Search Results (5)

Cinnabar has been used as a red pigment for centuries, but its degradation significantly impacts the aesthetic quality of historical paintings, particularly murals. Therefore, investigating the preparation method and transformation process of HgS is highly significant for mural research. In this study, we compared different sulfur sources for HgS synthesis and precisely synthesized α-HgS and β-HgS by adjusting the S/HgCl₂ ratio. SEM and XRD analyses under optimal conditions demonstrated that spherical β-HgS-1.2 exhibited significant morphological differences in comparison with α-HgS-1.0 and α-HgS-1.5. Elemental analysis of HgS was conducted using XPS and ICP-MS for qualitative and quantitative insights. Based on the potential mechanism of cinnabar discoloration, two strategies for converting black β-HgS to α-HgS were proposed and successfully implemented by adding sulfur or HgCl₂. Full article

The exploration initiated by the discovery of the topological insulator (Bi_xSb_1−x)₂Te₃ has extended to unlock the potential of quantum anomalous Hall effects (QAHEs), marking a revolutionary era for topological quantum devices, low-power electronics, and spintronic applications. In this study, we present the epitaxial growth of Cr-doped (Bi_0.4Sb_0.6)₂Te₃ (Cr:BST) thin films via molecular beam epitaxy, incorporating various Cr doping concentrations with varying Cr/Sb ratios (0.025, 0.05, 0.075, and 0.1). High-quality crystalline of the Cr:BST thin films deposited on a c-plane sapphire substrate has been rigorously confirmed through reflection high-energy electron diffraction (RHEED), X-ray diffraction (XRD), and high-resolution transmission electron microscopy (HRTEM) analyses. The existence of a Cr dopant has been identified with a reduction in the lattice parameter of BST from 30.53 ± 0.05 to 30.06 ± 0.04 Å confirmed by X-ray diffraction, and the valence state of Cr verified by X-ray photoemission (XPS) at binding energies of ~573.1 and ~583.5 eV. Additionally, the influence of Cr doping on lattice vibration was qualitatively examined by Raman spectroscopy, revealing a blue shift in peaks with increased Cr concentration. Surface characteristics, crucial for the functionality of topological insulators, were explored via Atomic Force Microscopy (AFM), illustrating a sevenfold reduction in surface roughness as the Cr concentration increased from 0 to 0.1. The ferromagnetic properties of Cr:BST were examined by a superconducting quantum interference device (SQUID) with a magnetic field applied in out-of-plane and in-plane directions. The Cr:BST samples exhibited a Curie temperature (T_c) above 50 K, accompanied by increased magnetization and coercivity with increasing Cr doping levels. The introduction of the Cr dopant induces a transition from n-type ((Bi_0.4Sb_0.6)₂Te₃) to p-type (Cr:(Bi_0.4Sb_0.6)₂Te₃) carriers, demonstrating a remarkable suppression of carrier density up to one order of magnitude, concurrently enhancing carrier mobility up to a factor of 5. This pivotal outcome is poised to significantly influence the development of QAHE studies and spintronic applications. Full article

To enhance the sorption efficacy of attapulgite for heavy metals, mercapto-functionalized attapulgite (ATP-SH) was synthesized with mercaptan functional groups. When the mass-to-volume ratio of calcined attapulgite (ATP-C) to 3-Mercapropyltrimethoxysilane (MPTMS) was 1 g:0.5 mL (ATP-SH-0.5) and the pH was set to 8, a strong adsorption capacity for Cd (II) and Pb (II) was demonstrated. This indicates excellent adsorption performance for these heavy metals. ATP-SH-0.5 exhibited a maximum adsorption capacity of 43.81 mg/g and 274.83 mg/g for Cd (II) and Pb (II), respectively, in a single ion system. In a binary ion system, the maximum adsorption capacity was 31.86 mg/L and 254.45 mg/L for Cd (II) and Pb (II), respectively. Various characterizations and experiments showed that the adsorption of Cd (II) and Pb (II) onto ATP-SH-0.5 involves ion exchange reactions involving hydroxyl and thiol functional group complexation reactions. This adsorption process follows a single-molecule layer adsorption mechanism. XPS results indicate that hydroxyl and grafted thiol functional groups on the surface of mercapto-functionalized attapulgite participated in surface complexation reactions with Cd (II) and Pb (II), resulting in the formation of Cd-S and Pb-S species. Overall, this study provides a promising mercapto-functionalized modification material for the remediation of polluted water and soil. Full article

Chronic wounds fail to heal and are accompanied by an ongoing infection. They cause suffering, shorten lifespans, and their prevalence is increasing. Unfortunately, the medical treatment of chronic wounds has remained unchanged for decades. A novel approach to break the biological vicious cycle is the long-lived radical (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl (TEMPO). TEMPO can be plasma polymerised (TEMPOpp) into thin coatings that have antimicrobial properties. However, due to its radical nature, quenching causes it to lose effectiveness over time. Our aim in this study was to extend the shelf-life of TEMPOpp coatings using various storage conditions: Namely, room temperature (RT), room temperature & vacuum sealed (RTV), freezer temperature & vacuum sealed (FTV). We have analysed the coatings’ quality via the surface analytical methods of X-Ray Photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR); finding marked differences among the three storage conditions. Furthermore, we have compared the antimicrobial efficacy of the stored coatings against two major bacterial pathogens, Staphylococcus aureus and Staphylococcus epidermidis, commonly found in chronic wounds. We did so both qualitatively via live/dead staining, as well as quantitatively via (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium (XTT) viability assay for up to 15 weeks in 5 weeks increments. Taken all together, we demonstrate that samples stored under FTV conditions retain the highest antimicrobial activity after 15 weeks and that this finding correlates with the retained concentration of nitroxides. Full article

The adsorption of cysteine on the pyrite (1 0 0) surface was evaluated by using first-principles-based density functional theory (DFT) and X-ray photoelectron spectroscopy (XPS) measurements. The frontier orbitals analyses indicate that the interaction of cysteine and pyrite mainly occurs between HOMO of cysteine and LUMO of pyrite. The adsorption energy calculation shows that the configuration of the -OH of -COOH adsorbed on the Fe site is the thermodynamically preferred adsorption configuration, and it is the strongest ionic bond according to the Mulliken bond populations. As for Fe site mode, the electrons are found transferred from cysteine to Fe of pyrite (1 0 0) surface, while there is little or no electron transfer for S site mode. Projected density of states (PDOS) is analyzed further in order to clarify the interaction mechanism between cysteine and the pyrite (1 0 0) surface. After that, the presence of cysteine adsorption on the pyrite (1 0 0) surface is indicated by the qualitative results of the XPS spectra. This study provides an alternative way to enhance the knowledge of microbe–mineral interactions and find a route to improve the rate of bioleaching. Full article