长期高温高压氢暴露对Cr-Mo钢断裂韧性和裂纹行为的影响

选用Cr-Mo钢经400℃,20 MPa,10⁴ h氢暴露后进行拉伸、断裂韧性和疲劳试验.结果表明:Cr-Mo钢已经发生了氢腐蚀,氢蚀使Cr-Mo钢强度、塑性和断裂韧性均有所降低,也使断裂机制由韧窝型转变为解理脆性.氢蚀使疲劳裂纹扩展行为也发生了变化,疲劳裂纹扩展速率增加,ΔK_th降低.Cr-Mo钢氢蚀后,随应力比增加,疲劳裂纹扩展门槛值大幅度降低.     

氧化芋头淀粉理化性质研究

以芋头淀粉为原料、过氧化氢为氧化剂,在碱性介质中制备了低氧化度芋头淀粉。经扫描电镜分析,氧化芋头淀粉颗粒呈多角状,平均颗粒直径18.09μm。X-射线衍射确定其晶体形貌为A型结构。流变学分析其糊化温度为79.5℃、特性粘度为2.505 Pa.s,粘弹性曲线显示其粘性大于弹性。其塑性测定结果符合Croass模型,稠度指数为85.56 s。     

钯钇合金膜分离器级联分离氢同位素理论计算

钯合金膜分离氢同位素具有分离能力强、氚滞留量小以及装置设计简单等优点,是一种很有发展潜力的氢同位素分离方法,但受膜及泵输系统等因素的制约,目前仍处于概念设计阶段。文中针对级联分离建立了考虑返混的近似模型。模型表明:各级的分流比和分离系数相同时,对含氚体积分数0.065%的氢同位素混合气体,在0.2分流比(体积比),分离系数为2.5时,经过3级富集和4级贫化就可以得到含氚体积分数1.5%的产品和含氚体积分数0.000 5%的贫料;相同分离系数下,分流比较大时分离系统的规模较小。     

High pressure organic colloid method for the preparation of high performance carbon nanotube-supported Pt and PtRu catalysts for fuel cell applications

Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 20...     

Hydrogen‐Bonding‐Assisted Intermolecular Charge Transfer: A New Strategy to Design Single‐Component White‐Light‐Emitting Materials

This study reveals the mechanism of the dual‐emission properties for asymmetrical diphenylsulfone and diphenylketone derivatives. A series of asymmetrical diphenylketone and diphenylsulfone derivatives with dual‐emission properties are designed and synthesized. By single crystal structure analyses, various photophysical studies, and 2D ¹H–¹H NOSEY NMR studies, the lower energy emission bands in the dual‐emission spectra are successfully assigned to hydrogen‐bonding‐assisted intermolecular charge transfer emission. The emission properties of these compounds can easily be tuned in both solid state and solution state by destroying or strengthening the intermolecular hydrogen bonding. In addition, thermally activated delayed fluorescence characteristics for the intermolecular charge transfer emissions are also observed. The control of the intermolecular and intramolecular charge transfers serves as the basis for the generation of the white‐light emission. For compound CPzPO, nearly pure white‐light emission with CIE coordinates of (0.31, 0.32) is easily achieved by precipitation from dichloromethane and hexane mixed solvent system. These results clearly give an insight into the dual‐emission properties and provide a rational strategy for the design and synthesis of single‐component white‐light‐emitting materials and mechanoresponsive light‐emitting materials.     

Kinetic‐Oriented Construction of MoS2 Synergistic Interface to Boost pH‐Universal Hydrogen Evolution

As a prerequisite for a sustainable energy economy in the future, designing earth‐abundant MoS₂ catalysts with a comparable hydrogen evolution catalytic performance in both acidic and alkaline environments is still an urgent challenge. Decreasing the energy barriers could enhance the catalysts' activity but is not often a strategy for doing so. Here, the first kinetic‐oriented design of the MoS₂‐based heterostructure is presented for pH‐universal hydrogen evolution catalysis by optimizing the electronic structure based on the simultaneous modulation of the 3d‐band‐offsets of Ni, Co, and Mo near the interface. Benefiting from this desirable electronic structure, the obtained MoS₂/CoNi₂S₄ catalyst achieves an ultralow overpotential of 78 and 81 mV at 10 mA cm^?2, and turnover frequency as high as 2.7 and 1.7 s^?1 at the overpotential of 200 mV in alkaline and acidic media, respectively. The MoS₂/CoNi₂S₄ catalyst represents one of the best hydrogen evolution reaction performing ones among MoS₂‐based catalysts reported to date in both alkaline and acidic environments, and equally important is the remarkable long‐term stability with negligible activity loss after maintaining at 10 mA cm^?2 for 48 h in both acid and base. This work highlights the potential to deeply understand and rationally design highly efficient pH‐universal electrocatalysts for future energy storage and delivery.     

Carbon Free and Noble Metal Free Ni2Mo6S8 Electrocatalyst for Selective Electrosynthesis of H2O2

Electrocatalytic two-electron reduction of oxygen is a promising method for producing sustainable H₂O₂ but lacks low-cost and selective electrocatalysts. Here, the Chevrel phase chalcogenide Ni₂Mo₆S₈ is presented as a novel active motif for reducing oxygen to H₂O₂ in an aqueous electrolyte. Although it has a low surface area, the Ni₂Mo₆S₈ catalyst exhibits exceptional activity for H₂O₂ synthesis with >90% H₂O₂ molar selectivity across a wide potential range. Chemical titration verified successful generation of H₂O₂ and confirmed rates as high as 90 mmol H₂O₂ g_cat⁻¹ h⁻¹. The outstanding activities are attributed to the ligand and ensemble effects of Ni that promote H₂O dissociation and proton-coupled reduction of O₂ to HOO*, and the spatial effect of the Chevrel phase structure that isolates Ni active sites to inhibit O O cleavage. The synergy of these effects delivers fast and selective production of H₂O₂ with high turn-over frequencies of ≈30 s⁻¹. In addition, the Ni₂Mo₆S₈ catalyst has a stable crystal structure that is resistive for oxidation and delivers good catalyst stability for continuous H₂O₂ production. The described Ni-Mo₆S₈ active motif can unlock new opportunities for designing Earth-abundant electrocatalysts to tune oxygen reduction for practical H₂O₂ production.     

A highly luminescent organic crystal with the well-balanced charge transport property: The role of cyano-substitution in the terminal phenyl unit of distyrylbenzene

1,4-bis(2-cyano styryl)benzene (2-CSB) crystal with cyano substituent groups introduced to the terminal phenyl rings of distyrylbenzene (DSB) has been prepared and its luminescence efficiency could be as high as ∼55%. Based on the analyses of cyclic voltammetry and crystal structure, cyano substituents not only lower the LUMO level but also result in a change of the packing mode from the herringbone arrangement to the face-to-face slipped π stacking motif. Then field-effect transistors (FETs) based on high-quality 2-CSB crystals grown by the physical vapor transport method have been fabricated and the highest hole and electron mobilities were measured as 0.66 and 0.29 cm²/Vs, which enhanced the corresponding values of DSB crystal by up to one and two orders of magnitude, respectively. 2-CSB crystal simultaneously combined the high luminescence and the well-balanced mobility is expected to be of interest for the fundamental research of organic light-emitting devices.     

Surface Oxygen Coordination of Hydrogen Bond Chemistry for Aqueous Ammonium Ion Hybrid Supercapacitor

Aqueous ammonium ion hybrid supercapacitor (A-HSC) combines the charge storage mechanisms of surface adsorption and bulk intercalation, making it a low-cost, safe, and sustainable energy storage candidate. However, its development is hindered by the low capacity and unclear charge storage fundamentals. Here, the strategy of phosphate ion-assisted surface functionalization is used to increase the ammonium ion storage capacity of an α-MoO₃ electrode. Moreover, the understanding of charge storage mechanisms via structural characterization, electrochemical analysis, and theoretical calculation is advanced. It is shown that NH₄⁺ intercalation into layered α-MoO₃ is not dominant in the A-HSC system; rather, the charge storage mainly depends on the adsorption energy of surface “O” to NH₄⁺. It is further revealed that the hydrogen bond chemistry of the coordination between “O” of surface phosphate ion and NH₄⁺ is the reason for the capacity increase of MoO₃. This study not only advances the basic understanding of rechargeable aqueous A-HSC but also demonstrates the promising future of surface engineering strategies for energy storage devices.