Relevant bibliographies by topics / 030304 Physical Chemistry of Materials

Academic literature on the topic '030304 Physical Chemistry of Materials'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "030304 Physical Chemistry of Materials"

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Fischlschweiger, Michael, and Sabine Enders. "Thermodynamic Principles for the Design of Polymers for Drug Formulations." Annual Review of Chemical and Biomolecular Engineering 10, no. 1 (June 7, 2019): 311–35. http://dx.doi.org/10.1146/annurev-chembioeng-060718-030304.

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Polymers play an essential role in drug formulation and production of medical devices, implants, and diagnostics. Following drug discovery, an appropriate formulation is selected to enable drug delivery. This task can be exceedingly challenging owing to the large number of potential delivery methods and formulation and process variables that can interact in complex ways. This evolving solubility challenge has inspired an increasing emphasis on the developability of drug candidates in early discovery as well as various advanced drug solubilization strategies. Among the latter, formulation approaches that lead to prolonged drug supersaturation to maximize the driving force for sustained intestinal absorption of an oral product, or to allow sufficient time for injection after reconstitution of a parenteral lyophile formulation, have attracted increasing interest. Although several kinetic and thermodynamic components are involved in stabilizing amorphous dispersions, it is generally assumed that maximum physical stability, defined in terms of inhibition of drug crystallization, requires that the drug and excipient remain intimately mixed. Phase separation of the drug from its excipient may be the first step that ultimately leads to crystallization. We discuss the role of advanced thermodynamics using two examples: ASD and vitamin E–stabilized ultrahigh–molecular weight polyethylene implants.
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Ghayeni, Hamid Reza, Reza Razeghi, and Abolfazl Olyaei. "Synthesis and characterization of nitro-functionalized hydroxyl-terminated polybutadiene using N-iodosuccinimide." Polymer Bulletin 77, no. 9 (October 25, 2019): 4993–5004. http://dx.doi.org/10.1007/s00289-019-03004-6.

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Rueda, Juan Carlos, Carlos Suárez, Hartmut Komber, Stefan Zschoche, and Brigitte Voit. "Synthesis and characterization of pH- and thermo-responsive hydrogels based on poly(2-cyclopropyl-2-oxazoline) macromonomer, sodium acrylate, and acrylamide." Polymer Bulletin 77, no. 10 (November 30, 2019): 5553–65. http://dx.doi.org/10.1007/s00289-019-03034-0.

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Goto, Kazuhiro. "Physical chemistry of functional materials." Bulletin of the Japan Institute of Metals 26, no. 7 (1987): 661–65. http://dx.doi.org/10.2320/materia1962.26.661.

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Wang, Moran. "The physical chemistry of materials." Materials Today 13, no. 3 (March 2010): 67. http://dx.doi.org/10.1016/s1369-7021(10)70043-2.

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Bulut, Niyazi. "Physical chemistry and functional materials: 2019." Journal of Thermal Analysis and Calorimetry 139, no. 6 (January 20, 2020): 3817–19. http://dx.doi.org/10.1007/s10973-019-09242-0.

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Quesnel, Etienne, Frédéric Roux, Fabrice Emieux, Pascal Faucherand, Emmanuel Kymakis, George Volonakis, Feliciano Giustino, et al. "Graphene-based technologies for energy applications, challenges and perspectives." 2D Materials 2, no. 3 (August 6, 2015): 030204. http://dx.doi.org/10.1088/2053-1583/2/3/030204.

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Morpurgo, Alberto F., and Björn Trauzettel. "Special issue on Graphene." Semiconductor Science and Technology 25, no. 3 (February 3, 2010): 030301. http://dx.doi.org/10.1088/0268-1242/25/3/030301.

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Kim, Jang-Joo, Min-Koo Han, and Yong-Young Noh. "Flexible OLEDs and organic electronics." Semiconductor Science and Technology 26, no. 3 (February 14, 2011): 030301. http://dx.doi.org/10.1088/0268-1242/26/3/030301.

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Suda, Jun. "Special issue on wide-bandgap semiconductor power electronics." Semiconductor Science and Technology 31, no. 3 (January 26, 2016): 030301. http://dx.doi.org/10.1088/0268-1242/31/3/030301.

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Dissertations / Theses on the topic "030304 Physical Chemistry of Materials"

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O'Brien, Stephen. "The chemistry of mesoporous materials." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390532.

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Ngabe, Barnabe. "Physical chemistry of sulphide self-heating." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123024.

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ABSTRACTA prerequisite step towards building a self-heating (SH) model for sulphide materials is the determination of physico-chemical parameters such as the specific heat capacity (Cp), and the energy of activation (Ea). The specific heat capacity of one copper and three nickel concentrates was determined over the temperature range 50 to 80oC in the presence of 6% moisture using the self-heating (SH) apparatus and confirmed by Drop Calorimetry. The Cp values from both techniques were comparable. The Cp values were similar for all concentrates increasing from 0.4 to 1.4 Jg-1K-1 as temperature increased from 50 to 80oC. From the Cp values, the enthalpy change (ΔH), the entropy change (ΔS) and the Gibbs free energy change (ΔG) for self-heating, were determined. The ΔG was negative, demonstrating that self-heating of the concentrates was spontaneous.Using the self-heating apparatus the, activation energy (Ea) was determined for the Ni-and Cu-concentrates and for pairs of sulphide minerals. The Ea ranged from 22 to 30 kJ.mol-1, implying a common reaction. Further support for a common reaction is the strong positive correlation between Ea and ln(QA/Cp) where Q (J.kg-1) is the heat of reaction causing self-heating and A the Arrhenius pre-exponential factor (s-1). Comparing to literature, the Ea values correspond to partial oxidation of hydrogen sulphide, supporting the contention that H2S may be an intermediate product in the self-heating of sulphide minerals. A positive relationship between Ea and the rest potential difference (ΔV) for the sulphide pairs and a negative relationship between Cp and ΔV were demonstrated which support a connection between self-heating and the galvanic effect.
RESUMÉLa réalisation d'un modèle mathématique de l'auto-échauffement des concentrés sulfurés de nickel et de cuivre et des mélanges des minerais sulfurés, enjoint à la détermination des paramètres physico-chimiques tels que les capacités de chaleur spécifiques (Cp), et les énergies d'activation (Ea). Les capacités de chaleur spécifiques d'un concentré de cuivre et de trois concentrés de nickel contenant 6% d'humidité, ont été déterminées par utilisation d'un instrument de mesure de vitesse d'auto – échauffement et validées par la calorimétrie de chute dans l'intervalle de températures allant de 50 à 80oC. Les Cp (0.4 à 1.4 Jg-1K-1) obtenues sont similaires pour tous les échantillons. A partir des valeurs des Cp, les variations de l'enthalpie (ΔH), l'entropie (ΔS) et de l'énergie libre de Gibbs (ΔG) de l'auto échauffement ont été déterminées. La valeur négative de ΔG confirme le caractère spontané de l'auto échauffement des minerais sulfurés.Les énergies d'activation (Ea) pour l'auto-échauffement des concentrés de nickel et cuivre et des paires de minerais sulfurés étaient déterminées en faisant usage de l'appareil d'auto-échauffement. Les Ea ainsi obtenues oscillent entre 22 et 30 kJ.mol-1 : Ce qui est suggestif d'une rèaction chimique commune gouvernant l'auto-échauffement de ces matériaux. Ce fait est corroboré par la forte corrélation obtenue entre Ea et ln(QA/Cp) (Q (J.kg-1) est la chaleur de la rèaction chimique responsable de l'auto-échauffement et A (s-1) la constante d'Arrhenius).Ensuite celles-ci sont similaires à celle de l'oxydation partielle du H2S. Il se pourrait, ce faisant, que H2S soit un composé intermediaire lors de l'auto–échauffement des sulfures.Enfin, la corrélation positive entre Ea et la difference de potential (ΔV) dans les paires de minerais sulfurés et celle negative entre Cp et ΔV sont une preuve qu'il existe bel et bien une connection entre l'auto-échauffement et l'effet galvanique.
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Frank, Robert A. "Physical chemistry of carbothermic reduction of alumina." Thesis, Massachusetts Institute of Technology, 1985. http://hdl.handle.net/1721.1/15150.

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Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1985.
MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE
Vita.
Bibliography: leaves 177-180.
by Robert A. Frank.
M.S.
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Tavener, P. "Electron spectroscopy of electrode materials." Thesis, University of Oxford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370304.

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Yager, Kevin G. "Investigation of photomechanical surface patterning in azobenzene materials." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103017.

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Detailed modeling and experiments were conducted in order to elucidate the nature of photo-induced surface patterning in azobenzene materials. Using a cellular automaton simulation, it was established that both the absolute temperature rise, and the thermal gradient, in a film during patterning are negligibly small. These results, confirmed experimentally by patterning samples on substrates of differing thermal conductivity, eliminate purely thermal mechanisms as candidate explanations for mass transport. The length-scale of patterning was probed by monitoring the formation and thermal erasure of gratings as a function of film thickness. In both cases, film dynamics deviate from bulk behavior when film thickness decreases below ~150 nm. Moreover, mass transport is completely hindered below 40 nm. This deviation of polymer dynamics implies that photo-induced mass transport involves the coordinated motion of many polymer chains in the depth of the material, and not merely surface diffusion of individual chains.
Neutron reflectometry was applied to measure in detail the photomechanical response of azobenzene materials. A significant photo-expansion effect, up to 17%, was observed at 25°C, attributed to the molecular free volume requirement of azo isomerization. Above a well-defined crossover temperature, which occurs at ~50°C for poly(disperse red 1 acrylate), the material response is inverted. At these elevated temperatures, photo-contraction effects, of more than -15%, were instead measured. In this case the combination of photo-induced motion and thermally-enabled mobility enables aggregation, aromatic stacking, and crystallization of the azobenzene dipoles. Using localized surface patterning experiments, it was confirmed that the mass transport phenomenon exhibits the same trend and phase relationship as the photomechanical effect. It is argued that the fundamental origin of surface mass transport in azo materials is in fact this newly identified photomechanical effect. This suggestion enables explanation of a variety of previously contradictory results in the literature.
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Pope, Chris. "Hyroxylic polymers as materials for permanent holograms." Thesis, Cranfield University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357054.

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Rocheleau, Marie-Josée. "Investigation of membrane materials for solid-state, ion-selective electrodes." Thesis, McGill University, 1990. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74675.

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The preparation and characterization of new materials to make ion-selective membranes are described. The usefulness of zinc orthophosphate and zinc mercuric thiocyanate to make a carbon-support electrode responsive to zinc was investigated. Better results were obtained with zinc orthophosphate. However, the electrode response was lowered by the formation of acidic oxides on the surface of the electrode, and interferences from copper(II), lead(II), and cadmium(II) were observed. An indirect potentiometric method based on the selective monitoring of chlorozincate(II) or cyanozincate(II) anions with a coated-wire ion-selective electrode was proposed as an alternative for monitoring zinc ion. The application of quaternary ammonium, phosphonium, and alkyl phosphate ionic polymer membranes to potentiometric and voltammetric analysis was also studied. Ionic polymer membranes offer a number of advantages, namely improved membrane lifetime and enhanced adherence to solid-substrate electrodes, when compared to conventional ion-selective membranes. The last stage of this research focused on the application of ionic polymer membrane electrodes in flow injection analysis.
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Shaw, Christopher P. "Polymeric materials for piezoelectricity and second harmonic generation." Thesis, Cranfield University, 1991. http://dspace.lib.cranfield.ac.uk/handle/1826/3674.

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Studies have been undertaken to utilise the possible potential of the rodlike, helical structures associated with polyglutamates and polyisocyanates for piezoelectric (PE) and nonlinear optical (second harmonic generation (SHG)) applications. Various techniques have been employed to form samples/films of these polymers containing oriented helices whose bulk structures are non-centrosymmetric, (an important criterium for the aforementioned applications). Owing to the poor yields obtained for certain intermediates in the synthetic stages of these polymers, only poly('S-benzyl-L-glutamate) (PBzLG) and poly(n- hexylisocyanate) (PHIC) were available for subsequent studies. Piezoelectric work was limited to hydrostatic measurements (d3h) made on electrically poled, composite (guest host), polymer samples. Phase separation was common in all the samples, but no piezoelectric response was observed. However, low concentration (not greater than 10% w/w) of active polymer (PBzLG or PHIC) and high conductivity during the poling stage, may have accounted for the lack of response. Electrically poled, homopolymer samples of PBzLG and PHIC were achieved using a solvent evaporation technique. Nonlinear optical studies of these poled samples revealed threshold fields above which detectable levels of SHG could be observed, (i.e. PBzLG > 40 V/mm, PHIC > 150 V/mm). The variation of SHG signal versus the angle of polarisation of the incident laser light (1064 nm) relative to the poling direction of the film, implied biaxial symmetry was present in the case of PBzLG, whereas the more conventional uniaxial symmetry was observed for PHIC. The variation in SHG signal observed for a fixed thickness was attributed to varying degrees of alignment, resulting from uneven poling. Although PHIC and PBzLG showed low SHG activity (less than value for urea), little ageing of this activity occurred over the 6 month testing period. Langmuir Blodgett studies carried out on chemically modified, low molecular weight PBzLG molecules showed poor transference of the monolayer to a quartz substrate once ten layers had been deposited. In addition, areas per molecule (or per residue) calculated from the pressure-area isotherms, proved inconclusive when deducing possible orientations for the PBzLG helices. No SHG signal was observed for the L.B. films.
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Dennis, J. S. "The desulphurisation of flue gases using calcareous materials." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372626.

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Simpson, W. Mark. "Solid state NMR studies of molecular crystalline materials." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362006.

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Books on the topic "030304 Physical Chemistry of Materials"

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Maier, Joachim. Physical Chemistry of Ionic Materials. Chichester, UK: John Wiley & Sons, Ltd, 2004. http://dx.doi.org/10.1002/0470020229.

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Pizzini, Sergio. Physical chemistry of semiconductor materials and processes. Chichester, West Sussex: John Wiley & Sons, Inc., 2015.

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Blasse, G. Luminescent materials. Berlin: Springer-Verlag, 1994.

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Pizzini, Sergio. Physical Chemistry of Semiconductor Materials and Processes. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118514610.

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Bulusu, Surya N. Chemistry and Physics of Energetic Materials. Dordrecht: Springer Netherlands, 1990.

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Saĭfullin, R. S. Physical chemistry of inorganic, polymeric, and composite materials. Edited by Kemp T. J. 1938-. New York: Ellis Horwood, 1992.

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Saifullin, Renat S. Physical chemistry of inorganic polymeric and composite materials. New York: Ellis Horwood, 1992.

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Laskar, A. L. Diffusion in Materials. Dordrecht: Springer Netherlands, 1990.

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Lazarev, P. I. Molecular Electronics: Materials and Methods. Dordrecht: Springer Netherlands, 1991.

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service), SpringerLink (Online, ed. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Book chapters on the topic "030304 Physical Chemistry of Materials"

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van der Put, Paul J. "Inorganic Physical Chemistry." In The Inorganic Chemistry of Materials, 345–80. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-0095-1_10.

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Cuevas-Diarte, M. À., and D. Mondieig. "Phase Change Materials." In Physical Chemistry in Action, 291–304. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68727-4_12.

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Pomogailo, Anatolii D., and Gulzhian I. Dzhardimalieva. "Physical Chemistry of Intercalated System." In Nanostructured Materials Preparation via Condensation Ways, 205–86. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-90-481-2567-8_5.

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Hawk, Jennifer L., and Stephen L. Craig. "Physical and Materials Applications of Pincer Complexes." In Topics in Organometallic Chemistry, 319–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-31081-2_11.

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Adler, David. "Chemistry and Physics of Covalent Amorphous Semiconductors." In Physical Properties of Amorphous Materials, 5–103. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-2260-1_2.

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Brunklaus, Gunther, Hans-Wolfgang Spiess, and Hellmut Eckert. "Solid State NMR: A Versatile Tool in Solid State Chemistry and Materials Science." In Methods in Physical Chemistry, 85–158. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527636839.ch4.

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Richter, J., and H. Behret. "Physical Chemistry — Overview and Selected Experiments." In Fluid Sciences and Materials Science in Space, 141–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-46613-7_4.

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Funke, Klaus. "Broadband Conductivity Spectroscopy for Studying the Dynamics of Mobile Ions in Materials with Disordered Structures." In Methods in Physical Chemistry, 191–229. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527636839.ch6.

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Klein, Andreas, Thomas Mayer, Andreas Thissen, and Wolfram Jaegermann. "Photoelectron Spectroscopy in Materials Science and Physical Chemistry: Analysis of Composition, Chemical Bonding, and Electronic Structure of Surfaces and Interfaces." In Methods in Physical Chemistry, 477–512. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527636839.ch15.

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Kusuhiro, Mukai, and Matsushita Taishi. "Interfacial Phenomena of High-Temperature Melts and Materials Processing." In Interfacial Physical Chemistry of High-Temperature Melts, 81–113. Boca Raton : Taylor & Francis, a CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa, plc, [2020]: CRC Press, 2019. http://dx.doi.org/10.1201/9780429265341-4.

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Conference papers on the topic "030304 Physical Chemistry of Materials"

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Stepanovskih, E. I., L. A. Brusnitsina, and T. A. Alekseeva. "Teaching physical chemistry: Electronic labs." In MODERN SYNTHETIC METHODOLOGIES FOR CREATING DRUGS AND FUNCTIONAL MATERIALS (MOSM2020): PROCEEDINGS OF THE IV INTERNATIONAL CONFERENCE. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0068501.

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HYDUTSKY, D. P., D. E. BERGERON, T. E. DERMOTA, J. R. STAIRS, K. L. KNAPPENBERGER, K. M. DAVIS, C. E. JONES, et al. "FUNDAMENTAL CLUSTER STUDIES OF MATERIALS AND ATMOSPHERIC CHEMISTRY." In Clusters and Nano-Assemblies - Physical and Biological Systems. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701879_0011.

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Hopper, Tom, Andrei Gorodetsky, Franziska Krieg, Maryna Bodnarchuk, Xiaokung Huang, Robert Lovrincic, Maksym V. Kovalenko, and Artem A. Bakulin. "Hot-carrier cooling in lead-bromide perovskite materials." In Physical Chemistry of Semiconductor Materials and Interfaces XVIII, edited by Daniel Congreve, Hugo A. Bronstein, Christian Nielsen, and Felix Deschler. SPIE, 2019. http://dx.doi.org/10.1117/12.2528131.

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Chernikov, Alexey. "Exciton propagation in monolayer semiconductors and hybrid materials." In Physical Chemistry of Semiconductor Materials and Interfaces IX, edited by Daniel Congreve, Christian Nielsen, and Andrew J. Musser. SPIE, 2020. http://dx.doi.org/10.1117/12.2568466.

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Bardeen, Christopher J. "Nanoscale interfaces in hybrid materials for exciton fission and fusion (Conference Presentation)." In Physical Chemistry of Interfaces and Nanomaterials XV, edited by Artem A. Bakulin, Natalie Banerji, and Robert Lovrincic. SPIE, 2016. http://dx.doi.org/10.1117/12.2237797.

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Refaely-Abramson, Sivan. "Excitons in functional materials: A computational many-body perspective." In Physical Chemistry of Semiconductor Materials and Interfaces IX, edited by Daniel Congreve, Christian Nielsen, and Andrew J. Musser. SPIE, 2020. http://dx.doi.org/10.1117/12.2567659.

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Clarke, Tracey M. "Understanding Triplets and Charge Carriers in Organic Photovoltaic Materials." In Physical Chemistry of Semiconductor Materials and Interfaces XX, edited by Daniel Congreve, Christian Nielsen, Andrew J. Musser, and Derya Baran. SPIE, 2021. http://dx.doi.org/10.1117/12.2594194.

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Prezhdo, Oleg V., and Carlos Mora Perez. "Ab Initio Quantum Dynamics in Nanoscale Materials and Interfaces." In Physical Chemistry of Semiconductor Materials and Interfaces XX, edited by Daniel Congreve, Christian Nielsen, Andrew J. Musser, and Derya Baran. SPIE, 2021. http://dx.doi.org/10.1117/12.2595741.

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Ehrler, Bruno. "Ion migration in methylammonium lead halide perovskites (Conference Presentation)." In Physical Chemistry of Semiconductor Materials and Interfaces XVII, edited by Hugo A. Bronstein and Felix Deschler. SPIE, 2018. http://dx.doi.org/10.1117/12.2320259.

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Zhao, Lianfeng, YunHui L. Lin, and Barry P. Rand. "Charge-transfer states at 2D metal halide perovskite/organic heterojunctions (Conference Presentation)." In Physical Chemistry of Semiconductor Materials and Interfaces XVII, edited by Hugo A. Bronstein and Felix Deschler. SPIE, 2018. http://dx.doi.org/10.1117/12.2320314.

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Reports on the topic "030304 Physical Chemistry of Materials"

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Dunn, Bruce. Physical Chemistry of Sol-Gel Materials Symposium Held during the 213th National Meeting of the American Chemical Society Held in Anaheim, California on March 21-25, 1999. Fort Belvoir, VA: Defense Technical Information Center, May 2000. http://dx.doi.org/10.21236/ada376790.

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Nechypurenko, Pavlo P., Viktoriia G. Stoliarenko, Tetiana V. Starova, Tetiana V. Selivanova, Oksana M. Markova, Yevhenii O. Modlo, and Ekaterina O. Shmeltser. Development and implementation of educational resources in chemistry with elements of augmented reality. [б. в.], February 2020. http://dx.doi.org/10.31812/123456789/3751.

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The purpose of this article is an analysis of opportunities and description of the experience of developing and implementing augmented reality technologies to support the teaching of chemistry in higher education institutions of Ukraine. The article is aimed at solving problems: generalization and analysis of the results of scientific research concerning the advantages of using the augmented reality in the teaching of chemistry, the characteristics of modern means of creating objects of augmented reality; discussion of practical achievements in the development and implementation of teaching materials on chemistry using the technologies of the augmented reality in the educational process. The object of research is augmented reality, and the subject - the use of augmented reality in the teaching of chemistry. As a result of the study, it was found that technologies of augmented reality have enormous potential for increasing the efficiency of independent work of students in the study of chemistry, providing distance and continuous education. Often, the technologies of the augmented reality in chemistry teaching are used for 3D visualization of the structure of atoms, molecules, crystalline lattices, etc., but this range can be expanded considerably when creating its own educational products with the use of AR-technologies. The study provides an opportunity to draw conclusions about the presence of technologies in the added reality of a significant number of benefits, in particular, accessibility through mobile devices; availability of free, accessible and easy-to-use software for creating augmented-reality objects and high efficiency in using them as a means of visibility. The development and implementation of teaching materials with the use of AR-technologies in chemistry teaching at the Kryvyi Rih State Pedagogical University has been started in the following areas: creation of a database of chemical dishes, creation of a virtual chemical laboratory for qualitative chemical analysis, creation of a set of methodical materials for the course “Physical and colloidal chemistry”.
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Yurovskaya, M. V., and A. V. Yushmanova. Complex Investigations of the World Ocean. Proceedings of the VI Russian Scientific Conference of Young Scientists. Edited by D. A. Alekseev, A. Yu Andreeva, I. M. Anisimov, A. V. Bagaev, Yu S. Bayandina, E. M. Bezzubova, D. F. Budko, et al. Shirshov Institute Publishing House, April 2021. http://dx.doi.org/10.29006/978-5-6045110-3-9.

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Abstract:
The collection contains materials of the VI All-Russian Scientific Conference of Young Scientists "Complex Investigations of the World Ocean", dedicated to the discussion of the main scientific achievements of young specialists in the field of oceanology, modern methods and means of studying the World Ocean. Within the framework of the conference, issues of modern oceanology were considered in sections: ocean physics, ocean biology, ocean chemistry, marine geology, marine geophysics, marine ecology and environmental management, oceanological technology and instrumentation, as well as interdisciplinary physical and biological research of the ocean. Along with the coverage of the results obtained in the course of traditional oceanological expeditionary research, attention was paid to the development of modern methods of studying the ocean: numerical modeling and remote sensing methods of the Earth from space.
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