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Two‐dimensional (2D)‐halide perovskites have been enriched over recent years to offer remarkable features from diverse chemical structures and environmental stability endowed with exciting functionalities in photoelectric detectors and phosphorescence systems. However, the low conversion efficiency of singlet to triplet in 2D hybrid halide perovskites reduces phosphorescence lifetimes. In this study, the long persistent luminescence of 2D all‐inorganic perovskites with a self‐assembled 2D interlayer galleries structure is investigated. The results show that the decay time of the long persistent luminescence increases from 450 s to 600 s, and the luminescence color changes from cyan to orange, and the thermal stability of photoluminescence enhances dramatically after replacing Cd2+ by appropriate Mn2+ ions in 2D Cs2CdCl4 Ruddlesden‐Popper phase perovskites. Furthermore, diversified anti‐counterfeiting modes are fabricated to highlight the promising applications of Cs2CdCl4 perovskite systems with tunable persistent luminescence in advanced anti‐counterfeiting. Therefore, our studies provide a novel model for realizing tunable long persistent luminescence of perovskite with 2D self‐assembled layered structure for advanced anti‐counterfeiting.

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To decrease the eutrophication caused by nitrogen (N) and phosphorus (P) in water, magnesium-modified corn stalk biochar (MgB) was prepared under the synergistic impact of the multi-pyrolysis temperatures and Mg2+ contents for the co-adsorption of ammonium (NH4+-N) and phosphate (PO43−). The co-adsorption mechanism, slow-release performance and plant application of MgB were systematically studied. The results showed that pyrolysis temperatures (350–650 °C) and Mg2+(0–3.6 g/L) contents not only altered the physicochemical properties of biochar, but also significantly affected the adsorption efficacy of MgB. The adsorption of NH4+-N and PO43− was in accordance with Langmuir–Freundlich and pseudo-second-order kinetic models (Qmax = 37.72 and 73.29 mg/g, respectively). Based on the characteristics, adsorption kinetics and isotherms results, the adsorption mechanism was determined and found to mainly involve struvite precipitation, ion exchange, and surface precipitation or electrostatic attraction. Compared with the leaching performance of chemical fertilizers (CF), after adsorption of NH4+-N and PO43− (MgB-A), MgB had a more stable pH and lower conductivity. Leaching of NH4+-N and PO43− by MgB-A was controlled by both the diffusion mechanism and the dissolution rate of struvite and Mg-P. The excellent long-term slow-release performance and abundant Mg2+ of MgB-A promoted the growth of Zea mays L. and Lolium perenne L. Overall, this study suggested that MgB could realize a win–win outcome of struvite biochar-based fertiliser production and wastewater treatment.