Multistep Micellization of Standard Surfactants Evidenced by Second Harmonic Scattering.

Processes involving in solution a reduced number of molecules are difficult to identify and characterize. Here, we show that micellization of standard surfactants, namely sodium dodecyl sulfate and trimethyl tetradecyl ammonium bromide, two nonefficient compounds for quadratic nonlinear optics, can be investigated by second harmonic scattering (SHS). In particular, the formation of aggregates at concentrations smaller than the critical micellar concentration is evidenced through a nonmonotonic behavior of the SHS intensity as a function of the surfactant concentration. A simple model based on chemical equilibria between monomers and micelles is proposed to account for the experimental observations. Signature of long-range molecular orientation correlation is revealed by polarization resolved experiments and is discussed regarding micellization and charge-induced effects.

Second harmonic generation from tryptophan-rich short peptides: W(n)K(m) and gramicidin A.

We report the first hyperpolarizability of a series of tryptophan-rich short peptides with the respective sequence KWK, KWWK, KWWWK, KWWKWWK, where W and K stand for tryptophan and lysine. The measurements were performed with the technique of hyper-Rayleigh scattering in the bulk of an aqueous Tris buffer solution at a pH of 8.5 and a salt concentration of 150 mM at the non-resonant fundamental wavelength of 784 nm. The first hyperpolarizability of the different peptides follows a simple additive model scaling with the number of tryptophan residues contained in the peptide. However, it appears that the first hyperpolarizability response of a single tryptophan residue in the peptide strongly differs from that of an isolated tryptophan. Hence, it is therefore demonstrated that the local environment of the tryptophan residues within the peptide strongly influences its nonlinear optical response. A comparison with the first hyperpolarizability of the natural peptide gramicidin A measured in trifluoroethanol (TFE) further confirms the key role of the local environment on the first hyperpolarizability of tryptophan residues in peptides.

Second harmonic generation monitoring of nitric acid extraction by a monoamide at the water-dodecane interface.

The interface dynamic properties of a monoamide extractant with potential for application to the front end of the nuclear cycle and to waste treatment are examined by second harmonic generation. The results are compared with bulk nitric ion titration and surface pressure measurements. SH static studies show the extractant reaching the interface and accurately match the IFT measurements. The main feature of the SH dynamic studies is a chaotic fluctuation period, strongly related to intense extraction. Fluctuations are a signature of the interface behaviour during the extraction process. Vertical development of the interface, often called protrusion, remains the most probable origin of the measured fluctuation. Additionally, interfacial measurements show a non-monotonic lag time during extraction, probably related to cooperative effects not observed in the bulk at the working concentration. Such mutual behaviour could be a supplementary prerequisite for the ion transfer across this liquid-liquid interface.

First hyperpolarizability of the natural aromatic amino acids tryptophan, tyrosine, and phenylalanine and the tripeptide lysine-tryptophan-lysine determined by hyper-Rayleigh scattering.

We report the first hyperpolarizability of tryptophan (Trp) and tyrosine (Tyr) and an upper limit for that of phenylalanine (Phe), three natural aromatic amino acids. The measurements were performed with hyper-Rayleigh scattering in an aqueous Tris buffer solution at a pH of 8.5 and 150 mM salt concentration with a fundamental wavelength of 780 nm. A value of (4.7 ± 0.7) × 10(-30) esu is found for Trp and (4.1 ± 0.7) × 10(-30) esu for Tyr whereas the upper limit of 1.4 × 10(-30) esu is found for that of Phe due to its limited solubility. The influence of the presence of lysine (Lys) in close vicinity of Trp is investigated with a measurement of the first hyperpolarizabilty of Trp in an excess of Lys and compared to the first hyperpolarizability obtained for the tripeptide Lys-Trp-Lys. The clear decrease of the values measured in these two cases indicates that the first hyperpolarizabilty of Trp is very sensitive to its local environment.

Interference between selected dipoles and octupoles in the optical second-harmonic generation from spherical gold nanoparticles.

Optical second-harmonic generation from gold nanoparticles is investigated both experimentally and theoretically. The contribution of octupoles is reported for the first time in the second-harmonic emission pattern, by using an harmonic polarization in the scattering plane. The experimental results presented here for particle sizes up to 100 nm are in excellent agreement with finite element method simulations involving the normal surface term only in the nonlinear polarization source. In addition, analytical calculations based on nonlinear Mie scattering theory clearly evidence the constructive and destructive interferences occurring between the dipolar and octupolar responses selected with this polarization configuration.

Fano profiles induced by near-field coupling in heterogeneous dimers of gold and silver nanoparticles.

The near-field coupling between a gold and a silver spherical nanoparticle is investigated theoretically. Fano profiles are observed in the absorption cross section of the gold nanoparticle due to the coupling between the spectrally localized surface plasmon resonance of the silver nanoparticle and the continuum of interband transitions of the gold one. The effect of dimer internal characteristics (particle sizes and distance), surrounding medium (through the refractive index), and external excitation (polarization and propagation directions) are addressed. In particular, it is shown that the near-field coupling can be tuned from the weak to the strong regime by rotating the polarization direction, and that the Fano profiles are sensitive to the shadowing effect even for small particle sizes.

Second harmonic generation from small gold metallic particles: from the dipolar to the quadrupolar response.

Hyper Raleigh scattering, a common technique to investigate the second harmonic light scattered from a liquid suspension of molecular compounds and to determine their quadratic hyperpolarizability, has been used for aqueous suspensions of gold nanoparticles, the diameter of which ranges from 20 up to 150 nm. The hyper Rayleigh signal intensity was recorded as a function of the angle of polarization of the incident fundamental wave. For the particles with a diameter smaller than 50 nm, the response is dominated by the dipolar contribution arising from the deviation of the particle shape from that of a perfect sphere. For larger diameter particles, retardation effects in the interaction of the electromagnetic fields with the particles cannot be neglected any longer and the response deviates from the pure dipolar response, exhibiting a strong quadrupolar contribution. It is then shown that in order to quantify the relative magnitude of these two dipolar and quadrupolar contributions, a weighting parameter zeta(V) which equals unity for a pure quadrupolar contribution and vanishes for a pure dipolar response, can be introduced.

Preparation of silver nanoparticles in solution from a silver salt by laser irradiation.

A new method is proposed for the fabrication of a well-defined size and shape distribution of silver nanoparticles in solution; the method employs direct laser irradiation of an aqueous solution containing a silver salt and a surfactant in the absence of reducing agents.

Second harmonic generation of glucose oxidase at the air/water interface.

We present a study of the adsorption of the glucose oxidase enzyme (GOx) at the air/water interface, using the nonlinear optical technique of surface second harmonic generation (SSHG). Resonant SSHG experiments were achieved by probing the pi-pi* transition of the flavin adenine dinucleotide (FAD) chromophores embedded in the GOx protein. Because of the subsequent resonance enhancement of the signal, the second harmonic (SH) wave arising from the GOx entities adsorbed at the interface was detectable for protein bulk aqueous concentrations as low as 70 nM. The protein adsorption was followed, and, at high GOx coverage, a change in the orientation of the FAD chromophore was observed, indicating either a rearrangement or a reorientation of the protein at the interface. Inasmuch as GOx is negatively charged at the biological pH of 7, its interactions with charged surfactants were also investigated. As expected, spreading positively charged surfactants onto a partial protein monolayer was found to increase the GOx surface concentration, whereas in the case of negatively charged surfactants, the GOx surface concentration decreased until the SH signal went back to the pure buffer solution response level. With the increasing GOx surface concentration, the rearrangement or reorientation of the protein was also observed.