efficiency of 13.1% in this new solar cell design. In addition to GaP as an electron-selective contact, MoOx was successfully implemented as a hole-selective contact in the n-GaP/n-Si heterojunction solar cell, increasing efficiency to 14.1% by improving the short wavelength response. The Si bulk lifetime is maintained during growth of GaP on Si by two different approaches and their effects on GaP/Si solar cell performance are also presented.

The novel visible-light-responsive direct solid-state Z-scheme g-C3N4/BiOI heterojunction has been synthesized successfully by means of a solid phase calcination method and used for the degradation of microcystin-LR (MC-LR). The layered g-C3N4 disperses on the surface of BiOI microspheres. The samples are characterized by FESEM, HRTEM, XRD, FT-IR, UV-vis spectroscopy, XPS, BET, PL, and Mott–Sckottky. The photocatalytic activity and photodegradation mechanism of the as-prepared g-C3N4/BiOI microsphere photocatalysts are conducted under visible light irradiation using MC-LR as the target pollutant. The g-C3N4/BiOI material exhibits superior photocatalytic performance when compared with pure BiOI, the possible reason is the efficient separation of photogenerated carriers at the interface between g-C3N4 and BiOI. The heterostructure is responsible for the improved separation efficiency of photogenerated electron–hole pairs and thus the higher photocatalytic activity. The possible photocatalytic mechanism is proposed based on relative band positions of these two semiconductors.

A series of Ag2S/Ag2WO4 composite microrods with different Ag2S contents (10–50 wt%) were synthesized via a facile successive precipitation route. The texture and optical properties of the pure Ag2S, Ag2WO4, and Ag2S/Ag2WO4 composites were intensively characterized by some physicochemical characterizations like N2 physical adsorption, x-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, Ultraviolet–visible spectroscopy, x‐ray photoelectron spectroscopy, photoluminescence spectroscopy, and photocurrent measurements. Under visible light irradiation, different organic dyes, e.g., methylene blue and methyl orange dye were applied to evaluate the photocatalytic performances by their photocatalytic degradation reactions. The Ag2S/Ag2WO4 composite microrods exhibited superior photocatalytic activity and stability. The high crystallinity of Ag2WO4 and improved texture properties of Ag2S/Ag2WO4 resulted in their enhanced photocatalytic property. More importantly, the Ag2S/Ag2WO4 heterojunctions with matching electronic band structures obviously enhanced the separation of photo‐generated electrons and holes, further promoting the photocatalytic reaction.

Visible-light responsive plasmonic Ag2O/Ag/g-C3N4 nanosheets (NS) were successfully prepared by a simple and green photodeposition method. The obtained composites were characterized by XRD, Fourier transform infrared, transmission electron microscopy, UV-vis, and the photoluminescence (PL) results indicated that the Ag2O/Ag/g-C3N4 NS composites showed better photoabsorption performance than g-C3N4 due to the surface plasmon resonance effect of Ag nanoparticles. Meanwhile, the composite exhibited excellent photocatalytic activities, which was ∼3.8 and ∼3.0 times higher than those of bulk g-C3N4 and pure g-C3N4 NS, respectively. Moreover, the as-prepared composites showed a high structural stability in the photodegradation of Rhodamine B. A possible photocatalytic and charge separation mechanism was suggested based on the PL spectra and the active species trapping experiment.

C3N4/Bi2WO6 heterojunction photocatalysts were successfully synthesized using consecutive hydrothermal and calcination processes. These photocatalysts were characterized using x-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet-visible diffuse reflectance spectroscopy, x-ray photoelectron spectroscopy, and photoluminescence measurements. The results of these measurements indicated that the Bi2WO6 nanoparticles were approximately 30–50 nm and uniformly distributed on the surface of C3N4 lamellar structures. The 20% C3N4/Bi2WO6 displayed enhanced visible-light absorption from 432 nm to 468 nm. Photocatalytic tests also revealed that the 20% C3N4/Bi2WO6 photocatalyst exhibited significantly enhanced photocatalytic activity compared to that of pure C3N4 and Bi2WO6 under irradiation by visible light (λ > 420 nm). Furthermore, the excellent photocatalytic efficiency of the 20% C3N4/Bi2WO6 photocatalyst was determined to be related to the formation of C3N4/Bi2WO6 heterojunctions, and their presence was found to be generally beneficial for the separation of photogenerated electron–hole pairs.

ZnO/TiO2 heterojunction composite fibers were prepared via a physical route, i.e., first electrospinning titanium dioxide (TiO2) fibers, then pulse plating zinc (Zn) on the fibers, and at last thermal treating the fibers. The morphologies, phase structures, and photocatalytic property of the composite fibers were characterized by using field-emission gun scanning electron microscope, x-ray diffractometer, high-resolution transmission electron microscope, and ultraviolet–visible spectrophotometer. It was found that a full or partial lattice coherent heterojunction was formed between the TiO2 fibers and zinc oxide (ZnO) particles, due to thermal treatment at 400 °C, which simultaneously resulted in the phase transformations including Zn to ZnO and amorphous TiO2 to anatase TiO2. The experimental results demonstrated that the photocatalytic activity of the composite fibers was improved and exhibited a value more than two times higher than that of TiO2 fibers.