Emerging Trends in CdS-Based Nanoheterostructures: From Type-II and Z-Scheme toward S-Scheme Photocatalytic H Production.

Cadmium sulfide (CdS) based heterojunctions, including type-II, Z-scheme, and S-scheme systems emerged as promising materials for augmenting photocatalytic hydrogen (H) generation from water splitting. This review offers an exclusive highlight of their fundamental principles, synthesis routes, charge transfer mechanisms, and performance properties in improving H production. We overview the crucial roles of Type-II heterojunctions in enhancing charge separation, Z-scheme heterojunctions in promoting redox potentials to reduce electron-hole (e/h) pairs recombination, and S-scheme heterojunctions in combining the merits of both type-II and Z-scheme frameworks to obtain highly efficient H production.

Interlayer Potassium Single-Atom-Coordinated g-CN for Significantly Boosted Visible Light Photocatalytic H Production.

In recent years, graphitic carbon nitride (g-CN) has attracted considerable attention because it includes earth-abundant carbon and nitrogen elements and exhibits good chemical and thermal stability owing to the strong covalent interaction in its conjugated layer structure. However, bulk g-CN has some disadvantages of low specific surface area, poor light absorption, rapid recombination of photogenerated charge carriers, and insufficient active sites, which hinder its practical applications. In this study, we design and synthesize potassium single-atom (K SAs)-doped g-CN porous nanosheets (CM-K, where X represents the mass of KHP added) via supramolecular self-assembling and chemical cross-linking copolymerization strategies.

Clinical applications and perspectives of circulating tumor DNA in gastric cancer.

Gastric cancer remains a leading cause of cancer-related death worldwide, largely due to inadequate screening methods, late diagnosis, and limited treatment options. Liquid biopsy has emerged as a promising non-invasive approach for cancer screening and prognosis by detecting circulating tumor components like circulating tumor DNA (ctDNA) in the blood. Numerous gastric cancer-specific ctDNA biomarkers have now been identified.

[Effects of Biochar on Antibiotic Environmental Behaviors in Soil: A Meta-analysis].

Biochar, as a soil amendment for synergizing the reduction of pollution and carbon emissions, shows great potential and future prospects in controlling antibiotic contamination. In order to research the effects of biochar on antibiotic behaviors in soil systematically, a Meta-analysis was conducted based on 20 studies published from 2011 to 2021. The results showed that the adsorption and degradation of antibiotics in the soil were significantly affected by the application rate and property of biochar.

Hierarchically hollow N-doped carbon-cobalt nanoparticle heterointerface for efficient bifunctional oxygen electrocatalysis.

The rational design and fabrication of high-performance and durable bifunctional non-noble-metal electrocatalysts for both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are still a great challenge in the practical applications of rechargeable zinc-air (Zn-air) batteries. Herein, we report a simple yet robust route to synthesize cobalt nanoparticles rooted in the hierarchically hollow nitrogen-doped carbon frameworks (Co@HNCs). This strategy employs the pyrolysis of nanostructured hollow Co-based metal-organic framework (ZIF-67) precursors produced by selective linker cleaving with pyrazino(2,3-)(1,10)phenanthroline-2,3-dicarboxylic acid molecules (HPPDA).

Novel luminescent homo/heterometallic platinum(ii) alkynyl complexes based on Y-shaped pyridyl diphosphines.

A series of dinuclear platinum(ii) alkynyl complexes [Pt2L2(C[triple bond, length as m-dash]CC6H4R-4)4] (R = H 1, CH32, But3) and unusual tetranuclear Pt(ii)-Ag(i) clusters [Pt2Ag2L(C[triple bond, length as m-dash]CC6H4R-4)6] (R = H, 4; CH3, 5; But, 6), together with novel polymer crystals [Pt2Ag2L(C[triple bond, length as m-dash]CC6H5)6]∞ ([4]∞), were synthesized by a self-assembly reaction between [NBu4]2[Pt(C[triple bond, length as m-dash]CC6H4-R-4)4] and [Ag6L6]6+ (L = 4-(3,5-(diphenylphosphine)phenyl)pyridine). These complexes were characterized by using a range of spectroscopic techniques and complexes 1, 3, 5, and [4]∞ were analysed by X-ray crystallography. Each platinum atom of the Pt(ii)-Ag(i) clusters shows an unusual asymmetric distorted square planar geometry with three alkynyl groups and one bridging L phosphorus atom.

Preparation and characterization of maltodextrin-based polyurethane.

Maltodextrin (MD) based polyurethane (MDPU) was prepared by the reaction of MD and polyethyleneglicol (PEG) polyurethane prepolymer (PUP). The structure and properties of the MDPU were investigated by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (H NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscope (SEM), Energy dispersive X-ray spectrometry (EDS), and tensile-testing machine in detail. Chemical structure of MDPU was confirmed by FTIR and H NMR.

Electrochemiluminescence properties of [Pt2Ag4(C≡CC6H4R)8]n (R = CH3, n = 1; R = H, n = 1 and 2) with amine (TPrA and DBAE) as the coreactant and determination of Sudan I.

Two hexanuclear clusters, [Pt(2)Ag(4)(C≡CC(6)H(4)R)(8)] (R = CH(3), 1; R = H, 2), together with dimer [Pt(2)Ag(4)(C≡CC(6)H(5))(8)](2) (3), have been synthesized and characterized by elemental analyses, electrospray ionization mass spectrometry, and (1)H NMR spectroscopy and by X-ray crystallography for 1 and 3. A considerable enhancement of photoluminescence (PL) and a notable red shift in the emission maximum of 1 (λ(max) 600 nm) relative to 2 (λ(max) 545 nm) are observed. Electrogenerated chemiluminescence (ECL) of 1 and 2 in the absence or presence of coreactant tri-n-propylamine (TPrA) or 2-(dibutylamino)ethanol (DBAE) at different working electrodes in different solvents (CH(2)Cl(2), CH(2)ClCH(2)Cl, or CH(3)CN) has been studied.

Synthesis, structure, photophysical and electrochemiluminescence properties of Re(I) tricarbonyl complexes incorporating pyrazolyl-pyridyl-based ligands.

Three rhenium carbonyl complexes 1-3 were synthesized by reaction of the appropriate bidentate pyrazolyl-pyridyl-based ligand L1, L2 (L1 = 2-[1-{4-(bromomethyl)benzyl}-1H-pyrazol-3-yl]pyridine; L2 = 1,4-bis(3-(2-pyridyl)pyrazol-1-ylmethyl)benzene) with [Re(CO)(5)Cl] in toluene. They were characterized by elemental analyses, ESI-MS, (1)H spectroscopy, and X-ray crystallography for 1 and 2. Compounds 1-3 exhibit bright yellow-green luminescence in the solid state and in solution at 298 K with the lifetimes in the microsecond range.