Enhanced photoelectrocatalytic performance for degradation of dimethyl phthalate over well-designed 3D hierarchical TiO2/Ti photoelectrode coupled dual heterojunctions.

A novel A/R-TiO2 NSs/NRs photoelectrode was constructed through electrodeposition of anatase TiO2 nanosheets (A-TiO2 NSs) with highly exposed {001} facet onto the 1D upright rutile TiO2 nanorods (R-TiO2 NRs). At first, A/R-TiO2 NSs/NRs exhibited enhanced adsorption of dimethyl phthalate (DMP) due to the specific recognition between Lewis acid sites of {001} facet and Lewis basic DMP. NH3-TPD and Py-IR revealed that the Lewis acidity on the {001} facet of A-TiO2 NSs was much stronger than that of R-TiO2 NRs, demonstrating superior adsorption capacity to DMP. DFT theoretical calculations coupled with in-situ ATR-FTIR spectra were performed to investigate the binding adsorption behavior of DMP on A/R-TiO2 NSs/NRs. Secondly, the rapid separation of excited charges and strong oxidation of h+ were achieved by the synergistic effect of dual heterojunctions (A/R "phase heterojunction" and {111}/{110} "facet heterojunction"). The A/R-TiO2 NSs/NRs exhibited 100% degradation efficiency for the target pollutant DMP within 3 h, whose rate constant (k) was 18.02 × 10-3 min-1, 2.16 times that of pure R-TiO2 NRs. In real wastewater application, A/R-TiO2 NSs/NRs achieved 93.8% elimination of DMP during 4 h and preserved excellent stability after 5 cycles, promising a wide-range of applications in water environment remediation.

Analysis on the difference of skin surface lipids during blue light therapy for acne by lipidomics.

Acne is a chronic inflammatory skin disease of the sebaceous glands of the hair follicles, caused by a variety of factors and tends to recur, causing skin damage and psychological stress to patients. Blue light (415nm) is a popular physical therapy for acne, however, studies on the effects of blue light on skin surface lipids (SSL) have not been exhaustively reported. So, we want to investigate the difference in SSL before and after acne treatment with blue light and to reveal the potential mechanism of acne treatment with blue light from the lipid level. SSL samples were collected and physiological indicators (moisture content, transepidermal water loss (TEWL), sebum content and pH) were measured. By using ultra performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) with multivariate data analysis methods to obtain specific information on the lipid composition. Analysis of the physiological index data showed a significant increase in moisture content (p = 0.042), pH (p = 0.000) and a significant decrease in sebum content(p = 0.008) in the after treatment area (AT group), while there was no significant change in TEWL values. A total of 2398 lipids were detected by lipidomics analysis and 25 differential lipids were screened. Triradylglycerols (TGs), isoprenoids and hopanoids being the potential differential lipids. Among the lipids associated with the skin barrier, only monounsaturated fatty acids (MUFA) (p = 0.045) were significantly increased. This study revealed significant changes in SSL after blue light treatment for acne, suggesting that blue light exposure may cause changes in the relative lipid content and redistribution of lipid components, and that whether it damages the skin barrier requires further study.

In situ construction of 3D TiO2 photoelectrode with multilevel facet heterojunctions towards the efficient removal of bisphenol A.

An innovative three-dimensional (3D) TiO2 photoelectrode with multilevel facet heterojunctions (FHs) is rationally designed based on in situ 1D rutile TiO2 nanorods with top {111} facets on a Ti mesh substrate. The 3D configuration composed of nanosheets and nanorods is provided with large specific area. The stepped band structure of the multilevel FH gives further impetus to spatial charge separation. The obtained FH-{111}TiO2/Ti photoelectrode achieves a 100% removal of bisphenol A (BPA) in only 20 min and presents an outstanding stability even after 10 cycles. Briefly, this work provides a reference pathway for the highly efficient removal of BPA.

Efficient photocatalytic removal of phthalates easily implemented over a bi-functional {001}TiO2 surface.

It is stubborn to remove the lowly concentrated phthalic acid esters (PAEs) that usually coexist with other highly concentrated but low-toxic pollutants in municipal sewage. Herein, we report a novel strategy for completely removing the PAEs over a bi-functional {001}TiO2 surface (with highly exposed {001} facet), which not only serve as functional sites to specifically adsorb the target PAEs pollutants, but also contribute to an enhanced oxidation ability. The adsorption behavior of PAEs on {001}TiO2 is analyzed deeply through kinetic experiments combining with in situ ATR-FTIR spectroscopy and theoretical calculations. The results reveal that the adsorption capacities of PAEs on {001}TiO2 are about 4-5 times higher than that on TiO2, both of which follow the pseudo-second-order and Langmuir model. This is mainly attributed to the interfacial Lewis Acid-Base Pair between {001} facet Ti5c sites and CO of PAEs. Benefitting from the specific adsorption capability toward target pollutant and enhanced oxidation ability of {001} facets, nearly 100% of DMP or DEP in simulated wastewater can be eliminated by {001}TiO2 within 2 h illumination, and the relevant degradation rate constants (k) (3.67 h-1 for DMP and 2.19 h-1 for DEP) are 5.73 and 3.08 folds higher than that of pure TiO2, respectively. In the application of municipal wastewater, nearly 76% of DMP and 85% DEP can be eliminated by {001}TiO2 within 2 h illumination, which are nearly 3-6 fold higher than that of pure TiO2.