Anne-Marie Dowgiallo

Controlled Plasmon Resonance Properties of Hollow Gold Nanosphere Aggregates

Hollow gold nanospheres (HGNs) ranging from 29.9 nm/8.5 nm (outer diameter/shell thickness) to 51.5 nm/4.5 nm and having aspect ratios spanning 3.5-11.7 were employed to investigate the ability to tailor charge oscillations of HGN aggregates by systematic variation of particle aspect ratio, interparticle gap, and nanosphere inner surface spatial separation. Altering these properties in aggregated HGNs led to control over the interparticle plasmon resonance. Thiol-mediated aggregation was accomplished using either ethanedithiol or cysteine, resulting in dimeric structures in which monomer subunits were spatially separated by <3 Å and 1.2 ± 0.7 nm, respectively. Particle dimensions and separation distances were confirmed by transmission electron microscopy. Experimental absorption spectra obtained for high-aspect ratio nanospheres dimerized using ethanedithiol exhibited an obvious blue shift of the surface plasmon resonance (SPR) relative to that observed for the native, monomeric HGN. This spectral difference likely results from a charge-transfer plasmon resonance at the dimer interface. The extent of the blue shift was dependent upon shell thickness. Dimers comprised of thin-shelled HGNs exhibited the largest shift; aggregates containing HGNs with thick shells (≥7 nm) did not display a significant SPR shift when the individual particles were in contact. By comparison, all cysteine-induced aggregates examined in this study displayed large interparticle gaps (>1 nm) and a red-shifted SPR, regardless of particle dimensions. This effect can be described fully by a surface mode coupling model. All experimental measurements were verified by finite difference time domain calculations. In addition, simulated electric field maps highlighted the importance of the inner HGN surface in the interparticle coupling mechanism. These findings, which describe structure-dependent SPR properties, may be significant for applications derived from the plasmonic nanostructure platform.

Charge Transfer Dynamics between Carbon Nanotubes and Hybrid Organic Metal Halide Perovskite Films

In spite of the rapid rise of metal organic halide perovskites for next-generation solar cells, little quantitative information on the electronic structure of interfaces of these materials is available. The present study characterizes the electronic structure of interfaces between semiconducting single walled carbon nanotube (SWCNT) contacts and a prototypical methylammonium lead iodide (MAPbI3) absorber layer. Using photoemission spectroscopy we provide quantitative values for the energy levels at the interface and observe the formation of an interfacial dipole between SWCNTs and perovskite. This process can be ascribed to electron donation from the MAPbI3 to the adjacent SWCNT making the nanotube film n-type at the interface and inducing band bending throughout the SWCNT layer. We then use transient absorbance spectroscopy to correlate this electronic alignment with rapid and efficient photoexcited charge transfer. The results indicate that SWCNT transport and contact layers facilitate rapid charge extraction and suggest avenues for enhancing device performance.

Structure-dependent coherent acoustic vibrations of hollow gold nanospheres.

Hollow gold nanospheres (HGNs) were excited with ultrashort laser pulses, and the coherent vibrational response was examined using femtosecond time-resolved transient absorption. The results indicated that HGNs support an isotropic mode, resulting in periodic modulation of the surface plasmon differential absorption. Two different categories of coherent acoustic vibrations, which depend on particle dimensions, were observed for HGNs. Further, the vibration launching mechanism was dependent upon the dimensions of the HGN. Coherent vibrations in HGNs characterized by small outer radii (<10 nm) and low cavity-radius-to-outer-shell radius aspect ratios (<0.5) were excited by a direct mechanism, whereas the vibrations observed for the larger particles (>25 nm OR) with higher aspect ratios (>0.5) resulted from an indirect mechanism. These findings may be significant for developing a predictive understanding of nanostructure optical and mechanical properties.

Electronic relaxation dynamics in isolated and aggregated hollow gold nanospheres.

Electronic relaxation and interparticle electromagnetic coupling processes in hollow gold nanospheres (HGNs) and HGN aggregates are described. These plasmon-tunable HGNs exhibit an unexpected, but systematic, blue shift of the surface plasmon resonance spectral position when the particles are aggregated. Femtosecond transient absorption measurements and finite-difference time-domain (FDTD) calculations are used to demonstrate that this blue shift is the result of delocalization of the Fermi-gas over multiple particles, an effect not observed with solid spherical particles. The ultrafast electron-phonon coupling lifetimes for the thin-shelled HGNs increase upon aggregation, indicating significant enhancement in interparticle electromagnetic coupling. For instance, a 48-nm HGN with a shell thickness of 7 nm shows ultrafast electron-phonon coupling with a lifetime of 300 +/- 100 fs, and upon aggregation, this lifetime increases to 730 +/- 140 fs. The experimental data strongly suggest that confinement effects in HGNs allow for enhanced energy transport over nanometer distances and this effect can be applied to developing more efficient devices, including photovoltaics.

Magnetic dipolar interactions in solid gold nanosphere dimers.

We report the first observation of a magnetic dipolar contribution to the nonlinear optical (NLO) response of colloidal metal nanostructures. Second-order NLO responses from several individual solid gold nanosphere (SGN) dimers, which we prepared by a bottom-up approach, were examined using polarization-resolved second harmonic generation (SHG) spectroscopy at the single-particle level. Unambiguous circular dichroism in the SH signal was observed for most of the dimeric colloids, indicating that the plasmon field located within the interparticle gap was chiral. Detailed analysis of the polarization line shapes of the SH intensities obtained by continuous polarization variation suggested that the effect resulted from strong magnetic-dipole contributions to the nanostructures optical properties.

Ultrafast electron–phonon coupling in hollow gold nanospheres

Electronic energy relaxation in hollow gold nanospheres (HGNs) was studied using femtosecond time-resolved transient absorption spectroscopy. A range of HGNs having outer diameter-to-shell thickness aspect ratios of 3.5 to 9.5 were synthesized by a galvanic replacement method. The HGNs exhibited electron-phonon relaxation times that decreased from 1.18 ± 0.16 to 0.59 ± 0.08 ps as the aspect ratio increased over this range. The corresponding electron-phonon coupling constants, G, ranged from (1.67 ± 0.22) to (3.33 ± 0.45) × 10(16) W m(-3) K(-1). Electron-phonon coupling was also determined for solid gold nanospheres (SGNs) with diameters spanning 20 nm to 83 nm; no size dependence was observed for these structures. The HGNs with high aspect ratios exhibited larger electron-phonon coupling constants than the SGNs, whose average G value was (1.9 ± 0.2) × 10(16) W m(-3) K(-1). By comparison, low-aspect ratio HGNs exhibited values comparable to SGNs. The electron-phonon coupling of high-aspect ratio HGNs was also influenced by the surrounding fluid dielectric; slightly smaller G values were obtained when methanol was the solvent as opposed to water. This coupling enhancement observed for high-aspect ratio HGNs was attributed to the large surface to volume ratio of these structures, which results in non-negligible contributions from the environment.

Probing the Structure–Property Interplay of Plasmonic Nanoparticle Transducers Using Femtosecond Laser Spectroscopy

The characteristic feature of noble metal nanoparticles is the localized surface plasmon resonance (LSPR). Plasmon-supporting nanoparticles can function as transducers because of the LSPRs ability to amplify electromagnetic fields and its sensitivity to changes in the surrounding dielectric. The performance of these materials in transducer applications is inherently related to nanoparticle structure. This Perspective describes the use of femtosecond laser-based spectroscopies to elucidate the nanoscale structure-property interplay. First, femtosecond time-resolved transient extinction measurements that probe the LSPR following nanoparticle photoexcitation are described. These measurements illustrate how nanostructure dimensions influence sensitivity to changes in the interfacial dielectric. The combination of single-particle nonlinear optical (NLO) measurements and electron microscopy is also used to describe the symmetry of plasmon surface fields in nanoparticle assemblies. In particular, the use of continuous polarization variation-detected second-harmonic generation to describe electric and magnetic dipolar contributions to NLO properties is discussed.

Influence of Confined Fluids on Nanoparticle-to-Surroundings Energy Transfer

Energy transfer from photoexcited nanoparticles to their surroundings was studied for both hollow and solid gold nanospheres (HGNs and SGNs, respectively) using femtosecond time-resolved transient extinction spectroscopy. HGNs having outer diameters ranging from 17 to 78 nm and fluid-filled cavities were synthesized by a sacrificial galvanic replacement method. The HGNs exhibited energy transfer half times that ranged from 105 ± 10 ps to 1010 ± 80 ps as the total particle surface area increased from 1005 to 28,115 nm(2). These data showed behaviors that were categorized into two classes: energy transfer from HGNs to interior fluids that were confined to cavities with radii <15 nm and ≥15 nm. Energy transfer times were also determined for solid gold nanospheres (SGNs) having radii spanning 9-30 nm, with a similar size dependence where the relaxation times increased from 140 ± 10 to 310 ± 15 ps with increasing nanoparticle size. Analysis of the size-dependent energy transfer half times revealed that the distinct relaxation rate constants observed for particle-to-surroundings energy transfer for HGNs with small cavities were the result of reduced thermal conductivity of confined fluids. These data indicate that the thermal conductivity of HGN cavity-confined fluids is approximately one-half as great as it is for bulk liquid water. For all HGNs and SGNs studied, energy dissipation through the solvent and transfer across the particle/surroundings interface both contributed to the energy relaxation process. The current data illustrated the potential of fluid-filled hollow nanostructures to gain insight into the properties of confined fluids.