Impact of an ion-flux non-uniformity on the sputtering of a target with a surface relief in a glow discharge plasma

The distribution of the sputtering yield averaged over the ion energy and flux density of sputtered atoms in a glow discharge plasma on a surface with a small-amplitude periodic relief has been calculated. The average sputtering yield of the target has a minimum at tops of the relief due to the energy separation of ions within the near-electrode discharge layer, while the flux density of sputtered atoms in this case is maximized due to the higher density of the ion flux on these areas.     

多自由度Maxwell阻尼器减震结构(Ⅰ)——随机响应特性

对多自由度带支撑Maxwell粘滞阻尼器减震结构的随机响应特性进行了系统研究。建立了结构一般运动方程;将运动方程按原结构振型展开,将运动方程化为振型广义坐标的微分和积分混合地震响应方程组;基于多自由度随机平均法理论,获得了结构随机平均It方程组的解析式,推导出耗能结构各振型振子的振幅与相位瞬态联合概率密度函数、位移与速度瞬态联合概率密度函数、位移与速度瞬态响应方差的一般解析解;根据SRSS组合方法,给出了耗能结构随机地震响应方差的一般解析式,从而建立了此类耗能结构随机响应特性分析的完备解析解法。     

Molecular Design of Calixarene,Part 4, Synthesis of Novel Double‐Armed p‐(tert‐Butyl)calix[4]arene‐Derived Amides and Their Lead(II)(Pb2+)‐Selective‐Electrode Properties

A series of novel double‐armed p‐(tert‐butyl)calix[4]arenes, carrying benzoylamido, 4‐nitrobenzoylamido, isonicotinamido, α‐naphthamido, acetamido, propionamido, or butyramido groups (see 2 – 8 , resp.) were synthesized in 80 – 86% yield by the reaction of the lower‐rim 1,3‐bis(aminoethoxy)‐substituted calix[4]arenediol 1 with the corresponding acylating agents. Their structures were established by elemental analysis, mass, IR, UV, and ¹H‐NMR spectroscopy. Ion‐selective electrodes (ISEs) for Pb²⁺, carrying 2 – 8 in a PVC membrane as neutral ionophore, were prepared, and their selectivity coefficients for Pb²⁺ (K) were determined against other heavy‐metal ions, alkali and alkaline earth metal ions, and ammonium ions by means of the separate‐solution method. The results obtained indicated that the electrodes based on the calix[4]arene‐derived amides 2 – 8 as the neutral ionophores were all Pb²⁺ selective and exhibited almost theoretical Nernstian slopes, except for 3 and 4 . Typically, the Pb²⁺‐selective electrode based on 6 – 8 exhibited almost Nernstian slopes for Pb²⁺ over a relatively wide concentration range and had a fast response time as well as a long lifetime, although the silver ion interfered strongly. These ISEs based on 6 – 8 showed a relatively good Pb²⁺ selectivity against most of the interfering cations examined, except for Ag⁺. The effect of the side‐arm functions of calix[4]arene derivatives 2 – 8 on the Nernstian slopes and on the selectivity coefficients for Pb²⁺ obtained with the Pb²⁺ ISEs based on 2 – 8 is discussed.     

Toward Two‐Dimensional π‐Conjugated Covalent Organic Radical Frameworks

Reported is the synthesis, characterization, and material properties of the first π‐conjugated two‐dimensional covalent organic radical framework (CORF), PTM‐CORF , based on the stable polychlorotriphenylmethyl (PTM) radical. The covalent organic framework (COF) precursor ( PTM‐H‐COF ) was first synthesized by liquid/liquid interfacial acetylenic homocoupling of a triethynylpolychlorotriphenylmethane monomer, and showed crystalline features with a hexagonal diffraction pattern matching that of A‐B‐C stacking. Subsequent deprotonation and oxidation of the PTM units in PTM‐H‐COF gave PTM‐CORF . Magnetic measurements revealed that the neighboring PTM radicals in the PTM‐CORF are anti‐ferromagnetically coupled each other, with a moderate exchange interaction (J=?375 cm^?1). The PTM‐CORF has a small energy gap (ca. 0.88 eV) and a low‐lying LUMO energy level (?4.72 eV), and exhibits high electrocatalytic activity and durability toward the oxygen reduction reaction.     

S-shaped para-Quinodimethane-Embedded Double [6]Helicene and Its Charged Species Showing Open-Shell Diradical Character

Helicenes and extended helical π-conjugated compounds have been widely studied, but most of the systems contain only aromatic benzene or heterocyclic rings, showing local aromatic character. Herein, new S-shaped double [6]helicene 1 , which has two embedded para-quinodimethane (p-QDM) units, is reported. Due to the existence of a proaromatic quinoidal substructure, it has open-shell diradical character. Its model compound, C-shaped single [6]helicene 2 containing one p-QDM unit, was also synthesized and compared. Their ground-state structures and electronic properties were systematically studied by a combination of various experimental methods assisted by theoretical calculations. Compound 1 has a double-helical structure in the crystal, with the two terminal [6]helicene units bent in opposite directions (i.e., anti form). However, an anti/syn isomerization process with a moderate interconversion energy barrier was observed on the NMR timescale. Compound 1 shows amphoteric redox behavior. It also exhibits open-shell diradical character (y₀=12.1 %) and a small singlet–triplet gap. On the other hand, compound 2 has a typical closed-shell nature. The dication and dianion of 1 also show open-shell diradical character. The dianion of 2 and the tetraanion of 1 exhibit similar electronic structures to their respective isoelectronic structures, that is, [6]helicene and a double [6]helicene. This work provides some insights into the design and synthesis of stable helical π systems with open-shell diradical character and magnetic activity.     

Aerodynamic modeling using an end-to-end learning attitude dynamics network for flight control

Acta Mechanica Sinica - A novel identification method of aerodynamic models using a physics neural network, named the attitude dynamics network, which incorporates the attitude dynamics of an...     

Deposition Process Based on Organosilicon Precursors in Dielectric Barrier Discharges at Atmospheric Pressure—A Comparison

Dielectric barrier discharges (DBD) at atmospheric pressure are presented as a tool to create organosilicon deposits on technical planar aluminium substrates (up to 15 × 8 cm²) by admixing small amounts of hexamethyldisiloxane (HMDSO) and tetraethoxysilane (TEOS) to the carrier gas of the discharges. Using barrier materials of different specific capacities (2.6 × 10⁴ and 3.2 pF/cm²) in two electrode arrangements operated at less than 1 W, the influence of the filament properties on the deposition is studied. In comparison to these arrangements, a third electrode setup with a barrier of the specific capacity of 2.9 pF/cm² is operated at approximately 50 W to study the influence of the specific energy of the plasma (energy per molecule) on the deposition process. The plasma chemical process was studied qualitatively by Gas Chromatography, and properties of the plasma-treated substrates were examined by means of X-ray Photoelectron Spectroscopy (XPS), Fourier Transform Infrared (FTIR) spectroscopy, as well as visually.