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Near-infrared (NIR) transparency windows have evoked considerable interest in biomedical thermal imaging owing to the superior tissue penetration and the high signal-to-noise ratio, allowing real-time temperature reading with nanometric spatial resolution. Here, we develop a multimode nonintrusive luminescent thermometer based on the YAlO (YAG):Cr/Ln (Ln = Ho, Er, Yb) phosphor, which covers three NIR biological transparency windows, enabling cross-checking readings with high sensitivity and a high penetration depth. Utilizing the energy transfer between lanthanide ions and transition-metal ions, the Cr/Ln-activated upconversion emissions provide ideal signals for ratiometric luminescent thermometry of the NIR-I mode. The phonon-assisted downshifting emissions of Er/Ho are used to construct the NIR-III/II mode, and the NIR-III mode is based on the thermal coupling between stark levels of I (Er). Three independent modes show distinct thermometric performance in different NIR transparency windows and temperature ranges, and the combination of the three modes is conducive to obtain more accurate temperature readings in a broad temperature range, which paves the way toward versatile luminescent thermometers.
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http://dx.doi.org/10.1021/acs.inorgchem.1c02311 | DOI Listing |
J Am Chem Soc
September 2025
Division of Chemistry and Chemical Engineering, Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, California 91125, United States.
Coherent electron spin states within paramagnetic molecules hold significant potential for microscopic quantum sensing. However, all-optical coherence measurements amenable to high spatial and temporal resolution under ambient conditions remain a significant challenge. Here we conduct room-temperature, picosecond time-resolved Faraday ellipticity/rotation (TRFE/R) measurements of the electron spin decoherence time in [IrBr].
View Article and Find Full Text PDFJ Chem Inf Model
September 2025
Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721-0041, United States.
The development of low-cost, high-performance materials with enhanced transparency in the long-wavelength infrared (LWIR) region (800-1250 cm/8-12.5 μm) is essential for advancing thermal imaging and sensing technologies. Traditional LWIR optics rely on costly inorganic materials, limiting their broader deployment.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Architecture, Southeast University, Nanjing, 210096, China.
Buildings are increasingly being conceived as dynamic systems that interact with their surroundings to optimize energy performance and enhance occupant comfort. This evolution in architectural thinking draws inspiration from biological systems, where the building envelope functions like a thermally responsive "skin" that can autonomously adjust its optical and thermal properties in response to environmental temperature changes. Among the many approaches developed for smart building envelopes, passive thermoresponsive spectral modulation systems have attracted growing interest due to their structural simplicity and low energy demand.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Department of Food Science and Agricultural Chemistry, McGill University, Quebec H9X 3V9, Canada.
Passive daytime radiative cooling (PDRC) offers a sustainable solution to global energy challenges by dissipating heat without energy input. However, conventional PDRC materials face trade-offs between biodegradability, color integration, optical transparency, and mechanical robustness. Herein, a biomimetic, structurally colored PDRC film fabricated via evaporation-induced self-assembly of cellulose nanocrystals (CNCs), betaine, and polyvinyl alcohol was developed.
View Article and Find Full Text PDFJ Mater Chem B
September 2025
The Avram and Stella Goldstein Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev, P.O.B. 653, Beer-Sheva 8410501, Israel.
The development of "smart" polymers capable of responding to physiologically relevant stimuli is essential for engineering dynamic sensing and actuation systems that leverage biological signals under specific (patho)physiological conditions. In this study, we present a general and versatile strategy to engineer novel stimuli-responsive behaviors in temperature-responsive protein-based polymers (PBPs) site-specific conjugation with self-immolative molecules. Specifically, we developed hydrogen peroxide (HO)- and β-galactosidase (β-gal)-responsive elastin-like polypeptides (ELPs) and resilin-like polypeptides (RLPs).
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