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The manipulation of excitation modes and resultant emission colors in luminescent materials holds pivotal importance for encrypting information in anti-counterfeiting applications. Despite considerable achievements in multimodal and multicolor luminescent materials, existing options generally suffer from static monocolor emission under fixed external stimulation, rendering them vulnerability to replication. Achieving dynamic multimodal luminescence within a single material presents a promising yet challenging solution. Here, we report the development of a phosphor exhibiting dynamic multicolor photoluminescence (PL) and photo-thermo-mechanically responsive multimodal emissions through the incorporation of trace Mn ions into a self-activated CaGaO host. The resulting phosphor offers adjustable emission-color changing rates, controllable via re-excitation intervals and photoexcitation powers. Additionally, it demonstrates temperature-induced color reversal and anti-thermal-quenched emission, alongside reproducible elastic mechanoluminescence (ML) characterized by high mechanical durability. Theoretical calculations elucidate electron transfer pathways dominated by intrinsic interstitial defects and vacancies for dynamic multicolor emission. Mn dopants serve a dual role in stabilizing nearby defects and introducing additional defect levels, enabling flexible multi-responsive luminescence. This developed phosphor facilitates evolutionary color/pattern displays in both temporal and spatial dimensions using readily available tools, offering significant promise for dynamic anticounterfeiting displays and multimode sensing applications.
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http://dx.doi.org/10.1038/s41467-024-47431-0 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing 100029, China.
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Recent quest for emulating lifelike smart materials for developing functional outcomes has been spurred by the unparalleled spatiotemporal control of natural systems. However, it is still highly challenging to replicate the progressive time-dependent programmable features of biological systems, such as adaptive broad-spectrum luminescence accompanying functions. Here in, a chemically-fueled transient hydrogel is created based on an aggregation-induced emission-active peptide conjugate (NI-VD).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, China.
All inorganic lead halide perovskite (CsPbX) has become a hot topic in chiral optics for its high quantum yield and tunable luminescence. The environmental degradation tendency and lack of magneto-optical coupling mechanism of lead-based perovskite severely restrict its chirality integrated application. Rare-earth ions (such as Gd, Eu), with their unique 4f electronic configuration, not only passivate the lattice defects to improve stability but also expand the spectral response range through electronic localization effects.
View Article and Find Full Text PDFNanoscale Adv
August 2025
Research Center for Applied Sciences (RCAS), Academia Sinica Taipei 11529 Taiwan
We demonstrate a dual-colored light-emitting device using 2D semiconductors by modulating AC carrier injection through independent electrodes with phase delay, enabling balanced emission from WSe and WS monolayers. This innovative approach allows balanced, dynamically controllable, and spectrally stable emissions from WSe and WS monolayers, significantly enhancing emission control and expanding possibilities in advanced multicolor optoelectronic applications, including integrated photonic circuits and high-resolution display technologies.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Tianjin Key Laboratory of Chemical Process Safety, Hebei Key Laboratory of Functional Polymers, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin, 300401, P. R. China.
Achieving multi-color tunable time-dependent afterglow color (TDAC) in pure organic materials under visible light excitation remains a significant challenge. Herein, TDAC composites (CDs/U) are prepared with multi-color tunability upon visible-light excitation. Furthermore, the TDAC mechanism is the coexistence of shorter-lived afterglow and longer-lived afterglow.
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