Secrecy Performance Analysis in STAR-RIS-Aided NOMA Networks

An analytical framework for physical layer security in simultaneous transmitting and reflecting reconfigurable intelligent surface (STAR-RIS) assisted non-orthogonal multiple access (NOMA) transmissions is proposed, where legitimate users and eavesdroppers are randomly deployed. To characterize system performance, the channel statistics are first provided, and the Gamma approximation is adopted for general cascaded κ-μ fading. Afterwards, the energy splitting (ES) protocol is considered and closed-form expressions of average secrecy capacity are derived. To obtain further insights, the asymptotic secrecy slope is deduced. The theoretical results show that the secrecy slope of the ES protocol is one. The numerical results demonstrate that: 1) there is an optimal resource allocation ratio of STAR-RIS to maximize the system performance; 2) the STAR-RIS-aided NOMA significantly outperforms the STAR-RIS-aided orthogonal multiple access

Debris cover effects on energy and mass balance of Batura Glacier in the Karakoram over the past 20 years

The influence of supraglacial debris cover on glacier mass balance in the Karakoram is noteworthy. However, understanding of how debris cover affects the seasonal and long-term variations in glacier mass balance through alterations in the glacier's energy budget is incomplete. The present study coupled an energy–mass balance model with heat conduction within debris layers on debris-covered Batura Glacier in Hunza Valley to demonstrate the influence of debris cover on glacial surface energy and mass exchanges during 2000–2020. The mass balance of Batura Glacier is estimated to be -0.262±0.561 m w.e. yr−1, with debris cover accounting for a 45 % reduction in the negative mass balance. Due to the presence of debris cover, a significant portion of incoming energy is utilized for heating debris, leading to a large energy emission to the atmosphere via thermal radiation and turbulent sensible heat. This, in turn, reduces the melt latent heat energy at the glacier surface. We found that the mass balance exhibits a pronounced arch-shaped structure along the elevation gradient, which is associated with the distribution of debris thickness and the increasing impact of debris cover on the energy budget with decreasing elevation. Through a comprehensive analysis of the energy transfer within each debris layer, we have demonstrated that the primary impact of debris cover lies in its ability to modify the energy flux reaching the surface of the glacier. Thicker debris cover results in a smaller temperature gradient within debris layers, consequently reducing energy reaching the debris–ice interface. Over the past 2 decades, Batura Glacier has exhibited a trend towards less negative mass balance, likely linked to a decrease in air temperature and reduced ablation in areas with thin or sparse debris cover.</p

Molecular-beam Epitaxy of Monolayer MoSe2: Growth Characteristics and Domain Boundary Formation

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Are Au nanoparticles on oxygen free supports catalytically active?

Gold nanoparticles Au NPs on oxygen free supports were examined using near ambient pressure X ray photoelectron spectroscopy NAP XPS under CO oxidation conditions, and ex situ using scanning electron microscopy SEM and transmission electron microscopy TEM . Our observations demonstrate that Au NPs supported on carbon materials are inactive, regardless of the preparation method. Ozone O3 treatment of carbon supports leads oxygen functionalization of the supports. When subsequently exposed to a CO feed, CO is oxidized by the functionalized sites of the carbon support via a stoichiometric pathway. Microscopy reveals that the reaction with CO does not change the morphology of the Au NPs. In situ XPS reveals that the O3 treatment gives rise to additional Au 4f and O 1s peaks at binding energies of 85.25 85.6 eV and 529.4 530 eV, respectively, which are assigned to the presence of Au oxide. A surface oxide phase is formed during the activation of Au NPs supported on Au foil by O3 treatment. However, this phase decomposes in vacuum and the remaining low coordinative atoms do not have sufficient catalytic properties to oxidize CO, so the size reduction of Au NPs and or oxidation of Au NPs is not sufficient to activate A

Serum Uric Acid Levels Are Associated with Polymorphism in the SAA1 Gene in Chinese Subjects

OBJECTIVE: Serum uric acid (SUA) is a cardiovascular risk marker associated with inflammation. The serum amyloid A protein (SAA) is an inflammatory factor and is associated with cardiovascular disease (CVD). However, the relationship between genetic polymorphisms of SAA and SUA levels has not been studied. The objective of this study was to investigate the association between SUA levels and SAA genetic polymorphisms. METHODS: All participants were selected from subjects participating in the Cardiovascular Risk Survey (CRS) study. The single nucleotide polymorphism (SNP) rs12218 of the SAA1 gene was genotyped by using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The association of SUA levels with genotypes was assessed by using the general liner mode. RESULTS: The SNP rs12218 was associated with SUA levels by analyses of a dominate model (P = 0.002) and additive model (P = 0.005), and the difference remained significant after adjustment of sex, age, obesity, ethnicity, HDL-C, alcohol intake, smoking, and creatinine (P = 0.006 and P = 0.023, respectively). The TT genotype was associated with an increased SUA concentration of 39.34 mmol/L (95% confidence interval [CI], 3.61-75.06, P = 0.031) compared with the CC genotype, and the TT genotype was associated with an increased SUA concentration of 2.48 mmol/L (95% CI, 6.86-38.10; P = 0.005) compared with the CT genotype. CONCLUSIONS: The rs12218 SNP in the SAA1 gene was associated with SUA levels in Chinese subjects, indicating that carriers of the T allele of rs12218 have a high risk of hyperuricemia

Spin-dependent thermoelectric transport through double quantum dots

We study thermoelectric transport through double quantum dots system with spin-dependent interdot coupling and ferromagnetic electrodes by means of the non-equilibrium Green function in the linear response regime. It is found that the thermoelectric coefficients are strongly dependent on the splitting of interdot coupling, the relative magnetic configurations and the spin polarization of leads. In particular, the thermoelectric efficiency can achieve considerable value in parallel configuration when the effective interdot coupling and tunnel coupling between QDs and the leads for spin-down electrons are small. Moreover, the thermoelectric efficiency increases with the intradot Coulomb interactions increasing and can reach very high value at an appropriate temperature. In the presence of the magnetic field, the spin accumulation in leads strongly suppresses the thermoelectric efficiency and a pure spin thermopower can be obtained.Comment: 5 figure

Nature of the N-Pd interaction in nitrogen-doped carbon nanotube catalysts

In this work, the geometric and electronic structure of N species in N-doped carbon nanotubes (NCNTs) is derived by X-ray photoemission (XPS) and absorption spectroscopy (NEXAFS) of the N 1s core excitation. Substitutional N species in pyridine-like configuration and another form of N with higher thermal stability are found in NCNTs. The structural configuration of the high thermally stable N species, in the literature often referred to as graphitic N, is assessed in this work by a combined theoretical and experimental study as a 3-fold substitutional N species in an NCNT basic structural unit (BSU). Furthermore, the nature of the interaction of those N species with a Pd metal center immobilized onto NCNTs is of σ-type donation from the filled π-orbital of the N atom to the empty d-orbital of the Pd atom and a π back donation from the filled Pd atomic d-orbital to the π* antibonding orbital of the N atom. We have found that the interaction of pyridine N with Pd is characterized by a charge transfer typical of a covalent chemical bond with partial ionic character, consistent with the chemical shift observed in the Pd 3d core level of divalent Pd. Graphitic N sites interact with Pd by a covalent bond without any charge redistribution. In this case, the electronic state of the Pd corresponds to metallic Pd nanoparticles electronically modified by the interaction with the support. The catalytic reactivity of these samples in hydrogenation, CO oxidation, and oxygen reduction reaction (ORR) allowed clarifying some aspects of the metal carbon support interaction in catalysis