arXiv subjects

Hong-fei Wang

Publications and source records attributed to Hong-fei Wang.

11 recordsLinked to original sources

arXiv2019

Beyond the Gouy-Chapman Model with Heterodyne-Detected Second Harmonic Generation

We report ionic strength-dependent phase shifts in second harmonic generation (SHG) signals from charged interfaces that verify a recent model in which dispersion between the fundamental and second harmonic beams modulates observed signal intensities. We show how phase information can be used to unambiguously separate the chi(2) and interfacial potential-dependent chi(3) terms that contribute to the total signal and provide a path to test primitive ion models and mean field theories for the electrical double layer with experiments to which theory must conform. Finally, we demonstrate the new method on supported lipid bilayers and comment on the ability of our new instrument to identify hyper-Rayleigh scattering contributions to common homodyne SHG measurements in reflection geometries.

physics.app-ph↗

arXiv2018

On Second-Order Vibrational Lineshapes of the Air/Water Interface

We explore by means of modeling how absorptive-dispersive mixing between the second- and third-order terms modify the imaginary chi(2)total responses from air/water interfaces under conditions of varying charge densities and ionic strength. To do so, we use published Im(chi(2)) and chi(3) spectra of the neat air/water interface that were obtained either from computations or experiments. We find that the chi(2)total spectral lineshapes corresponding to experimentally measured spectra contain significant contributions from both interfacial chi(2) and bulk chi(3) terms at interfacial charge densities equivalent to less than 0.005% of a monolayer of water molecules, especially in the 3100 wavenumber to 3300 wavenumber frequency region. Additionally, the role of short-range static dipole potentials is examined under conditions mimicking brine. Our results indicate that surface potentials, if indeed present at the air/water interface, manifest themselves spectroscopically in the tightly bonded H-bond network observable in the 3200 wavenumber frequency range.

cond-mat.other↗

arXiv2017

Second-Order Spectral Lineshapes from Charged Interfaces

Second-order nonlinear spectroscopy has proven to be a powerful tool in elucidating key chemical and structural characteristics at a variety of interfaces. However, the presence of interfacial potentials may lead to complications regarding the interpretation of second harmonic and vibrational sum frequency generation responses from charged interfaces due to mixing of absorptive and dispersive contributions. Here, we examine by means of mathematical modeling how this interaction influences second-order spectral lineshapes. We discuss our findings in the context of reported nonlinear optical spectra obtained from charged water/air and solid/liquid interfaces and demonstrate the importance of accounting for the interfacial potential-dependent \c{hi}(3) term in interpreting lineshapes when seeking molecular information from charged interfaces using second-order spectroscopy.

cond-mat.mtrl-sci↗

arXiv2016

Phase-referenced Nonlinear Spectroscopy of the alpha-Quartz/Water Interface

Probing the polarization of water molecules at charged interfaces by second harmonic generation spectroscopy has been heretofore limited to isotropic materials. Here, we report non-resonant nonlinear optical measurements at the interface of anisotropic z-cut α-quartz and water under conditions of dynamically changing ionic strength and bulk solution pH. We find that the product of the third-order susceptibility and the interfacial potential, \c{hi}(3). Φ(0), is given by ( \c{hi}(3)-i\c{hi}(3)). Φ(0), and that the interference between this product and the second-order susceptibility of bulk quartz depends on the rotation angle of α-quartz around the z-axis. Our experiments show that this newly identified term, i\c{hi}(3). Φ(0), which is out of phase from the surface terms, is of bulk origin. The possibility of internally phase referencing the interfacial response for the interfacial orientation analysis of species or materials in contact with α-quartz is discussed along with the implications for conditions of resonance enhancement.

cond-mat.other↗

arXiv2008

Specific Na+ and K+ Cation Effects on the Interfacial Water Molecules at the Air/Aqueous Salt Solution Interfaces Probed with Non-resonant Second Harmonic Generation (SHG)

Here we report the polarization dependent non-resonant second harmonic generation (SHG) measurement of the interfacial water molecules at the aqueous solution of the following salts: NaF, NaCl, NaBr, KF, KCl, and KBr. Through quantitative polarization analysis of the SHG data,the orientational parameter D value and the relative surface density of the interfacial water molecules at these aqueous solution surfaces were determined. From these results we found that addition of each of the six salts caused increase of the thickness of the interfacial water layer at the surfaces to a certain extent. Noticeably, both the cations and the anions contributed to the changes, and the abilities to increase the thickness of the interfacial water layer were in the following order: KBr > NaBr > KCl > NaCl ~ NaF > KF. Since these changes can not be factorized into individual anion and cation contributions, there are possible ion pairing or association effects, especially for the NaF case. We also found that the orientational parameter D values of the interfacial water molecules changed to opposite directions for the aqueous solutions of the three sodium salts versus the aqueous solutions of the three potassium salts. These findings clearly indicated unexpected specific Na+ and K+ cation effects at the aqueous solution surface. These effects were not anticipated from the recent molecular dynamics (MD) simulation results, which concluded that the Na+ and K+ cations can be treated as small non-polarizable hard ions and they are repelled from the aqueous interfaces. These results suggest that the electrolyte aqueous solution surfaces are more complex than the currently prevalent theoretical and experimental understandings.

physics.chem-ph↗

arXiv2007

Treatment of Linear and Nonlinear Dielectric Property of Molecular Monolayer and Submonolayer with Microscopic Dipole Lattice Model: I. Second Harmonic Generation and Sum-Frequency Generation

In the currently accepted models of the nonlinear optics, the nonlinear radiation was treated as the result of an infinitesimally thin polarization sheet layer, and a three layer model was generally employed. The direct consequence of this approach is that an apriori dielectric constant, which still does not have a clear definition, has to be assigned to this polarization layer. Because the Second Harmonic Generation (SHG) and the Sum-Frequency Generation vibrational Spectroscopy (SFG-VS) have been proven as the sensitive probes for interfaces with the submonolayer coverage, the treatment based on the more realistic discrete induced dipole model needs to be developed. Here we show that following the molecular optics theory approach the SHG, as well as the SFG-VS, radiation from the monolayer or submonolayer at an interface can be rigorously treated as the radiation from an induced dipole lattice at the interface. In this approach, the introduction of the polarization sheet is no longer necessary. Therefore, the ambiguity of the unaccounted dielectric constant of the polarization layer is no longer an issue. Moreover, the anisotropic two dimensional microscopic local field factors can be explicitly expressed with the linear polarizability tensors of the interfacial molecules. Based on the planewise dipole sum rule in the molecular monolayer, crucial experimental tests of this microscopic treatment with SHG and SFG-VS are discussed. Many puzzles in the literature of surface SHG and SFG spectroscopy studies can also be understood or resolved in this framework. This new treatment may provide a solid basis for the quantitative analysis in the surface SHG and SFG studies.

physics.chem-ph↗

arXiv2007

A New Type of Two-photon Forward Radiation in Pure Liquids

Unexpected spectral features are observed in the two photon spectrum of the pure water in the forward direction when an 80 femtosecond laser pulse is focused at 10^10Wcm-2 or less. Such intensity is much lower than the breakdown or stimulated threshold of the liquid water. The two broad features are about 2700cm-1 and 5000cm-1 red shifted from the hyper-Rayleigh wavelength, respectively, and they are quadratic with the laser intensity. They do not match the known Raman or hyper-Raman frequencies of water, and they are both centered at a narrow angle in the forward direction. Several other liquids also exhibited similar but molecular specific spectral features.

physics.chem-ph↗

arXiv2006

An Empirical Approach to the Bond Additivity Model in Quantitative Interpretation of Sum Frequency Generation Vibrational Spectra

A complete empirical approach from known Raman and IR spectra is used to make corrections to the bond additivity model for quantitative interpretation of Sum Frequency generation Vibrational Spectra (SFG-VS) from molecular interfaces. This empirical correction successfully addresses the failures of the simple bond additivity model. This empirical approach not only provides new understandings of the effectiveness and limitations of the bond additivity model, but also provides a practical roadmap for its application in SFG-VS studies of molecular interfaces.

physics.chem-ph↗

arXiv2005

Reconsideration of Second Harmonic Generation from neat Air/Water Interface: Broken of Kleinman Symmetry from Dipolar Contribution

It has been generally accepted that there are significant quadrupolar and bulk contributions to the second harmonic generation (SHG) reflected from the neat air/water interface, as well as common liquid interfaces. Because there has been no general methodology to determine the quadrupolar and bulk contributions to the SHG signal from a liquid interface, this conclusion was reached based on the following two experimental phenomena. Namely, the broken of the macroscopic Kleinman symmetry, and the significant temperature dependence of the SHG signal from the neat air/water interface. However, because sum frequency generation vibrational spectroscopy (SFG-VS) measurement of the neat air/water interface observed no apparent temperature dependence, the temperature dependence in the SHG measurement has been reexamined and proven to be an experimental artifact. Here we present a complete microscopic analysis of the susceptibility tensors of the air/water interface, and show that dipolar contribution alone can be used to address the issue of broken of the macroscopic Kleinman symmetry at the neat air/water interface. Using this analysis, the orientation of the water molecules at the interface can be obtained, and it is consistent with the measurement from SFG-VS. Therefore, the key rationales to conclude significantly quadrupolar and bulk contributions to the SHG signal of the neat air/water interface can no longer be considered as valid as before. This new understanding of the air/water interface can shed light on our understanding of the nonlinear optical responses from other molecular interfaces as well.

cond-mat.other↗

arXiv2005

Polarization and Experimental Configuration Analysis of Sum Frequency Generation Vibrational Spectra of Air/Water Interface

Here we report a detailed study on spectroscopy, structure and dynamics of water molecules at air/water interface, investigated with Sum Frequency Generation Vibrational Spectroscopy (SFG-VS). Quantitative polarization and experimental configuration analysis of the SFG data in different polarizations with four sets of experimental configurations can shed new lights on our present understanding of the air/water interface. Firstly, we concluded that the motion of the interfacial water molecules can only be in a limited angular range, instead rapidly varying over a broad angular range in the vibrational relaxation time suggested previously. Secondly, because different vibrational modes of different molecular species at the interface has different symmetry properties, polarization and symmetry analysis of the SFG-VS spectral features can help assignment of the SFG-VS spectra peaks to different interfacial species. These analysis concluded that the narrow 3693cm-1 and broad 3550cm-1 peaks belong to C_ v symmetry, while the broad 3250cm-1 and 3450cm-1 peaks belong to the symmetric stretching modes with C_2v symmetry. Thus, the 3693cm-1 peak is assigned to the free OH, the 3550cm-1 peak is assigned to the single hydrogen bonded OH stretching mode, and the 3250cm-1 and 3450cm-1 peaks are assigned to interfacial water molecules as two hydrogen donors for hydrogen bonding (with C_2v symmetry), respectively. Thirdly, analysis of the SFG-VS spectra concluded that the singly hydrogen bonded water molecules at the air/water interface have their dipole vector direct almost parallel to the interface, and is with a very narrow orientational distribution. The doubly hydrogen bond donor water molecules have their dipole vector point away from the liquid phase.

cond-mat.other↗

arXiv2005

Orientation and Motion of Water Molecules at Air/Water Interface

Analysis of SFG vibrational spectra of OH stretching bands in four experimental configurations shows that orientational motion of water molecule at air/water interface is libratory within a limited angular range. This picture is significantly different from the previous conclusion that the interfacial water molecule orientation varies over a broad range within the vibrational relaxation time, the only direct experimental evidence for ultrafast and broad orientational motion of a liquid interface by Wei et al. [Phys. Rev. Lett. 86, 4799, (2001)] using single SFG experimental configuration.

cond-mat.other↗