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Academic literature on the topic 'Crystal structure of metals'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Crystal structure of metals"

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Носенко, Владимир, Vladimir Nosenko, Александр Фетисов, Alexander Fetisov, С. Носенко, S. Nosenko, Валентин Харламов, and Valentin Kharlamov. "Contact interaction intensity and material transfer at grinding and refractory metal micro-scratching." Science intensive technologies in mechanical engineering 2, no. 10 (October 4, 2017): 9–18. http://dx.doi.org/10.12737/article_59d496eb7ba532.91441180.

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Peculiarities in the contact surfaces formation and material transfer at micro-scratching and grinding of refractory metals are investigated. There is shown a connection of metal quantity transferred to the area of crystal wear, a degree of ground surface charging with silicon carbide crystals and wear of an abrasive tool with the electron structure of atoms in refractory metals. It is defined, that the intensity of metal transfer in a crystal surface layer decreases with the increase of a principle quantum number of metal valence electrons. According to the intensity of the interaction silicon carbide during grinding and micro-cutting the refractory metals are classified into adhesion-active metals of IVB, VB sub-groups and inert metals of VIB subgroup of the Periodic Table.

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Gärtner, Stefanie. "Spotlight on Alkali Metals: The Structural Chemistry of Alkali Metal Thallides." Crystals 10, no. 11 (November 7, 2020): 1013. http://dx.doi.org/10.3390/cryst10111013.

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Alkali metal thallides go back to the investigative works of Eduard Zintl about base metals in negative oxidation states. In 1932, he described the crystal structure of NaTl as the first representative for this class of compounds. Since then, a bunch of versatile crystal structures has been reported for thallium as electronegative element in intermetallic solid state compounds. For combinations of thallium with alkali metals as electropositive counterparts, a broad range of different unique structure types has been observed. Interestingly, various thallium substructures at the same or very similar valence electron concentration (VEC) are obtained. This in return emphasizes that the role of the alkali metals on structure formation goes far beyond ancillary filling atoms, which are present only due to charge balancing reasons. In this review, the alkali metals are in focus and the local surroundings of the latter are discussed in terms of their crystallographic sites in the corresponding crystal structures.

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Widom, M., and M. Mihalkovic. "Stability of Fe-Based Alloys With Structure Type C6Cr23." Journal of Materials Research 20, no. 1 (January 2005): 237–42. http://dx.doi.org/10.1557/jmr.2005.0028.

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Bulk metallic glass forms when liquid metal alloys solidify without crystallization. In the search for iron-based bulk glass-forming alloys of the metal–metalloid type (Fe–B- and Fe–C-based), crystals based on the structural prototype C6Cr23 often preempt the amorphous phase. Destabilizing this competing crystal structure could enhance glass formability. We carried out first-principles total energy calculations of enthalpy of formation to identify third elements that can effectively destabilize C6Cr23. Yttrium appears optimal among transition metals, and rare earths also are suitable. Atomic size is the dominant factor.

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Макарова, О. В., М. Н. Палатников, И. В. Бирюкова, and Н. В. Сидоров. "Влияние электронного строения примеси на физические свойства, дефектную структуру и особенности технологии легирования кристаллов ниобата лития." Журнал технической физики 89, no. 12 (2019): 1971. http://dx.doi.org/10.21883/jtf.2019.12.48498.230-18.

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Macro- and microstructure were researched for doped LiNbO3 crystals. The transmission spectra and the effective distribution coefficients of the dopant were studied. The analysis of literature data on ternary phase diagrams of systems Li2O-Nb2O5-dopant oxide and electronic configurations of dopants has revealed a possibility to predict technological growth conditions and quality of doped lithium niobate crystals. At this p-elements (boron) provide growth of structurally and compositionally uniform LiNbO3 crystals without incorporation of a dopant into the structure. Metals, s- and d-elements (magnesium and zinc) influence the melts and the crystal properties similar. At this non-periodical domain structures and similar types of point defects appear. Metals of f-elements (cerium) order the melt structure in such a way that provide forming of growth regular domain structure in LiNbO3 crystals due to their electron configurations. Keywords: crystal, lithium niobate, doping, optical microscopy.

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Radka, Christopher D., Lawrence J. DeLucas, Landon S. Wilson, Matthew B. Lawrenz, Robert D. Perry, and Stephen G. Aller. "Crystal structure ofYersinia pestisvirulence factor YfeA reveals two polyspecific metal-binding sites." Acta Crystallographica Section D Structural Biology 73, no. 7 (June 30, 2017): 557–72. http://dx.doi.org/10.1107/s2059798317006349.

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Gram-negative bacteria use siderophores, outer membrane receptors, inner membrane transporters and substrate-binding proteins (SBPs) to transport transition metals through the periplasm. The SBPs share a similar protein fold that has undergone significant structural evolution to communicate with a variety of differentially regulated transporters in the cell. InYersinia pestis, the causative agent of plague, YfeA (YPO2439, y1897), an SBP, is important for full virulence during mammalian infection. To better understand the role of YfeA in infection, crystal structures were determined under several environmental conditions with respect to transition-metal levels. Energy-dispersive X-ray spectroscopy and anomalous X-ray scattering data show that YfeA is polyspecific and can alter its substrate specificity. In minimal-media experiments, YfeA crystals grown after iron supplementation showed a threefold increase in iron fluorescence emission over the iron fluorescence emission from YfeA crystals grown from nutrient-rich conditions, and YfeA crystals grown after manganese supplementation during overexpression showed a fivefold increase in manganese fluorescence emission over the manganese fluorescence emission from YfeA crystals grown from nutrient-rich conditions. In all experiments, the YfeA crystals produced the strongest fluorescence emission from zinc and could not be manipulated otherwise. Additionally, this report documents the discovery of a novel surface metal-binding site that prefers to chelate zinc but can also bind manganese. Flexibility across YfeA crystal forms in three loops and a helix near the buried metal-binding site suggest that a structural rearrangement is required for metal loading and unloading.

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Eberhart, Mark. "From topology to geometry." Canadian Journal of Chemistry 74, no. 6 (June 1, 1996): 1229–35. http://dx.doi.org/10.1139/v96-138.

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A systematic study of the charge density topologies corresponding to a number of transition metal aluminides with the B2 structure indicates that unstable crystal structures are sometimes associated with uncharacteristic topologies. This observation invites the speculation that the "distance" to a topological instability might relate to a metals phase behavior. Following this speculation, a metric is imposed on the topological theory of Bader, producing a geometrical theory, where it is now possible to assign a distance from a calculated charge density topology to a topological instability. For the cubic transition metals, these distances are shown to correlate with single crystal elastic constants, where the metals that are furthest from an instability are observed to be the stiffest. Key words: crystal structure, charge density topology, mechanical properties, brittle/ductile failure.

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Degtyareva, Olga. "Crystal structure of simple metals at high pressures." High Pressure Research 30, no. 3 (September 2010): 343–71. http://dx.doi.org/10.1080/08957959.2010.508877.

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Gulay, Nataliya, Yuriy Tyvanchuk, Marek Daszkiewicz, Bohdan Stel’makhovych, and Yaroslav Kalychak. "Crystal structure of Sc3Co1.64In4 and Sc10Co9In20 from single-crystal data." Zeitschrift für Naturforschung B 74, no. 3 (March 26, 2019): 289–95. http://dx.doi.org/10.1515/znb-2018-0275.

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AbstractTwo compounds in the Sc-Co-In system were obtained by arc-melting of the pure metals and their crystal structures have been determined using single crystal X-ray diffraction data. The structure of Sc3Co1.64In4 (space group P6̅, а=7.6702(5), c=3.3595(2) Å, Z=1, R1=0.0160, wR2=0.0301) belongs to the Lu3Co2−xIn4 type structure, which is closely related to the ZrNiAl and Lu3CoGa5 types. The structure of Sc10Co9In20 (space group P4/nmm, а=12.8331(1), c=9.0226(1) Å, Z=2, R1=0.0203, wR2=0.0465) belongs to the Ho10Ni9In20 type, which is closely related to HfNiGa2.

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Heying, Birgit, Oliver Niehaus, Ute Ch Rodewald, and Rainer Pöttgen. "Indides RE3T2In4 (RE = Y, Gd–Tm, Lu; T = Ni, Ru, Rh) with a ZrNiAl superstructure." Zeitschrift für Naturforschung B 71, no. 12 (December 1, 2016): 1261–67. http://dx.doi.org/10.1515/znb-2016-0167.

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AbstractThree series of rare earth-transition metal-indides RE3T2In4 (RE=Y, Gd–Tm, Lu; T=Ni, Ru, Rh) were synthesized from arc-melted RE3T2 precursor compounds and indium tear shot in sealed niobium ampoules using different annealing sequences. The new indides crystallize with the hexagonal Lu3Co2In4-type structure, space group P6̅. All samples were characterized on the basis of Guinier powder patterns and six structures were refined from single crystal X-ray diffractometer data. The RE3T2In4 structures are derived from the ZrNiAl type through RE/In ordering, paralleled by a symmetry reduction from P6̅2m to P6̅. This induces twinning for some of the investigated crystals. The main crystal chemical motifs of the RE3T2In4 structures are trigonal prisms of rare earth, respectively indium atoms that are filled by the transition metals.

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Tyvanchuk, Yuriy, Nataliya Gulay, Inna Bigun, Yaroslav Galadzhun, and Yaroslav Kalychak. "The crystal structure of Sc5Co2In4." Zeitschrift für Naturforschung B 70, no. 4 (April 1, 2015): 283–87. http://dx.doi.org/10.1515/znb-2014-0216.

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AbstractThe new intermetallic compound Sc5Co2In4 was synthesized by arc melting of the pure metals. Its crystal structure was investigated from single-crystal X-ray data: Pbam, a = 17.3400(7), b = 7.5940(5), c = 3.3128(2) Å, R1 = 0.0337, wR2 = 0.0620 for 1502 independent reflections with [I >2 σ(I)]. It is the first representative of the Lu5Ni2In4 type with cobalt.

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Dissertations / Theses on the topic "Crystal structure of metals"

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Ponnada, Pradeepthi. "Crystal Structure Determination and Spectral Characterization of Dipeptides with Metals." Youngstown State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1343762067.

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Day, S. "Neutron and optical spectroscopy of alkaline earth metals." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234944.

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Eng, Hank W. "The crystal and electronic structures of oxides containing d0 transition metals in octahedral coordination." Connect to this title online, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1070570079.

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Thesis (Ph. D.)--Ohio State University, 2003.
Title from first page of PDF file. Document formatted into pages; contains xx, 180 p.; also includes graphics. Includes bibliographical references (p. 139-145).

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Kauser, N. "Low temperature anomalies in plastic response of crystalline materials with special reference to dilute solid solutions." Thesis, Brunel University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233340.

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Belot, Céline. "Synthesis, crystal structure and physico-chemical studies on thienyl-substituted alkoxides of the rare earth metals." Besançon, 2009. http://www.theses.fr/2009BESA2016.

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Ce travail porte sur la synthèse, la détermination des structures cristallographiques, l'étude des propriétés électrochimiques et la luminescence de méthoxydes contenant des groupements thiophéniques de métaux alcalins, d' étain(II) et de terres rares. La première partie est consacrée à la synthèse et aux études RMN et cristallographiques des nouveaux composés. Afin de corréler les effets structuraux et stéréoélectroniques sur la géométrie moléculaire, une série d'alcoxydes métalliques a été préparée. La seconde partie traite des propriétés électrochimiques des composés. Les voltammogrammes cycliques sont dominés par la vague d'oxydation des unités thiophéniques. Aucune réduction ou oxydation due aux centres métalliques n'a été constatée. Contrairement aux autres composés, après cyclage de la rampe de potentiels, la formation d'un film électroactif a été observée dans le cas des produits HO-C(CgHsSV3 (1), {Nd[OC(CgHsS2)3]3(thf)3}. 4 thf(10) et Er[OC(CgHsS2)3]3(thf) (11). La troisième partie concerne les propriétés de luminescence des produits. Les spectres d'absorption UV -Vis sont dominés par les ligands organiques. Les spectres d'émission des composés du potassium, sodium et yttrium révèlent de larges bandes attribuées aux transitions [Py*→Py]des groupements aromatiques. En outre, les spectres de luminescence des alcoxydes de Nd3+ et de Sm3+ mettent en évidence un transfert d'énergie (effet d'antenne) entre le ligand et le lanthanide
The present work focuses on the synthesis, crystal structure determination, electrochemical and luminescence studies of thienyl-substituted methoxides of alkali, tin(II) and rare earth metals. The first part is devoted to the synthesis, NMR and crystallographic investigations of the new products. To correlate structural and stereoelectronic effects on the molecular geometry, a series of rare earth metal alkoxides was prepared. The second part deals on the electrochemical properties of the novel compounds. The cyclic voltammograms are dominated by the oxidation wave of the thiophene groups. No reduction or oxidation of the metal centres bas been noticed. Contrarily to the other compounds, the repetitive cycling ofpotentials ofHO-C(CgHsS2)3 (1), {Nd[OC(CgHsS2)3]3(thf)3}. Thf (10) and Er[OC(CgHsS2)3]3(thf) (11) leads to the formation of electroactive polymeric film. The third part concerns the luminescence properties of the novel compounds. The UV-Vis absorption spectra are dominated by the organic ligands. The emission spectra of the potassium, sodium and yttrium compounds reveal broad bands attributed to the [Py* → Py] transitions of the aromatic ligands. Furthermore, the luminescence spectra of the Nd3+ and Sm3+ alkoxides exhibit an energy transfer ("antenna effect") from the Iigand to the lanthanide centre

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Ovchinnikov, Alexander. "Nitridomanganates of alkaline-earth metals." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-215891.

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The main goal of the present work was the synthesis of alkaline-earth nitridomanganates (AExMnyNz) with extended anionic structures and the characterization of their electronic and magnetic properties. Up to now, only compounds with isolated nitridomanganate anions have been reported in the discussed ternary systems. A systematic exploratory synthesis, employing high-temperature treatment of AE nitrides and Mn under controlled N2 pressure, yielded more than ten new nitridomanganates. Their crystal structures contain anionic building blocks of different dimensionalities, ranging from isolated species to three-dimensional frameworks. In general, the formation of Mn-rich compositions was found to be driven by the emergence of Mn-Mn interactions, which creates a link between nitridometalates and transition-metal-rich binary nitrides. The obtained nitridomanganates display a plethora of interesting phenomena, such as large spin-orbit coupling, magnetic frustration, quenching of magnetism due to Mn-Mn interactions, and metal-insulator transition.

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Chan, Eric J. "Structural systematics of complexes of lanthanoid picrates with unidentate O-donor ligands and other related arrays." University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2006. http://theses.library.uwa.edu.au/adt-WU2006.0075.

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Structures as determined by single crystal X-ray methods for lanthanoid(III) compounds for series of simple homoleptic species with diverse ligands frequently display variations entailing a diminution in coordination number (‘C.N.’), a consequence of the variation in the size of the atoms/ions due to the ‘lanthanoid contraction’. A change from C.N. nine to eight is common, clearly separating compounds of the light/‘early’ or heavy/‘later’ metal atoms. Earlier work on the complexes of the lanthanoid(III) picrates arose out of the exploration of simple reagents which might usefully exploit lanthanoid ion properties for purposes such as solvent extraction. They are also of potential synthetic utility because of their relatively high solubility in apolar solvents. This thesis encompasses a systematic structural study of hydrated lanthanoid picrate complexes (including those of yttrium) with a selection of dipolar aprotic solvent ligands, namely trimethylphosphate (‘tmp’), dimethylsulfoxide (‘dmso’), hexamethylphosphoramide (‘hmpa’), N,N´-dimethylacetamide (‘dma’), N-methylpyrrolidinone (‘nmp’) and octamethylpyrophosphoramide (‘ompa’), all liquids at room temperature and all unidentate, with the exception of ompa which can be considered in some cases to behave as the equivalent of two unidentate ligands, in others as a chelate. Structures of adducts of these ligands with scandium picrate are also included in order to gain further insight into the coordination behavior of the totality of the group ‘3’ transition metals, and, for similar reasons, a study of the structures of complexes of Eu(dipivaloylmethanide)3 with the same (solvent) ligands as a ‘baseline’. In the course of these studies, hydrolysis of the aprotic solvent trimethylphosphate was found to lead to novel adducts of the dimethylphosphate (‘dmp’) ligand; the introduction of polycyclic aromatic nitrogen base ligand complexes resulted in further novel mixed ligand compounds, supplemented by a study of protonated base picrate salts. This work aims not only to establish structural ‘domains of existence’ with a concomitant consideration of the associated stereochemistry for these related series of rare earth complexes, but, also, to enhance our understanding of metal ion solvation and the interactions of aromatic groups within these types of crystal structures.

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Koedtruad, Anucha. "SYNTHESIS OF NOVEL METAL HALIDES AND THEIR STRUCTURE-PROPERTY RELATIONS." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263484.

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Liu, Hui-Ping. "Magnetic ordering and crystal structure in selected transition-metal compounds /." Uppsala : Acta Universitatis Upsaliensis, 1999. http://catalogue.bnf.fr/ark:/12148/cb402057270.

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Lyle, Matthew John. "Crystal structure prediction and its application to novel metal oxides." Thesis, University of Cambridge, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708224.

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Books on the topic "Crystal structure of metals"

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Szytuła, Andrzej. Handbook of crystal structures and magnetic properties of rare earth intermetallics. Boca Raton, Fla: CRC Press, 1994.

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Khatamian, D. Crystal structure of thin oxide films grown on Zr-Nb alloys studied by RHEED. Chalk River, Ont: Chalk River Laboratories, 1996.

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Daams, J. L. C. Atlas of crystal structure types for intermetallic phases. Materials Park, OH: ASM International, 1991.

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Daams, J. L. C. Atlas of crystal structure types for intermetallic phases. Materials Park, OH: ASM International, 1991.

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Daams, J. L. C. Atlas of crystal structure types for intermetallic phases. Materials Park, OH: ASM International, 1991.

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Daams, J. L. C. Atlas of crystal structure types for intermetallic phases. Materials Park, OH: ASM International, 1991.

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Daams, J. L. C. Atlas of crystal structure types for intermetallic phases. Materials Park, OH: ASM International, 1991.

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G, Roberts S., Holt D. B, and Wilshaw P. R, eds. Structure and properties of dislocations in semiconductors 1989: Proceedings of the Sixth International Symposium on the Structure and Properties of Dislocations in Semiconductors held at the University of Oxford, 5-8 April 1989. Bristol: Institute of Physics, 1989.

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Satdarova, Faina. DIFFRACTION ANALYSIS OF DEFORMED METALS: Theory, Methods, Programs. xxu: Academus Publishing, 2019. http://dx.doi.org/10.31519/monography_1598.

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General analysis of the distribution of crystals orientation and dislocation density in the polycrystalline system is presented. Recovered information in diffraction of X-rays adopting is new to structure states of polycrystal. Shear phase transformations in metals — at the macroscopic and microscopic levels — become a clear process. Visualizing the advances is produced by program included in package delivered. Mathematical models developing, experimental design, optimal statistical estimation, simulation the system under study and evolution process on loading serves as instrumentation. To reduce advanced methods to research and studies problem-oriented software will promote when installed. Automation programs passed a testing in the National University of Science and Technology “MISIS” (The Russian Federation, Moscow). You score an advantage in theoretical and experimental research in the field of physics of metals.

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Massa, Werner. Crystal structure determination. 2nd ed. Berlin: Springer, 2003.

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Book chapters on the topic "Crystal structure of metals"

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Bolton, William, and R. A. Higgins. "The crystal structure of metals." In Materials for Engineers and Technicians, 51–60. Seventh edition. | Abingdon, Oxon ; New York, NY : Routledge, 2021.: Routledge, 2020. http://dx.doi.org/10.1201/9781003082446-4.

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Overhauser, A. W. "Crystal Structure of Lithium at 4.2 K." In Anomalous Effects in Simple Metals, 424–26. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631469.ch51.

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Bo, Wang, Zong Shufeng, Sun Huilan, Zhang Jianxin, Zhang Yubing, Liu Dongdong, and Liu Jiajia. "Crystal Structure and Alumina Leaching Property of Na2O Doped C12A7." In Light Metals 2014, 77–80. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-48144-9_13.

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Bo, Wang, Zong Shufeng, Sun Huilan, Zhang Jianxin, Zhang Yubing, Liu Dongdong, and Liu Jiajia. "Crystal Structure and Alumina Leaching Property of Na2O Doped C12A7." In Light Metals 2014, 77–80. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118888438.ch13.

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Meijer, Michel D., Robertus J. M. Klein Gebbink, and Gerard van Koten. "Solid-Gas Interactions Between Small Gaseous Molecules and Transition Metals in the Solid State. Toward Sensor Applications." In Crystal Design: Structure and Function, 375–86. Chichester, UK: John Wiley & Sons, Ltd, 2003. http://dx.doi.org/10.1002/0470868015.ch9.

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Chambers, R. G. "Crystal Structures and the Reciprocal Lattice." In Electronics in Metals and Semiconductors, 35–45. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0423-1_3.

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Bo, Wang, Zhang Jianxin, Zong Shufeng, and Sun Huilan. "Effect of Calcium/Aluminium Ratio on Crystal Structure and Al2O3Leaching Property of 12CaO-7Al2O3." In Light Metals 2014, 87–90. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118888438.ch15.

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Bo, Wang, Zhang Jianxin, Zong Shufeng, and Sun Huilan. "Effect of Calcium/Aluminium Ratio on Crystal Structure and Al2O3 Leaching Property of 12CaO·7Al2O3." In Light Metals 2014, 87–90. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-48144-9_15.

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Jankowski, Joseph, Michael Kaufman, Amy Clarke, Krish Krishnamurthy, and Paul Wilson. "Determination of the Intermetallic α-Phase Crystal Structure in Aluminum Alloys Solidified at Rapid Cooling Rates." In Light Metals 2019, 121–27. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-05864-7_17.

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Yin, Jianguo, Wangxing Li, Zhanwei Liu, Zhaohui Su, Zhonglin Yin, and Wentang Xia. "Effect of Crystal Growth Modifier on the Structure of Sodium Aluminate Liquors Analyzed by Raman Spectroscopy." In Light Metals 2012, 125–28. Cham: Springer International Publishing, 2012. http://dx.doi.org/10.1007/978-3-319-48179-1_22.

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Conference papers on the topic "Crystal structure of metals"

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Song, H. H., A. V. Fratini, M. Chabinyc, A. K. AgrawaI, and C. S. Wang. "Crystal structure and thin film morphology of BBL ladder polymer." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835393.

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Fast, Lars, and Per Söderlind. "Crystal structure of a actinide metals at high compression." In Proceedings of the conference of the American Physical Society topical group on shock compression of condensed matter. AIP, 1996. http://dx.doi.org/10.1063/1.50737.

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Jung-Si Lee, Kuo-Chih Huang, Wen-Jwu Wang, and Gene-Hsiang Lee. "Crystal structure and physical properties of 1,3,6,8-tetrakis(etinlthio)pyrene-QMNT coniplex." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835496.

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Green, M. A., M. Kurmoo, P. Day, and J. Stalick. "Crystal structure ans magnetism of the spin-peierls compound GeCuO/sub 3/." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835927.

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Pokrovskii, V. Ya, and S. V. Zaitsev-Zotov. "The effect of crystal-structure defects on tbe low-tenterature conduction of TaS/sub 3/." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835976.

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Yang, C. Y., Y. Yang, and S. Hotta. "Crystal structure and polymorphism of dimethyl-oligothiophenes crystallized epitaxially on highly oriented PTFE thin films." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835400.

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Hosokoshi, Y., M. Tamura, K. Nozawa, S. Suzuki, N. Kinoshita, H. Sawa, and R. Kato. "Magnetic properties and crystal structures of 2-hydro and 2-halo nitronyl nitroxide radical crystals." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835484.

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Rovira, C., J. Tarres, J. Veciana, E. Molins, M. Mas, D. O. Cowan, and S. Yang. "New organic conductors derived from trans-BET-TTF. crystal structure and electrical, optical and magnetic properties." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835536.

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Matsumura, Y., S. Wang, T. Kasuh, and T. Maeda. "Dependence of reversible capacity in the lithium rechargeable batteries on the crystal structure of the carbon electrode." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.836109.

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Sawa, H., Y. Okano, S. Aonuma, and R. Kato. "Crystal and electronic structure of (BPDT-TSeF)-ni(dmit)/sub 2/ system BPDT-TSeF = bis(propylenedithio)-tetraselenafulvalene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834913.

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Reports on the topic "Crystal structure of metals"

1

Fast, L., and P. Soederlind. Crystal structure of actinide metals at high compression. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/113969.

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2

Roberts, Joel Glenn. Surface structure determinations of crystalline ionic thin films grown on transition metal single crystal surfaces by low energy electron diffraction. Office of Scientific and Technical Information (OSTI), May 2000. http://dx.doi.org/10.2172/764397.

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Chin, Bryan A. Crystal Structures of Ordered Carbon Metal Alloys. Fort Belvoir, VA: Defense Technical Information Center, January 1988. http://dx.doi.org/10.21236/ada195597.

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4

Zhang, Xiongzhi, Robert Bau, Jeffrey A. Sheehy, and Karl O. Christe. Crystal Structure of Hexamethylguanidinium Hexafluorosilicate Hexahydrate. Fort Belvoir, VA: Defense Technical Information Center, March 1999. http://dx.doi.org/10.21236/ada408584.

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Zhang, Xiongzhi, Robert Bau, Jeffrey A. Sheehy, and Karl O. Christe. Crystal Structure of Hexamethylguanidinium Hexafluorosilicate Hexahydrate. Fort Belvoir, VA: Defense Technical Information Center, January 1998. http://dx.doi.org/10.21236/ada386864.

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6

Galloway, Heather Claire. Thin films of metal oxides on metal single crystals: Structure and growth by scanning tunneling microscopy. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/219542.

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7

Young, L., C. Kurtz, and S. Hasegawa. Hyperfine structure studies of transition metals. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/166498.

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8

Lee, John. Crystal and Solution Structure of the Photoprotein Obelin. Fort Belvoir, VA: Defense Technical Information Center, October 2002. http://dx.doi.org/10.21236/ada407919.

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Zhang, Rong-Guang, M. L. Westbrook, S. Nance, B. D. Spangler, D. L. Scott, and E. M. Westbrook. The three-dimensional crystal structure of cholera toxin. Office of Scientific and Technical Information (OSTI), February 1996. http://dx.doi.org/10.2172/205782.

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Ho, H. M. Crystal structure and microstructure of el-Fe2O3 particles. Office of Scientific and Technical Information (OSTI), August 1985. http://dx.doi.org/10.2172/6303280.

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