UbiQD (United States)

Core/shell nanostructures of type I and type II band-offset materials have been pivotal in improving photoluminescence and imparting charge separation in well-established colloidal quantum dots. In addition to these features, the multishell motif provides a simple means to expand the emission spectral range and spatially fine-tune electron and hole wave functions. Here, we explore the CdSe/CdTe/CdSe core/shell/shell structure with a total diameter of ≲7 nm, within the practical limits of readily accessible synthesis capabilities. Systematic variations of the dimensions of the core and the shells are carried out to examine how each of these structural parameters affects optical properties. Emission in the red to near-infrared range from 677 to 1057 nm (1.83 to 1.17 eV), photoluminescence quantum yields of up to 88%, and line widths as narrow as 109 meV (41.8 nm for the peak position of 677 nm) are achieved. Even with a total size limit of ∼7 nm with an ∼1 nm thick CdTe shell, the reddest emission energy can approach the expected energy separation between the bulk CdSe conduction band edge and CdTe valence band edge to within tens of millielectronvolts. Comparison to simple effective mass approximation provides insights and guidelines on achieving independent control over the effective band gap and the electron-hole overlap.

The major challenges in designing a Hybrid Renewable Energy System (HRES) include selecting appropriate renewable energy sources and storage systems, accurately sizing each component, and defining suitable optimization criteria. This study addresses these challenges by employing Particle Swarm Optimization (PSO) within a multi-criteria optimization framework to design an HRES in Kern County, USA. The proposed system integrates wind turbines (WTS), photovoltaic (PV) panels, Biomass Gasifiers (BMGs), batteries, electrolyzers (ELs), and fuel cells (FCs), aiming to minimize Annual System Cost (ASC), minimize Loss of Power Supply Probability (LPSP), and maximize renewable energy fraction (REF). Results demonstrate that the PSO-optimized system achieves an ASC of USD6,336,303, an LPSP of 0.01%, and a REF of 90.01%, all of which are reached after 25 iterations. When compared to the Genetic Algorithm (GA) and hybrid GA-PSO, PSO improved cost-effectiveness by 3.4% over GA and reduced ASC by 1.09% compared to GAPSO. In terms of REF, PSO outperformed GA by 1.22% and GAPSO by 0.99%. The PSO-optimized configuration includes WT (4669 kW), solar PV (10,623 kW), BMG (2174 kW), battery (8000 kWh), FC (2305 kW), and EL (6806 kW). Sensitivity analysis highlights the flexibility of the optimization framework under varying weight distributions. These results highlight the dependability, cost-effectiveness, and sustainability for the proposed system, offering valuable insights for policymakers and practitioners transitioning to renewable energy systems.

Abstract Bioregenerative life-support systems (BLSS) involving plants will be required to realize self-sustaining human settlements beyond Earth. To improve plant photosynthetic efficiency in BLSS, the quality of the solar spectrum can be modified by lightweight, luminescent films. CuInS2/ZnS quantum dot (QD) films with peak emissions at 600 and 660 nm were used to redshift ultraviolet and blue photons to increase biomass accumulation in red romaine lettuce. Plant growth parameters, except spectral quality, were held constant among three equivalent production environments. Lettuce grown under the 600 and 660 nm-emitting QD films respectively increased edible dry mass (13% and 9%), edible fresh mass (11% each), and total leaf area (8% and 13%) compared to under a control film that contained no QDs. Spectral modifications by the luminescent QD films improved photosynthetic efficiency in lettuce and could enhance crop productivity in greenhouses on Earth or in space, where further improvements are expected from greater availability of ultraviolet photons for conversion.

CuInS2 (CIS) quantum dots (QDs) have emerged as one of the most promising candidates for application in a number of new technologies, mostly due to their heavy-metal-free composition and their unique optical properties. Among those, the large Stokes shift and the long-lived excited state are the most striking ones. Although these properties are important, the physical mechanism that originates them is still under debate. Here, we use two-photon absorption spectroscopy and ultrafast dynamics studies to investigate the physical origin of those phenomena. From the two-photon absorption spectroscopy, we observe yet another unique property of CIS QDs, a two-photon absorption transition below the one-photon absorption band edge, which has never been observed before for any other semiconductor nanostructure. This originates from the inversion of the 1S and 1P hole level order at the top of the valence band and results in a blue-shift of the experimentally measured one photon absorption edge by nearly 100 to 200 meV. However, this shift is not large enough to account for the Stokes shift observed, 200-500 meV. Consequently, despite the existence of the below band gap optical transition, photoluminescence in CIS QDs must originate from trap sites. These conclusions are reinforced by the multiexciton dynamics studies. From those, we demonstrate that biexciton Auger recombination behaves similarly to negative trion dynamics on these nanomaterials, which suggests that the trap state is an electron donating site.

Building-integrated sunlight harvesting utilizing laminated glass luminescent solar concentrators (LSCs) is proposed. By incorporating high quantum yield (>90%), NIR-emitting CuInS2/ZnS quantum dots into the polymer interlayer between two sheets of low-iron float glass, a record optical efficiency of 8.1% is demonstrated for a 10 cm × 10 cm device that transmits ∼44% visible light. After completing prototypes by attaching silicon solar cells along the perimeter of the device, the electrical power conversion efficiency was certified at 2.2% with a black background and at 2.9% using a reflective substrate. This “drop-in” LSC solution is particularly attractive because it fits within the existing glazing industry value chain with only modest changes to typical glazing products. Performance modeling predicts >1 GWh annual electricity production for a typical urban skyscraper in most major U.S. cities, enabling significant energy cost savings and potentially “net-zero” buildings.

Luminescent solar concentrators serving as semitransparent photovoltaic windows could become an important element in net zero energy consumption buildings of the future. Colloidal quantum dots are promising materials for luminescent solar concentrators as they can be engineered to provide the large Stokes shift necessary for suppressing reabsorption losses in large-area devices. Existing Stokes-shift-engineered quantum dots allow for only partial coverage of the solar spectrum, which limits their light-harvesting ability and leads to colouring of the luminescent solar concentrators, complicating their use in architecture. Here, we use quantum dots of ternary I-III-VI2 semiconductors to realize the first large-area quantum dot-luminescent solar concentrators free of toxic elements, with reduced reabsorption and extended coverage of the solar spectrum. By incorporating CuInSexS2-x quantum dots into photo-polymerized poly(lauryl methacrylate), we obtain freestanding, colourless slabs that introduce no distortion to perceived colours and are thus well suited for the realization of photovoltaic windows. Thanks to the suppressed reabsorption and high emission efficiencies of the quantum dots, we achieve an optical power efficiency of 3.2%. Ultrafast spectroscopy studies suggest that the Stokes-shifted emission involves a conduction-band electron and a hole residing in an intragap state associated with a native defect.