The rapid photochemical conversion of materials from liquid to solid (i.e., curing) has enabled the fabrication of modern plastics used in microelectronics, dentistry, and medicine. However, industrialized photocurables remain restricted to unimolecular bond homolysis reactions (Type I photoinitiations) that are driven by high-energy UV light. This narrow mechanistic scope both challenges the production of high-resolution objects and restricts the materials that can be produced using emergent manufacturing technologies (e.g., 3D printing). Herein we develop a photosystem based on triplet-triplet annihilation upconversion (TTA-UC) that efficiently drives a Type I photocuring process using green light at low power density (<10 mW/cm) and in the presence of ambient oxygen. This system also exhibits a superlinear dependence of its cure depth on the light exposure intensity, which enhances spatial resolution. This enables for the first-time integration of TTA-UC in an inexpensive, rapid, and high-resolution manufacturing process, digital light processing (DLP) 3D printing. Moreover, relative to traditional Type I and Type II (photoredox) strategies, the present TTA-UC photoinitiation method results in improved cure depth confinement and resin shelf stability. This report provides a user-friendly avenue to utilize TTA-UC in ambient photochemical processes and paves the way toward fabrication of next-generation plastics with improved geometric precision and functionality.
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http://dx.doi.org/10.1021/acscentsci.3c01263 | DOI Listing |
Mater Adv
January 2025
Department of Materials Science and Metallurgy, University of Cambridge CB3 0FS UK
The ability to convert light to higher energies through triplet-triplet annihilation upconversion (TTA-UC) is attractive for a range of applications including solar energy harvesting, bioimaging and anti-counterfeiting. Practical applications require integration of the TTA-UC chromophores within a suitable host, which leads to a compromise between the high upconversion efficiencies achievable in liquids and the durability of solids. Herein, we present a series of methacrylate copolymers as TTA-UC hosts, in which the glass transition temperature ( ), and hence upconversion efficiency can be tuned by varying the co-monomer ratios (-hexyl methacrylate (HMA) and 2,2,2-trifluoroethyl methacrylate (TFEMA)).
View Article and Find Full Text PDFSmall
January 2025
College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310014, P. R. China.
Developing single-particle nanocomposite with aqueous-phase orthogonal multicolor phosphorescence or multimodal luminescence holds great significance for optical coding, anti-counterfeiting encryption, bioimaging, and biosensing. However, it faces challenges such as a limited range of emission wavelengths and difficulties in controlling the synthesis process. In this work, a conjugate structure manipulation integrated luminophor confinement strategy is proposed to prepare carbon dots@upconversion nanoparticles (CDs@UCNPs) featuring aqueous-phase orthogonal multicolor room-temperature phosphorescence-upconversion luminescence (RTP-UCL) through wet-chemical synthetic methods.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry, University of Illinois Chicago, Chicago, Illinois 60607, United States.
Donor-acceptor dyads are promising materials for improving triplet-sensitized photon upconversion due to faster intramolecular energy transfer (ET), which unfortunately competes with charge transfer (CT) dynamics. To circumvent the issue associated with CT, we propose a novel purely organic donor-acceptor dyad, where the CT character is confined within the donor moiety. In this work, we report the synthesis and characterization of a stable organic radical donor-triplet acceptor dyad () consisting of the acceptor perylene () linked to the donor (4--carbazolyl-2,6-dichlorophenyl)-bis(2,4,6-trichlorophenyl)methyl radical ().
View Article and Find Full Text PDFACS Nano
December 2024
Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada.
Pirquitasite AgZnSnS (AZTS) nanocrystals (NCs) are emergent, lead-free emissive materials in the coinage chalcogenide family with applications in optoelectronic technologies. Like many multinary nanomaterials, their phase-pure synthesis is complicated by the generation of impurities, e.g.
View Article and Find Full Text PDFChimia (Aarau)
December 2024
Dept. of Chemistry, Dept. of Physics and Astronomy, Dept. of Materials Science and Nanoengineering, Rice Advanced Materials Institute, Rice University, Houston, Texas 77005, USA.
Photon interconversion promises to alleviate thermalization losses for high energy photons and facilitates utilization of sub-bandgap photons - effectively enabling the optimal use of the entire solar spectrum. However, for solid-state device applications, the impact of intermolecular interactions on the energetic landscape underlying singlet fission and triplet-triplet annihilation upconversion cannot be neglected. In the following, the implications of molecular arrangement, intermolecular coupling strength and molecular orientation on the respective processes of solid-state singlet fission and triplet-triplet annihilation are discussed.
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