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1.
It is well known that symmetry plays a key role in chemical reactivity. Here we explore its role in vibrational strong coupling (VSC) for a charge‐transfer (CT) complexation reaction. By studying the trimethylated‐benzene–I2 CT complex, we find that VSC induces large changes in the equilibrium constant KDA of the CT complex, reflecting modifications in the ΔG° value of the reaction. Furthermore, by tuning the microfluidic cavity modes to the different IR vibrations of the trimethylated benzene, ΔG° either increases or decreases depending only on the symmetry of the normal mode that is coupled. This result reveals the critical role of symmetry in VSC and, in turn, provides an explanation for why the magnitude of chemical changes induced by VSC are much greater than the Rabi splitting, that is, the energy perturbation caused by VSC. These findings further confirm that VSC is powerful and versatile tool for the molecular sciences.  相似文献   
2.
We report the experimental proof of molecular count rate enhancement (up to 6.5-fold) and lifetime reduction for single fluorescent molecules diffusing in subwavelength apertures milled in aluminum films. The observed enhancement dependence with the aperture diameter agrees qualitatively with numerical electromagnetic computations of the excitation power density into the aperture volume.  相似文献   
3.
We present results of the transmitted, reflected, and absorbed power associated with the enhanced transmittance of light through a silver film pierced by a periodic array of subwavelength holes. Comparing experimentally acquired dispersion curves under different polarization conditions shows that the transmission features of the array are consistent with p-polarized resonant modes of the structure. By exploring the regime in which no propagating diffracted orders are allowed, we further show that the transmittance maxima are associated with both reflectance minima and absorption maxima. These new results provide strong experimental evidence for transmission based on diffraction, assisted by the enhanced fields associated with surface plasmon polaritons.  相似文献   
4.
In this Letter, we explore transmission properties of a single subwavelength slit flanked by a finite array of grooves made on a thick metallic film. We identify three main mechanisms that can enhance optical transmission: groove cavity mode excitation (controlled by the depth of the grooves), in-phase groove reemission (controlled by the period of the groove array), and slit waveguide mode (controlled by the thickness of the metal film). By tuning these geometrical parameters, enhancements of transmission of light by up to 2 orders of magnitude can be achieved when all three mechanisms coincide. Experimental verification of these findings is also shown for structured silver films fabricated by focused-ion-beam milling.  相似文献   
5.
We present a theoretical foundation for the beaming of light displayed by a single subwavelength aperture in an appropriately corrugated metal film [H. J. Lezec, Science 297, 820 (2002)]]. Good agreement is found between calculations and experimental data. We show that beaming is due to the formation of electromagnetic surface resonances and that the beam direction, width, and wavelength at which it occurs can be selected by tuning geometrical parameters of the structure.  相似文献   
6.
IR spectroscopy has been an important tool for studying detailed interactions of reactants and reaction-intermediates with catalyst surfaces. Studying reactions in water is, however, far from trivial, due to the excessive absorption of infrared light by water. One way to deal with this is the use of Attenuated Total Reflection spectroscopy (ATR-IR) minimizing the path length of infrared light through the water. Moreover, ATR-IR allows for a direct comparison of reactions in gas and water on the same sample, which bridges the gap between separate catalyst investigations in gas and liquid phase. This tutorial review describes recent progress in using ATR-IR for studying heterogeneous catalysts in water. An overview is given of the important aspects to be taken into account when using ATR-IR to study heterogeneous catalysts in liquid phase, like the procedure to prepare stable catalyst layers on the internal reflection element. As a case study, CO adsorption and oxidation on noble metal catalysts is investigated with ATR-IR in gas and water. The results show a large effect of water and pH on the adsorption and oxidation of CO on Pt/Al(2)O(3) and Pd/Al(2)O(3). From the results it is concluded that water affects the metal particle potential as well as the adsorbed CO molecule directly, resulting in higher oxidation rates in water compared to gas phase. Moreover, also pH influences the metal particle potential with a clear effect on the observed oxidation rates. Finally, the future outlook illustrates that ATR-IR spectroscopy holds great promise in the field of liquid phase heterogeneous catalysis.  相似文献   
7.
We investigate the potential of a single subwavelength aperture milled in an aluminium film to enhance the local electromagnetic field. We compare the Raman scattering of unadsorbed chlorobenzene molecules and the fluorescence emission of Cyanine-5 dyes, having the same excitation and collection setup for both experiments. For the optimal nanoaperture diameter, we report a clear enhancement factor of about 5 of the Raman scattering intensity per unit volume. Since Raman scattering probes the molecular vibrational levels and avoids the resonant pumping of a real excited state, the observed Raman enhancement is disconnected from the effects of the molecular energy levels alteration previously reported for fluorescent dyes. The observations are similar for both Raman and fluorescence experiments, and stand in good agreement with numerical electromagnetic computations of the excitation intensity inside the nanoaperture.  相似文献   
8.
This study describes a versatile strategy combining reversible addition fragmentation transfer (RAFT) polymerization and click chemistry to synthesize well‐defined, reactive copolymers of N‐(2‐hydroxypropyl)methacrylamide (HPMA) for drug delivery applications. A novel azide containing monomer N‐(3‐azidopropyl)methacrylamide (AzMA) was synthesized and copolymerized with HPMA using RAFT polymerization to provide p(HPMA‐co‐AzMA) copolymers with high control of molecular weight (~10–54 kDa) and polydispersity (≤1.06). The utility of the side‐chain azide functionality by Cu(I)‐catalyzed azide‐alkyne cycloaddition (CuAAC) was demonstrated by efficient conjugation (up to 92%) of phosphocholine, a near infrared dye, and poly(ethylene glycol) (PEG) with different substitution degrees, either alone or in combination. This study introduces a novel and versatile method to synthesize well‐defined click‐reactive HPMA copolymers for preparing a panel of bioconjugates with different functionalities needed to systemically evaluate and tune the biological performance of polymer‐based drug delivery. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 5091–5099  相似文献   
9.
10.
The transmission spectrum of a metal that is perforated with a periodic array of subwavelength holes exhibits well-defined maxima and minima resulting from, respectively, a transmission enhancement by surface plasmons and Wood's anomaly, a diffraction effect. These features occur at wavelengths determined by the geometry of the hole arrays, the refractive index of the adjacent medium, and the angle of incidence. We demonstrate control of the transmission through variation of these parameters and show that perforated metal films may form a novel basis for electro-optic devices such as flat-panel displays, spatial light modulators, and tunable optical filters.  相似文献   
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