Phosphor-converted white light-emitting diodes (pc-WLEDs) are excellent energy-efficient light sources for artificial lighting applications. One goal of artificial lighting is to make objects/images look natural – as they look under the sunlight. The ability of a light source to accurately render the natural color of an object is gauged by the parameter – color rendering index (CRI). A conventional pc-WLED has an average CRI ~ 80, which is very low for accurate color reproduction. To utilize the pc-WLEDs for artificial lighting applications, all the CRI points (R1 – R15) should be above 95. However, there is a trade-off between CRI and luminous efficacy (LER), and it is challenging to increase both CRI and LER. Herein we propose a novel LED package (PKG) design to achieve CRI points ≥95 and efficiency ~100 lm/W by introducing two blue LEDs and a UV LED in combination with green and red phosphors. The silicone encapsulant, the current through the LEDs, and the green/red phosphor ratio were optimized for achieving high CRI and LER. Our re-designed LED PKG will find applications in stadium lighting as well as for ultra-high-definition television production where high CRI points are required for the artificial light source.
Mechanisms of molecular transport across oil-water interfaces covered by nonionic surfactants are investigated using coarse-grained molecular dynamics simulations. Resistance of the surfactant monolayer to the solute transport is shown to be controlled by dense regions in the monolayer. The dense regions are formed on both sides of the dividing surface and the barrier to the solute transport is created by those of them experiencing unfavorable interactions with the solute. Resistance to the transport of a hydrophobic (hydrophilic) solute increases with the excess density of the head (tail) group region of the monolayer, which in turn increases with the length of the surfactant head (tail) group. Barriers for solute transport through surfactant monolayers are also influenced by the solute size. However, the extent of this influence is determined by the monolayer thickness and the solute structure and composition. For example, it is shown that resistance offered by thin monolayers to transport of linear oligomers is relatively insensitive to the solute length. The barrier sensitivity to the length of these solutes increases with the monolayer thickness. In addition to the static barriers, the solute transport is shown to be affected by dynamic barriers due to a nonadiabatic coupling of the monolayer surface with the solute position and configuration. This coupling leads to deviations of the system dynamics from the minimum energy path. The deviations are most significant in the neighborhood of the static energy barrier, which effectively leads to an increase of the barrier for the solute transport.
The generation of renewable energy is a promising solution to counter the rapid increase in energy consumption. Nevertheless, the availability of renewable resources (e.g., wind, solar, and tidal) is non-continuous and temporary in nature, posing new demands for the production of next-generation large-scale energy storage devices. Because of their low cost, highly abundant raw materials, high safety, and environmental friendliness, aqueous rechargeable multivalent metal-ion batteries (AMMIBs) have recently garnered immense attention. However, several challenges hamper the development of AMMIBs, including their narrow electrochemical stability, poor ion diffusion kinetics, and electrode instability. Transition metal dichalcogenides (TMDs) have been extensively investigated for applications in energy storage devices because of their distinct chemical and physical properties. The wide interlayer distance of layered TMDs is an appealing property for ion diffusion and intercalation. This review focuses on the most recent advances in TMDs as cathode materials for aqueous rechargeable batteries based on multivalent charge carriers (Zn2+, Mg2+, and Al3+). Through this review, the key aspects of TMD materials for high-performance AMMIBs are highlighted. Furthermore, additional suggestions and strategies for the development of improved TMDs are discussed to inspire new research directions.
The adhesion behavior of perfluoropolyether (PFPE) on rough silica surfaces is investigated by steered molecular dynamics simulations. To reproduce bond breakage during sliding of PFPE, a dynamic bond breaking method is developed and applied to the PFPE−silica interface. Calculated results reveal that nanoscale roughness is a critical parameter that affects the adhesion strength due to the PFPE film thickness of 1 nm, and the adhesion strength also depends on the molecular density of PFPE on the silica surface. The effect of roughness amplitude, spacing, and molecular weight of PFPE are individually analyzed to find a key parameter for adhesion enhancement. Adhesion strength on a flat surface is highest and decreases with increasing roughness within the considered conditions. When R a = 17.5 Å, adhesion strength is 3 times lower than the flat surface, and vacant pores at the interface are observed, which implies a reduced molecular density of PFPE from 0.31 to 0.27 molecules/nm 2 . Increasing the roughness spacing removes vacant pores at the interface and hence, adhesion enhances up to 50% of the original interface. Decreased molecular weight is another way to increase surface density of PFPE, and the highest adhesion is observed with the lowest molecular weight of PFPE. Comparing the change of adhesion strength, both roughness amplitude and molecular weight are determined as key parameters for enhancing adhesion strength.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.