The near-infrared (NIR) light source is desirable for realtime nondestructive examination applications, which include the analysis of foodstuffs, health monitoring, iris recognition, and infrared cameras. The emission spectra of such an infrared light source should also be as broad as possible for effective performance, in view of the fact that the broad absorption and reflection of light by the organic elements present in foodstuffs and human health fall in the blue and NIR regions of the electromagnetic spectrum, respectively. In this letter, a blue light-emitting diode (LED) excitable super broadband NIR phosphor light source is developed with a high fwhm of 330 nm and radiant flux of 18.2 mW for the first time. The observation of superbroad-band luminescence from two distinct luminescence centers is studied and evidenced by electron paramagnetic resonance, X-ray absorption near-edge structure, steady-state luminescence, and timeresolved luminescence at ambient and high-pressure environments. Finally, the luminescence mechanism is discussed with the relevant configurational coordinate diagrams.

Spinel LiNi0.5Mn1.5O4 (LNMO) is a promising cathode candidate for the next‐generation high energy‐density lithium‐ion batteries (LIBs). Unfortunately, the application of LNMO is hindered by its poor cycle stability. Now, site‐selectively doped LNMO electrode is prepared with exceptional durability. In this work, Mg is selectively doped onto both tetrahedral (8a) and octahedral (16c) sites in the Fdtrue3‾ m structure. This site‐selective doping not only suppresses unfavorable two‐phase reactions and stabilizes the LNMO structure against structural deformation, but also mitigates the dissolution of Mn during cycling. Mg‐doped LNMOs exhibit extraordinarily stable electrochemical performance in both half‐cells and prototype full‐batteries with novel TiNb2O7 counter‐electrodes. This work pioneers an atomic‐doping engineering strategy for electrode materials that could be extended to other energy materials to create high‐performance devices.

Recently, infrared (IR) light-emitting diodes (LEDs) have attracted considerable interest in the research field worldwide. IR phosphors, the basic materials utilized in LEDs, have become a research hotspot as well. Here, we introduce the high-quantum-efficiency IR ScBO 3 :Cr 3+ phosphor, which provides a spectral range of emission from 700 to 1000 nm with a peak maximum at 800 nm. Electron paramagnetic resonance spectroscopy, with high element selectivity, was used to elucidate the unusual small peak in the photoluminescence spectrum. Phonon structure and electron−lattice interaction were well observed and discussed via temperature-dependent measurements. Moreover, the high quantum efficiency of 72.8% was achieved. To evaluate their potential practical application, phosphor-converted LED packages were designed, which revealed high stability and high output power of 39.11 mW. Furthermore, the fabricated IR LED demonstrated a remarkable ability to penetrate biological tissues. This study provides insights into the luminescent properties and the practical applications of IR LEDs.

We aim to conduct a complete study on the unexpected structure evolution behavior in Cr 3+ -doped phosphors. A series of Ga 2−x Sc x O 3 :Cr 3+ phosphors are successfully synthesized and confirmed through structural studies, while the lattice parameters change unexpectedly. The unique partial substitution (∼87%) of Sc 3+ in the octahedral site is demonstrated via Rietveld refinement. Therefore, the bond valence sum calculation explains the reason for this particular Sc 3+ concentration. The photoluminescent bandwidth and electron−lattice coupling energy initially increase and then decrease, implying an inhomogeneous broadening effect. Time-resolved spectra and electron paramagnetic resonance are utilized to further examine the subtle change in the microstructures and the second coordination sphere effect of Cr 3+ . Ga 1.594 Sc 0.4 O 3 :0.006Cr 3+ exhibits high internal quantum efficiency (99%) and high phosphor-converted light-emitting diode output power (66.09 mW), demonstrating its capability as an outstanding infrared phosphor. This work will motivate further research on unexpected partial substitution during the solid solution process.

Portable near-infrared (NIR) light sources are in high demand for applications in spectroscopy, night vision, bioimaging, and many others. Typical phosphor designs feature isolated Cr 3+ ion centers, and it is challenging to design broadband NIR phosphors based on Cr 3+ −Cr 3+ pairs. Here, we explore the solidsolution series SrAl 11.88−x Ga x O 19 :0.12Cr 3+ (x = 0, 2, 4, 6, 8, 10, and 12) as phosphors featuring Cr 3+ −Cr 3+ pairs and evaluate structure−property relations within the series. We establish the incorporation of Ga within the magentoplumbite-type structure at five distinct crystallographic sites and evaluate the effect of this incorporation on the Cr 3+ −Cr 3+ ion pair proximity. Electron paramagnetic measurements reveal the presence of both isolated Cr 3+ and Cr 3+ − Cr 3+ pairs, resulting in NIR luminescence at approximately 650−1050 nm. Unexpectedly, the origin of broadband NIR luminescence with a peak within the range 740−820 nm is related to the Cr 3+ −Cr 3+ ion pair. We demonstrate the application of the SrAl 5.88 Ga 6 O 19 :0.12Cr 3+ phosphor, which possesses an internal quantum efficiency of ∼85%, a radiant flux of ∼95 mW, and zero thermal quenching up to 500 K. This work provides a further understanding of spectral shifts in phosphor solid solutions and in particular the application of the magentoplumbites as promising next-generation NIR phosphor host systems.