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      Revealing the Intrinsic Decay of Mechanoluminescence for Achieving Ultrafast‐Response Stress Sensing

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          Abstract

          Converting mechanical energy into photon emission provides a promising route for intelligent sensing, self‐powered lighting, and distributed energy harvesting, which is of great significance for finding a feasible solution to the current sensing technical bottleneck and energy crisis. As the basis for understanding the conversion mechanism and realizing high‐frequency mechanical energy utilization, elucidating the dynamic process of intensity variation in the mechano‐to‐photon conversion remains a great challenge. Herein, a time‐domain characterization scheme that enables to unravel the intrinsic decay of mechanoluminescence (ML) with lifetimes from milliseconds down to tens of microseconds is constructed. It is demonstrated that ML decay characterization is an important tool to reveal the dynamics of charge migration in ML materials. The ML decay in a typical self‐reproducible ML material ZnS:Mn 2+ shows temperature dependence and stress fluctuation resistance, which opens up a new reliable approach for self‐powered and remote temperature sensing. Finally, benefiting from the shortest ML lifetime recorded to date, an ultrafast‐response stress sensor that enables to detect individual pulses of ultrasonic waves with ML sensing technology is developed.

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          Maximizing and stabilizing luminescence from halide perovskites with potassium passivation

          Metal halide perovskites are of great interest for various high-performance optoelectronic applications. The ability to tune the perovskite bandgap continuously by modifying the chemical composition opens up applications for perovskites as coloured emitters, in building-integrated photovoltaics, and as components of tandem photovoltaics to increase the power conversion efficiency. Nevertheless, performance is limited by non-radiative losses, with luminescence yields in state-of-the-art perovskite solar cells still far from 100 per cent under standard solar illumination conditions. Furthermore, in mixed halide perovskite systems designed for continuous bandgap tunability (bandgaps of approximately 1.7 to 1.9 electronvolts), photoinduced ion segregation leads to bandgap instabilities. Here we demonstrate substantial mitigation of both non-radiative losses and photoinduced ion migration in perovskite films and interfaces by decorating the surfaces and grain boundaries with passivating potassium halide layers. We demonstrate external photoluminescence quantum yields of 66 per cent, which translate to internal yields that exceed 95 per cent. The high luminescence yields are achieved while maintaining high mobilities of more than 40 square centimetres per volt per second, providing the elusive combination of both high luminescence and excellent charge transport. When interfaced with electrodes in a solar cell device stack, the external luminescence yield-a quantity that must be maximized to obtain high efficiency-remains as high as 15 per cent, indicating very clean interfaces. We also demonstrate the inhibition of transient photoinduced ion-migration processes across a wide range of mixed halide perovskite bandgaps in materials that exhibit bandgap instabilities when unpassivated. We validate these results in fully operating solar cells. Our work represents an important advance in the construction of tunable metal halide perovskite films and interfaces that can approach the efficiency limits in tandem solar cells, coloured-light-emitting diodes and other optoelectronic applications.
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            Fluorescence lifetime measurements and biological imaging.

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              Long-Lived Emissive Probes for Time-Resolved Photoluminescence Bioimaging and Biosensing

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Advanced Functional Materials
                Adv Funct Materials
                Wiley
                1616-301X
                1616-3028
                July 08 2023
                Affiliations
                [1 ] State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Provincial Key Laboratory of Materials Genome and College of Materials Xiamen University Simingnan‐Road 422 Xiamen 361005 China
                [2 ] iRay Technology Company Limited Shanghai 201206 China
                [3 ] iRay Technology (Taicang) Limited Taicang 215434 China
                [4 ] College of Physics and Optoelectronic Engineering Shenzhen University Shenzhen 518060 China
                [5 ] International Center for Young Scientists (ICYS) National Institute for Materials Science (NIMS) Tsukuba 305‐0044 Japan
                Article
                10.1002/adfm.202304917
                665bdd33-97ac-45f6-a970-4cc2e01ff5d3
                © 2023

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