以磷化铁为添加剂沿(111)面生长磷掺杂金刚石大单晶

掺杂是调控金刚石性能的一种重要手段。本文采用温度梯度法,在5.6 GPa、1 312 ℃的条件下,选用Fe₃P作为磷源进行磷掺杂金刚石大单晶的合成。金刚石样品的显微光学照片表明,随着Fe₃P添加比例的增加,金刚石晶体的颜色逐渐变深,包裹体数量逐渐增加,晶形由板状转变为塔状直至骸晶。金刚石晶形的变化表明Fe₃P的添加使生长金刚石的V形区向右偏移,这是Fe₃P改变触媒特性的缘故。红外光谱分析表明,Fe₃P的添加使金刚石晶体中氮含量上升,这说明磷的进入诱使氮原子更容易进入金刚石晶格中。激光拉曼光谱测试表明,随着Fe₃P添加比例的增加,所合成的掺磷金刚石的拉曼峰位变化不大,其半峰全宽(FWHM)值变大,这说明磷的进入使得金刚石晶格畸变增加。XPS测试结果显示,随着Fe₃P添加比例的增加,金刚石晶体中磷相对碳的原子百分含量也会增加,这意味着添加Fe₃P所合成的金刚石晶体中有磷存在。     

Terahertz Dual-Band Near-Zero Effective Index Metamaterial Based on Double-Sided Metal Microstructure

Journal of Russian Laser Research - The zero-refractive-index metamaterials have excellent electromagnetic properties, which provide new ideas and methods to realize the control of electromagnetic...     

射频等离子制备石墨烯负载Co3O4催化剂及其析氧性能研究

氢能的引入能有效提升配电网的供电可靠性,而电解水制氢是实现低碳转型的关键技术,开发高效的电解水催化剂势在必行。过渡金属氧化物储量大、催化活性高,是具有广阔应用前景的析氧反应催化剂。本文通过射频等离子体处理制备石墨烯上负载Co₃O₄析氧催化剂,XRD、Raman和XPS测试结果显示,二维结构石墨烯的引入加速表面电子迁移,增大了反应面积。等离子体处理促进了纳米粒子在石墨烯上的负载,利用等离子体刻蚀作用在催化剂表面制造出大量碳结构缺陷和氧空位结构,改善了活性位点分布,有效调控Co₃O₄电子结构,提高析氧催化活性。电化学测试表明,本文中合成的Co₃O₄@rGO在电流密度为50 mA·cm^-2时的过电位为410 mV,动力学反应速率较快,表现出优于商业IrO₂的析氧催化活性。     

Stability of Multiplier Ideal Sheaves

Chinese Annals of Mathematics, Series B - In the present article, the authors find and establish stability of multiplier ideal sheaves, which is more general than strong openness.     

Synthesis of deuterium-labeled DL-threo-thiamphenicol

Journal of Radioanalytical and Nuclear Chemistry - A convenient and inexpensive approach for the synthesis of deuterium-labeled thiamphenicol was described. DL-threo-Thiamphenicol-methyl-d3 was...     

DYNAMIC RESPONSE OF HIGH SPEED TRAIN MEETING IN OPEN AIR,MEETING IN TUNNEL AND PASSING TUNNEL1)

明线会车、隧道会车和过隧道工况下的气动压力波对高速列车的动力响应和运行安全产生很大影响,本文建立了三辆编组的高速列车动力学模型,通过数值仿真得到了列车在三种工况下的车体所受的气动力,基于数值积分分析了列车的动力响应和脱轨系数。研究发现：明线会车和隧道会车工况相比,车辆的侧向运动相反。 明线会车和过隧道时,气动载荷对列车的脱轨系数影响较小,而隧道会车时,气动载荷作用对尾车的安全性影响较大。     

Facile room-temperature coprecipitation of uniform barium chlorapatite nanoassemblies as a host photoluminescent material

As an emerging host phosphor material, barium chlorapatite (Ba₅(PO₄)₃Cl), is attracting growing attention. However, rare earth-doped Ba₅(PO₄)₃Cl phosphors have mainly been obtained via high temperature-based, energy-consuming techniques. In this contribution, we developed a straightforward, facile room-temperature coprecipitation method in the presence of a specific amount of ethylenediaminetetraacetic acid disodium salt that provided Ba₅(PO₄)₃Cl nanoparticles self-assembled to construct uniform Ba₅(PO₄)₃Cl nanoassemblies (diameter: 80–120 nm) as well as rare earth Tb³⁺-doped Ba₅(PO₄)₃Cl:xTb³⁺ nanophosphors. The nanoassemblies were transparent within the ultraviolet and visible spectral range. The Ba₅(PO₄)₃Cl:xTb³⁺ nanophosphors exhibited four emission peaks under 228-nm excitation, and the optimal doping amount of Tb³⁺ was 4.0%. In contrast to traditional energy-consuming, high-temperature techniques, the facile room-temperature coprecipitation method developed here represents an attractive alternative route to obtain uniform Ba₅(PO₄)₃Cl nanoassemblies and Ba₅(PO₄)₃Cl:xTb³⁺ nanophosphors that are candidate luminescent hosts.     

Two new aromadendrane sesquiterpenes from Verticillium psalliotae

The chemical constituents of the fungus Verticillium psalliotae were studied. Two new aromadendrane sesquiterpenes inonotin M (1) and inonotin N (2) were isolated from the EtOAc extract of the fungal culture broth. The structures of compounds were elucidated mainly by HRESIMS experiments, and 1D, 2D-NMR spectroscopy analysis.     

Improvement in thermodynamic characteristics of sodium acetate trihydrate composite phase change material with expanded graphite

In this study, three different volume expansion ratios of expanded graphite (EG) are prepared and investigated to enhance the heat transfer efficiency of the sodium acetate trihydrate (SAT) composites. A series of SAT composite phase change materials (CPCMs) with EG were prepared. The influence of volume expansion ratio and mass fraction of EG on thermodynamic characteristics of SAT CPCMs was examined, including thermal conductivity, phase change temperature, enthalpy, latent heat storage and release time, and the degree of supercooling. Results showed that SAT CPCMs can be absorbed adequately by EG, and EG could enhance the heat transfer efficiency effectively. But it also brought some problems with the addition of all the three volume expansion ratios of EG, such as the poor enthalpy and serious supercooling. Particularly, the situation gets worse with the increase in mass and expansion ratio of EG. Therefore, it is better to choose the EG with proper expansion ratio or reduce the proportion of the EG which possesses higher expansion ratio. Besides, thermal cycling test and thermogravimetric analysis revealed that the SAT CPCMs with 3 mass% EG showed a good thermal stability.

     

Solubilization of C60 using ultrasound and amphiphilic block copolymers in acidic aqueous solutions

Fullerene (C₆₀), the third carbon allotrope, has shown great potential in photoelectric materials and drug delivery. However, the low solubility of C₆₀ in polar solvents, especially in water, is the major limiting factor for further applications. The use of ultrasound and amphiphilic block copolymers, poly(ethylene glycol)-block-poly(4-vinylpyridine) (PEG-b-P4VP), helped to disperse C₆₀ in acidic aqueous solutions. As characterized by dynamic light scattering, transmission electron microscopy, and UV-visible spectroscopy, the C₆₀ colloids had a core-shell structure with C₆₀ aggregated in the micellar cores. The photosensitized generation of singlet oxygen using C₆₀-bound polymer micelle was confirmed by the iodide method. More importantly, C₆₀ and metalloporphyrin complexes could be synthesized by the self-assembly between PEG-b-P4VP/C₆₀ micelle and metalloporphyrin. The stability of metalloporphyrin increased in the presence of the PEG-b-P4VP/C₆₀ micelle. This study provides a method for the solubilization of C₆₀ with many potential applications in biomedicals and photovoltaics.