Rational Design of Charge‐Neutral,Near‐Infrared‐Emitting Osmium(II) Complexes and OLED Fabrication

A new series of charge neutral Os(II) isoquinolyl triazolate complexes ( 1 – 4 ) with both trans and cis arrangement of phosphine donors are synthesized, and their structural, electrochemical and photophysical properties are established. In sharp contrast to the cis‐arranged complexes 2 – 4 , the trans derivative 1 , which shows a planar arrangement of chromophoric N‐substituted chelates, offers the most effective extended π‐delocalization and hence the lowest excited state energy gap. These complexes exhibit phosphorescence with peak wavelengths ranging from 692–805 nm in degassed CH₂Cl₂ at room temperature. Near‐infrared (NIR)‐emitting electroluminescent devices employing 6 wt % of 1 (or 4 ) doped in Alq₃ host material are successfully fabricated. The devices incorporating 1 as NIR phosphor exhibit fairly intense emission with a peak wavelength at 814 nm. Forward radiant emittance reaches as high as 65.02 µW cm^?2, and a peak EQE of ～1.5% with devices employing Alq₃, TPBi and/or TAZ as electron‐transporting/exciton‐blocking layers. Upon switching to phosphor 4 , the electroluminescence blue shifts to 718 nm, while the maximum EQE and radiance increase to 2.7% and 93.26 (μW cm^?2) respectively. Their performances are optimized upon using TAZ as the electron transporting and exciton‐blocking material. The OLEDs characterized represent the only NIR‐emitting devices fabricated using charge‐neutral and volatile Os(II) phosphors via thermal vacuum deposition.     

Lithiophilic MXene-Guided Lithium Metal Nucleation and Growth Behavior

The positive effects of a lithiophilic substrate on the electrochemical performance of lithium metal anodes are confirmed in several reports, while the understanding of lithiophilic substrate-guided lithium metal nucleation and growth behavior is still insufficient. In this study, the effect of a lithiophilic surface on lithium metal nucleation and growth behaviors is investigated using a large-area Ti₃C₂T_x MXene substrate with a large number of oxygen and fluorine dual heteroatoms. The use of the MXene substrate results in a high lithium-ion concentration as well as the formation of uniform solid–electrolyte-interface (SEI) layers on the lithiophilic surface. The solid–solid interface (MXene-SEI layer) significantly affects the surface tension of the deposited lithium metal nuclei as well as the nucleation overpotential, resulting in the formation of uniformly dispersed lithium nanoparticles ( ≈ 10–20 nm in diameter) over the entire MXene surface. The primary lithium nanoparticles preferentially coalesce and agglomerate into larger secondary particles while retaining their primary particle shapes. Subsequently, they form close-packed structures, resulting in a dense metal layer composed of particle-by-particle microstructures. This distinctive lithium metal deposition behavior leads to highly reversible cycling performance with high Columbic efficiencies >  99.0% and long cycle lives of over 1000 cycles.     

Spare node cooperative method for IEEE 802.11 networks

Most of the existing cooperation methods select relay node(s) mainly based on the channel state information, but do not consider whether the selected relay nodes work or not. If the selected relays are invalidated, the performance of cooperative communication will deteriorate. To resolve the above problem, this paper investigates cooperative communication in IEEE 802.11 networks, and proposes a novel Spare Cooperative Method (SCM). SCM chooses a spare cooperation node to enhance the reliability of communication, and uses an enhanced handshaking mechanism to coordinate the access of source nodes and cooperation nodes to the wireless channel. The performance of SCM is comprehensively analyzed in terms of outage probability and saturated throughput. The analysis shows that SCM improves the performance of IEEE 802.11.     

大型MOX燃料快堆钠空泡反应性微扰理论研究

钠空泡反应性效应是钠冷快堆核设计和安全分析的重要内容。本文基于多群节块扩散法,采用微扰理论推导出钠空泡反应性的计算方法,对1 000 MWe钠冷快堆MOX燃料堆芯的总钠空泡反应性、空间分布、物理分项进行了计算。结果表明,钠空泡反应性主要来源于中子泄漏的增加和能谱的硬化,两者一正一负,且空间分布规律相反,导致钠空泡反应性具有强烈的空间依赖性;对于所计算的MOX燃料堆芯钠空泡反应性高达3 $左右。计算和分析结果阐明了钠空泡反应性的产生机理和分布规律,可为低钠空泡的设计提供参考。     

加热面朝下的池沸腾汽泡动态行为研究

基于Matlab软件开发了自动识别气液两相流界面程序,程序可获得气液界面变化、汽膜厚度、汽膜脱离周期和汽膜法向速度等特征。利用该程序对沟槽结构加热表面朝下布置时,在不同倾角、不同热流密度下的汽泡动态数据进行了处理和分析。结果表明：加热表面朝下发生核态沸腾时,汽膜厚度随热流密度的增大而增大,汽泡脱离周期随热流密度的增大先减小,而后维持在一稳定值;汽膜脱离周期随倾角的增大而减小,倾角为5°时的汽膜脱离周期稳定在0.27 s左右。当发生沸腾危机时,汽膜厚度迅速减小,这可作为动态监测加热表面沸腾状态的依据。     

富集硼酸在压水堆一回路水化学中的应用研究

压水堆核电厂一般采用天然硼来控制反应性。在核电厂实施长循环燃料管理后,寿期初硼浓度较高,增加了水化学控制的压力。本文开展了富集硼酸(EBA)在一回路水化学中的应用可行性及其对相关水质处理系统的影响分析。研究表明一回路采用EBA有助于降低结构材料的腐蚀和堆外辐射场,提高在役核电厂的经济性。     

Effect of Pressure on Moisture Transfer During Moisture Adsorption

ABSTRACT

A set of coupled heat, mass, and pressure transfer equations was used to describe the moisture adsorption process in gmn kernels. The finite element method was used to solve the system of equations. The technique was applied to analyze the temperature, moisture, and pressure distribution in a barley kernel during soaking with steep water. The temperature and moisture distributions with (heat, mass, and pressure transfer model) and without (heat and mass uansfer) the effect of pressure were simulated for assumed conditions. The results obtained from the heat, mass, and pressure transfer model show a marked difference from the results obtained from the heat and mass transfer model. This indicated that a pressure gradient exists during the transfer Process, causing additional moisture movement due to filtration effect. Hence. the pressure tern cannot be assumed constant during the moisture adsorption process. The simulated temperature, moisture and pressure profiles and gradients can be used for determining the optimum time required for solking kernels with sleep water to produce barley malt.     

1‐Arylsulfonyl‐5‐(N‐hydroxyacrylamide)indolines Histone Deacetylase Inhibitors Are Potent Cytokine Release Suppressors

A series of 1‐arylsulfonyl‐5‐(N‐hydroxyacrylamide)indolines ( 7 – 15 ) has been developed; the compounds exhibited potent histone deacetylase (HDAC) inhibitory activities. Notably, almost all of this series exhibited better HDAC‐inhibitory and antiproliferative activities than 3‐(1‐benzenesulfonyl‐1H‐indol‐5‐yl)‐N‐hydroxyacrylamide ( 6 ), as reported in a previous study. Among these compounds, 3‐[1‐(4‐methoxybenzenesulfonyl)‐2,3‐dihydro‐1H‐indol‐5‐yl]‐N‐hydroxyacrylamide ( 9 ) showed a two‐ to tenfold increase in activity compared to SAHA ( 1 ) in the suppression of lipopolysaccharide‐induced cytokine production. Compound 9 also caused a marked reduction in carrageenan‐induced acute inflammation in a rat model. Taken together, these data indicated that 1‐arylsulfonyl‐5‐(N‐hydroxyacrylamide)indolines HDAC inhibitors exhibit potent anti‐inflammatory activity.