The biotemplating technique is an environmental-protective high-efficiency new technology by which the resulting TiO2 may simultaneously attain the duplication of structure and self-doping elements from biotemplate materials, which is highly desirable for photocatalytic applications. In this paper, aquatic plant leaves—including reed, water hyacinth, and duckweed—were used as both templates and silicon precursors to successfully synthesize biomorphic TiO2/SiO2 composite with mesoporous structures. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, N2 adsorption–desorption, and UV–visible diffuse reflectance spectra were applied to characterize the microstructures of the samples. The results show that all TiO2/SiO2 composites are mainly composed of an anatase phase with mesoporous structure and possess high specific surface area. Compared with commercial Degussa P25 TiO2, all TiO2/SiO2 samples display intensive light-harvesting efficiency, particularly in the visible light range. The activities were evaluated by using gentian violet as a target for photocatalytic degradation experiments under simulated solar irradiation. The TiO2/SiO2 samples templated by reed and water hyacinth leaves exhibit high activity, while the TiO2/SiO2 samples obtained from duckweed are inferior to P25 in the degradation of gentian violet. A synergistic effect of SiO2 incorporation and structural construction through biotemplating is proposed to be beneficial to photocatalytic activity.

ZnIn₂S₄, a novel two-dimensional visible light-responsive photocatalyst, has attracted much attention in the photocatalytic evolution of H₂ under visible light irradiation due to its attractive intrinsic photoelectric properties and geometric configuration. However, ZnIn₂S₄ still has severe charge recombination, which results in moderate photocatalytic performance. Herein, we report the successful synthesis of 2D/2D ZnIn₂S₄/Ti₃C₂ nanocomposites by a facile one-step hydrothermal method. The efficiency of the nanocomposites in photocatalytic hydrogen evolution under visible light irradiation was also evaluated for different ratios of Ti₃C₂, and the optimal photocatalytic activity was achieved at 5% Ti₃C₂. Importantly, the activity was significantly higher than that of pure ZnIn₂S₄, ZnIn₂S₄/Pt, and ZnIn₂S₄/graphene. The enhanced photocatalytic activity is mainly due to the close interfacial contact between Ti₃C₂ and ZnIn₂S₄ nanosheets, which amplifies the transport of photogenerated electrons and enhances the separation of photogenerated carriers. This research describes a novel approach for the synthesis of 2D MXenes for photocatalytic hydrogen production and expands the utility of MXene composite materials in the fields of energy storage and conversion.

N-doped TiO₂ with oxygen vacancies exhibits many advantages for photocatalysis, such as enhanced visible light absorbency, inhibition of the photogenerated charge carrier recombination, etc. However, preparation of N-doped TiO₂ with oxygen vacancies under mild conditions is still a challenge. Herein, N-doped TiO₂ nanospheres with tetrahedral Ti⁴⁺ sites were synthesized by using dodecylamine as template and assisted by l-alanine acids. The obtained samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV–Vis diffuse reflectance spectra (UV–Vis DRS). It was found that the dodecylamine as a neutral surfactant controlled the structure of TiO₂ spherical, while l-alanine acids provided a nitrogen source. The existence of tetrahedral Ti⁴⁺ sites in N-doped TiO₂ was also confirmed. The N-doped TiO₂ sample with tetrahedral Ti⁴⁺ sites exhibited significantly improved photocatalytic performance for degradation of methylene blue solution under UV light or visible light irradiation. A combined time-resolved infrared (IR) spectroscopy study reveals that the enhanced photocatalytic performance could be attributed to a large amount of photogenerated charge carriers and efficient charge separation. It is demonstrated that the shallow donor state produced by oxygen vacancies of tetrahedral Ti⁴⁺ sites can effectively promote separation of charge carriers besides capturing electrons.

In the last few decades, many new synthesis techniques have been developed in order to obtain an effective visible-light responsive photocatalyst for hydrogen production by water splitting. Among these new approaches, the biotemplated synthesis method has aroused much attention because of its unique advantages in preparing materials with special morphology and structure. In this work, Hydrilla verticillata (L. f.) Royle was used as a biotemplate to synthesize a CdS photocatalyst. The as-synthesized sample had the microstructure of nano-scaled aggregate networks and its activity for photocatalytic hydrogen production was six times higher than that of CdS synthesized without a template in an Na₂S-Na₂SO₃ sacrificial system. The use of Pt and PdS as cocatalysts further improved the hydrogen production rate to 14.86 mmol/g·h under visible-light (λ ≥ 420 nm) irradiation, so the hydrogen production can be directly observed by the naked eye. The results of characterization showed that the as-synthesized CdS photocatalyst has a high specific surface area and narrow band gap, which is favorable for light absorption and photocatalytic reaction. This work provides a new way to search for efficient visible-light catalysts and confirms the uniqueness of a biotemplated synthesis method in obtaining specially structured materials.

A series of ceria-zirconia solid solutions were synthesized using tobacco leaves, stems and stem-silks as biotemplates. A combination of physicochemical techniques such as powder X-ray diffraction (XRD), N₂ adsorption/desorption measurement, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to characterize the as-synthesized samples. The results show that the morphologies of the templates were well replicated in the obtained ceria-zirconia solid solutions. Catalytic oxidation activities of CO over the ceria-zirconia solid solutions were then investigated. The catalyst templated by tobacco stem-silk exhibited higher conversion of CO at lower temperature than that of ceria-zirconia solid solutions templated by tobacco leaves and stems or without templates due to its special morphology. The catalyst even showed similar CO conversion when compared to ceria-zirconia solid solutions doped with 1.0 wt % noble metals such as Pt, Ag and Au. The results highlighted the advantages of using tobacco as biotemplate.