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Colloidal quantum dots (QDs) exhibit size-dependent, tuneable optical properties that render them useful in a wide range of technological applications. However, integration of QDs into structured materials remains a significant challenge due to their susceptibility to degradation under chemical or physical perturbations. Here, we present a facile, scalable one-pot co-assembly strategy to embed commercially available CdSe/ZnS core-shell quantum dots into photonic microparticles the confined self-assembly of a poly(styrene)--poly(2-vinylpyridine) block copolymer in emulsion droplets. The resulting hybrid particles exhibit a well-defined concentric lamellar structure and the quantum dots are selectively incorporated into the domains formed by the poly(2-vinylpyridine) blocks. This design enables two different optical responses, , vivid, non-iridescent structural colouration from photonic bandgap effects and stable engineered photoluminescence from the embedded QDs. The use of swelling agents provides an effective means to tune the photonic bandgap spectral position, extending the optical range to the entire visible region. Optical experiments reveal a subtle interplay between the photonic structure and QD emission, and the emission properties remain intact despite variations in the structural periodicity and matrix refractive index. This work highlights a robust platform for the integration of functional nanomaterials into photonic architectures, offering significant potential for applications in advanced light sources, displays, and sensing technologies. The simplicity of the approach, combined with its scalability, sets the stage for future exploration into hybrid photonic materials with tailored optical properties.
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http://dx.doi.org/10.1039/d5nr00216h | DOI Listing |
RSC Adv
September 2025
Department of Physics, University of Hull Cottingham Road UK
[This corrects the article DOI: 10.1039/D5RA04583E.].
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
October 2024
Department of Chemistry and Biochemistry, Nanoscale & Quantum Phenomena Institute, Ohio University, Athens, Ohio 45701, United States.
Carbon-based quantum dots (CQDs) have been around for a few decades. Low cell toxicity, good water solubility, excellent and tunable fluorescence properties, and the ability to dope and modify the surface of these CQDs make them an incredible choice for the visualization and treatment of various cancers. This perspective analyzes some recent progress on size-color correlation, modification, and cancer treatment applications of CQDs.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Nanoscience and Nanoengineering, Istanbul Technical University, 34469, Maslak, Istanbul, Turkey; Department of Chemistry, Faculty of Science and Letters, Istanbul Technical University, 34469, Maslak, Istanbul, Turkey. Electronic address:
This study presents the development of multifunctional starch-based biopolymer films reinforced with nitrogen-doped carbon quantum dots (N-CQDs), synthesized via a hydrothermal method, and exhibiting a high quantum yield (~70 %). N-CQDs were incorporated into the starch matrix at varying concentrations (0.1-1.
View Article and Find Full Text PDFNano Lett
September 2025
Department of Diagnostic Radiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119074, Singapore.
Discov Nano
September 2025
Department of Rehabilitation Medicine, Rehabilitation Medical Center, Key Laboratory of Rehabilitation Medicine in Sichuan Province, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Immunoelectron Microscopy (IEM) is a technique that combines specific immunolabeling with high-resolution electron microscopic imaging to achieve precise spatial localization of biomolecules at the subcellular scale (< 10 nm) by using high-electron-density markers such as colloidal gold and quantum dots. As a core tool for analyzing the distribution of proteins, organelle interactions, and localization of disease pathology markers, it has irreplaceable value, especially in synapse research, pathogen-host interaction mechanism, and tumor microenvironment analysis. According to the differences in labeling sequence and sample processing, the IEM technology system can be divided into two categories: the first is pre-embedding labeling, which optimizes the labeling efficiency through the pre-exposure of antigenic epitopes and is especially suitable for the detection of low-abundance and sensitive antigens; the second is post-embedding labeling, which relies on the low-temperature resin embedding (e.
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