Tuning electronic structure for enhanced photocatalytic performance: theoretical and experimental investigation of CuM1-xM'xO2 (M, M' = B, Al, Ga, In) solid solutions.

This study introduces robust screening methodology for the efficient design of delafossite CuM1-xM'xO2 solid-solution photocatalysts using band-structure engineering. The investigation not only reveals the formation rules for various CuM1-xM'xO2 solid solutions but also highlights the dependence on both lattice compatibility and thermodynamic stability. Moreover, the study uncovers the nonlinear relationship between composition and band gaps in these solid solutions, with the bowing coefficient determined by the substitution constituents. By optimizing the constituent elements of the conduction band edge and adjusting solubility, the band structure of CuM1-xM'xO2 samples can be fine-tuned to the visible light region. Among the examined photocatalysts, CuAl0.5Ga0.5O2 exhibits the highest H2 evolution rate by striking a balance between visible-light absorption and sufficient reduction potential, showing improvements of 28.8 and 6.9 times those of CuAlO2 and CuGaO2, respectively. Additionally, CuGa0.9In0.1O2 demonstrates enhanced electron migration and surpasses CuGaO2 in H2 evolution due to a reduction in the effective mass of photogenerated electrons. These findings emphasize the pivotal role of theoretical predictions in synthesizing CuM1-xM'xO2 solid solutions and underscore the importance of rational substitution constituents in optimizing light absorption, reduction potentials, and effective mass for efficient hydrogen production.

DFT calculations for single-atom confinement effects of noble metals on monolayer g-C3N4 for photocatalytic applications.

Graphitic carbon nitride, as a very promising two-dimensional structure host for single atom catalysts (SACs), has been studied extensively due to its significant confinement effects of single atoms for photocatalytic applications. In this work, a systematic investigation of g-C3N4 confining noble metal single atoms (NM1@g-C3N4) will be performed by using DFT calculations. The geometric structure calculations indicate that the most favorable anchored sites for the NM1 is located in the six-fold cavity, and the deformed wrinkle space of g-C3N4 helps the NM1 to be stabilized in the six-fold cavity. The electronic structure calculations show that the conduction band of NM1@g-C3N4 moved down and crossed through the Fermi level, resulting in narrowing the band gap of the NM1@g-C3N4. Moreover, the confined NM1 provide a new channel of charge transport between adjacent heptazine units, resulting in a longer lifetime of photo-generated carriers except Ru, Rh, Os and Ir atoms. Furthermore, the d-band centres of NM1 in NM1@g-C3N4 show that Rh1@, Pd1@, Ir1@ and Pt1@g-C3N4 SACs may have better photocatalytic performance than other NM1@g-C3N4 SACs. Finally, Pt1@g-C3N4 SACs are considered to have higher photocatalytic activity than other NM1@g-C3N4 SACs. These results demonstrate that the confinement effects of noble metals on monolayer g-C3N4 not only makes the single atom more stable to be anchored on g-C3N4, but also enhances the photocatalytic activity of the system through the synergistic effect between the confined NM1 and the monolayer g-C3N4. These detailed research may provide theoretical support for engineers to prepare photocatalysts with higher activity.

[Dexamethasone Blocks Adriamycin-induced Podocytes'Mobility via Impacting Nephrin Expression].

OBJECTIVE: To explore how dexamethasone (Dex) directly restores kidney podocyte function in adriamycin (ADR)-induced nephrotic model and the effects of Dex on the motility of podocytes, to analyze whether nephrin is a key signal molecule in the process. METHODS: The cultured podocytes were divided into three growps: ADR treated group, ADR+Dex group, blank control group. The analyses of podocytes function were performed using scrape-wound, Transwell migration assays and FITC-BSA. Quantitative real-time PCR and Western blot were used to test the expression of nephrin. Male SD rats were used to generate ADR-induced nephrology model, and randomly divided into three groups: ADR group, ADR+Dex group and normal group. At 7 d, 14 d, 21 d and 28 d after ADR injection, 24 h urine protein was measured as well. Podocyte foot process effacement was observed under transmission electron microscopy. RESULTS: Podocytes' motility, permeability of a monolayer of podocytes incubated with FITC-BSA, the expression of nephrin were higher in ADR group than those in blank control group (P<0.05); on the contrary, the indexes above in Dex+ADR group were decreased when compared with ADR group (P<0.05). 24 h urine protein increased significantly at day 14 (vs. normal group P<0.001) and peaked at day 28 in ADR rats (vs. normal group P<0.001), whereas decreased at day 14, 21 and 28 in Dex+ADR group (vs. ADR group, P<0.001). The FWP of ADR-treated rats was greater than normal group and Dex+ADR group (P<0.01). CONCLUSION: Dex impacts the expression of nephrin, relieves the enhanced motility induced by ADR and decreases urine protein level.

Synergistic effects of nonmetal co-doping with sulfur in anatase TiO2: a DFT + U study.

Using DFT + U calculations, the crystal structure and electronic properties of nonmetal co-doping with sulfur in anatase TiO2 are systematically investigated. The initial purpose of this work is to improve the photocatalytic performance of S mono-doped TiO2, in which S occupies the lattice Ti site and acts as a recombination center. Among eight nonmetal impurities that occupy the interstitial site of a TiO6 octahedron, the synergistic effects of B, C, and O with S could achieve this purpose: suppressing the recombination of photogenerated electron-hole pairs by inducing a local inner built-in electric field and eliminating the deep impurity energy bands of S mono-doped TiO2. Furthermore, the photon absorption could be extended to the visible-light region, owing to the overlap of impurity energy bands with the top of the valence band or the bottom of the conduction band. Thus, Ti1-xO2SxBy, Ti1-xO2SxCy and Ti1-xO2SxOy could be considered as promising efficient photocatalysts. Furthermore, the underlying mechanism and tendency of these synergistic effects have been discussed, according to the relationship between the photocatalytic performance and the crystal or electronic structure.