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Ultrathin Plasmonic Tungsten Oxide Quantum Wells with Controllable Free Carrier Densities
摘要： We report the colloidal synthesis of ~3 tungsten-oxygen (W-O) layer thick (~1 nm), two-dimensional (2D) WO3-x nanoplatelets (NPLs) (x ~ 0.55 — 1.03), which display tunable near-infrared localized surface plasmon resonances (LSPR) spectra and high free electron density (Ne) that arises predominantly from their large shape factor. Importantly, the W to O composition ratios inferred from their LSPR measurements show much higher percentage of oxygen vacancies than those determined by X-ray diffraction analysis, suggesting that the aspect ratio of ultrathin WO3-x NPLs is the key to producing an unprecedentedly large Ne, although synthesis temperature is also an independent factor. We find that NPL formation is kinetically controlled, whereas thermodynamic parameter manipulation leads to Ne as high as 4.13 X 1022 cm-3, which is close to that of plasmonic noble metals, and thus our oxide-based nanostructures can be considered as quasi-metallic. The unique structural properties of 2D nanomaterials along with the high Ne of WO3-x NPLs provide an attractive alternative to plasmonic noble metal nanostructures for energy conversions.
关键词： Ultrathin Plasmonic Tungsten Oxide,Quantum Wells,Colloidal Synthesis,Localized Surface Plasmon Resonances,Free Carrier Densities
更新于2025-09-23 15:19:57
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Scalable Synthesis of InAs Quantum Dots Mediated through Indium Redox Chemistry
摘要： Next-generation optoelectronic applications centered in the near-infrared (NIR) and short-wave infrared (SWIR) wavelength regimes require high-quality materials. Among these materials, colloidal InAs quantum dots (QDs) stand out as an infrared-active candidate material for biological imaging, lighting, and sensing applications. Despite significant development of their optical properties, the synthesis of InAs QDs still routinely relies on hazardous, commercially unavailable precursors. Herein, we describe a straightforward single hot injection procedure revolving around In(I)Cl as the key precursor. Acting as a simultaneous reducing agent and In source, In(I)Cl smoothly reacts with a tris(amino)arsenic precursor to yield colloidal InAs quantitatively and at gram scale. Tuning the reaction temperature produces InAs cores with a first excitonic absorption feature in the range of 700?1400 nm. A dynamic disproportionation equilibrium between In(I), In metal, and In(III) opens up additional flexibility in precursor selection. CdSe shell growth on the produced cores enhances their optical properties, furnishing particles with center emission wavelengths between 1000 and 1500 nm and narrow photoluminescence full-width at half-maximum (FWHM) of about 120 meV throughout. The simplicity, scalability, and tunability of the disclosed precursor platform are anticipated to inspire further research on In-based colloidal QDs.
关键词： colloidal synthesis,InAs quantum dots,short-wave infrared,optoelectronic applications,near-infrared
更新于2025-09-23 15:19:57
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Lead chalcogenide quantum dots for photoelectric devices
摘要： The review concerns the state of the art in methods of synthesis of colloidal lead chalcogenide quantum dots (QDs). The most recent data on the mechanisms of chemical transformations involving various precursors are discussed. Particular attention is paid to the influence of (i) trace impurities in the reactants used and (ii) post-synthesis treatment on the physicochemical properties of QDs used in photoelectric devices. The bibliography includes 129 references.
关键词： photoelectric devices,quantum dots,colloidal synthesis,lead chalcogenide,synthesis methods
更新于2025-09-16 10:30:52
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AN EXPLORATION INTO THE QUANTUM CONFINEMENT OF CTS/NATURAL DYE CORE- SHELL QUANTUM DOTS
摘要： In this work, we have presented a simple way of changing the confinement energies of Copper Tin Sulphide (CTS) quantum dots using natural dyes as shell material. Tetragonal CTS quantum dots in the size range of 1.7nm- 2.2nm, of bandgaps of 2.48eV and 5.0 eV were prepared by means of a green colloidal synthesis technique. These quantum dots were treated with natural dyes such as onion and beetroot skin dyes. Pelargonidin and Betanin (pigments of onion and beetroot skin dye respectively) formed hydrogen bonding with the capping agent, thus forming a shell around the CTS quantum dots. The change in confinement due to the effect of dye as shell was studied from absorption, photoluminescence and infrared spectroscopic techniques. The transitions occurring were analysed using a theoretical approach. CTS quantum dots, with its high transmittance in a wide range of wavelengths find promising applications in the buffer layer of solar cells.
关键词： Betanin,Copper tin sulphide,quantum dots,Pelargonidin,colloidal synthesis,quantum confinement
更新于2025-09-12 10:27:22
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Size-Programmed Synthesis of PbSe Quantum Dots via Secondary Phosphine Chalcogenides
摘要： In the most common syntheses of colloidal nanocrystal quantum dots (QDs) the size of the particle increases monotonically with reaction time. We have discovered a PbSe QD synthesis whereby size can be easily controlled by varying the side-chains of a secondary phosphine selenide precursor. The reaction runs to completion, and thus a desired QD diameter can be achieved by simply selecting an appropriate secondary phosphine. Quenching of the reaction to select a desired QD size is not required. For different secondary phosphine selenides, measurements of the precursor conversion rate show a direct relationship with final QD size, while P=Se bond strength calculations show an unexpected inverse relationship between QD size and P=Se bond strength. Finally, it is also demonstrated that secondary phosphine selenide precursors can provide an effective route for IV-VI QD syntheses on the large scale.
关键词： colloidal synthesis,size control,IV-VI QDs,secondary phosphine selenide,PbSe quantum dots
更新于2025-09-12 10:27:22
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Functional Macromolecule‐Enabled Colloidal Synthesis: From Nanoparticle Engineering to Multifunctionality
摘要： The synthesis of well-defined inorganic colloidal nanostructures using functional macromolecules is an enabling technology that offers the possibility of fine-tuning the physicochemical properties of nanomaterials and has contributed to a broad range of practical applications. The utilization of functional reactive polymers and their colloidal assemblies leads to a high level of control over structural parameters of inorganic nanoparticles that are not easily accessible by conventional methods based on small-molecule ligands. Recent advances in polymerization techniques for synthetic polymers and newly exploited functions of natural biomacromolecules have opened up new avenues to monodisperse and multifunctional nanostructures consisting of integrated components with distinct chemistries but complementary properties. Here, the evolution of colloidal synthesis of inorganic nanoparticles is revisited. Then, the new developments of colloidal synthesis enabled by functional macromolecules and practical applications associated with the resulting optical, catalytic, and structural properties of colloidal nanostructures are summarized. Finally, a perspective on new and promising pathways to novel colloidal nanostructures built upon the continuous development of polymer chemistry, colloidal science, and nanochemistry is provided.
关键词： polymer chemistry,nanochemistry,multifunctionality,colloidal synthesis,functional macromolecules,nanoparticle engineering,colloidal science
更新于2025-09-11 14:15:04
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Stability of Sn based inorganic perovskite quantum dots
摘要： Metal halide perovskite crystal structures have emerged as a class of optoelectronic materials, which combine the ease of solution processability with excellent optical absorption and emission qualities. However, the most promising perovskite structures rely on lead as a cationic species, thereby hindering commercial application. The replacement of lead with non-toxic alternatives such as tin has been studied in bulk but not in nanocrystals. In this work, we synthesize Sn and Pb based alloy perovskite nanocrystals by direct synthesis method by of taking mixture of Pb and Sn precursors in the desired ratio leading to quantum dots (QDs) of CsPb1-xSnxBryI3-y with successful Sn incorporation into the host lattice. As colloidal stability of these QDs is a crucial factor for device applications, we have studied the stability of the QDs under different conditions for these Sn based QDs and have found them to degrade faster upon using anti-solvents during washing process. In order to stabilize them, we have devised a purification method that is also discussed. Further, even though the optical and crystal structure stability in some of the inorganic perovskites leaves much room for improvement, so far there has been no studies on the structure property correlation. Here we study their structural purity and their optical stability after understanding the structure property correlation in CsPbI3 and CsPbBr3 perovskite structures. The stability of Sn doped perovskites obtained from a logical understanding of structure property correlations is found to be extremely stable across the series of compounds for upto three months.
关键词： Colloidal synthesis,Sn based perovskite nanocrystals
更新于2025-09-11 14:15:04
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Colloidal ReO3 Nanocrystals: Extra Re d-electron instigating a plasmonic response
摘要： Rhenium (+6) oxide (ReO3) is metallic in nature, which means it can sustain localized surface plasmon resonance (LSPR) in its nanocrystalline form. Herein, we describe the colloidal synthesis of nanocrystals (NCs) of this compound, through a hot-injection route entailing the reduction of rhenium (+7) oxide with a long chain ether. This synthetic protocol is fundamentally different from the more widely employed nucleophilic lysing of metal alkylcarboxylates for other metal oxide NCs. Owing to this difference, the NC surfaces are populated by ether molecules through an L-type coordination along with covalently bound (X-type) hydroxyl moieties, which enables easy switching from nonpolar to polar solvents without resorting to cumbersome ligand exchange procedures. These as-synthesized NCs exhibit absorption bands at around 590 nm (≈2.1 eV) and 410 nm (≈3 eV), which were respectively ascribed to their LSPR and interband absorptions by Mie theory simulations and Drude modeling. The LSPR response arises from the oscillation of free electron density created by the extra Re d-electron per ReO3 unit in the NC lattice, which resides in the conduction band. Further, the LSPR contribution facilitates the observation of dynamic optical modulation of the NC films as they undergo progressive electrochemical charging via ion (de)insertion. Ion (de)insertion leads to distinct dynamic optical signatures, and these changes are reversible in a wide potential range depending on the choice of the ion (lithium or tetrabutylammonium). Nanostructuring in ReO3 and the description of the associated plasmonic properties of these NCs made this optical modulation feasible, which were hitherto not reported for the bulk material. We envisage that the synthetic protocol described here will facilitate further exploration of such applications and fundamental studies of these plasmonic NCs.
关键词： Localized surface plasmon resonance,Colloidal synthesis,ReO3 nanocrystals,Electrochemical charging,Optical modulation
更新于2025-09-11 14:15:04
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Cs Oleate Precursor Preparation for Lead Halide Perovskite Nanocrystal Synthesis: The Influence of Excess Oleic Acid on Achieving Solubility, Conversion, and Reproducibility.
摘要： In the colloidal synthesis of inorganic perovskite materials, cesium oleate (CsOL) is the most commonly used Cs precursor. Yet despite its ubiquitous use in literature, CsOL has been observed to be insoluble at room temperature and leads to surprisingly inconsistent results in CsPbX3 nanocrystal synthesis depending on the Cs salt from which the precursor is derived. We show that under the conditions used in most reports, the amount of oleic acid (OA) added, while stoichiometrically sufficient, still leads to incomplete conversion of the Cs salts to CsOL. This results in a mixture of Cs sources being present during the reaction, causing decreased homogeneity and reproducibility. When a 1:5 Cs:OA ratio is used, complete conversion is readily obtained even under mild conditions, resulting in a precursor solution that is soluble at room temperature and yields identical synthetic results regardless of the initial Cs source. Further, 1H nuclear magnetic resonance (NMR) of solutions prepared using varying Cs:OA ratios shows that the maximum ratio of Cs:OA obtainable in solution is 1:5, with any excess Cs present in the precipitate. We believe the use of a soluble, fully converted CsOL reagent will improve reproducibility for Cs-based perovskite synthesis and directly benefit synthetic methods based on microfluidics.
关键词： reproducibility,inorganic perovskite materials,microfluidics,CsPbX3 nanocrystal synthesis,colloidal synthesis,oleic acid,solubility,cesium oleate
更新于2025-09-04 15:30:14