TiO2 with exposed (001) facets/Bi4O5Br2 nanosheets heterojunction with enhanced photocatalytic for NO removal.

A TiO2 with exposed (001) facets/Bi4O5Br2 nanosheets heterojunction (TNS/BOB) was fabricated via a hydrothermal and electrostatic self-assembly method. The photocatalytic activity for NO removal was evaluated under simulated solar light irradiation. Through optimizing the content of TNS nanosheets, the photo-oxidative NO removal rate of 15% TNS/BOB was increased by up to 54.3%. This value is much higher than that of the individual components TNS (31.1%) and BOB (37.7%). Through capturing experiments and electron spin resonance (ESR) measurements, the main active species in the photocatalytic process were identified as ·[Formula: see text] and ·OH. Discrete Fourier transform computation results and ESR tests revealed that the photo-induced electrons in TNS should recombine with the holes in BOB, leading to effectively promoted charge separation at the TNS/BOB interface through the Z-type charge transfer. This work showed that with appropriate facet control and heterojunction design TiO2 can be used as an effective visible-light photocatalyst material.

Oxygen vacancy rich Bi2O4-Bi4O7-BiO2-x composites for UV-vis-NIR activated high efficient photocatalytic degradation of bisphenol A.

To fully utilize the solar light, photocatalyst with broad spectrum response from UV to near-infrared (NIR) is desirable. In this work, ternary mixed valent Bi2O4-Bi4O7-BiO2-x with rich oxygen vacancy has been synthesized through one-pot hydrothermal treatment of NaBiO3. The results showed that through adjusting the hydrothermal conditions, oxygen vacancy-rich Bi2O4-Bi4O7-BiO2-x nanocomposites with much higher efficiency than single or mixed bismuth oxides (Bi2O4, Bi4O7, BiO2-x and Bi4O7-BiO2-x,) can be synthesized for photocatalytic degradation of bisphenol A (BPA) under UV, visible, and NIR light irradiation. In addition, the liquid chromatography-mass spectrometer (LC-MS) characterization demonstrated that BPA was oxidized to 4-isopropenyphenol first and the rings were opened sequentially under NIR light irradiation. Further detection of reactive species indicated that holes, O2-, and OH were the main oxidizing species in the degradation system. The experimental observations and density functional theory (DFT) calculations suggested that both type-II and the Z-scheme charge transfer with oxygen vacancies as electrons and holes mediators were formed at the interfaces of Bi2O4, Bi4O7, and BiO2-x, resulting in a very efficient separation of photogenerated charge carriers in the composite. This work adds to the growing potential of mixed valent bismuth oxides based photocatalysts and is expected to accelerate the pace of the development of new-generation photocatalysts with high efficiency utilizing full-spectrum solar light.

Synergetic Effects of Pd0 Metal Nanoparticles and Pd2+ Ions on Enhanced Photocatalytic Activity of ZnWO4 Nanorods for Nitric Oxide Removal.

Doping and novel metallic nanoparticles loading on the photocatalyst are two effective means to enhance its photocatalytic activity. In our study, Pd0/Pd2+-co-modified ZnWO4 nanorods were fabricated by a two-step hydrothermal process and room-temperature reduction method. The performance of the as-prepared samples was evaluated through the photocatalytic nitric oxide (NOx) removal under simulated solar and visible-light irradiation. Pd0/Pd2+-co-modified ZnWO4 nanorods present a significantly enhanced photocatalytic activity for NOx removal compared with Pd0-loaded or Pd2+-doped ZnWO4 under simulated sunlight irradiation owing to a narrower band gap of Pd2+ doping compared with that of pure ZnWO4. The role of Pd0 nanoparticles is to act as an electron reservoir to restrain the recombination of e-/h+ pairs. According to the trapping measurements, the photoinduced holes and electrons play critical roles during the photocatalytic process. In addition, electron spin resonance (ESR) results further confirm that •O2- and •OH radicals are present and assist in the photocatalysis under simulated solar light irradiation. Stability test demonstrated that 1.5% Pd0/0.5% Pd2+-co-modified ZnWO4 nanorods as photocatalyst have high photocatalytic stability in NOx removal. This work proved that Pd0/Pd2+-co-modified ZnWO4 nanorods can be considered as an efficient photocatalyst for NOx removal.

Magnetically separable sulfur-doped SnFe2O4/graphene nanohybrids for effective photocatalytic purification of wastewater under visible light.

In this report, magnetically recoverable sulfur-doped SnFe2O4/graphene (S-SFO/GR) nanohybrids have been successfully developed via a facile solvothermal method. The characterizations on the structural, morphology, and optical properties of the nanohybrids indicate that S-SFO particles are successfully embedded on the GR nanosheets. The photocatalytic activity has been evaluated by photocatalytic degradation of chlorotetracycline under visible light irradiation. Among the composites with various mass ratios, the quasi-first-order rate constant of the nanohybrids formed with 9wt% S in SFO and 15wt% GR (9S-SFO/GR-15) can reach as high as 1.83min-1, which is much higher than that of SFO (0.68min-1) and SFO/GR (0.91min-1), confirming the important role of S and GR for the photocatalytic process. The combination of the three components of S, SFO, and GR has enhanced the visible light absorption capability and inhibited the recombination of photogenerated electron-hole. The 9S-SFO/GR-15 nanohybrids can be recovered easily by a magnet and reused for five times with remained photocatalytic efficiency about 70%. A possible catalytic mechanism explaining the efficient photocatalytic performances of the prepared nanohybrids has been proposed.

Magnetic core-shell ZnFe2O4/ZnS nanocomposites for photocatalytic application under visible light.

Magnetic core-shell ZnFe2O4/ZnS composites were synthesized through a two-step chemical process including the hydrothermal and the co-precipitation methods. The structural characterization revealed that the composites consisted of a layer of ZnS clusters on the surface of ZnFe2O4 nanoparticles. The band gap energy of the composite was estimated to be 2.2eV through the Kubelka-Munk plot, implying the possible application as a photocatalyst under the visible light radiation. The improved photocatalytic efficiency of the ZnFe2O4/ZnS composites was confirmed through the photocatalytic degradation of Methyl Orange. The increased absorption of the visible light and the enhanced separation of the electron-hole pairs due to the relative energy band positions in ZnFe2O4 and ZnS are considered as the main advantages. Additionally, the moderate magnetization of the ZnFe2O4 core insured the easy magnetic collection of the composite materials without affecting the photocatalytic performance. Our results showed that ZnFe2O4-based nanocomposites could be used as an effective and magnetic retrievable photocatalyst.