Metal ions with smaller radii than Pb can stabilize CsPbBr NCs' cubic structure by lattice shrinkage, but lacking sensing research. Herein, Ni-substituting CsPbBr NCs were prepared to rapidly and accurately detect water content (WC) in edible oils. CsPbNiBr NCs had the highest fluorescence intensity, approximately 125 % of CsPbBr NCs. The results displayed that CsPbNiBr NCs were uniformly quadrilateral crystalline packing (8.78 ± 0.28 nm particle size) with inter-planar distances of 0.41, 0.33, and 0.29 nm. Given the fluorescence quenching behavior, a superior linear curve between fluorescence-decreased ratio and WC was established within 0-3 ‰ (/v) and a detection limitation of 0.042 ‰. Furthermore, excellent precision and accuracy were verified in various oils with a relative error of 2.06 %. It was suggested that water destroyed and dissolved CsPbNiBr NCs' crystal structure to induce fluorescence quenching. Thus, Pb-site substitutions of CsPbBr NCs enhanced the sensing performance, enlightening other elements-substituted CsPbBr NCs for sensing.
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http://dx.doi.org/10.1016/j.fochx.2025.102196 | DOI Listing |
J Am Chem Soc
March 2025
Polymer Science and Engineering Department, Conte Center for Polymer Science Research, University of Massachusetts Amherst, 120 Governors Drive, Amherst, Massachusetts 01003, United States.
The ability to arrange brightly fluorescent nanoscale materials into well-defined patterns is critically important in advanced optoelectronic structures. Traditional methods for doing so generally involve depositing different color quantum dot "inks," irradiating reactive (e.g.
View Article and Find Full Text PDFNano Lett
March 2025
State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, School of New Energy, North China Electric Power University, Beijing 102206, China.
Heteronanocrystals (HNCs) composed of colloidal lead halide perovskites and chalcogenides always offer unique photoelectric properties. Nevertheless, synthesizing perovskite-chalcogenide HNCs has been a tough challenge due to their completely different growth dynamics. Here, we present an effective strategy to synthesize Janus CsPbBr-AgBiS HNCs by in situ growth of CsPbBr NCs on prepared AgBiS quantum dot (QDs).
View Article and Find Full Text PDFLangmuir
March 2025
Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan.
All-inorganic perovskite (CsPbX, X = Cl, Br, I) nanomaterials as novel optoelectronic semiconductors have attracted much attention due to their unique photoelectric properties in lighting, display, and photovoltaic applications. Meanwhile, green and red light-emitting diodes (LEDs) based on bromine and iodine groups have developed rapidly, in which the high external quantum efficiency (EQE) is close to that of the current commercial green and red LEDs. However, the EQE of perovskite-based blue LEDs is far behind.
View Article and Find Full Text PDFNanoscale
February 2025
Key Laboratory of Automobile Materials MOE, School of Materials Science and Engineering, Jilin University, Changchun, 130012, P. R. China.
Inorganic lead halide perovskite nanocrystals (NCs), particularly CsPbBr, have attracted considerable attention due to their remarkable optical properties, positioning them as promising candidates for optoelectronics and bioimaging. Despite their potential, challenges such as environmental degradation and structural instability persist. Core-shell architectures and encapsulation have emerged as effective strategies to address these issues.
View Article and Find Full Text PDFACS Appl Mater Interfaces
February 2025
Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh 208016, India.
Metal halide perovskite nanocrystals (NCs), known for their strong visible-light absorption and tunable optoelectronic properties, show significant promise for photocatalytic applications. However, their efficiency is often hindered by rapid charge recombination and insufficient exciton dissociation, limiting effective catalysis. Excited-state interactions at the NC interface are critical in determining photocatalytic performance, underscoring the need for strategies that enhance charge separation and minimize recombination.
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