Opportunities for enhancing solar energy harvesting using photon upconversion are reviewed. The increasing prominence of bifacial solar cells is an enabling factor for the implementation of upconversion, however, when the realistic constraints of current best-performing silicon devices are considered, many challenges remain before silicon photovoltaics operating under nonconcentrated sunlight can be enhanced via lanthanide-based upconversion. A photophysical model reveals that >1–2 orders of magnitude increase in the intermediate state lifetime, energy transfer rate, or generation rate would be needed before such solar upconversion could start to become efficient. Methods to increase the generation rate such as the use of cosensitizers to expand the absorption range and the use of plasmonics or photonic structures are reviewed. The opportunities and challenges for these approaches (or combinations thereof) to achieve efficient solar upconversion are discussed. The opportunity for enhancing the performance of technologies such as luminescent solar concentrators by combining upconversion together with micro-optics is also reviewed. Triplet–triplet annihilation-based upconversion is progressing steadily toward being relevant to lower-bandgap solar cells. Looking toward photocatalysis, photophysical modeling indicates that current blue-to-ultraviolet lanthanide upconversion systems are very inefficient. However, hope remains in this direction for organic upconversion enhancing the performance of visible-light-active photocatalysts.
The production of upconverting nanostructures with tailored optical properties is of major technological interest, and rapid progress toward the realization of such production has been made in recent years. Ultimately, accurate understanding of nanostructure organization will lead to design rules for accurately tailoring optical properties. Here, the context of open questions still of general importance to the upconversion and nanocrystal communities is presented, with a particular emphasis on the structure–property relationships of core–shell upconverting nanocrystals. Although the optical properties of the latter have been thoroughly investigated, little is known regarding their atomic‐scale organization. Indeed, solving the atomic‐scale structure of such nanomaterials is challenging because of their intrinsic nonperiodic nature. Familiar concepts of crystallography are no longer appropriate; chemical and structural modulation waves must be introduced. To reveal the exact core–shell structures, innovative characterization techniques need to be applied and developed, as discussed herein. The continued development and application of structural characterization techniques will be vital to consolidate the currently incomplete link between atomic‐scale structure and upconversion properties. This will ultimately provide a valuable contribution to the emerging detailed guidelines on how to better design upconverting nanostructures to achieve given optical properties in terms of efficiency, absorption, spectral emission, and dynamics.
The world's plastic production reached 269 million tons p.a. in 2015. The EU fraction of this was 50 million tons, with 40% of this attributed to product packaging. [1] Even though packaging exhibits the highest recycling rate for any plastic product, this recycling rate in the EU is less than 40%. [1,2] Overall, 29.7% of the plastic within the EU was recycled, with the remainder either burnt for energy recovery (39.5%) or dumped in landfills (30.8%). Recently adopted EU legislative proposals on waste management put pressure on the industry to find solutionsThe demand for more efficient and complete sorting techniques for plastic waste is growing, and one possible solution isbased on fluorescent labeling. Novel fluorescent labels based on trivalent lanthanide (Ln 3+ ) activated inorganic up-conversion (UC) materials offer a promising technological solution for plastic recycling. UC is a nonlinear, anti-Stokes process of combining two or more low energy near-infrared (NIR) photons to obtain the emission of a single higher energy photon. While Ln 3+ based UC materials possess one key disadvantage -low quantum yield, they also exhibit many unique features, such as high signal/noise ratio, tailored emission color, long photoluminescent lifetime, and low toxicity. These unique features endear them for a diverse range of applications and offer many new opportunities. Herein, we review the recent advances in the Ln 3+ activated inorganic micro-sized UC materials from the perspective of tailoring UC emission color and intensity for plastic recycling applications.
In photon upconversion (UC) based on triplet−triplet annihilation, the upconversion photoluminescent quantum yield (UC-PLQY) depends on the excitation power density in a way that can be described by a single figure of merit. This figure of merit, the threshold value, allows the excitation power density required for efficient UC-PLQY to be compared between different triplet−triplet annihilation systems. Here, we investigate the excitation power density dependence of two-photon UC processes in a series of four lanthanide-doped inorganic host materials (oxides, fluorides, and chlorides) all doped with 18 mol % Yb 3+ sensitizer ions and 2 mol % Er 3+ activator ions. We demonstrate that an analogous figure of merit, which we call the critical power density (CPD), accurately describes the UC power dependence of these samples. Better CPD values are obtained when the lifetime of the intermediate states is long. The UC-PLQY at the CPD is linked to the saturation UC-PLQY. Thus, a measurement of the UC-PLQY at this low power density can be used to estimate the theoretical saturation UC-PLQY in the absence of deleterious effects such as laser-induced heating. This is compared to another method to estimate the saturation based on the CPD model, namely, taking half of the level's PLQY under direct excitation. Our careful analysis of the upconversion spectra as a function of excitation power density gives several insights into the differing upconversion pathways in the hosts and proves to be a useful tool for their comparison.
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.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.