Single molecule force spectroscopy on poly(vinyl alcohol) by atomic force microscopy

The elastic properties of poly(vinyl alcohol) (PVA) were investigated on the nanoscale using the new technique of single molecule force spectroscopy by atomic force microscopy (AFM). It was found that the elastic properties of PVA molecules scale linearly with their contour lengths. This finding corroborates that the deformation of individual PVA chains is measured. The force spectra of PVA show a kink at around 200 pN and cannot be fitted by an extended Langevin function. The deviation of the elastic behavior of PVA from a freely jointed chain model may indicate the presence of a suprastructure of PVA in NaCl solution.     

Post‐Treatment of CH3NH3PbI3/PbI2 Composite Films with Methylamine to Realize High‐Performance Photoconductor Devices

Organometallic halide perovskites have attracted great research interest as light‐active materials for use in optoelectronics. Here, we report a high‐performance photoconductor based on a methylammonium lead iodide (MAPbI₃) film that was prepared from a methylamine‐treated MAPbI₃/PbI₂ perovskite film. An ultrahigh responsivity of 3.6 A W^?1 and detectivity of 5.4×10¹² Jones were obtained for the film under 0.5 mW cm^?2 white‐light illumination. In addition, under 420 nm light irradiation, the film exhibited its highest responsivity and detectivity of 30 A W^?1 and 2.4×10¹⁴ Jones, respectively. The excellent photo‐response performance results from the improved electronic quality and suppressed nonradiative recombination channels of the treated perovskite thin film.     

A Ratiometric Fluorescent Probe for Hypochlorite Based on a Deoximation Reaction

The first ratiometric fluorescent probe for hypochlorite has been developed through regulation of the electron‐withdrawing ability of the electron acceptor in an intramolecular charge‐transfer (ICT) system by a deoximation reaction (see figure; EWG=electron‐withdrawing group).

     

Effects of film structure on electrochromic properties of the multilayer films containing polyoxometalates

Multilayer films of tungstophosphate anion (P₂W₁₈) and poly(allylamine hydrochloride) (PAH) were fabricated on quartz and ITO substrates by layer-by-layer self-assembly method. These films were characterized by UV–vis spectroscopy, cyclic voltammetry (CV), chronoamperometric (CA), chronocoulometry (CC) and atomic force microscopy (AFM). The effects of film structure on multilayer electrochromic properties were investigated. The electrochromic responses of the composite films were related to the surface coverage of anion and multilayer thickness. It was found that higher concentration of polycation and anion, or adding salt to the polycation solution used for multilayer film preparation led to thicker and denser film structure which improved optical contrast and coloration efficiency whereas prolonged response time.     

Hydrothermal synthesis and characterization of micro/nanostructured ZnSn(OH)6/ZnO composite architectures

Micro/nanostructured ZnSn(OH)₆/ZnO composite architectures were synthesized through a simple one‐step hydrothermal method. Phase structure and morphology of the products were characterized by using X‐ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscope (TEM). ZnSn(OH)₆ microcubes and ZnO nanorods with uniform size were interconnected to form the micro/nanostructured architectures. ZnO nanorods preferentially grow at edges and corners of the microcubes. Morphology of the products was susceptible to concentration of the reactants. With increasing reactant concentration, the ZnO nanorods grown on the surfaces of ZnSn(OH)₆ microcubes disappeared. Meanwhile, the smooth surfaces of the ZnSn(OH)₆ microcubes become coarsened and were etched to spherical outlines. Growth mechanism of the micro/nanostructured ZnSn(OH)₆/ZnO composite architectures was discussed and thermal decomposition properties of the micro/nanostructured ZnSn(OH)₆/ZnO composite architectures at high temperature were examined. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

带有限反馈下层的二层规划问题的部分合作模型

对下层最优反馈为离散有限多个的二层规划问题的部分合作模型进行探讨. 当下层的合作程度依赖于上层的决策变量时, 给出一个确定合作系数函数的一般方法, 进而得到一个新的部分合作模型. 在适当地假设下, 可保证所给的部分合作模型一定可以找到比悲观解要好的解, 并结合新的部分合作模型对原不适定问题进行分析, 得到了一些有益的结论. 最后以实际算例说明了所给部分合作模型的可行性.     

反射波对预混气体爆炸过程与管壁动态响应的影响

为研究管道内甲烷/空气混合气体火焰和压力波的传播规律,对内载压力波作用下管壁的动态响应进行实验。结果表明,末端闭口实验中,管道末端的反射激波会引起当地火焰亮度的增大,而前端反射激波则有可能导致火焰内部的分离从而出现熄灭与复燃现象。相对于末端开口工况,末端闭口实验时管道两端产生的往复反射激波对管壁具有叠加加载作用,导致管壁产生较大的环向应变。     

非线性呼吸行为对带横向裂纹Jeffcott转子稳定性的影响

在分析现有力学模型局限性的基础上,考虑转子在失稳转速附近复杂的涡动状态,构建了不依赖于重力占优假设的含横向裂纹的Jeffcott转子的通用运动方程和一种拟合的裂纹呼吸模型。根据Floquet稳定性理论,用打靶法分析了该裂纹转子模型运动的稳定性。结果表明,刚度相对变化量、系统阻尼、裂纹相位角等系统参数对模型的运动稳定性都有较大影响,特别是裂纹相位角对稳定性的影响很复杂;在临界转速附近,裂纹的非线性呼吸行为可以提高转子的稳定性,且改变了失稳发散的行为;在亚临界转速附近,裂纹的非线性呼吸行为会降低转子的稳定性,使周期运动发生结构失稳。     

Anion Solvation Reconfiguration Enables High-Voltage Carbonate Electrolytes for Stable Zn/Graphite Cells

Conventional carbonate solvents with low HOMO levels are theoretically compatible with the low-cost, high-voltage chemistry of Zn/graphite batteries. However, the nucleophilic attack of the anion on carbonates induces an oxidative breakdown at high potentials. Here, we restore the inherent anodic stability of carbonate electrolytes by designing a micro-heterogeneous anion solvation network. Based on the addition of a strongly electron-donating solvent, trimethyl phosphate (TMP), the oxidation-vulnerable anion-carbonate affinities are decoupled because of the preferential sequestration of anions into solvating TMP domains around the metal cations. The hybridized electrolytes elevate the electrochemical window of carbonate electrolytes by 0.45 V and enable the operation of Zn/graphite dual-ion cells at 2.80 V with a long cycle life (92 % capacity retention after 1000 cycles). By inheriting the non-flammability from TMP and the high ion-transport kinetics from the carbonate systems, this facile strategy provides cells with the additional benefits of fire retardancy and high-power capability.     

Influence of impurity hydrogen on the structure and properties of bulk Li and pressure effects

The structure and properties of a 16-atom body-centered cubic lithium cell with an interstitial hydrogen atom are studied using a pseudopotential-plane-wave method within the density functional theory at 0 K and high pressures. The host lattice is dramatically distorted by the introduction of H. Although the hydrogen atom is stable at the tetragonal site in perfect bcc host lattice, it favors the octahedral site formed by six non-equivalent Li atoms after full relaxation of the cell, showing P4/mmm symmetry within the pressures ranging from 0 to 6 GPa. The lattice ratio (a/c) changes irregularly with external pressure at about 3 GPa. The hydrogen band lies in the bottom of the valence band, separated by a gap from the metallic bands, illustrating the electronegativity of hydrogen. High reflectivity in the low frequency area induced by the impurity hydrogen is observed when only interband transitions are taken account of. A dip in reflectivity due to parallel band transitions is observed at ∼0.4 eV. Another dip at ∼4.3 eV appears when external pressure increases over 4 GPa.