Daniel C. Schinca

Silver-silver oxide core-shell nanoparticles by femtosecond laser ablation: core and shell sizing by extinction spectroscopy

The generation of small silver metal nanoparticles (Nps) by ultrashort pulsed laser ablation has been an active area of research in recent years due to their interest in several fields of applied research such as biotechnology and material research, in particular those with sizes smaller than 10 nm. In general, laser ablation tends to produce environmentally clean metal Nps compared with wet chemical methods. However, since silver may be oxidized in the presence of water or ethanol, core–shell silver–silver oxide (Ag–Ag2O) Nps can be formed, whose size and thickness must be determined and characterized for functionalization related to future applications. This work analyses the size characteristics of core–shell Ag–Ag2O colloid nanostructures (smaller than 10 nm) obtained by femtosecond laser ablation of solid silver targets in different liquid media (water or ethanol) through the study of their optical extinction spectra. A fit of full experimental spectrum using Mie theory allows the determination of core size and shell thickness distributions as a function of fluence. The red-shift of the plasmon peak wavelength with respect to the bare-core peak wavelength at 400 nm, produced by the oxide shell, may be easily measured even for very small thicknesses. It was found that the dominant Ag2O effective thickness is inversely proportional to the fluence, reaching a maximum of 0.2 nm for a fluence of 60 J cm−2 and a minimum of 0.04 nm for a fluence of 1000 J cm−2.

Analysis of the structure, configuration, and sizing of Cu and Cu oxide nanoparticles generated by fs laser ablation of solid target in liquids

We report on the analysis of structure, configuration, and sizing of Cu and Cu oxide nanoparticles (Nps) produced by femtosecond (fs) laser ablation of solid copper target in liquids. Laser pulse energy ranged between 500 μJ and 50 μJ. Water and acetone were used to produce the colloidal suspensions. The study was performed through optical extinction spectroscopy using Mie theory to fit the full experimental spectra, considering free and bound electrons size dependent contributions to the metal dielectric function. Raman spectroscopy and AFM technique were also used to characterize the sample. Considering the possible oxidation of copper during the fabrication process, two species (Cu and Cu2O) arranged in two structures (bare core or core-shell) and in two configuration types (Cu-Cu2O or Cu2O-Cu) were considered for the fitting depending on the laser pulse energy and the surrounding media. For water at high energy, it can be observed that a Cu-Cu2O configuration fits the experimental spectra of the collo...

Quantitative optical extinction-based parametric method for sizing a single core–shell Ag–Ag2O nanoparticle

This paper develops a parametric method for determining the core radius and shell thickness in small silver?silver-oxide core?shell nanoparticles (Nps) based on single particle optical extinction spectroscopy.The method is based on the study of the relationship between plasmon peak wavelength, full width at half maximum (FWHM) and contrast of the extinction spectra as a function of core radius and shell thickness. This study reveals that plasmon peak wavelength is strongly dependent on shell thickness, whereas FWHM and contrast depend on both variables. These characteristics may be used for establishing an easy and fast stepwise procedure to size core?shell NPs from single particle absorption spectrum. The importance of the method lies in the possibility of monitoring the growth of the silver-oxide layer around small spherical silver Nps in real time.Using the electrostatic approximation of Mie theory, core?shell single particle extinction spectra were calculated for a silver particles core size smaller than about 20?nm and different thicknesses of silver oxide around it. Analysis of the obtained curves shows a very particular characteristic of the plasmon peak of small silver?silver-oxide Nps, expressed in the fact that its position is strongly dependent on oxide thickness and weakly dependent on the core radius. Even a very thin oxide layer shifts the plasmon peak noticeably, enabling plasmon tuning with appropriate shell thickness.This characteristic, together with the behaviour of FWHM and contrast of the extinction spectra can be combined into a parametric method for sizing both core and shell of single silver Nps in a medium using only optical information. In turn, shell thickness can be related to oxygen content in the Nps surrounding media.The method proposed is applied to size silver Nps from single particle extinction spectrum. The results are compared with full optical spectrum fitting using the electrostatic approximation in Mie theory. The method may be the basis for developing a plasmonic sensor for O2 concentration based on Ag single NP spectroscopy.

Analysis of the main optical mechanisms responsible for fragmentation of gold nanoparticles by femtosecond laser radiation

Studies of fragmentation process of gold nanoparticles (Nps) in deionized water after generation by femtosecond laser ablation were performed. To analyze the fragmentation process, direct IR ultrafast pulses or super-continuum (SC) radiation focused in the colloidal solution were used in separate steps. IR pulses and SC generated externally in a sapphire crystal or directly inside the water were applied under low fluence regime. In the latter cases, to evaluate the effect on fragmentation of the different spectral bands present in the SC, we have determined different efficiency regions characterized by means of the product between the spectral response and the optical extinction spectrum corresponding to the initial Nps solution. From the analysis of this product function, we can conclude that the main fragmentation mechanism is due to linear absorption in the visible region. Likewise, the SC generated in water resulted more efficient than the SC obtained externally by a sapphire crystal. This fact may be...

Influence of size-corrected bound-electron contribution on nanometric silver dielectric function. Sizing through optical extinction spectroscopy

The study of metal nanoparticles (NPs) is of great interest due to their ability to enhance optical fields on the nanometric scale, which makes them interesting for various applications in several fields of science and technology. In particular, their optical properties depend on the dielectric function of the metal, its size, shape and surrounding environment.This work analyses the contributions of free and bound electrons to the complex dielectric function of spherical silver NPs and their influence on the optical extinction spectra. The contribution of free electrons is usually corrected for particle size under 10?nm, introducing a modification of the damping constant to account for the extra collisions with the particles boundary.For the contribution of bound electrons, we considered the interband transitions from the d-band to the conduction band including the size dependence of the electronic density states for radii below 2?nm. Bearing in mind these specific modifications, it was possible to determine optical and band energy parameters by fitting the bulk complex dielectric function. The results obtained from the optimum fit are: Kbulk?=?2???1024 (coefficient for bound-electron contribution), Eg?=?1.91?eV (gap energy), EF?=?4.12?eV (Fermi energy), and ?b?=?1.5???1014?Hz (damping constant for bound electrons).Based on this size-dependent dielectric function, extinction spectra of silver particles in the nanometric?subnanometric radius range can be calculated using Mies theory, and its size behaviour analysed. These studies are applied to fit experimental extinction spectrum of very small spherical particles fabricated by fs laser ablation of a solid target in water. From the fitting, the structure and size distribution of core radius and shell thickness of the colloidal suspension could be determined. The spectroscopic results suggest that the colloidal suspension is composed by two types of structures: bare core and core?shell. The former is composed by Ag, while the latter is composed by two species: silver?silver oxide (Ag?Ag2O) and hollow silver (air?Ag) particles. High-resolution transmission microscopy and atomic force microscopy analysis performed on the dried suspension agree with the sizing obtained by optical extinction spectroscopy, showing that the latter is a very good complementary technique to standard microscopy methods.

Determination of plasma frequency, damping constant, and size distribution from the complex dielectric function of noble metal nanoparticles

This paper develops a novel method for simultaneously determining the plasma frequency ωP   and the damping constant γfree in the bulk damped oscillator Drude model, based on experimentally measured real and imaginary parts of the metal refractive index in the IR wavelength range, lifting the usual approximation that restricts frequency values to the UV-deep UV region. Our method was applied to gold, silver, and copper, improving the relative uncertainties in the final values for ωp (0.5%–1.6%) and for γfree (3%–8%), which are smaller than those reported in the literature. These small uncertainties in ωp and γfree determination yield a much better fit of the experimental complex dielectric function. For the case of nanoparticles (Nps), a series expansion of the Drude expression (which includes ωp and γfree determined using our method) enables size-dependent dielectric function to be written as the sum of three terms: the experimental bulk dielectric function plus two size corrective terms, one for free el...

The luminescent quantum efficiency of Cr3+ ions in Cs2NaAlF6 single crystals

Abstract The luminescent quantum efficiency of Cr3+ ions in single fluoride crystal Cs2NaAlF6 was determined by using the simultaneous multiple-wavelength photoacoustic and luminescent experiments method, based on the generation of photoacoustic and luminescence signals after pulsed laser excitation. The luminescent quantum yield for the most important transition between the 4 T 2 → 4 A 2 vibronic levels was found to be 68±3%. This value agrees with that obtained from the ratio of the lifetimes of the corresponding transition at different temperatures.Abstract The luminescent quantum efficiency of Cr3+ ions in single fluoride crystal Cs2NaAlF6 was determined by using the simultaneous multiple-wavelength photoacoustic and luminescent experiments method, based on the generation of photoacoustic and luminescence signals after pulsed laser excitation. The luminescent quantum yield for the most important transition between the 4 T 2 → 4 A 2 vibronic levels was found to be 68±3%. This value agrees with that obtained from the ratio of the lifetimes of the corresponding transition at different temperatures.

Size dependent Cu dielectric function for plasmon spectroscopy: Characterization of colloidal suspension generated by fs laser ablation

Copper metal nanoparticles (Nps) have received increasing interest during the last years due to their potential applications in several fields of science and technology. Their optical properties depend on the characteristics of the dielectric function of the metal, their size, and the type of environment. The contribution of free and bound electrons on the dielectric function of copper Nps is analyzed as well as their influence on its plasmonic properties. The contribution of free electrons is corrected for particle size under 10 nm, introducing a term inversely proportional to the particles radius in the damping constant. For bound electron contribution, interband transitions from the d-band to the conduction band are considered. For particles with sizes below 2 nm, the larger spacing between electronic energy levels must be taken into account by making the electronic density of states in the conduction band size-dependent. Considering these specific modifications, optical parameters and band energy val...

Optical analysis of the fine crystalline structure of artificial opal films.

Herein, we present a detailed analysis of the structure of artificial opal films. We demonstrate that, rather than the generally assumed face centered cubic lattice of spheres, opal films are better approximated by rhombohedral assemblies of distorted colloids. Detailed analysis of the optical response in a very wide spectral range (0.4 < or = a/lambda < or = 2, where a is the conventional lattice constant), as well as at perpendicular and off-normal directions, unambiguously shows that the interparticle distance coincides very approximately with the expected diameter only along directions contained in the same close-packed plane but differs significantly in directions oblique to the [111] one. A full description of the real and reciprocal lattices of actual opal films is provided, as well as of the photonic band structure of the proposed arrangement. The implications of this distortion in the optical response of the lattice are discussed.

Alternative method for concentration retrieval in differential optical absorption spectroscopy atmospheric-gas pollutant measurements

Differential optical absorption spectroscopy is a widely used technique for open-column atmospheric-gas pollution monitoring. The concentration retrieval is based on the fitting of the measured differential absorbance through the Lambert-Beer law. We present an alternative method for calculating the gas concentration on the basis of the proportionality between differential absorbance and differential absorption cross section of the gas under study. The method can be used on its own for single-component analysis or as a complement to the standard technique in multicomponent cases. The performance of the method for the case of cross interference between two gases is analyzed. The procedure can be used with differential absorption cross sections measured in the laboratory or taken from the literature. In addition, the method provides a criterion to discriminate against different species having absorption features in the same wavelength range.