RESUMEN
Sum frequency generation (SFG) spectroscopy is an interface-selective spectroscopic technique that enables us to selectively observe the vibrational or electronic resonances of molecules within a very thin interface layer. The interfacial properties probed by SFG are contained in a complex quantity called the second-order nonlinear susceptibility (χ2). It is usually believed that the imaginary part of χ2 (Im χ2) exhibits the resonant responses of the system, whereas the nonresonant responses appear solely in the real part of χ2 (Re χ2). However, it was recently theoretically pointed out that a portion of the nonresonant responses actually contributes to the observed Im χ2 spectra when the finite thickness of the interface layer is taken into account. In this study, by considering a simple air/liquid interface without any solutes as a model system, we theoretically evaluate the nonresonant contribution to experimentally accessible Im χ2 as well as to Re χ2, from which the complex phase of the nonresonant background is estimated. It is shown that the deviation of the complex phase from 0° or 180° is less than 1° even if the thickness of the interface layer is taken into account. This means that the nonresonant contribution to Im χ2 is practically negligible, and it is a very good approximation to think that the nonresonant background appears solely in Re χ2 in the case of air/liquid interfaces. This result implies that Im χ2 practically contains only the resonant responses of the system, and molecular resonances at the interface can be conveniently studied using Im χ2 spectra at such interfaces.
RESUMEN
Scanning probe microscopes scan and manipulate a sharp tip in the immediate vicinity of a sample surface. The limited bandwidth of the feedback mechanism used for stabilizing the separation between the tip and the sample makes the fragile nanoscopic tip very susceptible to mechanical instabilities. We propose, demonstrate, and characterize an alternative device based on bulging a thin substrate against a second substrate and rolling them with respect to each other. We showcase the power of this method by placing gold nanoparticles and semiconductor quantum dots on the two opposite substrates and positioning them with nanometer precision to enhance the fluorescence intensity and emission rate. Furthermore, we exhibit the passive mechanical stability of the system over more than 1 h. Our design concept finds applications in a variety of other scientific and technological contexts, where nanoscopic features have to be positioned and kept near contact with each other.
RESUMEN
Absorption spectroscopy is one of the most widely used spectroscopic methods. The signal-to-noise ratio in conventional absorption spectroscopy is ultimately limited by the shot noise, which arises from the statistical property of the light used for the measurement. Here we show that the noise in absorption spectra can be suppressed below the shot-noise limit when entangled photon pairs are used for the light source. By combining broadband entangled photon pairs and multichannel detection, we realize the acquisition of sub-shot-noise absorption spectra in the entire visible wavelength. Furthermore, we demonstrate the strength of sub-shot-noise absorption spectroscopy for the identification and quantification of chemical species, which are two primary aims of absorption spectroscopy. For highly diluted binary mixture solutions, sub-shot-noise absorption spectroscopy enables us to determine the concentration of each chemical species with precision beyond the limit of conventional absorption spectroscopy. That is, sub-shot-noise absorption spectroscopy achieves superresolution in concentration measurements.
RESUMEN
Organic compounds present a powerful platform for nanotechnological applications. In particular, molecules suitable for optical functionalities such as single photon generation and energy transfer have great promise for complex nanophotonic circuitry due to their large variety of spectral properties, efficient absorption and emission, and ease of synthesis. Optimal integration, however, calls for control over position and orientation of individual molecules. While various methods have been explored for reaching this regime in the past, none satisfies requirements necessary for practical applications. Here, we present direct non-contact electrohydrodynamic nanoprinting of a countable number of photostable and oriented molecules in a nanocrystal host with subwavelength positioning accuracy. We demonstrate the power of our approach by writing arbitrary patterns and controlled coupling of single molecules to the near field of optical nanostructures. Placement precision, high yield and fabrication facility of our method open many doors for the realization of novel nanophotonic devices.
RESUMEN
Multiexcitonic transitions and emission of several photons per excitation comprise a very attractive feature of semiconductor quantum dots for optoelectronics applications. However, these higher-order radiative processes are usually quenched in colloidal quantum dots by Auger and other nonradiative decay channels. To increase the multiexcitonic quantum efficiency, several groups have explored plasmonic enhancement, so far with moderate results. By controlled positioning of individual quantum dots in the near field of gold nanocone antennas, we enhance the radiative decay rates of monoexcitons and biexcitons by 109 and 100 folds at quantum efficiencies of 60 and 70%, respectively, in very good agreement with the outcome of numerical calculations. We discuss the implications of our work for future fundamental and applied research in nano-optics.
RESUMEN
Hydrated electrons are the most fundamental anion species, consisting only of electrons and surrounding water molecules. Although hydrated electrons have been extensively studied in the bulk aqueous solutions, even their existence is still controversial at the water surface. Here, we report the observation and characterization of hydrated electrons at the air/water interface using new time-resolved interface-selective nonlinear vibrational spectroscopy. With the generation of electrons at the air/water interface by ultraviolet photoirradiation, we observed the appearance of a strong transient band in the OH stretch region by heterodyne-detected vibrational sum-frequency generation. Through the comparison with the time-resolved spectra at the air/indole solution interface, the transient band was assigned to the vibration of water molecules that solvate electrons at the interface. The analysis of the frequency and decay of the observed transient band indicated that the electrons are only partially hydrated at the water surface, and that they escape into the bulk within 100 ps.
RESUMEN
We report a new phenomenon that may possibly enable the selective detection of solvent/surface interactions on a buried TiO(2) surface. A mechanism based on intermolecular Fano resonance involving a solvent vibrational mode and a TiO(2) phonon mode is proposed, which suggests that the strong electronic character of the TiO(2) phonon mode plays an important role. The solvent vibrational mode that takes part in Fano resonance can be significantly enhanced with the help of the intense resonance hyper-Raman band of a TiO(2) phonon mode, and this allows us to selectively detect the solvent/surface interactions even from a buried surface.
RESUMEN
The interface selectivity of vibrational sum frequency generation (VSFG) spectroscopy is explained under the dipole approximation as resulting from the breakdown of inversion symmetry at the interface. From this viewpoint, VSFG is not expected to occur at the interface consisting of centrosymmetric molecules, because the inversion symmetry is preserved even at the interface. In reality, however, VSFG at the nonpolar benzene/air interface has been observed with traditional homodyne-detected VSFG. Here we report a heterodyne-detected VSFG study of the benzene/air interface. The result strongly indicates that VSFG at this interface cannot be explained within the framework of the dipole approximation. The selection rule and polarization dependence of the observed VSFG signal show that the quadrupole transition plays an essential role because of the field discontinuity at the interface. This finding implies the applicability of interface-selective VSFG to the nonpolar interfaces comprising centrosymmetric molecules, which opens a new possibility of VSFG spectroscopy.
RESUMEN
We have developed a superresolution vibrational imaging method by simultaneous detection of Raman and hyper-Raman scattering. Raman and hyper-Raman images obtained with the same laser spot carry independent information on the sample spatial distribution, owing to different signal dependence (linear in Raman and quadratic in hyper-Raman) on the incident light intensity. This information can be quantitatively analyzed to recover the incident light intensity distribution at the focal plane. A superresolution vibrational image is then derived by the constrained deconvolution of the images by the obtained incident light intensity distribution. This method has been applied to a TiO2 nanostructure and the obtained superresolution image was compared with a scanning electron microscopy image. The spatial resolution achieved by the present method is evaluated to be 160 nm, which is more than twice better than the diffraction limited resolution.