神经网络余／十转换的数学原理

本文提出了孙子定理的微分方程求解法，讨论了系数为求余算子的非线性微分方程的稳定平衡点和最佳解的误差。本文构造的非线性微分方程可以唯一地收敛于孙子定理的解，其误差可任意小。该微分方程可用人工神经网络实时计算，实现余／十转换。计算机模拟结果证实了本文理论的正确性。     

压电复合材料PT－P（VDF／TeFE）的静水压压电性

用热轧辊机制备了压电复合材料ＰＴ－Ｐ（ＶＤＦ／ＴｅＦＥ），并利用ＬＣＲ电桥和Ｂｅｒｌｉｎｃｏｕｒｔ电路分别测量了其介电常数和压电常数，实验结果表明它具有良好的静水压压电特性。最后讨论了该复合材料在水听器中的应用     

ECCP干法刻蚀条件下的TFT基板绝缘层过孔腐蚀的改善

过孔搭接失效一直是TFT-LCD行业中重点改善的不良之一。为了解决该不良,本文分析了不同刻蚀模式(ICP和ECCP)对过孔形貌的影响,利用四因子法研究ECCP模式刻蚀参数(压力、偏置/源极射频功率及O_2/SF_6气体比例)对刻蚀速率和均一性的影响,并得出ECCP过孔改善的最佳刻蚀参数。结果表明:ECCP模式下,氮化硅刻蚀过程中物理轰击对GI截面的下沿与Cu接触区域形成损伤后产生的缺陷,是诱发过孔腐蚀的主要因素,ICP模式无腐蚀。反应腔压力增大刻蚀速率增大,均一性下降;偏置射频功率增大,速率增大,均一性提高;源极射频功率增大,速率变化小,均一性下降;O_2/SF_6气体比例对速率影响小,O_2含量越高,均一性越高。为达到PR胶保护GI下沿截面的目的,反应压力增大到1.7Pa,偏置射频功率减小到30kW,源极功率增加到30kW,O_2/SF_6气体保持比例1∶1后,增加了氮化硅的刻蚀量,减小PR胶的内缩量,避免物理溅射表面损伤;同时刻蚀速率达到750nm/s,均一性达到10%,腐蚀发生率为10%～0,使ECCP刻蚀模式对过孔的腐蚀影响得到有效解决。     

激光偏振拉曼的CVD多晶石墨烯表征

石墨烯具有优异的物理化学性质,在MEMS器件、光电检测材料、柔性显示屏、新能源电池、复合材料等方面成为研究热点。目前大面积石墨烯制备主要依赖于化学气相沉积技术(chemical vapor deposition, CVD),但其生长的晶体质量直接影响到电化学特性和实际应用,因此需要一种快速而准确的表征方法。实验利用背向散射的偏振激光散射装置测量CVD生长的石墨烯拉曼光谱。通过分析实验获得的300 nm SiO2/Si基底上的单层、五层和十层左右的石墨烯角分辨偏振拉曼光谱,发现单层生长的石墨烯偏振特性与机械剥离单晶石墨烯一致;随着层数的增加,G峰偏振响应差异更加明显,表现出明显的椭圆特性;在不同石墨烯层数上的D峰也呈现出一定的偏振响应差异性。偏振拉曼测试结果表明目前CVD生长的缺陷和多晶特性与石墨烯层数呈现正相关特征。     

层状双金属氢氧化物及其复合材料加速电解水制氢的研究进展

随着经济社会的不断发展和能源的不断消耗,开发清洁能源已引起研究者们的广泛关注。层状双金属氢氧化物(LDH)具有典型的层状结构、制备难度低、组成易调节等优点,在电催化分解水方面表现出可与贵金属催化剂相媲美的性能。目前LDH催化剂仍然存在稳定性不足、活性位点辨别不明、电催化反应机理模糊不清等科学问题亟待解决。本文首先介绍了LDH材料的性质和制备方法,重点从元素和化合物对LDH材料结构和性能的调控、取代阳极OER以及海水氧化三个方面综述了LDH材料在电催化制氢方面的研究进展,阐述了LDH复合材料的形貌、界面作用及化合物之间的协同作用。最后对LDH材料更深层次的研究方向作出展望。     

Three Dimensionally Ordered Mesoporous Carbon as a Stable,High‐Performance Li–O2 Battery Cathode

Enabled by the reversible conversion between Li₂O₂ and O₂, Li–O₂ batteries promise theoretical gravimetric capacities significantly greater than Li‐ion batteries. The poor cycling performance, however, has greatly hindered the development of this technology. At the heart of the problem is the reactivity exhibited by the carbon cathode support under cell operation conditions. One strategy is to conceal the carbon surface from reactive intermediates. Herein, we show that long cyclability can be achieved on three dimensionally ordered mesoporous (3DOm) carbon by growing a thin layer of FeO_x using atomic layer deposition (ALD). 3DOm carbon distinguishes itself from other carbon materials with well‐defined pore structures, providing a unique material to gain insight into processes key to the operations of Li–O₂ batteries. When decorated with Pd nanoparticle catalysts, the new cathode exhibits a capacity greater than 6000 mAh g_carbon^?1 and cyclability of more than 68 cycles.     

Synthesis,Structure, and Energetic Properties of 1,5‐Diaminotetrazolium Sulfate Salts

1,5‐diaminotetrazolium chloride (DATC) and 1,5‐diaminotetrazolium sulfate (DATS) were synthesized in this work. The structures of DATS and DATC were characterized. The single crystal of DATS was first cultured, and its structure was analyzed. The thermal behavior of DATS was investigated. The activation energy and pro‐exponential factor were calculated, E_k = 120.86 KJ/mol, A_k = 10^12.96 s^?1. The density, heat of formation, detonation pressure, and detonation velocity of DATS were first calculated. The detonation pressure and detonation velocity of DATS are P = 11.877 GPa, D = 5.617 km s^?1, which are smaller than those of 1,5‐diaminotetrazolium nitrate (DATN) (P = 33.3GPa, D = 8.77 km s^?1).     

A Multi‐signal Fluorescent Probe with Multiple Binding Sites for Simultaneous Sensing of Cysteine,Homocysteine, and Glutathione

A novel fluorescent probe was developed by integrating chlorinated coumarin and benzothiazolylacetonitrile and exploited for simultaneous detection of cysteine (Cys), homocysteine (Hcy), and glutathione (GSH). Featuring four binding sites and different reaction mechanisms for different biothiols, this probe exhibited rapid fluorescence turn‐on for distinguishing Cys, Hcy, and GSH with 108‐, 128‐, 30‐fold fluorescence increases at 457, 559, 529 nm, respectively, across different excitation wavelengths. Furthermore, the probe was successfully applied to the fluorescence imaging of endogenous Cys and GSH and exogenous Cys, Hcy, and GSH in living cells.     

“Ghost peaks” of olmesartan medoxomil: Two solution degradation products of olmesartan medoxomil via oxidation mediated by metal ions

Two unknown solution degradants were found during the dissolution testing in 0.1-M HCl for olmesartan medoxomil (OLM) tablets. The structure of the degradants was identified and characterized by liquid chromatography–ultraviolet (LC–UV), liquid chromatography with tandem mass spectrometry (LC–MS/MS), and nuclear magnetic resonance (NMR) and demonstrated to be cyclization of tetrazole and benzene in the olmesartan (OL) and OLM structures. A series of studies including stress studies, simulation studies, and mechanism-based studies were performed to reveal the potential mechanisms that lead to the formation of the unknown degradants. The study results demonstrated that the degradation was catalyzed with radicals that originated from the metal ions leached from the inner surface of high-performance liquid chromatography (HPLC) glass vials with dissolved oxygen under acidic condition. Prerinsing the glass vials with acidic solution dissolved with EDTA can effectively avoid the generation of such oxidative impurities. The present work provides new insights into the understanding of degradation pathways of OLM, which might support the development of OLM tablets.     

担载材料对TiO2薄膜光催化活性的影响

TiO_2 nanocrystalline films were prepared on glass, ITO and p-Si substrates. Degradation of Rhodamine B was used to assess the photocatalytic activity of the films. It was found that photocatalytic activity of TiO2 films on ITO and p-Si are higher than that on glass, and the film grown on ITO is the best. In addition, crystalline phases and surface morphology of TiO_2films were also affected by different substrates. Surface Photovoltage Spectra was used to analyze surface states and energy levels of the films. Separation of photogenerate electrons and holes was promoted due to matching of the energy levels between TiO_2 films and ITO as well as p-Si. High photocatalytic activity was then obtained because more photogenerate electrons and holes took part in photocatalytic reaction on TiO_2 surfaces.