Sylvain G. Cloutier

Figures of merit for high-performance transparent electrodes using dip-coated silver nanowire networks

Homogeneous, highly conductive, and transparent silver nanowire thin films were fabricated using a simple dip-coating technique and a subsequent annealing step. Silver nanowires with two different average lengths (11 µm and 19µm) were used in the sample preparation to analyze the dependence of the sheet resistance on the length of the one-dimensional nanostructures. The best sample had a sheet resistance of 10.2Ω/D with optical transmittance of 89.9%. Two figures of merit, the electrical to optical conductivity ratio (σDC/σOP) and ϕTC, were obtained for all the samples in order to measure their performance as transparent conductive materials.

Efficient exciton funneling in cascaded PbS quantum dot superstructures.

Benzenedithiol (BDT) and ethanedithiol (EDT) ligand-exchange treatments can be used to cross-link colloidal PbS quantum dots into nanocrystalline film structures with distinct optoelectronic properties. Such structures can provide a unique platform to study the energy transfer between layers of quantum dots with different sizes. In this report, efficient exciton funneling and recycling of surface state-bound excitons is observed in cascaded PbS quantum dot-based multilayered superstructures, where the excitons transfer from the larger band gap or donor layers to the smallest band gap or acceptor layers. In this system, both the BDT- and EDT-treated cascaded structures exhibit dramatically enhanced photoluminescence from the acceptor layers. As we show, the energy transfer mechanisms involved and their efficiencies are significantly different depending on the ligand-exchange treatment. In the future, we believe these efficient exciton recycling and funneling mechanisms could be used to improve significantly the photocurrent, charge-transport, and conversion efficiencies in low-cost nanocrystalline and hybrid solar cells and the emission efficiencies in hybrid light-emitting devices.

Synthesis of diamond nanowires using atmospheric-pressure chemical vapor deposition.

We report diamond nanowires grown in an atmospheric pressure chemical vapor deposition process. These diamond nanowires are straight, thin and long, and uniform in diameter (60-90 nm) over tens of micrometers. Spectroscopic analysis, electron diffraction, and transmission electron microscopy provided confirmation that these nanowires are diamond with high crystallinity and high structural uniformity. They further revealed that these diamond nanowires are encased within multiwalled carbon nanotubes.

Graphene below the percolation threshold in TiO2 for dye-sensitized solar cells

We demonstrate a fast and large area-scalable methodology for the fabrication of efficient dye sensitized solar cells (DSSCs) by simple addition of graphene micro-platelets to TiO2 nanoparticulate ...

Direct-bandgap luminescence at room-temperature from highly-strained Germanium nanocrystals

Efficient room-temperature luminescence at optical telecommunication wavelengths and originating from direct band-to-band recombination has been observed in tensile-strained germanium nanocrystals synthesized by mechanical grinding techniques. Selected area electron diffraction, micro-Raman and optical-absorption spectroscopy measurements indicate high tensile-strains while combined photoluminescence spectroscopy, excitation-power evolution and time-resolved measurements suggest direct band-to-band recombination. Such band-engineered germanium nanocrystals offer great possibilities for silicon-photonics integration due to their superb light-emission properties, facile fabrication and compatibility with standard microelectronic processes.

Functionalized multi-wall carbon nanotubes/TiO2 composites as efficient photoanodes for dye sensitized solar cells

We report on the effects of incorporation of different concentrations of carboxyl group (COOH)-functionalized multi-wall carbon nanotubes (F-MWCNTs) into TiO2 active layers for dye-sensitized solar cells (DSSCs). Standard DSSCs with bare TiO2 exhibit a photo-conversion efficiency (PCE) of 6.05% and a short circuit current density (Jsc) of 13.3 mA cm−2. The presence of 2 wt% F-MWCNTs in the photoanodes increases the PCE up to 7.95% and Jsc up to 17.5 mA cm−2. The photoanodes were characterized using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy and Raman spectroscopy. The electrochemical behaviour of the solar cells was investigated by electrochemical impedance spectroscopy (EIS). We attribute the improved performances to the combined effect of increased dye loading and reduced charge recombination (as clarified by dye loading and EIS measurements), due to the conformal coverage of F-MWCNTs, which allows fast and efficient charge collection in operating solar cells. These results can help in improving the PCE in DSSCs in an elegant and straightforward way, minimizing the need of additional steps (e.g. pre- and post-treatment with TiCl4) for photoanode preparation.

Structure-property correlations in hybrid polymer-nanoparticle electrospun fibers and plasmonic control over their dichroic behavior

Electrospinning constitutes a simple and versatile approach of fabricating polymer heterostructures composed of nanofibers. A preferred alignment of polymer crystallites stems from complex shear elongational forces and generates a strong intrinsic optical anisotropy in typical electrospun fibers of semicrystalline polymers. While it can prove useful for certain devices, this intrinsic anisotropy can be extremely detrimental for other key applications such as high-performance polymer-based lighting and solar-energy harvesting platforms. We report a dramatic reduction in the intrinsic dichroism of electrospun poly(ethylene oxide) fibers resulting from the incorporation of inorganic nanoparticles in the polymer matrix. This effect is shown to originate from a controllable randomization of the orientational ordering of the crystalline domains in the hybrid nanofibers and not merely from a reduction in crystallinity. This improved understanding of the crystalline structure-optical property correlation then leads to a better control over the intrinsic anisotropy of electrospun fibers using localized surface-plasmon enhancement effects around metallic nanoparticles.

Impact of Different Surface Ligands on the Optical Properties of PbS Quantum Dot Solids

The engineering of quantum dot solids with low defect concentrations and efficient carrier transport through a ligand strategy is crucial to achieve efficient quantum dot (QD) optoelectronic devices. Here, we study the consequences of various surface ligand treatments on the light emission properties of PbS quantum dot films using 1,3-benzenedithiol (1,3-BDT), 1,2-ethanedithiol (EDT), mercaptocarboxylic acids (MPA) and ammonium sulfide ((NH4)2S). We first investigate the influence of different ligand treatments on the inter-dot separation, which mainly determines the conductivity of the QD films. Then, through a combination of photoluminescence and transient photoluminescence characterization, we demonstrate that the radiative and non-radiative recombination mechanisms in the quantum dot films depend critically on the length and chemical structure of the surface ligands.

Two-dimensional vectorial photonic crystals formed in azo-dye-doped liquid crystals

A 2D, square lattice, vectorial photonic crystal is formed by vectorial holography using an azo-dye-doped liquid-crystal material. Four coherent beams are interfered to generate a highly stable, switchable polarization holography structure. The formation of the vectorial lattice by the liquid-crystal molecular orientation is confirmed by diffraction pattern and polarization microscopy analysis. Simulations of the alignment and diffraction pattern are in good agreement with the experimental results. Polarization sensitive diffraction behavior is also consistent with the Kakichashvili model.

Effects of boron and phosphorus doping on the photoluminescence of self-assembled germanium quantum dots

The doping of Ge quantum dots grown on Si (100) was investigated using atomic force microscopy and photoluminescence spectroscopy. The dots produced photoluminescence in the energy range from 0.75 to 0.95 eV. Compared to the undoped dots, the boron and phosphorus doped dots demonstrated a shift in peak emission toward lower energy by 60–80 meV, which is attributed to the decrease in density of the smaller sized dots. Increased photoluminescence intensity with temperature indicated higher activation energy with doping, suggesting a higher probability of radiative transitions at elevated temperatures, potentially important for various applications.