基于Ka波段毫米波云雷达多普勒谱的降雪微物理过程的分析

云中过冷水滴的识别对于预警飞机积冰及云-降水物理研究具有重要意义。本文利用美国ARM-AMF2在芬兰的35GHz测云雷达多普勒谱数据,建立了谱峰识别算法,对全局谱进行了谱分离,识别出了过冷水滴然后,经过谱矩计算得到不同类型粒子的反射率因子、多普勒速度、谱宽,最后根据经验关系反演云中液态水含量,并与微波辐射计探测结果进行对比。结果表明：(1)混合云中,雪花主导了毫米波雷达总回波强度,因此根据总雷达反射率因子反演液态水含量会造成低估;(2)冰雪晶粒子在过冷水层(SWL)中多普勒速度随反射率因子的变化梯度比在冰雪层(ISL)中大;(3)多普勒谱反演得到过冷水的液态水路径(LWP)与微波辐射计反演结果一致性较好,说明毫米波雷达能够有效估量云中液态水路径。     

防暴水炮对舰艇电站的影响及解决方法

通过对舰艇防暴水炮和电站的认识,分析了舰艇防暴水炮和船艇电站的作用、结构及主要组成部分,以及水炮作为大功率负载启动、运行时对电站所造成的影响,最后,针对舰艇实际情况,提出一些改进措施和方法。     

Hierarchical Nanowire Arrays Based on ZnO Core−Layered Double Hydroxide Shell for Largely Enhanced Photoelectrochemical Water Splitting

Well‐aligned hierarchical nanoarrays containing ZnO core and layered double hydroxide (LDH) nanoplatelets shell have been synthesized via a facile electrosynthesis method. The resulting ZnO@CoNi–LDH core?shell nanoarray exhibits promising behavior in photoelectrochemical water splitting, giving rise to a largely enhanced photocurrent density as well as stability; much superior to those of ZnO‐based photoelectrodes. This is attributed to the successful integration of photogenerated electron–hole separation originating from the ZnO core and the excellent electrocatalytic activity of LDH shell. This work provides a facile and cost‐effective strategy for the fabrication of multifunctional nanoarrays with a hierarchical structure, which can be potentially used in energy storage and conversion devices.     

High Performance Core/Shell Ni/Ni(OH)2 Electrospun Nanofiber Anodes for Decoupled Water Splitting

Decoupled water splitting is a promising new path for renewable hydrogen production, offering many potential advantages such as stable operation under partial-load conditions, high-pressure hydrogen production, overall system robustness, and higher safety levels. Here, the performance of electrospun core/shell nickel/nickel hydroxide anodes is demonstrated in an electrochemical-thermally activated chemical decoupled water splitting process. The high surface area of the hierarchical porous electrode structure improves the utilization efficiency, charge capacity, and current density of the redox anode while maintaining high process efficiency. The anodes reach average current densities as high as 113 mA cm⁻² at a working potential of 1.48 V_RHE and 64 mA cm⁻² at 1.43 V_RHE, with a Faradaic efficiency of nearly 100% and no H₂/O₂ intermixing in a membrane-free cell.     

Reconstructed Water Oxidation Electrocatalysts: The Impact of Surface Dynamics on Intrinsic Activities

Electroreduction of small molecules such as H₂O, CO₂, and N₂ for producing clean fuels or valuable chemicals provides a sustainable approach to meet the increasing global energy demands and to alleviate the concern on climate change resulting from fossil fuel consumption. On the path to implement this purpose, however, several scientific hurdles remain, one of which is the low energy efficiency due to the sluggish kinetics of the paired oxygen evolution reaction (OER). In response, it is highly desirable to synthesize high-performance and cost-effective OER electrocatalysts. Recent advances have witnessed surface reconstruction engineering as a salient tool to significantly improve the catalytic performance of OER electrocatalysts. In this review, recent progress on the reconstructed OER electrocatalysts and future opportunities are discussed. A brief introduction of the fundamentals of OER and the experimental approaches for generating and characterizing the reconstructed active sites in OER nanocatalysts are given first, followed by an expanded discussion of recent advances on the reconstructed OER electrocatalysts with improved activities, with a particular emphasis on understanding the correlation between surface dynamics and activities. Finally, a prospect for clean future energy communities harnessing surface reconstruction-promoted electrochemical water oxidation will be provided.     

Theoretical and Experimental Insight into the Mechanism for Spontaneous Vertical Growth of ReS2 Nanosheets

Rhenium disulfide (ReS₂) differs fundamentally from other group‐VI transition metal dichalcogenides (TMDs) due to its low structural symmetry, which results in its optical and electrical anisotropy. Although vertical growth is observed in some TMDs under special growth conditions, vertical growth in ReS₂ is very different in that it is highly spontaneous and substrate‐independent. In this study, the mechanism that underpins the thermodynamically favorable vertical growth mode of ReS₂ is uncovered. It is found that the governing mechanism for ReS₂ growth involves two distinct stages. In the first stage, ReS₂ grows parallel to the growth substrate, consistent with conventional TMD growth. However, subsequent vertical growth is nucleated at points on the lattice where Re atoms are “pinched” together. At such sites, an additional Re atom binds with the cluster of pinched Re atoms, leaving an under‐coordinated S atom protruding out of the ReS₂ plane. This under‐coordinated S is “reactive” and binds to free Re and S atoms, initiating growth in a direction perpendicular to the ReS₂ surface. The utility of such vertical ReS₂ arrays in applications where high surface‐to‐volume ratio and electric‐field enhancement are essential, such as surface enhanced Raman spectroscopy, field emission, and solar‐based disinfection of bacteria, is demonstrated.     

Interfacial Connections between Organic Perovskite/n+ Silicon/Catalyst that Allow Integration of Solar Cell and Catalyst for Hydrogen Evolution from Water

The rapidly increasing solar conversion efficiency (PCE) of hybrid organic–inorganic perovskite (HOIP) thin-film semiconductors has triggered interest in their use for direct solar-driven water splitting to produce hydrogen. However, application of these low-cost, electronic-structure-tunable HOIP tandem photoabsorbers has been hindered by the instability of the photovoltaic-catalyst-electrolyte (PV+E) interfaces. Here, photolytic water splitting is demonstrated using an integrated configuration consisting of an HOIP/n⁺silicon single junction photoabsorber and a platinum (Pt) thin film catalyst. An extended electrochemical (EC) lifetime in alkaline media is achieved using titanium nitride on both sides of the Si support to eliminate formation of insulating silicon oxide, and as an effective diffusion barrier to allow high-temperature annealing of the catalyst/TiO₂-protected-n⁺silicon interface necessary to retard electrolytic corrosion. Halide composition is examined in the (FA_1-xCs_x)PbI₃ system with a bandgap suitable for tandem operation. A fill factor of 72.5% is achieved using a Spiro-OMeTAD-hole-transport-layer (HTL)-based HOIP/n⁺Si solar cell, and a high photocurrent density of −15.9 mA cm⁻² (at 0 V vs reversible hydrogen electrode) is attained for the HOIP/n⁺Si/Pt photocathode in 1 m NaOH under simulated 1-sun illumination. While this thin-film design creates stable interfaces, the intrinsic photo- and electro-degradation of the HOIP photoabsorber remains the main obstacle for future HOIP/Si tandem PEC devices.     

Bimetal-Incorporated Black Phosphorene with Surface Electron Deficiency for Efficient Anti-Reconstruction Water Electrolysis

Surface reconstruction (SRC) is a common phenomenon and a promotion manner for Ni/Co-based precatalysts during the water splitting process. However, the catalytic surface reconstruction will in turn complicate the streamlined prediction and modeling on the catalytic activity. Hence, the rational design of anti-SRC catalysts is highly desirable, but challengeable. In this article, a series of affordable bimetal-incorporated black phosphorene (BP) catalysts are constructed by an in situ electro-exfoliation/insertion method for anti-SRC water electrolysis. It is found that the bimetals (e.g., NiFe, NiPd) are of cationic and covalent incorporation with electron-deficient state in few-layer BP. The optimized bimetal-BP structures present excellent and stable catalytic performances with low overpotentials in hydrogen evolution (HER, 53 mV, NiPd-BP) and oxygen evolution (OER, 268 mV, NiFe-BP) reactions at 10 mA cm⁻² in 1 m KOH. The anti-SRC behaviors are elucidated by in situ Raman studies during HER/OER, probably due to the balanced electron transfer pathway on Ni sites. This research opens interesting possibilities for designing the anti-SRC catalysts for efficient hydrogen production and authentic structure-activity understandings.     

Solar-Driven Interfacial Evaporation Accelerated Electrocatalytic Water Splitting on 2D Perovskite Oxide/MXene Heterostructure

The rational design of economic and high-performance electrocatalytic water-splitting systems is of great significance for energy and environmental sustainability. Developing a sustainable energy conversion-assisted electrocatalytic process provides a promising novel approach to effectively boost its performance. Herein, a self-sustained water-splitting system originated from the heterostructure of perovskite oxide with 2D Ti₃C₂T_x MXene on Ni foam (La_1-xSr_xCoO₃/Ti₃C₂T_x MXene/Ni) that shows high activity for solar-powered water evaporation and simultaneous electrocatalytic water splitting is presented. The all-in-one interfacial electrocatalyst exhibits highly improved oxygen evolution reaction (OER) performance with a low overpotential of 279 mV at 10 mA cm⁻² and a small Tafel slope of 74.3 mV dec⁻¹, superior to previously reported perovskite oxide-based electrocatalysts. Density functional theory calculations reveal that the integration of La_0.9Sr_0.1CoO₃ with Ti₃C₂T_x MXene can lower the energy barrier for the electron transfer and decrease the OER overpotential, while COMSOL simulations unveil that interfacial solar evaporation could induce OH⁻ enrichment near the catalyst surfaces and enhance the convection flow above the catalysts to remove the generated gas, remarkably accelerating the kinetics of electrocatalytic water splitting.     

水中气泡界面的光强研究

通过菲涅耳公式,对气泡内外界面的光强进行了计算,得出气泡界面第2次反射光强I′2s和I′2p(内表面)、折射光强I2s和I2p(外表面)的一般规律,及不同偏振态的光线在界面第n次反射和折射后的光强与第2次光强的关系。理论和实验均表明,光在气泡界面连续反射4次后基本消失。最后通过激光和CCD相机抓拍到水中气泡的图像,能明显获得出射光线轨迹,实验测量出射光强的值与理论计算值相吻合。