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This work provides an insight into the relationship between the structure and the function of bone at a multilevel under load, specifically the role of the ordered MCF arrays in the lamellar structure.Transition metal dichalcogenides (TMDs) have attracted wide attention due to their quasi-two-dimensional layered structure and exotic properties. Plenty of efforts have been done to modulate the interlayer stacking manner for novel states. However, as an equally important element in shaping the unique properties of TMDs, the effect of intralayer interaction is rarely revealed. Here, we report a particular case of pressure-tuned re-arrangement of intralayer atoms in distorted 1T-NbTe2, which was demonstrated to be a new type of structural phase transition in TMDs. The structural transition occurs in the pressure range of 16-20 GPa, resulting in a transformation of Nb atomic arrangement from the trimeric to dimeric structure, accompanied by a dramatic collapse of unit cell volume and lattice parameters. Simultaneously, a charge density wave (CDW) was also found to collapse during the phase transition. The strong increase in the critical fluctuations of CDW induces a significant decline in the electronic correlation and a change of charge carrier type from hole to electron in NbTe2. Our finding reveals a new mechanism of structure evolution and expands the field of pressure-induced phase transition.Triazole-based g-C3N5, a potential catalyst, has received little attention over the years. We prepared phosphorus-doped g-C3N5 with one triazole and two triazine units for the first time to investigate its photoelectrochemical (PEC) and photocatalytic properties. The doping states and crystalline structures of the samples were determined using X-ray techniques, namely, X-ray diffraction, X-ray photoelectron spectroscopy, and X-ray absorption fine structure analysis. compound library chemical Our results suggested that the phosphorus was substituted into carbon sites form P-N/P═N bonds with four coordination, which contribute P 2p level donor states in the band gap to enhance light absorption and reduce charge separation. Therefore, P-doped g-C3N5 exhibited higher PEC current density and better photocatalytic efficiency toward the degradation of rhodamine B dye or tetracycline under light irradiation compared to the undoped g-C3N5 sample. However, excess phosphorus doping resulted in the formation of impurities and disrupted the triazine and triazole units, reducing the PEC and photocatalytic efficiency. In summary, P-doped g-C3N5 was successfully prepared in the present study and represents a promising, facile, and effective catalyst for energy applications and environmental remediation.With the rapid development in wearable electronics, self-powered devices have recently attracted tremendous attention to overcome the restriction of conventional power sources. In this regard, a simple, scalable, and one-pot electrospinning fabrication technique was utilized to construct an all-fiber-structured triboelectric nanogenerator (TENG). Ethyl cellulose was co-electrospun with polyamide 6 to serve as the triboelectric positive material, and a kind of strongly electronegative conductive material of MXene sheet was innovatively incorporated into poly(vinylidene fluoride) nanofiber to act as a triboelectric negative material. The assembled all-fiber TENG exhibited excellent durability and stability, as well as excellent output performance, which reached a peak power density of 290 mW/m2 at a load resistance of 100 MΩ. More importantly, the TENG was capable of harvesting energy to power various light-emitting diodes (LEDs) and monitoring human movements as a self-powered sensor, providing a promising application prospect in wearable electronics.HU is a bacterial nucleoid-associated protein. Two homologues, known as HU-A, and HU-B, are found in Escherichia coli within which the early, late, and stationary phases of growth are dominated by HU-AA, HU-BB, and HU-AB dimers, respectively. Here, using genetic manipulation, mass spectrometry, spectroscopy, chromatography, and electrophoretic examination of glutaraldehyde-mediated cross-linking of subunits, in combination with experiments involving mixing, co-expression, unfolding, and refolding of HU chains, we show that the spontaneous formation of HU-AB heterodimers that is reported to occur upon mixing of wild-type HU-AA and HU-BB homodimers does not occur if chains possess N-terminal extensions. We show that N-terminal extensions interfere with the conversion of homodimers into heterodimers. We also show that heterodimers are readily formed at anticipated levels by chains possessing N-terminal extensions in vivo, when direct chain-chain interactions are facilitated through production of HU-A and HU-B chains from proximal genes located upon the same plasmid. From the data, two explanations emerge regarding the mechanism by which N-terminal extensions happen to adversely affect the conversion of homodimers into heterodimers. (1) The disappearance of the α-amino group at HU’s N-terminus impacts the intersubunit stacking of β-sheets at HU’s dimeric interface, reducing the ease with which subunits dissociate from each other. Simultaneously, (2) the presence of an N-terminal extension appears to sterically prevent the association of HU-AA and HU-BB homodimers into a critically required, heterotetrameric intermediate (within which homodimers could otherwise exchange subunits without releasing monomers into solution, by remaining physically associated with each other).Ag(I)-insulin complex formation was investigated using electrospray quadrupole ion trap mass spectrometry (ESI-QIT-MS), and Ag(I) ion binding to an insulin molecule was evaluated. The Ag(I) binding ratios were measured in the range of pH 3-8. The highest binding ratio of the Ag(I) ions was obtained at pH 7. Spectrometric titration was carried out at varied molar ratios of Ag(I) ions to insulin from 20/1 to 250/1. It was observed that four Ag(I) ions were bound effectively to an insulin molecule to form Ag(I)1-4-insulin complexes. The formation equilibrium constants of Ag(I)1-4-insulin complexes were calculated from the ESI-QIT-MS peak intensities. The equilibrium constants were found as Kf1 = (2.92 ± 0.18) × 104 M-1, Kf2 = (1.03 ± 0.07) × 104 M-1, Kf3 = (6.67 ± 0.46) × 103 M-1, and Kf4 = (2.00 ± 0.16) × 103 M-1. The tandem MS/MS spectroscopies were studied to evaluate the stability of the Ag(I) complexes. The different flow rates with nano-ESI were performed to determine the binding of Ag(I) ions in solution or gas phase.