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A novel approach to nanoscale broadband viscoelastic spectroscopy is presented. The proposed approach utilizes the recently developed modeling-free inversion-based iterative control (MIIC) technique to achieve accurate measurement of the material response to the applied excitation force over a broad frequency band. Scanning probe microscope (SPM) and nanoindenter have become enabling tools to quantitatively measure the mechanical properties of a wide variety of materials at nanoscale. Current nanomechanical measurement, however, is limited by the slow measurement speed: the nanomechanical measurement is slow and narrow-banded and thus not capable of measuring rate-dependent phenomena of materials. As a result, large measurement (temporal) errors are generated when material is undergoing dynamic evolution during the measurement. The low-speed operation of SPM is due to the inability of current approaches to (1) rapidly excite the broadband nanomechanical behavior of materials, and (2) compensate for the convolution of the hardware adverse effects with the material response during high-speed measurements. These adverse effects include the hysteresis of the piezo actuator (used to position the probe relative to the sample); the vibrational dynamics of the piezo actuator and the cantilever along with the related mechanical mounting; and the dynamics uncertainties caused by the probe variation and the operation condition. In the proposed approach, an input force signal with frequency characteristics of band-limited white-noise is utilized to rapidly excite the nanomechanical response of materials over a broad frequency range. The MIIC technique is used to compensate for the hardware adverse effects, thereby allowing the precise application of such an excitation force and measurement of the material response (to the applied force). The proposed approach is illustrated by implementing it to measure the frequency-dependent plane-strain modulus of poly(dimethylsiloxane) (PDMS) over a broad frequency range extending over 3 orders of magnitude (~1 Hz to 4.5 kHz).  相似文献   
146.
Pyridinium 1,4-zwitterionic thiolates were applied to a formal [3 + 2] annulation reaction with modified activated alkynes, affording various tetrasubstituted thiophenes with aryl, alkenyl, alkyl or silyl group at the special position. The structural modification of alkyne substrates enabled the synthesis of diverse thiophenes to be achieved using the pyridinium 1,4-zwitterionic thiolates as the sulfur-containing building blocks. This approach is metal-free and catalyst-free.  相似文献   
147.
A study of the Nd-Fe-Ti phases at the Fe-rich end of the phase diagram has been carried out using57Fe Mössbauer spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDAX). In particular,57Fe Mössbauer spectroscopy has been used to characterize the phases present in these samples. In addition to the two well-known 217 and 112 phases, twonovel phases have been identified, with compositions denoted by3–29 and9–94, which are closely linked to the orthorhombic ScFe6Ga6-type and the hexagonal TbCu7-type structures, respectively. The possible crystal structures of these new phases will be discussed in terms of the dumbbell substitution sequence in the CaCu5 structure.  相似文献   
148.
Effects of electron-phonon interaction on the interaction between electrons in semiconductor quantum wells are considered. It is found that the direct Coulomb potential between electrons in a quantum well is smaller than that in bulk semicondutors. The antisymmetric modes of the confined bulk phonons and interface phonons have no contribution to the effective interaction of electrons. If a well is narrow enough, the effective interaction between electrons caused by interaction with interface phonons may exceed that by interaction with confined bulk phonons. In narrower wells the effective interaction potential of electrons produced by phonons is stronger, but decreases rapidly with increasing distance between electrons.  相似文献   
149.
某些含氮有机物光催化氧化产生的自由基中间体   总被引:3,自引:0,他引:3  
本文用自旋捕捉技术与ESR相结合的方法研究了某些含氮有机物TiO2光催化降解的过程中形成的活泼中间体.选择的化合物中有丁胺、戊胺、庚胺、六氢吡啶、吡啶、2-甲基吡啶、2,6-二甲基吡啶,这些分子中的氮原子分别作为初级脂肪胺、饱和环中的二级胺以及芳环中的三级胺出现,实验中观察到N-中心自由基及C-中心自由基与自旋捕捉剂加合物的ESR信号,表明这些自由基参与这些化合物光降解的初始过程,对深入了解其光降机理是有意义的.  相似文献   
150.
高掺镁LiNbO3晶体折射率温度系数的表示式   总被引:2,自引:0,他引:2  
徐浩  沈鸿元 《光学学报》1994,14(4):93-397
推导了掺5mol%MgO的LiNbO3晶体折射率温度系数的表示式。利用这些表示式可以计算293~428K温度和0.5398μm~1.3414μm波长范围内的折射率温度系度,结果表明:计算值和实验值的最大相对偏差是12%,用具有最大相对偏差的折射率温度系数的计算值,计算1.0795μm波长的非临界相位匹配温度,其值为382.4K,它与实验值仅差6K。因此,本文得到的表示式,对于采用这种晶体,设计在上  相似文献   
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