可伸缩复合材料悬臂梁的非线性动力学建模及分析

首先,根据Reddy给出的考虑高阶剪切效应的层合理论,气动弹性活塞理论,利用Hamilton原理,对考虑采用基于活塞理论的一阶非线性气动力和面内参数激励的联合作用下的轴向可伸缩复合材料悬臂梁进行非线性动力学进行建模,得到其偏微分动力学控制方程.然后对控制方程无量纲化,利用Galerkin方法对控制方程进行了截断,得到三个可反映可伸缩悬臂梁横向振动的无量纲形式的常微分非线性动力学方程,只要选取适合的复合材料及其相关参数,使用数值方法就对模型在外伸和回收过程中的相关振动特性进行了分析.     

改进的模块2DPCA人脸识别算法

提出一种改进的模块2DPCA人脸识别算法,即基于子距离的模块2DPCA人脸识别算法。该算法对图像进行分块,对每一子块独立地利用2DPCA进行处理,求出测试样本子块与训练样本对应子块间的子距离,将所有子距离相加得到测试样本与训练样本的距离,用最近距离分类器分类。在ORL人脸库上的实验结果表明,该算法在识别性能上优于普通的模块2DPCA算法和修正的模块2DPCA算法。     

Spin-polarized transport properties of Fe-oligoporphyrin dimer-based molecular device

By applying the density functional theory and the nonequilibrium Green’s function formalism, we investigate the spin-polarized transport properties of a Fe-oligoporphyrin dimer (Fe-P2TA) sandwiched between two armchair single-walled carbon nanotube electrodes. The results show that the system can present high-efficiency magnetoresistance, spin-filtering, and low-bias negative differential resistance effects with the help of magnetic field modulation. The above results are explained by the evolution of the spin-polarized transmission spectra and the molecular projected self-consistent Hamiltonian eigenstates with applied bias. Therefore, the system provides the possibilities for a multifunctional molecular spintronic device design.     

Reduced water vapor transmission rates of low-temperature-processed and sol-gel-derived titanium oxide thin films on flexible substrates

Sol-gel-derived, crack-free, and condensed TiO_x thin films with improved barrier properties were successfully fabricated on polymeric substrates with a simple two-step heat treatment at low temperatures. To assess the barrier properties of the TiO_x thin films, Ca corrosion tests were conducted and their water vapor transmission rates (WVTRs) were measured. We found that the two-step heat treatment (at 45 °C for 90 min and 110 °C for 60 min) produces a close-packed TiO_x structure that substantially reduces the WVTRs of the coated polymeric substrates. The WVTRs of 86 nm thick TiOx thin films on polyethylene naphthalate (PEN) substrates at a relative humidity (RH) of 90% were found to be 0.133 g m⁻² day⁻¹ at 38 °C and 0.0387 g m⁻² day⁻¹ at 25 °C. In addition, the WVTR value of the TiO_x thin films on PEN substrates are stable with respect to bending: it was found to increase by only ∼13% after 100 repetitions of bending with a 20 mm radius.     

Band alignment in organic light emitting diodes - On the track of thickness dependent onset voltage shifts

In this paper we report on an unclear effect in the IV characteristics of organic light emitting diodes (OLEDs). When the thickness of the emitter layer based on a modified phenyl carbozole triplet host material (TH) in the device is increased, a significant shift of the onset voltage to higher values can be noticed. The voltage shift is not observed if the TH is substituted by an isomer with only minor variation of the molecular structure. In a previous publication we could already show that an electric interface field is necessary to describe the onset voltage behaviour. To find the origin of this interface field in the present publication the two isomers are characterized and the band alignment at the interfaces to the emitter layer is investigated using photoelectron spectroscopy. The interface energy diagrams have been measured on stepwise prepared model interfaces. A further simplification of the bipolar to a hole only device stack proofs, that band bending at the hole injecting interface to the TH layer is the origin of the interface field. In contrast an entire flat band situation is measured in case of the device using the other isomer showing no onset voltage shift.     

Molecular packing correlated fluorescence in TIPS-pentacene films

The molecular packing and optical properties of exposed and buried layers (i.e. the layers at the top surface and near the substrate, respectively) were systematically studied in 6,13-Bis(triisopropylsilylethynyl)pentacene (TIPS-pentacene) films coated by spin-coated (SC) and droplet-pinned-crystallization (DPC) methods. Buried layers in both films exhibit intense photoluminescence (PL) resembling the behaviors of the molecules in dilute solution ascribing to weak π-π stacking, while the exposed layers show extremely weak PL due to strong crystallinity. Polarized excitation PL spectra demonstrate that molecular orientation of the buried layers is quasi-ordered in the film coated by DPC method and completely disordered in the film coated by SC method. Besides, the strong crystallinity of the exposed TIPS-pentacene is verified by grazing incident wide-angle X-ray scattering measurement. The distinct differences in optical and structural properties between the exposed and buried layers indicate that TIPS-pentacene films are inhomogeneous in vertical direction due to interfacial effect, which affects the performance of photodiode fabricated with both films. The understanding of the molecular packing correlated fluorescence in TIPS-pentacene films is vital for optimizing the film structure to achieve high performance organic electronic devices.     

Enhanced power factor of poly (3,4-ethyldioxythiophene):poly (styrene sulfonate) (PEDOT:PSS)/RTCVD graphene hybrid films

The thermoelectric generator has been an attractive alternative power source to operate a wireless sensor node. Usually, inorganic compounds are most often used in thermoelectric devices, and hence, are extensively studied due to their superior thermoelectric performance. We have investigated a novel interfacial technique to fabricate a hybrid film of highly conductive PEDOT:PSS (poly 3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) and graphene. Organic materials PEDOT doped with PSS exhibits outstanding electrical properties due to its high conductivity, low bandgap, and energy migration. Furthermore, we utilized graphene fabricated by rapid thermal chemical vapor deposition (RTCVD) as a thermoelectric material. Our results show that the interfacial technique between substrate and hybrid film could be clearly improved due to the UV plasma treatment. The thermoelectric hybrid film of PEDOT:PSS and RTCVD graphene (P/RTG) exhibited an enhanced power factor of 56.28 μW m⁻¹ K⁻² with a Seebeck coefficient of 54.0 μV K⁻¹.     

粉末渗锌钢渗层的形成机理及影响因素研究进展

粉末渗锌工艺是一种热扩散表面改性技术,将渗锌剂与钢构件在高温条件下接触,利用原子扩散作用,在构件表面形成一层合金保护层。作为一种工艺简单、环境友好的高效表面防腐处理工艺,粉末渗锌技术可有效改善金属材料的耐磨、耐蚀和耐氧化等性能,具有广泛的应用前景而备受研究者的关注。首先分析了粉末渗锌层的形成机理,并重点讨论了渗层的组织结构;然后,综述了保温温度、保温时间以及合金元素等因素对渗层形成的影响。研究者发现,升高温度和延长时间有益于渗层厚度的增加,但要合理控制,温度过高或时间过长不仅使渗层性能变差,还会增加能耗和降低生产率。此外,通过调整渗剂中合金元素的添加量以及种类,能够改善渗锌层的性能,但各类元素的最佳添加量以及其对渗层的改性机理还有待于进一步探究。目前,粉末渗锌生产中存在效率低的问题,在渗锌工艺中应用机械能助渗技术和纳米技术,可有效提高渗锌效率、改善渗层性能。最后,结合当前的研究现状,对粉末渗锌工艺的研究方向进行了探讨。     

The formation of supramolecular liquid-crystal gels for enhancing the electro-optical properties of twisted nematic liquid crystals

We report that the supramolecular liquid-crystal (LC) physical gel can be formed through the fibrous self-assembly of the polyfluorene-based π-conjugated polymer, poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT), in twisted nematic LC system for the first time. With the utility of alignment layers, the F8BT molecules can be aligned and formed the LC physical gels with the formation of self-assembled supramolecular structures in the twisted nematic LCs. In contrast to conventional LC physical gels, the presence of anisotropic π-conjugated structure makes the twisted nematic LC system exhibit excellent electro-optical properties of driving voltage reduction and contrast ratio enhancement owing to the conjugated polymer having a high π-electron delocalization degree which can efficiently drive LC molecules in much lower operating voltages. The self-assembled supramolecular network has revealed the potential for applying in various LC display devices with the ability of improving their electro-optical performance.     

Light-induced electron spin resonance study of galvinoxyl-doped P3HT/PCBM bulk heterojunctions

We report the effects of doping of P3HT/PCBM layers with spin 1/2 radicals of galvinoxyl (Gx) based on light-induced electron spin resonance (LESR), photoluminescence-detected magnetic resonance (PLDMR), and post-annealing experiments.LESR showed both a P3HT⁺ and PCBM⁻ signal for undoped P3HT/PCBM; however, as Gx doping increased (above ∼1 wt%), only the P3HT⁺ signal was evident in the LESR spectra, with no PCBM⁻ signal.The PLDMR exhibited a strong narrow signal at g = 2.002 that originates from nongeminate polaron pairs; no triplet PLDMR signal has been observed throughout the whole range of Gx concentrations (x = 0, 0.1, 1, 2, 4, 12 wt%). Adding Gx to ∼3 wt% led to a decrease of the PL-enhancement.There was big difference between the slow-dried P3HT/PCBM samples and the post-annealed samples. For the slow-dried samples, efficiency monotonously decreased with Gx additives. When post-annealed, however, an enhancement in η was observed at ∼2 wt% for P3HT/PCBM(1:2) samples.The LESR spectra for post-annealed samples revealed disappearance of Gx spin signals, and thus no spin interactions with PCBM⁻ spins. It is unlikely that the increase of efficiency after Gx doping of P3HT/PCBM solar cell is due to an increase of triplet states.