Gotowe bibliografie tematyczne / Inorganic Quantum Dots

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Gotowa bibliografia na temat „Inorganic Quantum Dots”

Autor: Grafiati

Data publikacji: 7 września 2023

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Artykuły w czasopismach na temat "Inorganic Quantum Dots"

Mitch Jacoby. "Superbright quantum dots with inorganic caps". C&EN Global Enterprise 101, nr 5 (6.02.2023): 6. http://dx.doi.org/10.1021/cen-10105-scicon4.

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Zunger, Alex. "Semiconductor Quantum Dots". MRS Bulletin 23, nr 2 (luty 1998): 15–17. http://dx.doi.org/10.1557/s0883769400031213.

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Semiconductor “quantum dots” refer to nanometer-sized, giant (103–105 atoms) molecules made from ordinary inorganic semiconductor materials such as Si, InP, CdSe, etc. They are larger than the traditional “molecular clusters” (~1 nanometer containing ≤100 atoms) common in chemistry yet smaller than the structures of the order of a micron, manufactured by current electronic-industry lithographic techniques. Quantum dots can be made by colloidal chemistry techniques (see the articles by Alivisatos and by Nozik and Mićić in this issue), by controlled coarsening during epitaxial growth (see the article by Bimberg et al. in this issue), by size fluctuations in conventional quantum wells (see the article by Gammon in this issue), or via nano-fabrication (see the article by Tarucha in this issue).

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Chawre, Yogyata, Lakshita Dewangan, Ankita Beena Kujur, Indrapal Karbhal, Rekha Nagwanshi, Vishal Jain i Manmohan L. Satnami. "Quantum Dots and Nanohybrids and their Various Applications: A Review". Journal of Ravishankar University (PART-B) 35, nr 1 (8.03.2022): 53–86. http://dx.doi.org/10.52228/jrub.2022-35-1-7.

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Organic/inorganic nanohybrids and quantum dots have attracted widespread interest due to their favorable properties and promising applications. Great efforts have been made to design and fabricate versatile nanohybrids. Processing structure-properties-performance relationships are reviewed for compound quantum dots. In this review, various methods for synthesizing quantum dots as well as their resulting properties are discussed. This review focuses on the design, properties, sensing as well as energy applications of organic/inorganic nanohybrids as well as quantum dots. In this article, strategies for the fabrication, properties, functions, characterization techniques, various synthesis strategies and application of nanohybrids and quantum dots are briefly deliberated.

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Gao, Ge, Qiaoyue Xi, Hua Zhou, Yongxia Zhao, Cunqi Wu, Lidan Wang, Pengran Guo i Jingwei Xu. "Novel inorganic perovskite quantum dots for photocatalysis". Nanoscale 9, nr 33 (2017): 12032–38. http://dx.doi.org/10.1039/c7nr04421f.

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Uniform CsPbX₃ quantum dots were synthesized via an emulsion fabrication and demulsion method at room temperature. The as-prepared CsPbX₃ QDs exhibit high synthetic yield and highly uniform morphology, as well as excellent photocatalytic activity toward the degradation of MO.

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GENG Wei-dong, 耿卫东, 郭嘉 GUO Jia, 唐静 TANG Jing i 刘会刚 LIU Hui-gang. "All-inorganic colloidal quantum dots display technology". Chinese Journal of Liquid Crystals and Displays 29, nr 4 (2014): 479–84. http://dx.doi.org/10.3788/yjyxs20142904.0479.

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Xu, Yuanhong, Xiaoxia Wang, Wen Ling Zhang, Fan Lv i Shaojun Guo. "Recent progress in two-dimensional inorganic quantum dots". Chemical Society Reviews 47, nr 2 (2018): 586–625. http://dx.doi.org/10.1039/c7cs00500h.

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Lobnik, Aleksandra, Špela Korent Urek i Matejka Turel. "Quantum Dots Based Optical Sensors". Defect and Diffusion Forum 326-328 (kwiecień 2012): 682–89. http://dx.doi.org/10.4028/www.scientific.net/ddf.326-328.682.

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Luminescent sensors are chemical systems that can deliver information on the presence of selected analytes through the variations in their luminescence emission. With the advent of luminescent nanoparticles several new applications in the field of chemical sensing were explored. Among them, quantum dots (QD) represent inorganic semiconductor nanocrystals that are advantageous over conventional organic dyes from many different points of view. In this short review, the optical detection of various analytes using QD-based probes/sensors is presented and significant sensors characteristics are discussed. The biosensing approaches are not included in this article.

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Li, Teng, Xinru Liu, Kai Wang i Zhengguo Zhang. "Preparation and Properties of Inorganic Perovskite Quantum Dots". IOP Conference Series: Earth and Environmental Science 300 (9.08.2019): 022123. http://dx.doi.org/10.1088/1755-1315/300/2/022123.

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Engelmann, A., V. I. Yudson i P. Reineker. "Hybrid excitons in organic-inorganic semiconducting quantum dots". Journal of Luminescence 76-77 (luty 1998): 214–16. http://dx.doi.org/10.1016/s0022-2313(97)00203-2.

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Pradeep, K. R., Saptarshi Chakraborty i Ranjani Viswanatha. "Stability of Sn based inorganic perovskite quantum dots". Materials Research Express 6, nr 11 (6.11.2019): 114004. http://dx.doi.org/10.1088/2053-1591/ab5121.

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Rozprawy doktorskie na temat "Inorganic Quantum Dots"

Hashim, Zeina. "Semiconducting polymer nanospheres : organic alternatives to inorganic quantum dots?" Thesis, King's College London (University of London), 2013. https://kclpure.kcl.ac.uk/portal/en/theses/semiconducting-polymer-nanospheres(c39fdbe6-f281-4472-94aa-d8e44f834b2e).html.

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Semiconducting polymer nanospheres are organic conjugated polymer nanoparticles which are synthesized from benign materials and exhibit excellent fluorescence properties. The nanoparticles are generally larger than inorganic quantum dots with a relatively broad size distribution. Quantum dots, on the other hand, which have extensively been developed and synthesized with precise and narrow distributions of a few nanometers in dimensions, are now being widely investigated as bio-imaging agents, despite the rising concerns about their toxic compositions. Therefore, advances in the synthesis of the organic nanoparticles and investigations into their suitability as alternatives to quantum dots need to be explored. The ‘size problem’ of semiconducting polymer nanospheres – polymer particles are significantly larger than quantum dots – was first tackled in this work. With modifications to the miniemulsion-evaporation synthesis method, narrowly distributed quantum dot-sized nanoparticles with diameters as small as 2 nm were synthesized. These organic nanoparticles which were capped/entwined with poly(ethylene) glycol (PEG), a Food and Drug Administration (FDA) approved surfactant, were found to conserve most of the optical properties of their constituent polymers, and are therefore expected to be useful in bio-imaging applications similar to their larger counterparts. A second nanoparticle system with a dual-modality was then prepared; semiconducting polymer nanospheres capped/entwined with three amphiphilic lipids one of which was gadolinium – diethylene triamine pentacetate, a Magnetic Resonance Imaging (MRI) active ligand. These bimodal nanoparticles also maintained their optical properties, were readily taken up by two cell lines, were distinguishable from the auto-fluorescence of animal tissue, and were found to be MRI-active as revealed by their MRI relaxivity measurements. Finally, the optimized organic nanoparticles and similarly coated quantum dots were investigated for their potential to interact with human blood components, a physiological system which may be very relevant for semiconducting polymer nanospheres used as medical diagnostic agents. The preliminary ex-vivo studies performed revealed that similarly coated organic nanoparticles and quantum dots did not induce platelet aggregation or alter aggregation behaviour in response to a physiological agonist. Further, no evidence of platelet activation, neutrophil activation or increases in platelet-monocyte adhesion was observed. This implied that introduction of the nanoparticles to the blood stream at the concentrations tested may not elicit acute pro-inflammatory effects or alter normal coagulation pathways, although further rigorous evaluation in this area is still required. Fluorescence imaging showed that the organic nanoparticles were taken up by different blood cells and also showed some evidence of adhesion to their surfaces, a property which might find an application in the future. Ultimately, more short-term and long-term safety studies (in-vitro, ex-vitro, and in-vivo) must be conducted before deriving any further conclusions.

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Yang, Mingrui. "Energy Transport in Colloidal Inorganic Nanocrystals". Bowling Green State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1616824530811137.

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Waggett, Jonathan. "The study of inorganic semiconductor quantum dots for solar cell applications". Thesis, University of Bristol, 2005. http://hdl.handle.net/1983/916bf29c-07eb-4601-be30-534e81635c1b.

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Garner, Brett William. "Multifunctional Organic-Inorganic Hybrid Nanophotonic Devices". Thesis, University of North Texas, 2008. https://digital.library.unt.edu/ark:/67531/metadc6108/.

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The emergence of optical applications, such as lasers, fiber optics, and semiconductor based sources and detectors, has created a drive for smaller and more specialized devices. Nanophotonics is an emerging field of study that encompasses the disciplines of physics, engineering, chemistry, biology, applied sciences and biomedical technology. In particular, nanophotonics explores optical processes on a nanoscale. This dissertation presents nanophotonic applications that incorporate various forms of the organic polymer N-isopropylacrylamide (NIPA) with inorganic semiconductors. This includes the material characterization of NIPA, with such techniques as ellipsometry and dynamic light scattering. Two devices were constructed incorporating the NIPA hydrogel with semiconductors. The first device comprises a PNIPAM-CdTe hybrid material. The PNIPAM is a means for the control of distances between CdTe quantum dots encapsulated within the hydrogel. Controlling the distance between the quantum dots allows for the control of resonant energy transfer between neighboring quantum dots. Whereby, providing a means for controlling the temperature dependent red-shifts in photoluminescent peaks and FWHM. Further, enhancement of photoluminescent due to increased scattering in the medium is shown as a function of temperature. The second device incorporates NIPA into a 2D photonic crystal patterned on GaAs. The refractive index change of the NIPA hydrogel as it undergoes its phase change creates a controllable mechanism for adjusting the transmittance of light frequencies through a linear defect in a photonic crystal. The NIPA infiltrated photonic crystal shows greater shifts in the bandwidth per ºC than any liquid crystal methods. This dissertation demonstrates the versatile uses of hydrogel, as a means of control in nanophotonic devices, and will likely lead to development of other hybrid applications. The development of smaller light based applications will facilitate the need to augment the devices with control mechanism and will play an increasing important role in the future.

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Royo, Romero Luis. "Optoelectronic Characteristics of Inorganic Nanocrystals and Their Solids". Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1555422820907262.

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Khozaee, Zahra. "Studies on organic/inorganic nanocomposites of lead sulphide quantum dots in solution- processed phthalocyanine films". Thesis, Queen Mary, University of London, 2012. http://qmro.qmul.ac.uk/xmlui/handle/123456789/8500.

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A unique organic/inorganic nanocomposite of lead sulphide (PbS) quantum dots (QDs) embedded in substituted metal-free phthalocyanine (C6H2Pc) has been prepared by a simple and low-cost method. The preparation procedure consists of exposure of a thin spun film of non-peripherally octa-hexyl lead phthalocyanine to hydrogen sulphide atmosphere. The formation of the PbS QDs has been verified using X-ray diffraction and transmission electron microscopy techniques. From the transmission electron microscopic measurements, the average size of the PbS QDs is found to be 4.5 nm, which is smaller than the exciton Bohr radius. Independent Xray diffraction and optical absorption studies provide supportive evidence for the size of QDs. Quantum confinement gives rise to a clear blue shift in the absorption spectrum with respect to the bulk PbS. The QDs band gap has been estimated to be 1.95 eV from Tauc's law and the frontier energy levels of the PbS QDs has been derived. About two orders of magnitude increase in ohmic conductivity, from 6.0×10−12 for C6H2Pc to 3.1×10−10 for the nanocomposite, is observed by steady-state electrical measurements in sandwich structure between indium tin oxide and aluminium. Temperature-dependence of the electrical conduction is studied aimed to calculate the activation energy and determine the type of conductivity. The incorporation of the PbS QDs decreases the activation energy by about 0.5 eV at temperatures higher than 240 K. It is found that the Poole-Frenkel mechanism is in good consistency with the superlinear electrical behaviour of the nanocomposite. The frequency response of alternating current (AC) conduction is found to obey the universal power-law. The cryogenic study of AC conduction reveals that the correlated barrier hopping (CBH) model closely fits to the experimental data at temperatures below 240 K. The parameters obtained by fitting the CBH model point out that the hopping process cannot take place directly between neighbouring PbS QDs but involves the localised states within the matrix.

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Dabbousi, Bashir O. (Bashir Osama). "Fabrication and characterization of hybrid organic/inorganic electroluminescent devices based on cadmium selenide nanocrystallites (quantum dots)". Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/10434.

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Lystrom, Levi Aaron. "Influence of Organic and Inorganic Passivation on the Photophysics of Cadmium Chalcogenide and Lead Chalcogenide Quantum Dots". Diss., North Dakota State University, 2020. https://hdl.handle.net/10365/31926.

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Quantum dots (QDs) are promising materials for photovoltaic (PV) and light-emitting diode (LED) applications due to their unique properties: photostability, size-tunable absorptivity, and narrow line-width emission. These properties are tailored by surface passivations by ligands. However, ligands used in the synthesis of colloidal QDs need to be exchanged with ligands designed for specific applications. The mechanism behind ligand exchange is not well understood. Density functional theory (DFT) is utilized to gain fundamental understanding of ligand exchange (LE) and the resulting effect on the photophysics of QDs. Experimental studies show that phenyldithiocarbamates (PTCs) derivatives can improve the photocurrent of QD-based PVs. Our calculations show that the PTC undergoes decomposition on the CdSe QD surface. Decomposed products of PTCs strongly interact with the surface of QDs, which could cause unforeseen challenges during the implementation of these functionalized QDs in PVs. Secondly, we studied the mechanism of photoluminescence (PL) enhancement by hydride treatment. In experiments, the PL increases by 55 times, but the mechanism is unclear. We found that hydride can interact with surface Se2- producing H2Se gas and passivate surface Cd2+. These interactions result in optically active QDs. Thiol derivatives can also improve PL when LE results in low surface coverage of thiols. The PL is quenched if LE is performed at high concentrations and acidic environments. DFT simulations reveal three scenarios for the thiol interacts with QDs: coordination of thiol, networking between surface and/or other ligands, or thiolate formation. It is the last scenario that was found to be responsible for PL quenching. Lastly, PbS(e)/CdS(e) core/shell QDs are investigated to obtain relaxation rates of electron and hole cooling via interactions with phonons. The band structure of the core/shell QDs facilitates carrier multiplication (CM), a process that generates multiple charge carrier pairs per one absorbed photon. It is thought that CM is facilitated because there are interface associated states that reduce carrier cooling. Non-Adiabatic Molecular Dynamics (NAMD) simulations show that this hypothesis is correct and PbSe/CdSe carrier cooling is about two times slower compared to PbS/CdS due to weaker coupling to optical phonons.

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Esteves, Richard J. "The Dawn of New Quantum Dots: Synthesis and Characterization of Ge1-xSnx Nanocrystals for Tunable Bandgaps". VCU Scholars Compass, 2016. http://scholarscompass.vcu.edu/etd/4637.

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Ge1-xSnx alloys are among a small class of benign semiconductors with composition tunable bandgaps in the near-infrared spectrum. As the amount of Sn is increased the band energy decreases and a transition from indirect to direct band structure occurs. Hence, they are prime candidates for fabrication of Si-compatible electronic and photonic devices, field effect transistors, and novel charge storage device applications. Success has been achieved with the growth of Ge1-xSnx thin film alloys with Sn compositions up to 34%. However, the synthesis of nanocrystalline alloys has proven difficult due to larger discrepancies (~14%) in lattice constants. Moreover, little is known about the chemical factors that govern the growth of Ge1-xSnx nanoalloys and the effects of quantum confinement on structure and optical properties. A synthesis has been developed to produce phase pure Ge1-xSnx nanoalloys which provides control over both size and composition. Three sets of Ge1-xSnx nanocrystals have been studied, 15–23 nm, 3.4–4.6 nm and 1.5–2.5 nm with Sn compositions from x = 0.000–0.279. Synthetic parameters were explored to control the nucleation and growth as well as the factors that have led to the elimination of undesired metallic impurities. The structural analysis of all nanocrystals suggests the diamond cubic structure typically reported for Ge1-xSnx thin films and nanocrystalline alloys. As-synthesized Ge1-xSnx nanoalloys exhibit high thermal stability and moderate resistance against sintering up to 400–500 °C and are devoid of crystalline and amorphous elemental Sn impurities.

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Haverinen, H. (Hanna). "Inkjet-printed quantum dot hybrid light-emitting devices—towards display applications". Doctoral thesis, University of Oulu, 2010. http://urn.fi/urn:isbn:9789514261275.

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Abstract This thesis presents a novel method for fabricating quantum dot light-emitting devices (QDLEDs) based on colloidal inorganic light-emitting nanoparticles incorporated into an organic semiconductor matrix. CdSe core/ZnS shell nanoparticles were inkjet-printed in air and sandwiched between organic hole and electron transport layers to produce efficient photon-emissive media. The light-emitting devices fabricated here were tested as individual devices and integrated into a display setting, thus endorsing the capability of this method as a manufacturing approach for full-colour high-definition displays. By choosing inkjet printing as a deposition method for quantum dots, several problems currently inevitable with alternative methods are addressed. First, inkjet printing promises simple patterning due to its drop-on-demand concept, thus overruling a need for complicated and laborious patterning methods. Secondly, manufacturing costs can be reduced significantly by introducing this prudent fabrication step for very expensive nanoparticles. Since there are no prior demonstrations of inkjet printing of electroluminescent quantum dot devices in the literature, this work dives into the basics of inkjet printing of low-viscosity, relatively highly volatile quantum dot inks: piezo driver requirements, jetting parameters, fluid dynamics in the cartridge and on the surface, nanoparticle assembly in a wet droplet and packing of dots on the surface are main concerns in the experimental part. Device performance is likewise discussed and plays an important role in this thesis. Several compositional QDLED structures are described. In addition, different pixel geometries are discussed. The last part of this dissertation deals with the principles of QDLED displays and their basic components: RGB pixels and organic thin-film transistor (OTFT) drivers. Work related to transistors is intertwined with QDLED work; ideas for surface treatments that enhance nanoparticle packing are carried over from self-assembled monolayer (SAM) studies in the OTFT field. Moreover, all the work done in this thesis project was consolidated by one method, atomic force microscopy (AFM), which is discussed throughout the entire thesis.

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Książki na temat "Inorganic Quantum Dots"

O'Brien, Paul, i Mark Green. Semiconductor Quantum Dots: Organometallic and Inorganic Synthesis. Royal Society of Chemistry, The, 2014.

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Semiconductor Quantum Dots: Organometallic and Inorganic Synthesis. Royal Society of Chemistry, The, 2014.

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Li, Jing, i Xiao-Ying Huang. Nanostructured crystals: An unprecedented class of hybrid semiconductors exhibiting structure-induced quantum confinement effect and systematically tunable properties. Redaktorzy A. V. Narlikar i Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.16.

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This article describes the structure-induced quantum confinement effect in nanostructured crystals, a unique class of hybrid semiconductors that incorporate organic and inorganic components into a single-crystal lattice via covalent (coordinative) bonds to form extended one-, two- and three-dimensional network structures. These structures are comprised of subnanometer-sized II-VI semiconductor segments (inorganic component) and amine molecules (organic component) arranged into perfectly ordered arrays. The article first provides an overview of II-VI and III-V semiconductors, II-VI colloidal quantum dots, inorganic-organic hybrid materials before discussing the design and synthesis of I-VI-based inorganic-organic hybrid nanostructures. It also considers the crystal structures, quantum confinement effect, bandgaps, and optical properties, thermal properties, thermal expansion behavior of nanostructured crystals.

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Części książek na temat "Inorganic Quantum Dots"

Gu, Kai, Mu Yang i Hongshang Peng. "Strategies Towards Improving the Stability of All-Inorganic Perovskite Quantum Dots". W Perovskite Quantum Dots, 347–72. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6637-0_13.

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Zang, Zhigang, i Dongdong Yan. "All-Inorganic Perovskite Quantum Dots: Ligand Modification, Surface Treatment and Other Strategies for Enhanced Stability and Durability". W Perovskite Quantum Dots, 51–106. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6637-0_3.

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Pietryga, Jeffrey M., Jennifer A. Hollingsworth, Fudong Wang i William E. Buhro. "Mid-Infrared Emitting Lead Selenide Nanocrystal Quantum Dots". W Inorganic Syntheses: Volume 36, 198–202. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118744994.ch37.

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Sridharan, Karthiyayini, Vijaya Ilango i R. Sugaraj Samuel. "Water Purification by Carbon Quantum Dots". W Inorganic-Organic Composites for Water and Wastewater Treatment, 113–60. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-5928-7_4.

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Blaudeck, Thomas. "Fluorescence Quenching of Semiconductor Quantum Dots by Multiple Dye Molecules". W Self-Assembled Organic-Inorganic Nanostructures, 201–13. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-4.

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Yue, Wenjin. "Organic-Inorganic Hybrid Solar Cells Based on Quantum Dots". W Printable Solar Cells, 65–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119283720.ch3.

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Kowerko, Danny. "Interrelation of Assembly Formation and Ligand Depletion in Colloidal Quantum Dots". W Self-Assembled Organic-Inorganic Nanostructures, 149–200. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-3.

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Fernández Argüelles, María Teresa, José M. Costa-Fernández, Rosario Pereiro i Alfredo Sanz-Medel. "Organically Modified Quantum Dots in Chemical and Biochemical Analysis". W The Supramolecular Chemistry of Organic-Inorganic Hybrid Materials, 377–403. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470552704.ch12.

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Uhrig, A., L. Banyai, S. Gaponenko, A. Wörner, N. Neuroth i C. Klingshirn. "Linear and nonlinear optical studies of CdS1−x Se x quantum dots". W Small Particles and Inorganic Clusters, 795–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76178-2_190.

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Mohan, Sneha, Jiji Abraham, Oluwatobi S. Oluwafemi, Nandakumar Kalarikkal i Sabu Thomas. "Rheology and Processing of Inorganic Nanomaterials and Quantum Dots/Polymer Nanocomposites". W Rheology and Processing of Polymer Nanocomposites, 355–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118969809.ch10.

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Streszczenia konferencji na temat "Inorganic Quantum Dots"

Gimenez, Sixto, Drialys Cardenas-Morcoso, Miguel Garcia-Tecedor, Seog Joon Yoon, Ivan Mora-Sero i Andres Gualdron. "Photocatalysis with All-Inorganic Perovskite Quantum Dots". W nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.fallmeeting.2018.110.

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Marcinkevicius, Saulius, Rosa Leon i Andreas Gaarder. "Ultrafast carrier dynamics in self-assembled semiconductor quantum dots". W Smart Optical Inorganic Structures and Devices. SPIE, 2001. http://dx.doi.org/10.1117/12.495846.

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Oron, Dan, i Ayelet Teitelboim. "All-inorganic colloidal upconversion quantum dots (Conference Presentation)". W Colloidal Nanoparticles for Biomedical Applications XII, redaktorzy Xing-Jie Liang, Wolfgang J. Parak i Marek Osiński. SPIE, 2017. http://dx.doi.org/10.1117/12.2250340.

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Li, Qing, Shikai Yan, Sheng Tang, Xu Zhang, Wei Lei i Jing Chen. "Photodetector Based on All-inorganic Perovskite Quantum Dots with Ring Electrode". W 2019 IEEE International Flexible Electronics Technology Conference (IFETC). IEEE, 2019. http://dx.doi.org/10.1109/ifetc46817.2019.9073761.

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Dhakal, Dileep. "Inorganic Nanowires Modulated with Quantum Dots to Store Qubit of Information". W 2008 8th IEEE Conference on Nanotechnology (NANO). IEEE, 2008. http://dx.doi.org/10.1109/nano.2008.162.

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Byoung-Ho Kang, Do-Eok Kim, Se-Hyuk Yeom, Kyu-Jin Kim, Jun-Seon Seo, Jae-Hyun Kim, Seong-Ho Kong, Jung-Hee Lee, Dae-Hyuk Kwon i Shin-Won Kang. "Fabrication of Organic/Inorganic LED device using nanocrystal quantum dots as active layer". W 2010 5th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS 2010). IEEE, 2010. http://dx.doi.org/10.1109/nems.2010.5592227.

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Yu, Chung-Ping, Meng-Ting Chung, Tzu-Yu Chen, Yu-Ming Huang, Chung-Ping Huang, Shu-Hsiu Chang, Shun-Chieh Hsu, Teng-Ming Chen, Hao-Chung Kuo i Chien-Chung Lin. "All Inorganic Perovskite Quantum Dots Hybrid Green Light-Emitting Diode with Stable Performance". W CLEO: Applications and Technology. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/cleo_at.2018.jth2a.89.

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Laera, Anna Maria, Emanuela Piscopiello, Leander Tapfer i Antonio Cardone. "Synthesis of New Organic/Inorganic Heterostructures from CdSe Quantum Dots and Tetracyanoquinodimethane Derivatives". W 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1121-n04-03.

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Di Benedetto, Pablo, Alessandro Martucci i Jochen Fick. "Photoluminescence properties of organic-inorganic sol-gel films doped with semiconductor quantum dots". W International Symposium on Optical Science and Technology, redaktor Zeno Gaburro. SPIE, 2002. http://dx.doi.org/10.1117/12.452214.

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Yasumatsu, Yuta, Yaohong Zhang, Chao Ding, Shen Qing, Feng Liu, Masamori Endo, Kiyoto Sasaki, Taizo Masuda i Mitsuhiro Iyoda. "Solar-pumped fiber laser with all-inorganic cesium lead halide perovskite quantum dots". W Fiber Lasers XVI: Technology and Systems, redaktorzy Liang Dong i Adrian L. Carter. SPIE, 2019. http://dx.doi.org/10.1117/12.2509756.

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Raporty organizacyjne na temat "Inorganic Quantum Dots"

and Moungi Bawendi, Vladimir Bulovic. Final Report for DE-FG36-08GO18007 "All-Inorganic, Efficient Photovoltaic Solid State Devices Utilizing Semiconducting Colloidal Nanocrystal Quantum Dots". Office of Scientific and Technical Information (OSTI), wrzesień 2011. http://dx.doi.org/10.2172/1048894.

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Weiss, Emily A. Chemical Control of Charge Trapping and Charge Transfer Processes at the Organic-Inorganic Interface within Quantum Dot-Organic Complexes. Office of Scientific and Technical Information (OSTI), listopad 2015. http://dx.doi.org/10.2172/1225212.

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