The discovery of highly efficient broadband near infrared (NIR) emission material is urgent and crucial for constructing NIR lighting sources and emerging applications. Herein, a series of NIR emission hexafluorides A2BMF6:Cr3+ (A = Na, K, Rb, Cs; B = Li, Na, K, Cs; M = Al, Ga, Sc, In) peaking at ≈733–801 nm with a full width at half maximum (FWHM) of ≈98–115 nm are synthesized by a general ammonium salt assisted synthesis strategy. Benefiting from the pre‐ammoniation of the trivalent metal sources, the Cr3+ can be more efficiently doped into the A2BMF6 and simultaneously prevent the generation of the competitive phase. Particularly, Na3ScF6:Cr3+ (λem = 774 nm, FWHM ≈ 108 nm) with optimal Cr3+‐doping concentration of 35.96% shows a high internal quantum efficiency of 91.5% and an external quantum efficiency of ≈40.82%. A lighting emitting diode (LED) device with a NIR output power of ≈291.05 mW at 100 mA driven current and high photoelectric conversion efficiency of 20.94% is fabricated. The general synthesis strategy opens up new avenues for the exploration of Cr3+‐doped high efficiency phosphors, and the as‐obtained record NIR output power demonstrates for NIR LED lighting sources applications.

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Mechanoluminescence (ML) materials, which can emit light under external mechanical stimuli, have aroused wide concern in diverse applications such as stress sensing, anti-counterfeiting and 3D signature. However, MLs located within...

Mechanoluminescent (ML) materials have shown promising prospects for various applications, e.g in stress sensing, information anti-counterfeiting and bio stress imaging fields. However, the development of the trap-controlled ML materials is...

Mechanoluminescence (ML) materials, which can emit light under external mechanical stimuli, have attracted wide attention in diverse applications such as display, anti-counterfeiting and 3D signature. However, weak ML intensity and...

Mechanical luminescence (ML) is the conversion of mechanical energy into light energy when a material is subjected to a force. It is challenging to develop ML materials with tunable luminescent properties by single ion doping, which have broad application prospects in the fields of stress sensing and dynamic signature anticounterfeiting. In this study, a Pr3+ doped Sr2Ga2GeO7 tunable ML material is reported. Due to the traps resulting from unequal substitution of Pr3+–Sr2+ in [SrO6] heptahedra, the deep/shallow traps redistribution occurs towards a multicolor ML from red to green. In addition, even after continuous friction sliding force (15 N), the ML intensities can be recovered after ultraviolet pre‐irradiation, indicating that Sr2Ga2GeO7: Pr3+ has excellent ML emission stability. Based on thermoluminescence analysis, potential PersL and ML mechanisms are further elaborated by a lattice engineering (trap regulation) strategy. In all, the development of single‐ion doped multicolor ML materials may have crucial research value and show a variety of potential applications in the fields of anticounterfeiting and information encryption.

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