Carbon nanotubes as electronic mediators combined with Bi2MoO6 and g-C3N4 to form Z-scheme heterojunctions to enhance visible light photocatalysis

In this paper, Z-scheme Bi2MoO6/CNTs/g-C3N4 composite-photocatalysts were prepared through a simple hydrothermal method. The analysis was performed by XRD, FT-IR, SEM, EDS, TEM, HRTEM, XPS, BET, UV-Vis diffuse reflectance and PL spectrums. Various analyses show that CNTs not only act as excellent charge transfer bridges, but also enable the formation of a Z-scheme of charge transfer mechanism between Bi2MoO6 and g-C3N4. This process not only effectively isolates electrons and holes, but also prolongs electron-hole pair lifetimes, resulting in a substantial improvement in the photocatalytic performance of the composite photocatalyst. Best photocatalytic degradation performance was shown by Bi2MoO6/CNTs/g-C3N4 composite photocatalyst under simulated sunlight, while the composite photocatalyst still maintained extremely high degradation performance in cycling tests.

Hydrothermal Fabrication of BiVO4/ Diatomite Composite Photocatalysts and their Photocatalytic Performance

A hydrothermal process was proposed to prepare BiVO4/ diatomite composite photocatalysts, where BiVO4 was grown from a precursor solution containing diatomite, and EDTA used as a chelating agent to prevent the precipitation of precursor solution compositions on diatomite before hydrothermal treatment. The effect of some processing parameters like diatomite percentage and Ag-loaded amount on their photocatalytic performance were also investigated in detail by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), BET, and UV‐Vis spectroscopy. The results show that BiVO4/ diatomite composite photocatalysts can be successfully prepared at 160 °C for the duration of 3h by the hydrothermal process. The diatomite has two significant impacts on their photocatalytic performance: (1) enhancing the dispersion of BiVO4 crystallites due to its high porosity and specific surface area to favor their photocatalytic performance, and (2) having a light screening effect to incident visible light to decrease their photocatalytic activity. Appropriately incorporating diatomite could improve their photocatalytic performance, but the overuse of diatomite would reduce that. Similarly, depositing Ag could effectively improve their photocatalytic activity because of its good light absorption and photosensitive characteristics, but excessive addition would result in their decrease since the overuse of Ag would also promote the electron-hole recombination.

Constructing g-C3N4/Cd1−xZnxS-Based Heterostructures for Efficient Hydrogen Production under Visible Light

Two types of photocatalysts, 1%Pt/Cd1−xZnxS/g-C3N4 (x = 0.2–0.3) and Cd1−xZnxS/1%Pt/g-C3N4 (x = 0.2–0.3), were synthesized by varying the deposition order of platinum, and a solid solution of cadmium and zinc sulfides onto the surface of g-C3N4. The characterization of photocatalysts showed that, for 1%Pt/Cd1−xZnxS/g-C3N4, small platinum particles were deposited onto a solid solution of cadmium and zinc sulfides; in the case of Cd1−xZnxS/1%Pt/g-C3N4, enlarged platinum clusters were located on the surface of graphitic carbon nitride. Based on the structure of the photocatalysts, we assumed that, in the first case, type II heterojunctions and, in the latter case, S-scheme heterojunctions were realized. The activity of the synthesized samples was tested in hydrogen evolution from triethanolamine (TEOA) basic solution under visible light (λ = 450 nm). A remarkable increase in hydrogen evolution rate compared to single-phase platinized 1%Pt/Cd1−xZnxS photocatalysts was observed only in the case of ternary photocatalysts with platinum located on the g-C3N4 surface, Cd1−xZnxS/1%Pt/g-C3N4. Thus, we proved using kinetic experiments and characterization techniques that, for composite photocatalysts based on Cd1−xZnxS and g-C3N4, the formation of the S-scheme mechanism is more favorable than that for type II heterojunction. The highest activity, 2.5 mmol H2 g−1 h−1, with an apparent quantum efficiency equal to 6.0% at a wavelength of 450 nm was achieved by sample 20% Cd0.8Zn0.2S/1% Pt/g-C3N4.

Fabrication of La2O3/g-C3N4 Heterojunction with Enhanced Photocatalytic Performance of Tetracycline Hydrochloride

In this study, La2O3/g-C3N4 heterojunction photocatalysts doped with different dosages of La2O3 were constructed by a facile ultrasound-assisted calcination approach. The as-prepared photocatalysts were characterized by XRD, FTIR, FESEM, TEM, XPS, PL and DRS to verify the composite photocatalysts’ purity and to investigate their structural, morphological and elemental composition, and their energy band. According to the results, a type of pure rod–sheet-shaped, heterostructured nanoparticle was successfully obtained. Decorated with 10% La2O3, 2 g/L of the composite sample had a 93% degradation rate for 20 mg/L tetracycline hydrochloride within 2 h under visible light at a pH of 7. After four successive photocatalytic runs, satisfactory stability and reusability was exhibited, with 70% of the tetracycline hydrochloride being removed in the final experiment. Electrons (e−), photogenerated holes (h+), superoxide radical anions (O2−) and hydroxyl radicals (OH) were the fundamental active species during the photocatalytic process and were investigated via quenching experiments. Furthermore, possible photocatalytic mechanisms were analyzed in this work.