Epitaxial growth of borophene on substrates

Borophene, a two-dimensional (2D) planar boron sheet, has attracted dramatic attention for its unique physical properties that are theoretically predicted to be different from those of bulk boron, such as polymorphism, superconductivity, Dirac fermions, mechanical flexibility and anisotropic metallicity. Nevertheless, it has long been difficult to obtain borophene experimentally due to its susceptibility to oxidation and the strong covalent bonds in bulk forms. With the development of growth technology in ultra-high vacuum (UHV), borophene has been successfully synthesized by molecular beam epitaxy (MBE) supported by substrates in recent years. Due to the intrinsic polymorphism of borophene, the choice of substrates in the synthesis of borophene is pivotal to the atomic structure of borophene. The different interactions and commensuration of borophene on various substrates can induce various allotropes of borophene with distinct atomic structures, which suggests a potential approach to explore and manipulate the structure of borophene and benefits the realization of novel physical and chemical properties in borophene due to the structure–property correspondence. In this review, we summarize the recent research progress in the synthesis of monolayer (ML) borophene on various substrates, including Ag(1 1 1), Ag(1 1 0), Ag(1 0 0), Cu(1 1 1), Cu(1 0 0), Au(1 1 1), Al(1 1 1) and Ir(1 1 1), in which the polymorphism of borophene is present. Moreover, we introduce the realization of bilayer (BL) borophene on Ag(1 1 1), Cu(1 1 1) and Ru(0 0 0 1) surfaces, which possess richer electronic properties, including better thermal stability and oxidation resistance. Then, the stabilization mechanism of polymorphic borophene on their substrates is discussed. In addition, experimental investigations on the unique physical properties of borophene are also introduced, including metallicity, topology, superconductivity, optical and mechanical properties. Finally, we present an outlook on the challenges and prospects for the synthesis and potential applications of borophene.     

Non-Interacting Ni and Fe Dual-Atom Pair Sites in N-Doped Carbon Catalysts for Efficient Concentrating Solar-Driven Photothermal CO2 Reduction

Solar-to-chemical energy conversion under weak solar irradiation is generally difficult to meet the heat demand of CO₂ reduction. Herein, a new concentrated solar-driven photothermal system coupling a dual-metal single-atom catalyst (DSAC) with adjacent Ni−N₄ and Fe−N₄ pair sites is designed for boosting gas-solid CO₂ reduction with H₂O under simulated solar irradiation, even under ambient sunlight. As expected, the (Ni, Fe)−N−C DSAC exhibits a superior photothermal catalytic performance for CO₂ reduction to CO (86.16 μmol g⁻¹ h⁻¹), CH₄ (135.35 μmol g⁻¹ h⁻¹) and CH₃OH (59.81 μmol g⁻¹ h⁻¹), which are equivalent to 1.70-fold, 1.27-fold and 1.23-fold higher than those of the Fe−N−C catalyst, respectively. Based on theoretical simulations, the Fermi level and d-band center of Fe atom is efficiently regulated in non-interacting Ni and Fe dual-atom pair sites with electronic interaction through electron orbital hybridization on (Ni, Fe)−N−C DSAC. Crucially, the distance between adjacent Ni and Fe atoms of the Ni−N−N−Fe configuration means that the additional Ni atom as a new active site contributes to the main *COOH and *HCO₃ dissociation to optimize the corresponding energy barriers in the reaction process, leading to specific dual reaction pathways (COOH and HCO₃ pathways) for solar-driven photothermal CO₂ reduction to initial CO production.     

快中子照相模拟分析与实验验证

首次系统地推导出快中子照相像素值形成解析式, 建立图像反差不等式, 并利用该不等式首次对图像对比度与源强、照射时间和散射之间的关系进行说明. 并在像素值解析式基础上编制快中子照相模拟程序, 利用该程序对空间分辨率和图像对比度进行模拟, 并与实验对照, 研究结果表明空间分辨率模拟效果好于实验, 图像对比度模拟效果与实验相当. 最后通过对狭缝、方孔以及多材质组成的复杂样品模拟并与实验对照, 结果显示模拟效果与实验照片在反差灵敏度效果上非常一致, 该模拟计算方法可为实验设计和工程应用提供参考.     

Voltage control of millimeter-wave ferromagnetic resonance in multiferroic heterostructures thin films

Multiferroic heterostructures thin films, SrBi₂Ta₂O₉/BaFe₁₂O₁₉ (SBT/BaM), were grown on Pt/TiO₂/SiO₂/Si substrates by using magnetron sputtering and Sol-gel ways. X-ray diffractometer (XRD) analysis showed that only SBT and BaM phases appeared in the multiferroic heterostructures. Magnetic hysteresis loops revealed that the saturated magnetization was 3.7 kG and the M-H characteristics of SBT/BaM were not influenced by the presence of the SBT layer. Ferromagnetic resonance (FMR) measurement showed the lowest FMR linewidth of 205 Oe at 50 GHz. Additionally, when direct-current electric field was applied to SBT layer, as a result of which mechanical deformation of the ferromagnetic layer occurred that leads to a frequency shift in ferromagnetic resonance and the magnetoelectric coupling effect (α) is 1.8 MHz*cm/kV. Our findings indicate that these SBT/BaM thin films have a significant potential for the usage in millimeter wave tunable devices.     

A pressure vessel for studying gas foaming of thermosetting polymers: sorption,synthesis and processing

We herein report the design of an apparatus for studying the concurrent chemo-physical processes occurring during gas foaming of thermosetting polymers. In particular, to address the recent interest in combining the gas (physical) foaming with the classical (chemical) polyurethane foaming, a novel instrumented pressure vessel was designed for investigating: i) gas sorption under high pressure on the different reactants, kept separate; ii) synthesis under high gas pressure, upon mixing and iii) foaming upon release of the pressure. The design of the new pressure vessel relies on two key features. From the processing side, we make use of a rubber impeller to keep the two reactants separate during gas sorption and to allow for an efficient mixing at the end of the sorption stage. From the analytic side, we utilized a sapphire window beneath the sample holder to use diffuse reflectance near-infrared spectroscopy to measure both the amount of sorbed gas and the reaction kinetics under gas pressure. Preliminary results are reported for the polyol-isocyanate/CO₂ system.     

Improved measurement of electron antineutrinodisappearance at Daya Bay

We report an improved measurement of the neutrino mixing angle θ₁₃ from the Daya Bay Reactor Neutrino Experiment. We exclude a zero value for sin² θ₁₃ with a significance of 7.7 standard deviations. Electron antineutrinos from six reactors of 2.9 GW_th were detected in six antineutrino detectors deployed in two near （flux-weighted baselines of 470 m and 576 m） and one far （1648 m） underground experimental halls. Using 139 days of data, 28909 （205308） electron antineutrino candidates were detected at the far hall （near halls）. The ratio of the observed to the expected number of antineutrinos assuming no oscillations at the far hall is 0.944±0.007（stat.）±0.003（syst.）. An analysis of the relative rates in six detectors finds sin² θ₁₃ =0.089±0.010（stat.）±0.005（syst.） in a three-neutrino framework.     

Good match exploration for thermal infrared face recognition based on YWF-SIFT with multi-scale fusion

Stable local feature detection is a critical prerequisite in the problem of infrared (IR) face recognition. Recently, Scale Invariant Feature Transform (SIFT) is introduced for feature detection in an infrared face frame, which is achieved by applying a simple and effective averaging window with SIFT termed as Y-styled Window Filter (YWF). However, the thermal IR face frame has an intrinsic characteristic such as lack of feature points (keypoints); therefore, the performance of the YWF-SIFT method will be inevitably influenced when it was used for IR face recognition. In this paper, we propose a novel method combining multi-scale fusion with YWF-SIFT to explore more good feature matches. The multi-scale fusion is performed on a thermal IR frame and a corresponding auxiliary visual frame generated from an off-the-shelf low-cost visual camera. The fused image is more informative, and typically contains much more stable features. Besides, the use of YWF-SIFT method enables us to establish feature correspondences more accurately. Quantitative experimental results demonstrate that our algorithm is able to significantly improve the quantity of feature points by approximately 38%. As a result, the performance of YWF-SIFT with multi-scale fusion is enhanced about 12% in infrared human face recognition.     

Sonochemical synthesis of CH3NH3PbI3 perovskite ultrafine nanocrystal sensitizers for solar energy applications

The organic–inorganic hybrid perovskite CH₃NH₃PbI₃ is becoming an interesting material in the field of energy harvesting. This material is one of the cleanest and cheapest components in solar cells which is available in ample amounts. However, most of the previous research work was done on thin film of this material. In the present work we describe the preparation of a powder containing nanoparticles of CH₃NH₃PbI₃ using a sonochemical method. Characterization of the product was done by various methods, such as HRTEM, FTIR, PL, DLS and XRD. The particles were found to be highly crystalline (tetragonal crystal structure), polygonal in shape and having diameters of 10–40 nm.     

Influence of aspect ratio and arrangement direction on the shear behavior of ellipsoids

This work studies the macroscopic and microscopic behaviors of ellipsoids under triaxial tests using 3D discrete element method (DEM) simulation. To avoid the boundary effect, a novel stress servo-controlled periodic boundary condition is proposed to maintain the confining pressure of samples during testing. The shape features of ellipsoids are investigated, including the aspect ratio of elongated/oblate ellipsoids and the initial arrangement directions of ellipsoids. The macroscopic properties of ellipsoidal particle samples, such as the deviatoric stress, volumetric strain, internal friction angle, as well as dilatancy angles are explored. Elongated and oblate ellipsoids with varying aspect ratios are investigated for the occurrence of stick-slips. In addition, it is demonstrated that the initial arrangement direction has a significant impact on the coordination number and contact force chains. The corresponding anisotropy coefficients of the entire contact network are analyzed to probe the microscopic roots of macroscopic behavior.