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Research on the core-shell design of rare earth-doped nanoparticles has recently gained significant attention, particularly in exploring the synergistic effects of combining active and inert shell layers. In this study, we successfully synthesized 8 types of spherical core-shell Na-based nanoparticles to enhance the efficiency of core-shell design in upconversion luminescence and temperature sensing through the strategic arrangement of inert and active layers. The most effective upconversion luminescence was observed under 980 nm and 808 nm laser excitation using NaYF inert shell NaYF:Yb, Er@ NaYF and NaYF@ NaYF4:Yb, Nd core-shell nanostructures. Moreover, the incorporation of the NaYbF active shell structure led to a significant increase in relative sensitivity in ratio luminescence thermometry. Notably, the NaYF:Yb, Nd, Er@ NaYbF core-shell structure demonstrated the highest relative sensitivity of 1.12 %K. This research underscores the crucial role of inert shell layers in enhancing upconversion luminescence in core-shell structure design, while active layers play a key role in achieving high-sensitivity temperature detection capabilities.
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http://dx.doi.org/10.1016/j.jcis.2024.06.071 | DOI Listing |
J Colloid Interface Sci
September 2025
Department of Radiation Oncology, Radiation Oncology Key Laboratory of Sichuan Province, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu 610041, China. Electronic address: Zhaoy
Lanthanide-doped fluoride nanoparticles show great potential for optical thermometry and bioimaging. However, their applications are still constrained by inherent limitations in luminescence intensity and functional versatility. To overcome these challenges, we propose a core-active shell-inert shell nanostructure that integrates multifunctional capabilities within a single platform.
View Article and Find Full Text PDFInt J Biol Macromol
August 2025
School of Materials and Chemical Engineering, Ningbo University of Technology, Ningbo 315211, PR China; Zhejiang Institute of Tianjin University, Ningbo 315211, PR China.
Cellulose-based paper, widely used in cultural heritage preservation and art, suffers from inherent flammability. Conventional phosphorus-based flame retardants, derived from depleting phosphate ores, necessitate sustainable alternatives. This study introduces an innovative layer-by-layer assembly strategy to fabricate biomass-derived MH-P@Mn and MH-P@Ni core-shell flame retardants.
View Article and Find Full Text PDFChem Sci
August 2025
School of Chemistry and Australian Centre for NanoMedicine, The University of New South Wales Sydney 2052 Australia
The specificity of enzymes for their substrate typically means there is one enzyme for one molecule. Nanozyme research has focussed on mimicking reactions that enzymes can perform, with far less emphasis on selectively reacting with species in complex biological fluids. Herein we ask the question, can a nanozyme be engineered to do what enzymes cannot do, detect and react selectively with two different substrates in the same blood sample? This is achieved using a nanoparticle that mimics the three-dimensional geometry of an enzyme with isolated substrate channels leading to an active site.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Department of Chemistry, School of Science and Key Laboratory for Quantum Materials of Zhejiang Province, Research Center for Industries of the Future, Westlake University, Hangzhou 310030, China; Institute of Natural Sciences, Westlake Institute for Advanced Study, Hangzhou 310024, China. Electroni
Site selectivity is fundamental to fabricating complex nanostructures. Herein, we introduce "In-Ex site selectivity," a novel mechanism for regulating deposition on a liquid template containing internal solid particles. The selectivity dictates whether deposition occurs on the interior (In) solid surface or the exterior (Ex) surface of the liquid template.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science and Engineering, Fudan University, Shanghai 200433, People's Republic of China.
The exceptional stability of carbon-fluorine (C-F) bonds in perfluorooctanoic acid (PFOA) presents a fundamental challenge in environmental remediation as traditional degradation methods struggle to break these bonds under mild conditions. Here, we demonstrate that the air-water interface in microdroplets can be strategically utilized to dramatically enhance PFOA ( = 20 mg L) degradation through a simple Fe(III)-Oxalate photochemical system, achieving complete destruction with 99% defluorination within 4 h at room temperature - a rate 2 orders of magnitude faster than conventional methods. Through comprehensive spectroscopic and computational investigations, we reveal that this remarkable enhancement stems from three synergistic interfacial effects: concentrated generation of superoxide radicals (O) from earth-abundant Fe(III)-Oxalate complexes, significantly enhanced O nucleophilicity due to disrupted solvation shells, and a strong interfacial electric field that catalyzes C-F bond activation.
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