Littérature scientifique sur le sujet « Organic and inorganic Lead »

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Articles de revues sur le sujet "Organic and inorganic Lead"

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Gonzalez-Carrero, Soranyel, Raquel E. Galian et Julia Pérez-Prieto. « Organic-inorganic and all-inorganic lead halide nanoparticles [Invited] ». Optics Express 24, no 2 (21 décembre 2015) : A285. http://dx.doi.org/10.1364/oe.24.00a285.

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Verity, M. A. « Comparative observations on inorganic and organic lead neurotoxicity. » Environmental Health Perspectives 89 (novembre 1990) : 43–48. http://dx.doi.org/10.1289/ehp.908943.

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Lemmerer, Andreas, et David G. Billing. « Lead halide inorganic–organic hybrids incorporating diammonium cations ». CrystEngComm 14, no 6 (2012) : 1954. http://dx.doi.org/10.1039/c2ce06498g.

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Ha, Son-Tung, Chao Shen, Jun Zhang et Qihua Xiong. « Laser cooling of organic–inorganic lead halide perovskites ». Nature Photonics 10, no 2 (21 décembre 2015) : 115–21. http://dx.doi.org/10.1038/nphoton.2015.243.

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Eperon, Giles E., Giuseppe M. Paternò, Rebecca J. Sutton, Andrea Zampetti, Amir Abbas Haghighirad, Franco Cacialli et Henry J. Snaith. « Inorganic caesium lead iodide perovskite solar cells ». Journal of Materials Chemistry A 3, no 39 (2015) : 19688–95. http://dx.doi.org/10.1039/c5ta06398a.

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The vast majority of perovskite solar cell research has focused on organic–inorganic lead trihalide perovskites; herein, we present working inorganic CsPbI3perovskite solar cells for the first time.
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Scally, Shaun, Hao Zhang et William Davison. « Measurements of Lead Complexation with Organic Ligands using DGT ». Australian Journal of Chemistry 57, no 10 (2004) : 925. http://dx.doi.org/10.1071/ch04076.

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The technique of diffusive gradients in thin films (DGT) was used to investigate the distribution of Pb between inorganic forms and organic complexes in various solutions that contained fulvic acid, humic acid, or nitrilotriacetic acid (NTA) over the pH range 4–8. Three types of DGT devices with diffusive gels of different pore sizes were used. When the diffusion coefficient of each species in each gel type was considered, the DGT measurements obtained agreed well with the distribution of species predicted by the ECOSAT equilibrium speciation model for all solutions and gel types. When an appreciable proportion of inorganic species was present in solution, direct measurements by DGT using the most restricted gel provided a reasonable estimate of the inorganic species in solution. This demonstrates that DGT is able to use differences in molecule mobility to distinguish between species in solution.
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Billing, D. G., et A. Lemerrer. « Structural diversity in lead-halide based organic-inorganic hybrids ». Acta Crystallographica Section A Foundations of Crystallography 61, a1 (23 août 2005) : c357. http://dx.doi.org/10.1107/s0108767305084795.

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Weber, Oliver J., Kayleigh L. Marshall, Lewis M. Dyson et Mark T. Weller. « Structural diversity in hybrid organic–inorganic lead iodide materials ». Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 71, no 6 (1 décembre 2015) : 668–78. http://dx.doi.org/10.1107/s2052520615019885.

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The structural chemistry of hybrid organic–inorganic lead iodide materials has become of increasing significance for energy applications since the discovery and development of perovskite solar cells based on methylammonium lead iodide. Seven new hybrid lead iodide compounds have been synthesized and structurally characterized using single-crystal X-ray diffraction. The lead iodide units in materials templated with bipyridyl, 1,2-bis(4-pyridyl)ethane, 1,2-di(4-pyridyl)ethylene and imidazole adopt one-dimensional chain structures, while crystallization from solutions containing piperazinium cations generates a salt containing isolated [PbI6]4−octahedral anions. Templating with 4-chlorobenzylammonium lead iodide adopts the well known two-dimensional layered perovskite structure with vertex shared sheets of composition [PbI4]2−separated by double layers of organic cations. The relationships between the various structures determined, their compositions, stability and hydrogen bonding between the protonated amine and the iodide ions of the PbI6octahedra are described.
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Wang, Bin, Dangwu Ma, Haixia Zhao, Lasheng Long et Lansun Zheng. « Room Temperature Lead-Free Multiaxial Inorganic–Organic Hybrid Ferroelectric ». Inorganic Chemistry 58, no 20 (26 septembre 2019) : 13953–59. http://dx.doi.org/10.1021/acs.inorgchem.9b01793.

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Green, Martin A., Yajie Jiang, Arman Mahboubi Soufiani et Anita Ho-Baillie. « Optical Properties of Photovoltaic Organic–Inorganic Lead Halide Perovskites ». Journal of Physical Chemistry Letters 6, no 23 (18 novembre 2015) : 4774–85. http://dx.doi.org/10.1021/acs.jpclett.5b01865.

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Thèses sur le sujet "Organic and inorganic Lead"

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SARRITZU, VALERIO. « Photophysics of organic/inorganic lead halide perovskites ». Doctoral thesis, Università degli Studi di Cagliari, 2018. http://hdl.handle.net/11584/255939.

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In keeping with their nature of hybrid materials, halide perovskites have been found to possess a particularly attractive blend of optoelectronic properties. A wealth of literature has been produced, that on some occasions raised questions just as readily as it answered them. In particular, my thesis addresses the following four key issues. First, the nature of the band gap. Long assumed to be the direct, according to recent reports the band gap supposedly has a dual nature. This fundamental matter is addressed through a study of the radiative recombination rates as a function of temperature. Data show that in perovskites radiative recombination becomes faster with decreasing temperature, as indeed in all direct-band gap materials. Second, exciton formation. Countless reports agree that free carriers are the majority photoexcited species under typical operating conditions of a solar cell, while evidence of exciton formation and dissociation processes is still elusive. A differential photoluminescence technique is employed to access extremely low injection levels at which emission from primary (geminate) excitons outshines that of free carriers. Third, efficiency loss. Understanding what processes limit the power conversion efficiency of perovskite solar cells is essential for the technology to mature. Shockley-Read-Hall and interface recombination are unambiguously identified as the main recombination mechanisms in perovskites and perovskite heterostructures, respectively. Fourth, solution processed nanostructures. A solution method developed by co-worker Dr Daniela Marongiu is shown to be able to form stable self-assembled MAPbI3-xBrx nanocrystals in a MAPbBr3 matrix. A thorough investigation on the photophysics of this material reveals that photoexcited charge carriers are funneled from the matrix to the nanocrystals, lifting quantum yield by one order of magnitude.
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Niu, Wendy Wanru. « Excitons in 2D organic-inorganic lead iodide perovskites ». Thesis, University of Cambridge, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708847.

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SESTU, NICOLA. « Optical properties of organic-inorganic lead halide perovskites ». Doctoral thesis, Università degli Studi di Cagliari, 2019. http://hdl.handle.net/11584/259899.

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One of the most important challenges for our society is to make more efficient devices in order to mitigate the rapidly increasing energy demand. In recent years a class of materials have attracted a great deal of attention in this perspective. Thanks to unique properties, including high absorption coefficient, broad absorption spectrum, high charge-carrier mobilities, long diffusion lengths, tunable band gap and low costs of fabrication, organic-inorganic lead halide perovskites have become very promising candidates for a new generation of potentially printable and efficient optoelectronic devices. The thesis aims to investigate some of the issues of optical properties of organic-inorganic lead halide perovskites. First, the nature of the band gap. Nevertheless for a long time it was considered direct, recent reports have proposed that the presence of heavy atoms in the crystal leads to Rashba-type effects. This crucial issue is addressed thanks to a study of the radiative recombination rates and photoluminescence decay dynamics as a function of temperature, the direct nature of band gap is demonstrated. Second, the exciton binding energy. Its knowledge is crucial for optoelectronic devices advances. Different measurement methods led to quite various each other values, even on the most widely studied materials, such as methylammonium lead iodide and methylammonium lead bromide. Thanks to a f-sum rule for integrated UV-vis absorption spectra, that allows to circumvent the pitfalls of least-squares fitting procedures, more accurate values of exciton binding energy is calculated and its dependence on temperature for these materials is shown. Third, the excitons formation and dissociation. Even though its understanding is of fundamental importance, many aspects of the processes of formation of an exciton population in perovskites are still elusive and some questions are still to be answered. The differential photoluminescence technique presented is able to provide a comprehensive picture of the kinetics of excitons in hybrid perovskites and to unveil the spectroscopic sign of excitons.
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Dooley, Joan Mary 1961. « LEAD MOBILIZING ACTIVITY OF DMPS, DMSA, AND DMPA FOLLOWING ORGANIC AND INORGANIC LEAD EXPOSURE ». Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/275507.

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Bhat, Jerome C. « Electroluminescent hybrid organic/inorganic quantum dot devices ». Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298766.

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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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Mannsfeld, Stefan. « Ordering in weakly bound molecular layers : organic-inorganic and organic-organic heteroepitaxy ». Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2004. http://nbn-resolving.de/urn:nbn:de:swb:14-1098888571984-95956.

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It is an aim of this work to provide insight into the energetic influence on the ordering of molecular thin films on crystalline substrates. Here, the term substrate either refers to inorganic crystal surfaces or highly ordered layers of another organic molecular species. In order to calculate the total interface potential of extended molecular domains, a new calculation technique (GRID technique) is developed in the first part of this work. Compared to the standard approach, this method accelerates the potential calculation drastically (times 10000). The other parts of the thesis are dedicated to the comparison of experimental results (obtained by scanning tunneling microscopy and electron diffraction) to the optimal layer structure as predicted by optimization calculations. Potential calculations which are performed for the system perylenetetracarboxylicdianhydride (PTCDA) on graphite demonstrate that point-on-line coincident structures correspond to energetically favorable alignments of the molecular lattice with respect to the substrate lattice. The capability of the GRID technique to predict the optimal layer structure is demonstrated for the system peri-hexabenzocoronene (HBC) on graphite. The organic-organic heteroepitaxy system PTCDA on HBC on graphite is investigated in order to clarify to which extent the ordering mechanism there differs from that of the organic-inorganic heteroepitaxy system PTCDA on graphite. As a result of this investigation, a new type of epitaxy, i.e., substrate induced ordering is found. This new epitaxy type is governed by the inner structure of the substrate lattice unit cell. Here, the substrate surface is a layer of organic molecules itself, hence the substrate surface unit cell does indeed exhibit a complex inner structure. A generalized classification scheme for epitaxial growth incorporating this new type of epitaxy is proposed. In the last chapter, the structure of the first layers of titanylphthalocyanine (TiOPc) on Au(111) is investigated and compared to potential optimization calculations. The correspondence of experimental and theoretical results provides evidence that the GRID technique can, in principle, also be applied to molecular layers on metal surfaces
Das Ziel der vorliegenden Arbeit ist es, Einblicke in die energetischen Einflüsse, die zur Ausbildung der Schichtstruktur organischer Moleküle auf kristallinen Substraten führen, zu geben. Diese Substrate sind entweder Oberflächen anorganische Kristalle oder selbst hochgeordnete Molekülschichten. Um das totale Grenzflächenpotential ausgedehnter Moleküldomänen berechnen zu können, wird im ersten Teil der Arbeit eine neue Berechnungsmethode (GRID Technik) vorgestellt. Im Vergleich mit herkömmlichen Berechnungsmethoden auf der Basis molekülmechanischer Kraftfelder ist diese neue Methode daher um ein Vielfaches schneller (Faktor 100000). Die folgenden Teile der Arbeit sind dem Vergleich experimenteller Ergebnisse (Rastertunnelmikroskopie und Elektronenbeugung) mit, durch Potentialoptimierungsrechnungen als energetisch günstig vorhergesagten, Schichtstrukturen gewidmet. So kann für das System Perylentetracarbonsäuredianhydrid (PTCDA) auf Graphit mittels Potentialberechnungen nachgewiesen werden, daß die experimentell gefundenen ?Point-on-line koinzidenten? Strukturen energetisch günstige Anordnungen des Molekülgitters bezüglich des Substratgitters darstellen. Die Eignung der neuen Berechnungsmethode zur Vorhersage der günstigsten Adsorbatgitterstruktur für ein gegebenes System aus Molekül und Substrat, wird anhand des Systems peri-Hexabenzocoronen (HBC) auf Graphit demonstriert. Das organisch-organische Heteroepitaxiesystem PTCDA auf HBC auf Graphit wird untersucht, um zu klären, inwieweit sich die dafür gültigen Ordnungsmechanismen von denen unterscheiden, die für das Wachstum des organisch-anorganischen Heteroepitaxiesystems PTCDA auf Graphit verantwortlich sind. Dabei gelingt es, eine bisher nicht klassifizierte Art von Epitaxie, d.h. substratinduzierter Ordnung, nachzuweisen. Dieser neue Epitaxietyp ist bedingt durch die innere Struktur einer Substrateinheitszelle - das Substrat ist ja hier selbst eine Schicht geordneter Moleküle, die natürlich eine innere Struktur aufweisen. Im folgenden wird ein verallgemeinertes Klassifizierungssystem für Epitaxietypen abgeleitet, welches den neuen Epitaxietyp beinhaltet. Im letzten Kapitel wird die Struktur von der ersten Lagen von Titanylphthalocyanin (TiOPc) auf Au(111) experimentell untersucht und mit entsprechenden Potentialoptimierungsrechnungen verglichen. Die Übereinstimmung von experimentellen und theoretischen Ergebnissen zeigt, daß die GRID Technik, zumindest prinzipiell, auch für Molekülschichten auf Metallsubstraten anwendbar ist
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Öz, Senol [Verfasser]. « Process-, Solvent- and Chemical Engineering for Solution Processed Organic-Inorganic Lead Halide Perovskite Solar Cells / Senol Öz ». München : Verlag Dr. Hut, 2018. http://d-nb.info/1170473601/34.

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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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Lini, Matilde. « Optoelectronic characterization of hybrid organic-inorganic halide perovskites for solar cell and X-ray detector applications ». Master's thesis, Alma Mater Studiorum - Università di Bologna, 2021. http://amslaurea.unibo.it/23213/.

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In the last 10 years, the research interest has been drawn towards the hybrid organic-inorganic halide perovskites, an innovative material characterized by remarkable optoelectronic properties and by its simplicity of fabrication; hybrid halide perovskites are currently being employed as active material in solar cells, X-ray photodetectors and light emitting devices. The following thesis presents the characterization of two perovskite-based materials. The first is a methylammonium lead iodide (MAPbI3) thin film solar cell, which has been fabricated and characterized at the University of Konstanz (Germany), with the aim to optimize the deposition procedure. The second material is a methylammonium lead bromide (MAPbBr3) single crystal that have been characterized at the University of Bologna with surface photovoltage and photocurrent spectroscopies, as a function of the deposited dose of X-rays in order to monitor the induced effects of radiation. After the exposure to X-rays, the exciton binding energy, calculated from the surface photovoltage spectra, has been found to increase by 20 meV with respect to the not irradiated sample. A similar result has been found with the photocurrent spectroscopy. The reasons for the increase in binding energy is discussed and attributed to a change in polarizability of the single crystal. The recovery of the crystals has been registered as well and has shown that the material is able to return to the initial condition after just few hours from the last X-ray's deposition.
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Livres sur le sujet "Organic and inorganic Lead"

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IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Inorganic and organic lead compounds. Lyon, France : International Agency for Research on Cancer, 2006.

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Programme, United Nations Environment, International Labour Organisation, World Health Organization, International Program on Chemical Safety. et WHO Task Group on Environmental Health Criteria., dir. Inorganic lead. Geneva : World Health Organization, 1995.

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Parnes, Robert. Organic & inorganic fertilizers. Mt. Vernon, ME : Woods End Agricultural Institute, 1986.

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Hearn, Leo C. Inorganic lead guidance document. Fairfax, Va : American Industrial Hygiene Association, 1995.

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V, Ramamurthy, et Schanze Kirk S, dir. Organic and inorganic photochemistry. New York : M. Dekker, 1998.

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Organic and inorganic nanostructures. Boston : Artech House, 2005.

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Kalia, Susheel, et Yuvaraj Haldorai, dir. Organic-Inorganic Hybrid Nanomaterials. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13593-9.

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Mark, J. E., C. Y.-C. Lee et P. A. Bianconi, dir. Hybrid Organic-Inorganic Composites. Washington, DC : American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0585.

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Brunet, Ernesto, Jorge L. Colón et Abraham Clearfield, dir. Tailored Organic-Inorganic Materials. Hoboken, NJ : John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118792223.

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Delville, Marie-Helene, et Andreas Taubert, dir. Hybrid Organic-Inorganic Interfaces. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527807130.

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Chapitres de livres sur le sujet "Organic and inorganic Lead"

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Seo, Seongrok, et Hyunjung Shin. « Electronic Properties of Organic–Inorganic Lead Halide Perovskite ». Dans Multifunctional Organic-Inorganic Halide Perovskite, 11–33. New York : Jenny Stanford Publishing, 2022. http://dx.doi.org/10.1201/9781003275930-2.

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Huber, F. « By Interaction of Lead (II) Salts with an Active Organometallic and an Organic Halide ». Dans Inorganic Reactions and Methods, 387–88. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch156.

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Johnson, Benjamin. « Advances in Organic Chemistry, Catalysis, and the Chemical Industry ». Dans Making Ammonia, 29–42. Cham : Springer International Publishing, 2012. http://dx.doi.org/10.1007/978-3-030-85532-1_3.

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AbstractAs we saw in the last section, the modern understanding of chemistry began in the second half of the eighteenth century with the advances of Antoine Lavoisier and others, and further contributions from John Dalton and Jöns Jacob Berzelius in the early 1800s. This period saw the emergence of organic chemistry, which, with the help of new conceptual and experimental tools, established itself as a discipline separate from inorganic chemistry over the next half century. The researchers of this period encountered considerable confusion due to the complexities and behavior of organic structures. Aided by increasingly accurate elementary analysis, they nevertheless made significant advances based on the empirical studies of structure chemistry. While these developments, along with other factors, helped the chemical and dye industries make large strides in chemical synthesis, the conceptual and experimental tools did not supply sufficient understanding of chemical systems to enable ammonia synthesis from the elements. Here we will focus on two developments that illustrate the experimentally-based approach to organic chemistry in the 1800s in order to frame the conceptual leap in physical chemistry toward the end of the century that led to Fritz Haber’s breakthrough.
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Benincasa, Fabrizio, Matteo De Vincenzi et Gianni Fasano. « Alexander von Humboldt, da 250 anni il teorizzatore dello studio interdisciplinare dell’ambiente ». Dans Proceedings e report, XVIII—XXIII. Florence : Firenze University Press, 2020. http://dx.doi.org/10.36253/978-88-5518-147-1.01.

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In 19th century birth of the term scientist led to beginning of Sciences professionalization and end of Nature eclectic scholar, of which Humboldt was the last exponent. Humboldt managed to connect all disciplines in a holistic vision of the world: organic and inorganic nature form a single system of active forces; all the organisms of Earth are linked as a family sharing same home. Today, given the anthropogenic damage caused to Nature, it needs to reconsider his unified vision, establishing connections between scholars of various disciplines, for an organic and global vision of Environment.
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Newell, Lyman C., R. N. Maxson et J. P. Mcreynolds. « Lead Dioxide ». Dans Inorganic Syntheses, 45–47. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch16.

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Bailar, John C., W. C. Fernelius et H. A. Skinner. « Lead Tetracetate ». Dans Inorganic Syntheses, 47–49. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch17.

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Olson, G. J., et F. E. Brinckman. « Lead ». Dans Inorganic Reactions and Methods, 429. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch179.

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Dräger, M., et N. Kleiner. « Formation of the Lead-Lead Bond ». Dans Inorganic Reactions and Methods, 96. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch61.

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Bellama, J. M. « With Lead ». Dans Inorganic Reactions and Methods, 157. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch123.

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Bellama, J. M. « With Lead ». Dans Inorganic Reactions and Methods, 159. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch128.

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Actes de conférences sur le sujet "Organic and inorganic Lead"

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Runina, K. I., O. B. Petrova, A. V. Khomyakov, M. P. Zykova, I. Ch Avetissov et M. N. Mayakova. « Organo-Inorganic Luminescent Hybrid Materials Based on Lead Fluoride and Organic Phosphors ». Dans 2019 IEEE 8th International Conference on Advanced Optoelectronics and Lasers (CAOL). IEEE, 2019. http://dx.doi.org/10.1109/caol46282.2019.9019423.

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Horvath, Endre, Massimo Spina, Bálint Náfrádi, Eric Bonvin, Márton Kollár, Andrzej Sienkievicz, Anastasiia Glushkova, Alla Aracheeva, Zsolt Szekrényes et Hajnalka Tóháti. « Organic-inorganic lead halide perovskite nanowires : formation mechanism and optoelectronic applications ». Dans 2nd Asia-Pacific Hybrid and Organic Photovoltaics. Valencia : Fundació Scito, 2017. http://dx.doi.org/10.29363/nanoge.ap-hopv.2018.041.

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Uratani, Hiroki, et Koichi Yamashita. « Inorganic Lattice Fluctuation Induces Charge Separation in Lead Iodide Perovskites : Theoretical Insights ». Dans 2nd Asia-Pacific Hybrid and Organic Photovoltaics. Valencia : Fundació Scito, 2017. http://dx.doi.org/10.29363/nanoge.ap-hopv.2018.031.

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Wang, Kaiyang, Zhiyuan Gu, Shuai Liu, Wenzhao Sun, Nan Zhang et Qinghai Song. « Organic-inorganic Lead Halide Perovskite CH3NH3PbBr3 Nanolaser Array based on Silicon Grating ». Dans CLEO : Science and Innovations. Washington, D.C. : OSA, 2017. http://dx.doi.org/10.1364/cleo_si.2017.sm4n.2.

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Deschler, Felix. « Photophysics of Organic-inorganic Lead Halide Perovskites for Optically Pumped Lasing Structures ». Dans CLEO : Science and Innovations. Washington, D.C. : OSA, 2016. http://dx.doi.org/10.1364/cleo_si.2016.sw1m.1.

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Singh, Rajan Kumar, Saumya R. Dash, Ranveer Kumar, Neha Jain et Jai Singh. « Role of organic and inorganic cations on thermal behavior of lead iodide perovskites ». Dans 9TH NATIONAL CONFERENCE ON THERMOPHYSICAL PROPERTIES (NCTP-2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5031736.

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Sachchidanand, Anil Kumar et Pankaj Sharma. « A comparative study of the organic and inorganic photovoltaic cells with/ without lead cation ». Dans 2021 International Conference on Control, Automation, Power and Signal Processing (CAPS). IEEE, 2021. http://dx.doi.org/10.1109/caps52117.2021.9730721.

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Abdou, Rana, Mohamed alHor, Zubair Ahmed et Noora Althani. « Development of organic–inorganic Halide Perovskites (OHPs) based Memristors ». Dans Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2021. http://dx.doi.org/10.29117/quarfe.2021.0017.

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Organic – inorganic halide perovskite (OHP) has drawn researchers’ attention working in the field of optoelectronics from last ten years due to its remarkable optical properties such as adjustable band gap, ambipolar charge transport, high optical absorption coefficients, and extended carrier diffusion lengths. OHP based memristors (memory + resistors) are a newly introduced passive two-terminal, nonlinear device used for information storage. In this work we have fabricated methyl ammonium lead iodide (MAPbI3) crystals-based device from MAPbI3 crystals. The crystals have been developed by simple solution process-based method. Developed crystals have shown highly porous geometry and trap charges across these pores facilitates higher conductivity. The fabricated device exhibits ~2.7 milli second response recovery time, which enabled elevated speed and showed hysteresis in the I-V characteristics thus demonstrating superior storage capacities. Hence, the developed device has been potential tool for next-generation non-volatile memories.
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Fruhling, Colton, Kang Wang, Sarah Chowdhury, Alexander Kildishev, Xiangeng Meng, Letian Dou, Alexandra Boltasseva et Vladimir M. Shalaev. « Demonstration of Coherent Random Lasing in Optically Thin Quasi-2D Lead-halide Perovskite ». Dans CLEO : QELS_Fundamental Science. Washington, D.C. : Optica Publishing Group, 2022. http://dx.doi.org/10.1364/cleo_qels.2022.fth5d.1.

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Random lasing in organic-inorganic lead halide quasi-2D perovskite was observed by measuring lasing threshold, spectral narrowing, spectral correlations and critical volume. The photon transport mean free path is found to be comparable to the lasing wavelength, suggesting a hybrid localized-diffusive lasing regime.
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Singh, Nitesh Kumar, Anshul Agarwal, Tirupathiraju Kanumuri et Tarun Varshney. « A Study of an Inorganic-Organic HTM on the Implementation of Lead based PSC Device ». Dans 2020 IEEE Students Conference on Engineering & Systems (SCES). IEEE, 2020. http://dx.doi.org/10.1109/sces50439.2020.9236734.

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Rapports d'organisations sur le sujet "Organic and inorganic Lead"

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Haddad, Timothy S., et Brent D. Viers. Organic Polymers Modified with Inorganic Polyhedra. Fort Belvoir, VA : Defense Technical Information Center, mai 2002. http://dx.doi.org/10.21236/ada410052.

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Brill, Thomas B. Organic-Inorganic Interactions in Hydrothermal Processing. Fort Belvoir, VA : Defense Technical Information Center, octobre 2002. http://dx.doi.org/10.21236/ada412728.

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Molina, Jean-Alex E., Aviva Hadas, C. Edward Clapp et Sala Feigenbaum. Nitrogen Exchange between Organic and Inorganic Pools in Soil-Organic Residues Systems. United States Department of Agriculture, novembre 1987. http://dx.doi.org/10.32747/1987.7568082.bard.

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Jewett, Kenneth L., William R. Blair, Frederick E. Brinckman et Francis W. Wang. Stability of aqueous inorganic lead solutions in polycarbonate containers. Gaithersburg, MD : National Institute of Standards and Technology, 1991. http://dx.doi.org/10.6028/nist.ir.4725.

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Phillips, S., R. Gonzales, K. Chaffee, T. Haddad et G. Hoflund. Remarkable AO Resistance of POSS Inorganic/Organic Polymers. Fort Belvoir, VA : Defense Technical Information Center, janvier 2000. http://dx.doi.org/10.21236/ada397900.

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Haddad, Tim, et Shawn Phillips. Nanostructured Hybrid Organic/Inorganic Materials. Silsesquioxane Modified Plastics. Fort Belvoir, VA : Defense Technical Information Center, décembre 1998. http://dx.doi.org/10.21236/ada409298.

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Francis, Matthew. Virus-Based Scaffolds for Organic/Inorganic Hybrid Materials. Fort Belvoir, VA : Defense Technical Information Center, janvier 2006. http://dx.doi.org/10.21236/ada455770.

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Haddad, Timothy S., Russell Stapleton, Hong G. Jeon, Patrick T. Mather et Joseph D. Lichtenhan. Nanostructured Hybrid Organic/Inorganic Materials, Silsesquioxane Modified Plastics. Fort Belvoir, VA : Defense Technical Information Center, janvier 1996. http://dx.doi.org/10.21236/ada386916.

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Phillips, Shawn H., Rene I. Gonzalez, Rusty L. Blanski, Brent D. Viers et Gar B. Hoflund. Hybrid Inorganic/Organic Reactive Polymers for Severe Environment Protection. Fort Belvoir, VA : Defense Technical Information Center, février 2002. http://dx.doi.org/10.21236/ada410034.

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Allcock, Harry L. Inorganic-Organic Polymers and Their Role in Materials Science. Fort Belvoir, VA : Defense Technical Information Center, mai 1994. http://dx.doi.org/10.21236/ada279715.

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