Unraveling the Electronic Effect of Transition-Metal Dopants (M = Fe, Co, Ni, and Cu) and Graphene Substrate on Platinum-Transition Metal Dimers for Hydrogen Evolution Reaction.

As an extension of single-atom catalysts, despite the increased opportunities to optimize the hydrogen evolution reaction (HER) activity with the variation of the composition, dual-metal-atom catalysts, i.e., dimers, are deeply trapped in a design blind spot due to the lack of the essential recognition of the intrinsic catalytic mechanism at the atomic level. Herein, based on first-principles calculations, a series of platinum-transition metal dimers were constructed on nitrogen-doped graphene (PtM-NDG, M = Fe, Co, Ni, Cu) to reveal the effects of the internal (i.e., M atom) and external (i.e., NDG substrate) environments on the HER activity. Computational results show that the original over-adsorption of hydrogen intermediate (H*) of PtM dimer is weakened after the introduction of NDG, and the optimal active site migrates from the Pt in PtM dimer to the Pt-M bridge in PtM-NDG, triggered by the redistribution of the charge density of the metal atoms. In particular, the M atom switches from tuning the d-band center of the Pt atom to indirectly assist the adsorption behavior of Pt in the PtM dimer to the direct participation in the bonding with H* in PtM-NDG via its own d-band to regulate the distribution of σ and σ*, which enables fine modulation of the bond strength with H*. Moreover, the overall hydrogen evolution performance of PtM-NDG is mainly determined by the d-band center of the M atom. Furthermore, PtFe-NDG with the lowest energy barrier of the rate-determining step stands out in the process of H2 desorption and water dissociation. The present work deepens our understanding of the effects of the metal dopant and substrate on the catalytic performance of platinum.

Ni-Coated Diamond-like Carbon-Modified TiO2 Nanotube Composite Electrode for Electrocatalytic Glucose Oxidation.

In this paper, a Ni and diamond-like carbon (DLC)-modified TiO2 nanotube composite electrode was prepared as a glucose sensor using a combination of an anodizing process, electrodeposition, and magnetron sputtering. The composition and morphology of the electrodes were analyzed by a scanning electron microscope and energy dispersive X-ray detector, and the electrochemical glucose oxidation performance of the electrodes was evaluated by cyclic voltammetry and chronoamperometry. The results show that the Ni-coated DLC-modified TiO2 electrode has better electrocatalytic oxidation performance for glucose than pure TiO2 and electrodeposited Ni on a TiO2 electrode, which can be attributed to the synergistic effect between Ni and carbon. The glucose test results indicate a good linear correlation in a glucose concentration range of 0.99-22.97 mM, with a sensitivity of 1063.78 µA·mM-1·cm-2 and a detection limit of 0.53 µM. The results suggest that the obtained Ni-DLC/TiO2 electrode has great application potential in the field of non-enzymatic glucose sensors.

Enhanced Methanol Electro-Oxidation Activity of Nanoclustered Gold.

Size-selected 3 nm gas-phase Au clusters dispersed by cluster beam deposition (CBD) on a conducting fluorine-doped tin oxide template show strong enhancement in mass activity for the methanol electro-oxidation (MEO) reaction compared to previously reported nanostructured gold electrodes. Density functional theory-based modeling on the corresponding Au clusters guided by experiments attributes this high MEO activity to the high density of exposed under-coordinated Au atoms at their faceted surface. In the description of the activity trends, vertices and edges are the most active sites due to their favorable CO and OH adsorption energies. The faceted structures occurring in this size range, partly preserved upon deposition, may also prevent destructive restructuring during the oxidation-reduction cycle. These results highlight the benefits of using CBD in fine-tuning material properties on the nanoscale and designing high-performance fuel cell electrodes with less material usage.

Transient transmission of THz metamaterial antennas by impact ionization in a silicon substrate.

The picosecond dynamics of excited charge carriers in the silicon substrate of THz metamaterial antennas was studied at different wavelengths. Time-resolved THz pump-THz probe spectroscopy was performed with light from a tunable free electron laser in the 9.3-16.7 THz frequency range using fluences of 2-12 J/m2. Depending on the excitation wavelength with respect to the resonance center, transient transmission increase, decrease, or a combination of both was observed. The transient transmission changes can be explained by local electric field enhancement, which induces impact ionization in the silicon substrate, increasing the local number of charge carriers by several orders of magnitude, and their subsequent diffusion and recombination. The studied metamaterials can be integrated with common semiconductor devices and can potentially be used in sensing applications and THz energy harvesting.

Ultrafast saturable absorption of BiOI nanosheets prepared by chemical vapor transport.

The saturable absorption properties of BiOI nanosheets with exposed {110} facets prepared by the chemical vapor transport were investigated by Z-scan with femtosecond pulse laser. The nonlinear absorption coefficient at 400 nm is stronger and more sensitive to photoexcitation than its nonlinear response at 800 nm. The small saturation intensity could have been achieved, which is one order of magnitude smaller than that of black phosphorus nanosheets, while the Imχ(3) are determined to be -4.35×10-12esu close to theoretical prediction. According to time-resolved photoluminescence spectrum results, this strong saturated absorption at 400 nm may be attributed to the interband recombination process, whose lifetime was 230 ps.

Tuning the electronic properties of van der Waals heterostructures composed of black phosphorus and graphitic SiC.

This study presents a new van der Waals (vdW) heterostructure composed of monolayer black phosphorus (BP) and monolayer graphitic SiC (g-SiC). Using first-principles calculations, the structural and electronic properties of the BP/SiC heterostructure were investigated. It was found that by stacking BP with SiC, weak type-I band alignment can be achieved with a band gap of 0.705 eV, where the direct band gap as well as linear dichroism features were well preserved. The electrostatic potential drop in the heterojunction was calculated to be 4.044 eV. By applying perpendicular electric field, the band alignment can be altered to either type-I or type-II, and the band gap can be effectively controlled by field intensity, hence making the heterostructure suitable for various applications.

Controllable Synthesis of Marks Decahedral Pd Nanoparticles via Etching.

Marks decahedral nanoparticles have attracted significant attention in recent years. In this work, a method of synthesizing Marks decahedron via etching regular decahedral nanoparticles is proposed and verified by Pd nanoparticles, which shows a high yield of Marks decahedron. The present work suggests that one can tune the concave size of Marks decahedral via controlling the etching time and the amount of Poly(vinyl pyrrolidone) (PVP). The thermal stability of Marks nanoparticles is explained by Bond-Energy model, which predicts the largest groove to be the most stable configuration. Moreover, the present method can be extended to synthesize Marks decahedral nanoparticles of other elements, and is of great significance for further studies and applications of Mark decahedral nanoparticles.

Structural assignment of small cationic silver clusters by far-infrared spectroscopy and DFT calculations.

The structures of small cationic silver clusters Agn+ (n = 3-13) are investigated by comparing measured far-infrared multiple photon dissociation spectra of cluster-argon complexes with the calculated harmonic vibrational spectra of different low-energy structural isomers. A global structure search was carried out using the CALYPSO structure prediction method, after which isomers were locally optimized with the meta GGA functional TPSS. The obtained structures of the cationic silver clusters are mostly consistent with earlier ion mobility measurements and photodissociation spectroscopy studies for Agn+ (n = 3-11) and allowed excluding several structural isomers that were considered in those earlier studies, which illustrates the strength of combining multiple experimental techniques for conclusive structural identification. The growth pattern of the cationic silver clusters is discussed and differences with other cationic coinage metal clusters are highlighted.

Nonlinear effects in infrared action spectroscopy of silicon and vanadium oxide clusters: experiment and kinetic modeling.

For structural assignment of gas phase compounds, infrared action spectra are usually compared to computed linear absorption spectra. However, action spectroscopy is highly nonlinear owing to the necessary transfer of the excitation energy and its subsequent redistribution leading to statistical ionization or dissociation. Here, we examine by joint experiment and dedicated modeling how such nonlinear effects affect the spectroscopic features in the case of selected inorganic clusters. Vibrational spectra of neutral silicon clusters are recorded by tunable IR-UV two-color ionization while IR spectra for cationic vanadium oxide clusters are obtained by IR multiphoton absorption followed by dissociation of the bare cluster or of its complex with Xe. Our kinetic modeling accounts for vibrational anharmonicities, for the laser interaction through photon absorption and stimulated emission rates, as well as for the relevant ionization or dissociation rates, all based on input parameters from quantum chemical calculations. Comparison of the measured and calculated spectra indicates an overall agreement as far as trends are concerned, except for the photodissociation of the V3O7(+)-Xe messenger complex, for which anharmonicities are too large and poorly captured by the perturbative anharmonic model. In all systems studied, nonlinear effects are essentially manifested by variations in the intensities as well as spectral broadenings. Differences in some band positions originate from inaccuracies of the quantum chemical data rather than specific nonlinear effects. The simulations further yield information on the average number of photons absorbed, which is otherwise unaccessible information: several to several tens of photons need to be absorbed to observe a band through dissociation, while three to five photons can be sufficient for detection of a band via IR-UV ionization.

The geometric structure of silver-doped silicon clusters.

Cationic silver-doped silicon clusters, Si(n)Ag(+) (n=6-15), are studied using infrared multiple photon dissociation in combination with density functional theory computations. Candidate structures are identified using a basin-hopping global optimizations method. Based on the comparison of experimental and calculated IR spectra for the identified low-energy isomers, structures are assigned. It is found that all investigated clusters have exohedral structures, that is, the Ag atom is located at the surface. This is a surprising result because many transition-metal dopant atoms have been shown to induce the formation of endohedral silicon clusters. The silicon framework of Si(n)Ag(+) (n=7-9) has a pentagonal bipyramidal building block, whereas the larger Si(n)Ag(+) (n=10-12, 14, 15) clusters have trigonal prism-based structures. On comparing the structures of Si(n)Ag(+) with those of Si(n)Cu(+) (for n=6-11) it is found that both Cu and Ag adsorb on a surface site of bare Si(n)(+) clusters. However, the Ag dopant atom takes a lower coordinated site and is more weakly bound to the Si(n)(+) framework than the Cu dopant atom.

Structure assignment, electronic properties, and magnetism quenching of endohedrally doped neutral silicon clusters, Si(n)Co (n = 10-12).

The structures of neutral cobalt-doped silicon clusters have been assigned by a combined experimental and theoretical study. Size-selective infrared spectra of neutral Si(n)Co (n = 10-12) clusters are measured using a tunable IR-UV two-color ionization scheme. The experimental infrared spectra are compared with calculated spectra of low-energy structures predicted at the B3P86 level of theory. It is shown that the Si(n)Co (n = 10-12) clusters have endohedral caged structures, where the silicon frameworks prefer double-layered structures encapsulating the Co atom. Electronic structure analysis indicates that the clusters are stabilized by an ionic interaction between the Co dopant atom and the silicon cage due to the charge transfer from the silicon valence sp orbitals to the cobalt 3d orbitals. Strong hybridization between the Co dopant atom and the silicon host quenches the local magnetic moment on the encapsulated Co atom.

Thermal radiation of laser heated niobium clusters Nb(+)(N), 8 ⩽ N ⩽ 22.

The thermal radiation from small, laser heated, positively charged niobium clusters has been measured. The emitted power was determined by the quenching effect on the metastable decay, employing two different experimental protocols. The radiative power decreases slightly with cluster size and shows no strong size-to-size variations. The magnitude is 40-50 keV/s at the timescale of several microseconds, which is the measured crossover time from evaporative to radiative cooling.

Interfacial Charge Transfer for Enhancing Nonlinear Saturable Absorption in WS2/graphene Heterostructure.

Interlayer charge-transfer (CT) in 2D atomically thin vertical stacks heterostructures offers an unparalleled new approach to regulation of device performance in optoelectronic and photonics applications. Despite the fact that the saturable absorption (SA) in 2D heterostructures involves highly efficient optical modulation in the space and time domain, the lack of explicit SA regulation mechanism at the nanoscale prevents this feature from realizing nanophotonic modulation. Here, the enhancement of SA response via CT in WS2/graphene vertical heterostructure is proposed and the related mechanism is demonstrated through simulations and experiments. Leveraging this mechanism, CT-induced SA enhancement can be expanded to a wide range of nonlinear optical modulation applications for 2D materials. The results suggest that CT between 2D heterostructures enables efficient nonlinear optical response regulation.

Polyaniline Induced Trivalent Ni in Laser-Fabricated Nickel Oxides for Efficient Oxygen Evolution Reaction.

Although it is generally acknowledged that transition metals at high oxidation states represent superior oxygen evolution reaction (OER) activity, the preparation and stability of such a high-valence state are still a challenge, which requires relatively harsh reaction conditions and is unstable under ambient conditions. Herein, we report the formation of trivalent nickel (Ni3+) in laser-fabricated nickel oxides induced by polyaniline (PANI) under electrochemical activation via a significant charge transfer between Ni and N, as confirmed by X-ray photoelectron spectroscopy and density functional theory calculations. Thereafter, the presence of Ni3+ and the improved conductivity by PANI effectively increase the electrochemical OER activity of the samples together with excellent long-term stability. This work provides new insights for the rational manufacture of high-valence metal for electrochemical reactions.

In-Site Grown NiFeOOH Nanosheets Foam Directly as Robust Electrocatalyst for Efficient Urea Oxidation Application.

In this work, a series of morphology-controlled NiFeOOH nanosheets were directly developed through a one-step mild in-situ acid-etching hydrothermal process. Benefiting from the ultrathin interwoven geometric structure and most favorable electron transport structure, the NiFeOOH nanosheets synthesized under 120 °C (denoted as NiFe_120) exhibited the optimal electrochemical performance for urea oxidation reaction (UOR). An overpotential of merely 1.4 V was required to drive the current density of 100 mA cm-2 , and the electrochemical activity remains no change even after 5000 cycles' accelerated degradation test. Moreover, the assembled urea electrolysis set by using the NiFe_120 as bifunctional catalysts presented a reduced potential of 1.573 V at 10 mA cm-2 , which was much lower than that of overall water splitting. We believe this work will lay a foundation for developing high-performance urea oxidation catalysts for the large-scale production of hydrogen and purification of urea-rich sewage.

Electronic Structure Modulation of Fe-N4-C for Oxygen Evolution Reaction via Transition Metal Dopants and Axial Ligands.

The popular single-atom catalyst (SAC) Fe-N4 is generally believed to be an excellent oxygen reduction reaction (ORR) electrocatalyst, which is less active in the oxygen evolution reaction (OER). Herein, FeM-N6 configuration catalysts (M = Fe, Co, Ni, Cu, Ag, and Au) were constructed for the oxygen evolution reaction by embedding M dopants on Fe-N4 systems based on the density functional theory. The electronic structure analysis reveals that the Fe-M metal interactions play dominant roles in regulating the d orbital distributions of Fe sites, which in turn alter the catalytic OER performance. Subsequent thermodynamic results indicate that the potential-determining step (PDS) for all catalysts is the formation of OOH*, which exhibits a tendency of decreased overpotentials with enhanced metal interactions. Apart from these, the effects of axial ligands on the OER activity of the catalysts in practical conditions were considered. Generally, most of the axial ligands are found to be thermodynamically favorable for the OER process. Interestingly, a competitive relationship of the electrons from the d orbital of Fe sites was found between the axial ligand and the adsorbed intermediate species during the reaction, which raises the energy barrier for OH* to O* conversion and can even alter the PDS in certain cases. The present work sheds new light on the design of future high-performance OER catalysts.

Unconventional Giant "Magnetoresistance" in Bosonic Semiconducting Diamond Nanorings.

The emergence of superconductivity in doped insulators such as cuprates and pnictides coincides with their doping-driven insulator-metal transitions. Above the critical doping threshold, a metallic state sets in at high temperatures, while superconductivity sets in at low temperatures. An unanswered question is whether the formation of Cooper pairsin a well-established metal will inevitably transform the host material into a superconductor, as manifested by a resistance drop. Here, this question is addressed by investigating the electrical transport in nanoscale rings (full loops) and half loops manufactured from heavily boron-doped diamond. It is shown that in contrast to the diamond half-loops (DHLs) exhibiting a metal-superconductor transition, the diamond nanorings (DNRs) demonstrate a sharp resistance increase up to 430% and a giant negative "magnetoresistance" below the superconducting transition temperature of the starting material. The finding of the unconventional giant negative "magnetoresistance", as distinct from existing categories of magnetoresistance, that is, the conventional giant magnetoresistance in magnetic multilayers, the colossal magnetoresistance in perovskites, and the geometric magnetoresistance in semiconductor-metal hybrids, reveals the transformation of the DNRs from metals to bosonic semiconductors upon the formation of Cooper pairs. DNRs like these could be used to manipulate Cooper pairs in superconducting quantum devices.

Fast and Deep Reconstruction of Coprecipitated Fe Phosphates on Nickel Foams for an Alkaline Oxygen Evolution Reaction.

Although there is a general consensus that the electrocatalysts will undergo reconstruction to generate (oxy)hydroxides as real active sites during the electrochemical oxygen evolution reaction (OER), the understanding of this process is still far from satisfactory. In particular, the reconstruction process of most of these electrocatalysts is either slow or occurs only on the surface, which thus restrains the OER performance of the electrocatalysts. Herein, we reveal a fast and deep reconstruction of the coprecipitated Fe phosphates on nickel foam, via in situ Raman spectroscopy together with electron microscopy, X-ray photoelectron spectroscopy, and electrochemical tests. The generated NiFe (oxy)hydroxide nanosheets after reconstruction behave as the real active sites for the OER in the alkaline condition, with a low overpotential and excellent durability. The present work provides deep insights on the reconstruction dynamics of OER electrocatalysts.

Pharmacokinetics effects of chuanxiong rhizoma on warfarin in pseudo germ-free rats.

Aim: In China, warfarin is usually prescribed with Chuanxiong Rhizoma for treating thromboembolism diseases. However, the reason for their combination is still being determined. The present study explored the pharmacokinetics interactions of warfarin, Chuanxiong Rhizoma, and gut microbiota in the rat model of middle cerebral artery occlusion (MCAO). Methods: A total of 48 rats were randomly divided into six groups: MCAO rats orally administered warfarin (W group), pseudo germ-free MCAO rats orally administered warfarin (W-f group), MCAO rats co-administered Chuanxiong Rhizoma and warfarin (C + W group), pseudo germ-free MCAO rats co-administered Chuanxiong Rhizoma and warfarin (C + W-f group), MCAO rats co-administered warfarin and senkyunolide I (S + W group); pseudo germ-free MCAO rats co-administered warfarin and senkyunolide I (S + W-f group). After treatment, all animals' blood and stool samples were collected at different time points. The stool samples were used for 16S rRNA sequencing analysis. Ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) method was established to quantify warfarin, internal standards, and the main bioactive components of Chuanxiong in blood samples. The main pharmacokinetics parameters of warfarin were calculated by DAS 2.1.1 software. Results: The relative abundance of Allobaculum and Dubosiella in the pseudo germ-free groups (W-f, C + W-f, S + W-f) was lower than that in the other three groups (W, C + W, S + W). The relative abundance of Lactobacillus in the W-f group was higher than that of the W group, while the relative abundance of Akkermansia decreased. The relative abundance of Ruminococcaceae_UCG-014 and Ruminococcaceae_NK4A214_group in the S + W-f group was lower than in the S + W group. Compared to the W group, the AUC0-t and Cmax of warfarin in the W-f group increased significantly to 51.26% and 34.58%, respectively. The AUC0-t and Cmax in the C + W group promoted 71.20% and 65.75% more than the W group. Compared to the W group, the AUC0-t and Cmax increased to 64.98% and 64.39% in the S + W group. Conclusion: Chuanxiong Rhizoma and senkyunolide I (the most abundant metabolites of Chuanxiong Rhizoma aqueous extract) might affect the pharmacokinetics features of warfarin in MCAO rats through, at least partly, gut microbiota.

External evaluation of published population pharmacokinetic models of posaconazole.

Population pharmacokinetic (PopPK) models of posaconazole have been established to promote the precision dosing. However, the performance of these models extrapolated to other centers has not been evaluated. This study aimed to conduct an external evaluation of published posaconazole PopPK models to evaluate their predictive performance. Posaconazole PopPK models screened from the PubMed and MEDLINE databases were evaluated using an external dataset of 213 trough concentration samples collected from 97 patients. Their predictive performance was evaluated by prediction-based diagnosis (prediction error), simulation-based diagnosis (visual predictive check), and Bayesian forecasting. In addition, external cohorts with and without proton pump inhibitor were used to evaluate the models respectively. Ten models suitable for the external dataset were finally included into the study. In prediction-based diagnostics, none of the models met pre-determined criteria for predictive indexes. Only M4, M6, and M10 demonstrated favorable simulations in visual predictive check. The prediction performance of M5, M7, M8, and M9 evaluated using the cohort without proton pump inhibitor showed a significant improvement compared to that evaluated using the whole cohort. Consistent with our expectations, Bayesian forecasting significantly improved the predictive per-formance of the models with two or three prior observations. In general, the applicability of these published posaconazole PopPK models extrapolated to our center was unsatisfactory. Prospective studies combined with therapeutic drug monitoring are needed to establish a PopPK model for posaconazole in the Chinese population to promote individualized dosing.