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      Highly efficient near-infrared phosphor LaMgGa 11O 19:Cr 3+

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          Abstract

          LaMgGa 11O 19:Cr 3+ phosphor was synthesized successfully, showing broadband NIR emission centered at ∼770 nm, high efficiency and excellent thermal quenching resistance for pc-LEDs.

          Abstract

          Near-infrared (NIR) phosphor-converted light-emitting diodes (pc-LEDs) are desirable for in vivo imaging and applications for nondestructive examination in the food industry. Accordingly, it is very important to exploit highly efficient and stable broad-band NIR phosphors. Herein we report a Cr 3+-activated LaMgGa 11O 19 phosphor via a simple solid-state reaction, showing broad-band emission centered at 770 nm with internal/external quantum efficiency of 82.6%/42.5%. There are three six-coordinated octahedral crystallographic sites in the structure for Cr 3+ occupancy, and changing the Cr 3+ concentration can tune the NIR emission with tunable band centers from 715 to 800 nm. This spectral red-shift is mainly ascribed to energy transfer among multiple Cr 3+ sites, which is further confirmed by decay lifetime analysis. The phosphor also shows excellent luminescence thermal stability, and the photoluminescence intensity at 410 K maintains 87% of that at room temperature. Our work provides a novel broadband NIR emission phosphor with high efficiency and excellent thermal quenching resistance for the field of NIR spectroscopy.

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          Sunlight-activated long-persistent luminescence in the near-infrared from Cr(3+)-doped zinc gallogermanates.

          Visible-light persistent phosphors are being widely used as self-sustained night-vision materials because of their sufficiently strong and long afterglow (>10 h) and their ability to be excited by sunlight as well as room light. In contrast, persistent phosphors for near-infrared (NIR) wavelengths are lacking. Here we report a series of Cr(3+)-doped zinc gallogermanate NIR persistent phosphors that exhibit strong emission at 650-1,000 nm, extending beyond the typical 690-750 nm, and with a super-long afterglow of more than 360 h. These new NIR persistent phosphors are all-weather materials that can be rapidly, effectively and repeatedly charged by natural sunlight in almost all kinds of outdoor environment. Seconds to minutes of sunlight activation can result in more than two weeks of persistent NIR light emission. This new series of NIR persistent materials have potential applications in night-vision surveillance, solar energy utilization and in vivo bio-imaging.
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            High contrast in vitro and in vivo photoluminescence bioimaging using near infrared to near infrared up-conversion in Tm3+ and Yb3+ doped fluoride nanophosphors.

            A new approach for photoluminescence imaging in vitro and in vivo has been shown utilizing near infrared to near infrared (NIR-to-NIR) up-conversion in nanophosphors. This NIR-to-NIR up-conversion process provides deeper light penetration into biological specimen and results in high contrast optical imaging due to absence of an autofluorescence background and decreased light scattering. Aqueous dispersible fluoride (NaYF4) nanocrystals (20-30 nm size) co-doped with the rare earth ions, Tm(3+) and Yb(3+), were synthesized and characterized by TEM, XRD, and photoluminescence (PL) spectroscopy. In vitro cellular uptake was shown by the PL microscopy visualizing the characteristic emission of Tm(3+) at approximately 800 nm excited with 975 nm. No apparent cytotoxicity was observed. Subsequent animal imaging studies were performed using Balb-c mice injected intravenously with up-converting nanophosphors, demonstrating the high contrast PL imaging in vivo.
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              WinPLOTR: A Windows Tool for Powder Diffraction Pattern Analysis

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                Author and article information

                Contributors
                Journal
                ICFNAW
                Inorganic Chemistry Frontiers
                Inorg. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1553
                March 17 2020
                2020
                : 7
                : 6
                : 1467-1473
                Affiliations
                [1 ]The Beijing Municipal Key Laboratory of New Energy Materials and Technologies
                [2 ]School of Materials Sciences and Engineering
                [3 ]University of Science and Technology Beijing
                [4 ]Beijing 100083
                [5 ]China
                Article
                10.1039/D0QI00063A
                db583d1c-c038-463d-9bb1-7aa432b6aae2
                © 2020

                http://rsc.li/journals-terms-of-use

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