A Scalable Video Multicast Scheme Based on User Demand Perception and D2D Communication.

With the widespread application of 5G technology, there has been a significant surge in wireless video service demand and video traffic due to the proliferation of smart terminal devices and multimedia applications. However, the complexity of terminal devices, heterogeneous transmission channels, and the rapid growth of video traffic present new challenges for wireless network-based video applications. Although scalable video coding technology effectively improves video transmission efficiency in complex networks, traditional cellular base stations may struggle to handle video transmissions for all users simultaneously, particularly in large-scale networks. To tackle this issue, we propose a scalable video multicast scheme based on user demand perception and Device-to-Device (D2D) communication, aiming to enhance the D2D multicast network transmission performance of scalable videos in cellular D2D hybrid networks. Firstly, we analyze user interests by considering their video viewing history and factors like video popularity to determine their willingness for video pushing, thereby increasing the number of users receiving multicast clusters. Secondly, we design a cluster head selection algorithm that considers users' channel quality, social parameters, and video quality requirements. Performance results demonstrate that the proposed scheme effectively attracts potential request users to join multicast clusters, increases the number of users in the clusters, and meets diverse user demands for video quality.

A Theoretical Study on Laser Cooling Feasibility of Group IVA Hydrides XH (X = Si, Ge, Sn, and Pb): The Role of Electronic State Crossing.

The feasibility of direct laser cooling of SiH, GeH, SnH, and PbH is investigated and assessed based upon first principles. The internally contracted multi-reference configuration interaction method with the Davidson correction is applied. Very good agreement is obtained between our computed spectroscopic constants and the available experimental data. We find that the locations of crossing point between the B2Σ- and A2Δ states have the tendency of moving downwards from CH to SnH relative to the bottom of the corresponding A2Δ potential, which precludes the laser cooling of GeH, SnH, and PbH. By including the spin-orbit coupling effects and on the basis of the A 2 Δ 5 / 2 → X 2 Π 3 / 2 transition, we propose a feasible laser cooling scheme for SiH using three lasers with wavelengths varying from 400 to 500 nm, which features a very large vibrational branching ratio (0.9954) and a very short radiative lifetime (575 ns). Moreover, similar studies are extended to carbon monosulfide (CS) with a feasible laser cooling scheme proposed. The importance of electronic state crossing in molecular laser cooling is underscored, and our work suggests useful caveats to the choice of promising candidates for producing ultracold molecules.

Solar thermochemical CO2 splitting with doped perovskite LaCo0.7Zr0.3O3: thermodynamic performance and solar-to-fuel efficiency.

The research of thermochemical CO2 splitting based on perovskites is a promising approach to green energy development. Performance evaluation was performed towards the doped perovskite LaCo0.7Zr0.3O3 (LCZ-73) based two-step thermochemical CO2 splitting process thermodynamically based on the experimentally derived parameters for the first time. The impacts of vacuum pump and inert gas purge to reduce oxygen partial pressure and CO2 heating on the performance parameter η solar-to-fuel have been analyzed. The results showed that at the P O2 of 10-5 bar, non-stoichiometric oxygen δ increased by more than 3 times as the reduction temperature varied from 1000 °C to 1300 °C, however, no significant deviation of δ was observed between 1300 °C and 1400 °C. The reaction enthalpy ranged from 60 to 130 kJ mol-1 corresponding to δ = 0.05-0.40. Comparing the abovementioned two ways to reduce the oxygen partial pressure, the η solar-to-fuel of 0.39% and 0.1% can be achieved with 75% and without heat recovery with the CO2 flow rate of 40 sccm under experimental conditions, respectively. The energy cost for CO2 heating during the thermodynamic process as the n CO2 /n LCZ-73 increases was obtained from the perspective of energy analysis. The ratio of n CO2 /n LCZ-73 at lower temperature required more demanding conditions for the aim of commercialization. Finally, the ability of perovskite to split CO2 and thermochemical performance were tested under different CO2 flow rates. The results showed that high CO2 flow rate was conducive to the production of CO, but at the cost of low η solar-to-fuel. The maximum solar-to-fuel efficiency of 1.36% was achieved experimentally at a CO2 flow rate of 10 sccm in the oxidation step and 75% heat recovery.

A water-soluble two-photon ratiometric triarylboron probe with nucleolar targeting by preferential RNA binding.

By functionalizing triarylboron with cyclen, we developed a two-photon fluorescence probe, TAB-2, which can selectively bind RNA with a ratiometric readout. We tested TAB-2 in NIH/3T3 fibroblast cells, and demonstrated its capability in visualizing nucleoli and analyzing microenvironment polarity by two-photon and fluorescence-lifetime imaging microscopy.

Laser cooling of CaBr molecules and production of ultracold Br atoms: A theoretical study including spin-orbit coupling.

Owing to the exciting potential applications of ultracold atoms and molecules in many fields, developing new cooling schemes has attracted great interests in recent years. Here, we investigate laser cooling of CaBr molecules and design a photonic scheme for the production of ultracold Br atoms using the highly accurate ab initio and dynamical methods. We find that the AΠ1/22(ν'=0)→X2Σ1/2+(ν=0) transition for CaBr features a large vibrational branching ratio, a significant photon-scattering rate, and no intermediate electronic-state interference, indicating that the ultracold CaBr could be produced through a three-laser cooling scheme. Moreover, an efficient four-pulse excitation scheme from the ground rovibrational level of the cooled CaBr molecules is proposed to yield ultracold Br atoms, in which a few spin-orbit excited states are utilized as the intermediate states. The importance of the spin-orbit coupling is underscored in this work.

Dynamical importance of van der Waals saddle and excited potential surface in C(1D)+D2 complex-forming reaction.

Encouraged by recent advances in revealing significant effects of van der Waals wells on reaction dynamics, many people assume that van der Waals wells are inevitable in chemical reactions. Here we find that the weak long-range forces cause van der Waals saddles in the prototypical C(1D)+D2 complex-forming reaction that have very different dynamical effects from van der Waals wells at low collision energies. Accurate quantum dynamics calculations on our highly accurate ab initio potential energy surfaces with van der Waals saddles yield cross-sections in close agreement with crossed-beam experiments, whereas the same calculations on an earlier surface with van der Waals wells produce much smaller cross-sections at low energies. Further trajectory calculations reveal that the van der Waals saddle leads to a torsion then sideways insertion reaction mechanism, whereas the well suppresses reactivity. Quantum diffraction oscillations and sharp resonances are also predicted based on our ground- and excited-state potential energy surfaces.

Extensive theoretical study on electronically excited states of calcium monochloride: Molecular laser cooling and production of ultracold chlorine atoms.

Nine doublet Λ-S states of calcium monochloride (CaCl) are calculated using the internally contracted multireference configuration interaction method with the Davidson correction. Both the core subvalence and spin-orbit coupling effects are taken into account. Laser cooling of CaCl and production of ultracold chlorine atoms are investigated and assessed. Our computed spectroscopic constants and radiative lifetimes match the available experimental data very well. The determined Franck-Condon factors and vibrational branching ratios of the A(2)Π1/2(ν('))←X(2)Σ1/2 (+)(ν) transition are highly diagonally distributed and the evaluated radiative lifetime for the A(2)Π1/2(ν' = 0) state is 28.2 ns, which is short enough for rapid laser cooling. Subsequently, detection of cold molecules via resonance enhanced multiphoton ionization to determine the final quantum state populations is discussed and the ionization energy calculated. A multi-pulse excitation scheme is proposed for producing ultracold chlorine atoms from zero-energy photodissociation of the cooled CaCl. Our results demonstrate the possibility of producing ultracold CaCl molecules and Cl atoms.

Nonlinear optical chromophores based on Dewar's rules: enhancement of electro-optic activity by introducing heteroatoms into the donor or bridge.

In this work, we investigated the enhancement of the electro-optic response by introducing electron-rich heteroatoms as additional donors into the donor or bridge of a conventional second-order nonlinear optical chromophore. A series of chromophores C2-C4 based on the same tricyanofuran acceptor (TCF) but with different heteroatoms in the alkylamino phenyl donor (C2 or C3) or thiophene bridge (C4) have been synthesized and systematically investigated. Density functional theory calculations suggested that chromophores C2-C4 had a smaller energy gap and larger first-order hyperpolarizability (ß) than traditional chromophore C1 due to the additional heteroatoms. Single crystal structure analyses and optimized configurations indicate that the rationally introduced heteroatom group would bring larger ß and weaker intermolecular interactions which were beneficial for translating molecular ß into macro-electro-optic activity in electric field poled films. The electro-optic coefficient of poled films containing 25 wt% of these new chromophores doped in amorphous poly-carbonate afforded values of 83 and 91 pm V(-1) at 1310 nm for chromophores C3 and C4, respectively, which are two times higher than that of the traditional chromophore C1 (39 pm V(-1)). High r33 values indicated that introducing heteroatoms to the donor and bridge of a conventional molecular structure can efficiently improve the electron-donating ability, which improves the ß. The long-chain on the donor or bridge part, acting as the isolation group, may reduce inter-molecular electrostatic interactions, thus enhancing the macroscopic EO activity. These results, together with good solubility and compatibility with the polymer, show the new chromophore's potential application in electro-optic devices.

Global analytical ab initio ground-state potential energy surface for the C((1)D)+H2 reactive system.

A new global ab initio potential energy surface (called ZMB-a) for the 1(1)A' state of the C((1)D)+H2 reactive system has been constructed. This is based upon ab initio calculations using the internally contracted multireference configuration interaction approach with the aug-cc-pVQZ basis set, performed at about 6300 symmetry unique geometries. Accurate analytical fits are generated using many-body expansions with the permutationally invariant polynomials, except that the fit of the deep well region is taken from our previous fit. The ZMB-a surface is unique in the accurate description of the regions around conical intersections (CIs) and of van der Waals (vdW) interactions. The CIs between the 1(1)A' and 2(1)A' states cause two kinds of barriers on the ZMB-a surface: one is in the linear H-CH dissociation direction with a barrier height of 9.07 kcal/mol, which is much higher than those on the surfaces reported before; the other is in the C((1)D) collinearly attacking H2 direction with a barrier height of 12.39 kcal/mol. The ZMB-a surface basically reproduces our ab initio calculations in the vdW interaction regions, and supports a linear C-HH vdW complex in the entrance channel, and two vdW complexes in the exit channel, at linear CH-H and HC-H geometries, respectively.