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Self‐recoverable mechanoluminescence (ML) is becoming a novel technology widely used in the fields of sensing, display, and artificial intelligence. The dominant ML material, ZnS: Mn2+, is reported to solely present a yellow emission color, which limits the applications of self‐recoverable ML materials to a large extent. Herein, an effective strategy to extend the ML emission range of ZnS: Mn2+ by the ferromagnetic coupling of Mn2+ ions are reported. Under the thermal carbon‐reduction atmosphere (TCRA), the emission ranges of ML, photoluminescence (PL), and persistent luminescence spectra of ZnS: Mn2+ phosphors are all successfully broadened from yellow to red. Furthermore, as for the PL and ML intensities of ZnS: Mn2+, they are intensified to 1.76 and 3.23 folds larger under the TCRA treatment than those in pure nitrogen, respectively. Various spectra and magnetic test results reveal that the red emission bands of ZnS: Mn2+ @TCRA phosphors originate from the ferromagnetic coupling of Mn2+ ions. This study is the first to realize strong red emission and tunable multicolor luminescence in the conventional ZnS‐based phosphors, which introduces opportunities for discovering the multiband emissions of Mn2+ ion in other compounds. Brightly multicolored ZnS: xMn2+ @TCRA elastic films have been fabricated to demonstrate their anti‐counterfeiting and security applications. [ABSTRACT FROM AUTHOR]

Promoting the interfacial Li+ transport and suppressing detrimental lithium dendrites are the main challenges for developing practical solid‐state lithium metal batteries. In this respect, interface rationalizing to synergize the enhancement of ion transport and suppression of lithium dendrites is of paramount significance. Herein, a novel strategy is demonstrated to address those issues by a designed multifunctional composite interlayer. The photocrosslinkable polymer is introduced in a scalable elastic skeleton, which promotes the migration and diffusion of Li+. Moreover, adding perfluoropolyether in the interlayer benefits to regulating the formation of LiF‐rich interface, sufficiently suppress the growth of lithium dendrites. Benefitting from the elasticity, high Li+ conductivity and the lithium dendrites suppression capability, the interlayer can significantly improve the interfacial performance of the solid electrolyte/lithium interface, thus leading to the greatly enhanced electrochemical performance of solid‐state lithium metal batteries. A high critical current density of 3.6 mA cm−2 and a long cycling life at 1.0 mA cm−2 for >400 h are achieved for the symmetric cells. Besides, when used in a pouch‐type full cell coupled with LiNi0.6Co0.2Mn0.2O2 cathode, a high charged capacity of 3.25 mAh cm−2 can be maintained through 20 cycles, demonstrating its great potentials for practical application. [ABSTRACT FROM AUTHOR]

Mechanoluminescence (ML), as an optical response to deformation stimuli, shows great potential in high‐end stress sensing, ultrasonic field visualization, and multidimensional anti‐counterfeiting. However, processive practical applications in bio‐medicine are constrained by the discovery of near‐infrared (NIR) ML materials. Unlike lanthanides (Ln3+) with sharp multiplets, two kinds of Cr3+‐doped NIR ML materials, gallate spinel (ZnGa2O4:Cr3+, Zn3Ga2GeO8:Cr3+) and gallate magnetoplumbite (SrGa12O19:Cr3+) are here reported. Owing to the intrinsic cation antisite defects and cation vacancies in the matrix, these materials exhibit bright NIR ML under a relatively low load (20 N). In particular for SrGa12O19:Cr3+ (750 nm, peak; 100 nm, FWHM) with low persistent luminescence (PersL) interference, the ML behavior can be further rejuvenated under UV and sunlight irradiation. SrGa12O19:Cr3+ also shows bright NIR emission under photo‐ and thermo‐stimulation. Owing to their excellent tissue penetration and concealment capability, NIR ML materials show great potential in the fields of bio‐medicine and anti‐counterfeiting. [ABSTRACT FROM AUTHOR]

Solid‐state batteries (SSBs) promise high energy density and strong safety due to using nonflammable solid‐state electrolytes (SSEs) and high‐capacity Li metal anode. Ta‐substituted Li7La3Zr2O12 (LLZT) SSE possesses superior ionic conductivity and stability with Li metal, yet the interfacial compatibility and lithium dendrite hazards still hinder its applications. Herein, an interfacial engineering is demonstrated by facile acid‐salt (AS) treatment on LLZT, constructing a 3D cross‐linking LiF‐LiCl (CF) network. Such structure facilitates Li wetting via capillary permeation. Notably, CF as electronically insulting phases block the electrons through the interface and ulteriorly suppress the dendrite formation. The assembled Li symmetric cell exhibited a low interfacial impedance (11.6 Ω cm2) and high critical current densities (CCDs) in the time‐constant mode, 1.8 mA cm−2 at 25 °C and 3.6 mA cm−2 at 60 °C, respectively. Meanwhile, by exploring the capacity‐constant mode of CCD measurement, the concept of critical areal capacity (CAC) is first proposed, obtaining its values of ≈0.5 mAh cm−2 at 25 °C and 1.2 mAh cm−2 at 60 °C. Moreover, the safety‐enhanced hybrid SSBs matched with LiFePO4 and LiNi0.6Co0.2Mn0.2O2 deliver a remarkable rate and cycling performances, validating the feasibility of this interfacial engineering in various SSB systems. [ABSTRACT FROM AUTHOR]