Electrochemiluminescence and Photoluminescence of Carbon Quantum Dots Controlled by Aggregation-Induced Emission, Aggregation-Caused Quenching, and Interfacial Reactions.

Carbon quantum dots (CQDs) show promise in optoelectronics as a light emitter due to simple synthesis, biocompatibility and strong tunable light emissions. However, CQDs commonly suffer from aggregation caused quenching (ACQ), inhibiting the full potential of these light emitters. Studies into different ideal light emitters have shown enhancements when converting common ACQ effects to aggregation induced emission (AIE) effects. We report CQD synthesis using citric acid and high/low thiourea concentrations, or sample 2/1. These two CQDs exhibited AIE and ACQ PL effects, respectively. CQD characterizations and photoluminescence interrogations of CQD films and solutions revealed that these unique emission mechanisms likely arose from different S incorporations into the CQDs. Furthermore, it was discovered that sample 2 emitted electrochemiluminescence (ECL) more intensely than sample 1 in a homogenous solution with S2O82- as a coreactant, due to aggregation and interactions of CQD species in solution. Very interestingly, sample 1's CQD film|S2O82- system achieved an ECL efficiency of 26% and emitted roughly 26 times more efficiently than sample 2 in the same conditions. Predominant interfacial reactions and surface state emission produced intense white light with a correlated color temperature of 2000 K. Spooling ECL spectroscopy was utilized to investigate emission mechanisms. Sample 2's CQD film|TPrA system had four times higher ECL intensity than that of sample 1, most likely due to π-cation interactions leading to a strong CQD•+ stability, thereby, enhancing ECL. It is anticipated that ECL enhancement of CQD films or solutions by means of AIE will lead to wide CQD optoelectronic applications.

Efficient White Electrochemiluminescent Emission From Carbon Quantum Dot Films.

Carbon quantum dots (CQDs) were manufactured from citric acid and urea in a gram-scale synthesis with a controlled size range between 1. 5 and 23.8 nm. The size control was realized by varying volume of the precursor solution in a hydrothermal synthesis method. The prepared CQDs were investigated using electrochemiluminescence (ECL) spectroscopy at interfaces of their electrode films and electrolyte solution containing coreactants rather than conventional optoelectronic tests, providing an in-depth analysis of light-emission mechanisms of the so-called half-cells. ECL from the CQD films with TPrA and K2S2O8 as coreactants provided information on the stability of the CQD radicals in the films. It was discovered that CQD•- has a powerful electron donating nature to sulfate radical to generate ECL at a relative efficiency of 96% to the Ru(bpy)3Cl2/K2S2O8 coreactant system, indicating a strong performance in light emitting applications. The smaller the CQD particle sizes, the higher the ECL efficiency of the film interface, most likely due to the increased presence of surface states per mass of CQDs. Spooling ECL spectroscopy of the system revealed a potential-dependent light emission starting from a deep red color to blue-shifted intensity maximum, cool bright white emission with a correlated color temperature of 3,200 K. This color temperature is appropriate for most indoor lighting applications. The above ECL results provide information on the performance of CQD light emitters in films, permitting preliminary screening for light emitting candidates in optoelectronic applications. This screening has revealed CQD films as a powerful and cost-effective light emitting layer toward lighting devices for indoor applications.

Electrogenerated Chemiluminescence and Electroluminescence of N-Doped Graphene Quantum Dots Fabricated from an Electrochemical Exfoliation Process in Nitrogen-Containing Electrolytes.

Artificial lighting sources are one of the most important technological developments for our modern lives; the search for cost-effective and efficient luminophores is therefore crucial to a sustainable future. Graphene quantum dots (GQDs) are carbon-based nanomaterials that exhibit exceptional optical and electronic properties, making them a prime candidate for a luminophore in a light-emitting device. Nitrogen-doped GQDs fabricated from a facile top-down electrochemical exfoliation process with a nitrogen-containing electrolyte in this report showed strong photoluminescent emission at 450 nm, and electrogenerated chemiluminescence at 660 nm in the presence of benzoyl peroxide as a coreactant. When introduced into solid-state light-emitting electrochemical cells, for the first time, the GQDs displayed a broad white emission centered at 610 nm, corresponding to Commision Internationale de l'eclairage (CIE) colour coordinates of (0.38, 0.36).

Preparation and characterization of CuInS2 nanocrystals for photovoltaic materials.

Copper indium disulphide (CIS) nanocrystals (NCs) were prepared using a one-pot synthesis. The stoichiometry was optimized based on its current density as measured by photoelectrochemical (PEC) experiments at interfaces between NC films deposited on ITO and 0.1 M methyl viologen dichloride (MV(2+)) solution. This method also offers insight into the kinetics of the photoreaction. A copper poor sulphur rich starting ratio was found to produce a copper-rich, indium-poor and slightly sulphur rich material. Further NC characterization was performed with SEM and TEM to investigate the morphology and crystallinity of the 30-70 nm NCs. The oxidation states of the individual elements were determined to be I, III, and 2- for Cu, In and S, respectively. Characteristics of optimal as-prepared NCs were found to be compatible among high functioning absorbing layers.

One-pot electrodeposition, characterization and photoactivity of stoichiometric copper indium gallium diselenide (CIGS) thin films for solar cells.

Herein we report the one-pot electrodeposition of copper indium gallium diselenide, CuIn(1-x)Ga(x)Se(2) (CIGS), thin films as the p-type semiconductor in an ionic liquid medium consisting of choline chloride/urea eutectic mixture known as Reline. The thin films were characterized by scanning electron microscopy with energy dispersive X-ray analysis, transmission electron microscopy, X-ray photoelectron spectroscopy, Raman microspectroscopy, and UV-visible spectroscopy. Based on the results of the characterizations, the electrochemical bath recipe was optimized to obtain stoichiometric CIGS films with x between 0.2 and 0.4. The chemical activity and photoreactivity of the optimized CIGS films were found to be uniform using scanning electrochemical microscopy and scanning photoelectrochemical microscopy. Low-cost stoichiometric CIGS thin films in one-pot were successfully fabricated.

Does health affect portfolio choice?

A number of recent studies find that poor health is empirically associated with a safer portfolio allocation. It is difficult to say, however, whether this relationship is truly causal. Both health status and portfolio choice are influenced by unobserved characteristics such as risk attitudes, impatience, information, and motivation, and these unobserved factors, if not adequately controlled for, can induce significant bias in the estimates of asset demand equations. Using the 1992-2006 waves of the Health and Retirement Study, we investigate how much of the connection between health and portfolio choice is causal and how much is due to the effects of unobserved heterogeneity. Accounting for unobserved heterogeneity with fixed effects and correlated random effects models, we find that health does not appear to significantly affect portfolio choice among single households. For married households, we find a small effect (about 2-3 percentage points) from being in the lowest of five self-reported health categories.