Focus of the figure: Cu₂O was synthesized via a one-step reduction method and combined with Bi₂WO₆ in varying proportions to create Cu₂O/Bi₂WO₆ composites for photocatalytic CO₂ reduction. Characterization techniques, including XRD, SEM, TEM, UV-vis, and XPS, analyzed the materials' properties. Under low-power blue and green LED light, the Cu₂O/Bi₂WO₆ (3:1) composite exhibited the highest performance, producing 27.4 μmol g⁻¹ CH₄ and 30.6 μmol g⁻¹ CO. More details about this figure will be discussed by Dr. Ren-Jang Wu and his co-workers on pages 27-36 in this issue.

The aspect ratio of 1:1 CL-20/4,5-MDNI crystal grown in methanol at a temperature of 313K is 1.680, while the aspect ratio of 1:3 CL-20/4,5-MDNI crystal grown in acetonitrile at a temperature of 313K is 1.936.

A systematic response profile of PTX and its chemically diverse analogues to various tubulin variations in GCs is created using an iSiV protocol, from which a number of resistant variations and few sensitive variations can be identified, and a considerable difference between the PTX response behaviors to α- and β-subunit variations is revealed.

The photoreduction of CO₂ using the prepared samples was studied under low-power visible LED lights irradiation (blue LED and green LED) to save energy. Experimental results showed that Cu₂O/Bi₂WO₆ with a 3:1 ratio possessed the optimal properties, yielding 27.4 μmol g⁻¹ of methane and 30.6 μmol g⁻¹ of carbon monoxide under green light.

Novel defective Fe-MOFs prepared by solvothermal method.

Fabrication of the separation bed was carried out by packing mosquito-repellent incense (MRI) ashes into a 5 mL plastic column, which was fixed by two stainless steel meshes as the support and cover. The as-prepared packed column was successfully used for the surfactant-stabilized O/W and W/O emulsion separation.

Application of PAMAM functional biomedical materials in the field of biomedicine.

MultiCP NMR for determination of lignin in tobacco was introduced. The measurement time of quantitative NMR was shortened from 59.0 h for DP spectra to 130 min. The interesting solid-state NMR method was rapid, practicable, and very promising.