Carley Corrado

Synthesis, Structural, and Optical Properties of Stable ZnS:Cu,Cl Nanocrystals †

Stable water-suspendable Cu+-doped ZnS nanocrystals (NCs) have been synthesized with mercaptopropionic acid (MPA) as a capping molecule. The nanocrystals have been characterized using a combination of experimental techniques including UV-vis and photoluminescence (PL) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), inductively coupled plasma (ICP), and extended X-ray absorption fine structure (EXAFS). The UV-vis electronic absorption spectrum shows an excitonic peak at 310 nm, characteristic of quantum-confined ZnS NCs. This excitonic peak does not change noticeably with Cu+ doping. XRD confirms the formation of ZnS nanocrystals, and the average size of the NCs has been determined to be around 6 nm by TEM. The incorporation of Cu+ into the ZnS is manifested as a substantial red-shift of the emission band in the PL spectra upon addition of Cu2+ that was reduced into Cu+ during the synthesis reaction. EXAFS data were obtained to confirm copper doping as well as determine the local structure about Cu+ and Zn2+ in the NCs. Fitting to the EXAFS data for Cu+ suggests that most Cu+ ions are located near the surface within the ZnS NCs and that a significant fraction may be in the form of CuS as found in bulk material. These combined optical and structural studies have provided important new insight into the relevant electronic energy levels and their correlation to the optical and structural properties of ZnS:Cu,Cl NCs. This has important implications in potential applications of this phosphor material for solid state lighting, imaging, and other photonic devices.

Characterization of Primary Amine Capped CdSe, ZnSe, and ZnS Quantum Dots by FT-IR: Determination of Surface Bonding Interaction and Identification of Selective Desorption

Surface ligands of semiconductor quantum dots (QDs) critically influence their properties and functionalities. It is of strong interest to understand the structural characteristics of surface ligands and how they interact with the QDs. Three quantum dot (QD) systems (CdSe, ZnSe, and ZnS) with primary aliphatic amine capping ligands were characterized primarily by FT-IR spectroscopy as well as NMR, UV-vis, and fluorescence spectroscopy, and by transmission electron microscopy (TEM). Representative primary amines ranging from 8 to 16 carbons were examined in the vapor phase, KBr pellet, and neat and were compared to the QD samples. The strongest hydrogen-bonding effects of the adsorbed ligands were observed in CdSe QDs with the weakest observed in ZnS QDs. There was an observed splitting of the N-H scissoring mode from 1610 cm(-1) in the neat sample to 1544 and 1635 cm(-1) when bound to CdSe QDs, which had the largest splitting of this type. The splitting is attributed to amine ligands bound to either Cd or Se surface sites, respectively. The effect of exposure of the QDs dispersed in nonpolar medium to methanol as a crashing agent was also examined. In the CdSe system, the Cd-bound scissoring mode disappeared, possibly due to methanol replacing surface cadmium sites. The opposite was observed for ZnSe QDs, in which the Se-bound scissoring mode disappeared. It was concluded that surface coverage and ligand bonding partners could be characterized by FT-IR and that selective removal of surface ligands could be achieved through introduction of competitive binding interactions at the surface.

Enhanced Cu emission in ZnS:Cu,Cl/ZnS core–shell nanocrystals

ZnS : Cu,Cl/ZnS core-shell nanocrystals (NCs) have been synthesized via a facile aqueous synthesis method. The shell growth of the NCs was observed via a red-shift in the UV-Vis absorption spectra with increasing NC size. The Cu photoluminescence (PL) emission was enhanced by capping with a thin ZnS shell. The ZnS : Cu (0.2%) and ZnS : Cu (0.5%) show a more pronounced red-shift in the apparent PL peak position as well as a 37% and 67% increase in emission intensity, respectively, in comparison to the undoped NCs. The observed red-shift is mainly due to an increase in intensity of the Cu PL emission. The 1% Cu-doped NCs exhibit very little red-shift because the observed emission is dominated by the Cu-dopant and thus nearly independent of the size of the NCs. The increase in Cu emission is evidence that Cu atoms occupying non-emissive surface sites in doped ZnS NCs were encapsulated by the ZnS shell. Extended X-Ray Absorption Fine Structure (EXAFS) data also suggests that the Cu had slightly more neighbors upon growth of a ZnS shell, indicating its encapsulation into the core of the NCs. The EXAFS Zn edge data also indicate greater disorder in the ZnS structure when the shell is grown, which may be attributed to the ZnS shell being more amorphous than the core NCs. This study demonstrates that core-shell structures can be used as a simple and yet powerful strategy to enhance PL properties of doped semiconductor NCs.

Probing the local structure of dilute Cu dopants in fluorescent ZnS nanocrystals using EXAFS

A local structure study of ZnS nanocrystals, doped with very low concentrations of Cu, was carried out using the EXAFS technique to better understand how Cu substitutes into the host lattice and forms Cu luminescence centers. We show that a large fraction of the Cu have three nearest neighbor S atoms and the Cu-S bond is significantly shortened compared to Zn-S, by ∼0.08 Å. In addition, the second neighbor Cu-Cu peak is extremely small. We propose that Cu occupies an interior site next to a S(2-) vacancy, with the Cu displaced towards the remaining S(2-) and away from the vacancy; such a displacement immediately explains the lack of a significant Cu-Cu peak in the data. There is no evidence for interstitial Cu sites (Cu(i)), indicating that no more than 2% of the Cu are Cu(i.) This study provides new insights into the local structure of the Cu dopant in ZnS without the presence of CuS nanoprecipitates that are present at higher Cu doping levels.

Analyzing luminescent solar concentrators with front-facing photovoltaic cells using weighted Monte Carlo ray tracing

Luminescent solar concentrators (LSC) collect ambient light from a broad range of angles and concentrate the captured light onto photovoltaic (PV) cells. LSCs with front-facing cells collect direct and indirect sunlight ensuring a gain factor greater than one. The flexible placement and percentage coverage of PV cells on the LSC panel allow for layout adjustments to be made in order to balance re-absorption losses and the level of light concentration desired. A weighted Monte Carlo ray tracing program was developed to study the transport of photons and loss mechanisms in the LSC to aid in design optimization. The program imports measured absorption/emission spectra of an organic luminescent dye (LR305), the transmission coefficient, and refractive index of acrylic as parameters that describe the system. Simulations suggest that for LR305, 8–10 cm of luminescent material surrounding the PV cell yields the highest increase in power gain per unit area of LSC added, thereby determining the ideal spacing betwe...

Power generation study of luminescent solar concentrator greenhouse

A Luminescent Solar Concentrator (LSC) greenhouse and an identical control greenhouse were constructed with photovoltaic (PV) cells attached to the roof panels of both structures. The placement and types of PV cells used in the LSC panels were varied for performance comparisons. Solar power generation was monitored continuously for one year, with leading LSC panels exhibiting a 37% increase in power production compared to the reference. The 22.3 m2 greenhouse was projected to generate a total of 1342 kWh per year, or 57.4 kWh/m2 if it were composed solely of the leading panel of Criss Cross panel design. The LSC panels showed no signs of degradation throughout the trial demonstrating the materials robustness in field conditions.

Monte Carlo ray-tracing simulations of luminescent solar concentrators for building integrated photovoltaics

Luminescent solar concentrators (LSCs) have the ability to receive light from a wide range of angles, concentrating the captured light onto small photo active areas. This enables greater incorporation of LSCs into building designs as windows, skylights and wall claddings in addition to rooftop installations of current solar panels. Using relatively cheap luminescent dyes and acrylic waveguides to effect light concentration onto lesser photovoltaic (PV) cells, there is potential for this technology to approach grid price parity. We employ a panel design in which the front facing PV cells collect both direct and concentrated light ensuring a gain factor greater than one. This also allows for flexibility in determining the placement and percentage coverage of PV cells during the design process to balance reabsorption losses against the power output and level of light concentration desired. To aid in design optimization, a Monte-Carlo ray tracing program was developed to study the transport of photons and loss mechanisms in LSC panels. The program imports measured absorption/emission spectra and transmission coefficients as simulation parameters with interactions of photons in the panel determined by comparing calculated probabilities with random number generators. LSC panels with multiple dyes or layers can also be simulated. Analysis of the results reveals optimal panel dimensions and PV cell layouts for maximum power output for a given dye concentration, absorbtion/emission spectrum and quantum efficiency.

Wavelength‐Selective Solar Photovoltaic Systems: Powering Greenhouses for Plant Growth at the Food‐Energy‐Water Nexus

Global renewable electricity generation capacity has rapidly increased in the past decade. Increasing the sustainability of electricity generation and the market share of solar photovoltaics (PV) will require continued cost reductions or higher efficiencies. Wavelength-Selective Photovoltaic Systems (WSPVs) combine luminescent solar cell technology with conventional silicon-based PV, thereby increasing efficiency and lowering the cost of electricity generation. WSPVs absorb some of the blue and green wavelengths of the solar spectrum but transmit the remaining wavelengths that can be utilized by photosynthesis for plants growing below. WSPVs are ideal for integrating electricity generation with glasshouse production, but it is not clear how they may affect plant development and physiological processes. The effects of tomato photosynthesis under WSPVs showed a small decrease in water use, whereas there were minimal effects on the number and fresh weight of fruit for a number of commercial species. Although more research is required on the impacts of WSPVs, they are a promising technology for greater integration of distributed electricity generation with food production operations, for reducing water loss in crops grown in controlled environments, as building-integrated solar facilities, or as alternatives to high-impact PV for energy generation over agricultural or natural ecosystems.