TY - GEN A1 - Rudorf, Wolfram W. A1 - Schmidt, Peer T1 - Studies on synthetic galloalunites AGa3(SO4)2(OH)6: Synthesis, Thermal analysis, and X-ray characterization T2 - Thermochimica Acta N2 - Stoichiometric end member galloalunites of the general formula AGa3(SO4)2(OH)6, with A = Na+, K+, Rb+, H3O+, and NH4+ have been synthesized under hydrothermal conditions. These galloalunites were characterized by chemical methods, thermal analysis (DSC, TG coupled with mass spectroscopy), and powder X-ray diffraction (XRD). The stages of thermal decomposition of sodium, potassium and rubidium galloalunite show a common decomposition mechanism forming β-Ga2O3 and A2SO4 (A = Na+, K+, and Rb+) while ammonium and oxonium galloalunite decompose under formation of pure β-Ga2O3. The thermogravimetric results confirmed the analytical results on the galloalunites and thereby verified the stoichiometry of these synthetic products. Galloalunites with different monovalent cations in A site (i.e. Na+, K+, Rb+, H3O+ and NH4+) crystallize in the rhombohedral space group R-3m (#166). The effects of substitution on the unit cell parameters are rationalized in terms of the structural arrangements in galloalunites. The unit cell parameter c increases with increasing effective ionic radii of the cation in the A site, whereas the parameter a changes to a much lesser degree. KW - Synthesis KW - Galloalunites KW - X-ray diffraction KW - Unit cell parameters KW - Thermal analysis Y1 - 2011 UR - http://www.sciencedirect.com/science/article/pii/S0040603111002310 U6 - https://doi.org/10.1016/j.tca.2011.04.013 VL - 521 IS - 1-2 SP - 112 EP - 120 ER - TY - GEN A1 - Zhang, Xi A1 - Herklotz, Frank A1 - Hieckmann, Ellen A1 - Weber, Jörg A1 - Schmidt, Peer T1 - Vapor phase growth of ZnO single crystals T2 - Journal of Vacuum Science and Technology : A N2 - Zinc oxide is a promising wide band gap semiconductor for future optoelectronic devices. Today ZnO bulk single crystals are grown by three different techniques: hydrothermally, from the melt, and by chemical vapor transport. For our studies, the authors employed in addition a simple and low cost vapor phase method which gives us good quality crystals and flexibility in crystal doping. The as-grown needle-shaped single crystals were characterized by resistivity measurements, scanning electron microscopy, electron backscatter diffraction, and low temperature photoluminescence spectroscopy. Y1 - 2011 UR - http://scitation.aip.org/content/avs/journal/jvsta/29/3/10.1116/1.3553461 U6 - https://doi.org/10.1116/1.3553461 VL - 29 SP - 03A107 ER - TY - GEN A1 - Tschulik, Kristina A1 - Hoffmann, Stefan A1 - Fokwa, Boniface P. T. A1 - Gilleßen, Michael A1 - Schmidt, Peer T1 - Studies regarding the homogeneity range of the zirconium phosphide telluride Zr2+xPTe2 T2 - Solid State Sciences N2 - The phosphide tellurides Zr2+δPTe2 (0 ≤ δ ≤ 1) can be synthesized from the elements in a solid state reaction or by thermal decomposition of Z. Zr2PTe2 decomposes under release of Te2(g) + P4(g) forming the homogeneity range Zr2+δPTe2. The growth of single crystals of Zr2+δPTe2 succeeded by chemical vapour transport using iodine as transport agent from 830 °C in direction of higher temperatures up to 900 °C. Zr2+δPTe2 crystallizes in the rhombohedral space group R-3m (no. 166) with lattice parameters a = 383(1)…386(1) pm and c = 2935(4)…2970(4) pm for δ = 0…1, respectively. Single crystal data have been determined for Zr2.40(2)PTe2 with lattice parameters a = 385.24(4) pm and c = 2967.8(4) pm. The electronic structure and chemical bonding in Zr2+δPTe2 was investigated by the linear muffin–tin orbital (LMTO) method. Both Zr2PTe2 and Zr3PTe2 show non-vanishing DOS values at the Fermi level (EF) indicating metallic character. According to COHP bonding analyses, mainly the heteroatomic Zr–P and Zr–Te bonds are responsible for the structural stability of Zr3PTe2. The new Zr2–Te bond, which is not present in Zr2PTe2, is stronger than Zr1–Te and is thought to be responsible for the stability of phases having Zr in excess. KW - Zirconium phosphide telluride KW - Homogeneity range KW - Thermal decomposition KW - Crystal structure KW - Chemical bonding Y1 - 2010 UR - http://www.sciencedirect.com/science/article/pii/S1293255810003614 U6 - https://doi.org/10.1016/j.solidstatesciences.2010.08.022 SN - 1293-2558 VL - 12 IS - 12 SP - 2030 EP - 2035 ER - TY - GEN A1 - Schöneich, Michael A1 - Schmidt, Marcus P. A1 - Schmidt, Peer T1 - Chemical Vapour Transport of Bismuth and Antimony Chalcogenides M2Q3 (M = Sb, Bi, Q = Se, Te) T2 - Zeitschrift für anorganische und allgemeine Chemie N2 - Thermodynamic modelling of the ternary systems M/Q/I (M = Sb, Bi, Q = Se, Te) indicated solid-gas equilibria suitable for chemical vapour transport of bismuth and antimony chalcogenides. The predictions of the modelling were confirmed by transport experiments on a transport balance. The optimum transport conditions using iodine as transport agent were determined for all systems to: ϑsource = 500 °C and ϑsink = 450 °C. For ΔT > 50 K the sequential transport of chalcogenide iodides MQI followed by M2Q3 occurs. Thermodynamic standard data of the gas species SbI(g) were concluded from equilibrium calculations: ΔH0f,298(SbI(g)) = 106 ± 3 kJ·mol–1; S0298(SbI(g)) = 255 ± 3 J·mol–1·K–1; Cp(SbI(g)) = 37 ± 1 J·mol–1·K–1 KW - Antimony KW - Bismuth KW - Selenium KW - Tellurium KW - Chemical vapor transport KW - Thermodynamic modelling Y1 - 2010 UR - http://onlinelibrary.wiley.com/doi/10.1002/zaac.201000149/full U6 - https://doi.org/10.1002/zaac.201000149 SN - 1521-3749 VL - 636 IS - 9-10 SP - 1810 EP - 1816 ER - TY - GEN A1 - Jahn, Stephan F. A1 - Blaudeck, Thomas A1 - Baumann, Reinhard R. A1 - Jakob, Alexander A1 - Ecorchard, Petra A1 - Rüffer, Tobias A1 - Lang, Heinrich A1 - Schmidt, Peer T1 - Inkjet Printing of Conductive Silver Patterns by Using the First Aqueous Particle-Free MOD Ink without Additional Stabilizing Ligands T2 - Chemistry of Materials N2 - The chemical and physical properties of [AgO2C(CH2OCH2)3H] (3) and its use as an aqueous, ligand-free MOD ink (MOD = metal−organic decomposition) for piezo inkjet printing is discussed. The printed, thermal, or photochemical sintered silver features are electrically conductive on glass (2.7 × 107 S m−1) and PET (PET = polyethylene terephthalate) substrates (1.1 × 107 S m−1) corresponding to 43% and 18% of the bulk silver conductivity. Conducted tape tests show the suitability of the ink for particularly polymer substrates. TG-MS studies demonstrate a two-step decomposition for the conversion of 3 to elemental silver. The structure of 3 in the solid state was determined by single X-ray structure determination. Y1 - 2010 UR - http://pubs.acs.org/doi/abs/10.1021/cm9036428 U6 - https://doi.org/10.1021/cm9036428 SN - 1520-5002 VL - 22 IS - 10 SP - 3067 EP - 3071 ER - TY - GEN A1 - Müller, Carola J. A1 - Schwarz, Ulrich A1 - Schmidt, Peer A1 - Schnelle, Walter A1 - Doert, Thomas T1 - High-Pressure Synthesis, Crystal Structure, and Properties of GdS2 with Thermodynamic Investigations in the Phase Diagram Gd-S, T2 - Zeitschrift für anorganische und allgemeine Chemie N2 - Gadolinium disulfide was prepared by high-pressure synthesis at 8 GPa and 1173 K. It crystallizes in the monoclinic space group P121/a1 (No. 14) with lattice parameters a = 7.879(1) Å; b = 3.936(1) Å, c = 7.926(1) Å and β = 90.08(1)°. The crystal structure is a twofold superstructure of the aristotype ZrSSi and consists of puckered cationic [GdS]+ double slabs that are sandwiched by planar sulfur sheets containing S22– dumbbells. The thermal decomposition of GdS2 proceeds via the sulfur-deficient polysulfides GdS1.9, GdS1.85 and GdS1.77 and eventually results in the sesquisulfide Gd2S3. GdS2 is a paramagnetic semiconductor which orders antiferromagnetically at TN = 7.7(1) K. A metamagnetic transition is observed in the magnetically ordered state. KW - Polysulfides KW - Gadolinium KW - High-pressure synthesis KW - X-ray diffraction KW - Phase diagrams Y1 - 2010 UR - http://onlinelibrary.wiley.com/doi/10.1002/zaac.201000015/full U6 - https://doi.org/10.1002/zaac.201000015 SN - 1521-3749 VL - 636 IS - 6 SP - 947 EP - 953 ER - TY - GEN A1 - Jahn, Stephan F. A1 - Jakob, Alexander A1 - Blaudeck, Thomas A1 - Schmidt, Peer A1 - Lang, Heinrich A1 - Baumann, Reinhard R. T1 - Inkjet printing of conductive patterns with an aqueous solution of [AgO2C(CH2OCH2)3H] without any additional stabilizing ligands T2 - Thin Solid Films N2 - The use of silver(I)-2-[2-(2-methoxyethoxy)ethoxy]acetate, [AgO2C(CH2OCH2)3H], and its application as an aqueous metal-organic decomposition (MOD) inkjet ink is reported. The chemical and physical properties of the silver carboxylate and the ink formulated thereof are discussed. The ink meets all requirements of piezo driven inkjet printing. The printed features were converted into electrically conducting silver patterns by thermal or photo-thermal treatment. The conversion of [AgO2C(CH2OCH2)3H] to elemental silver follows a two-step decomposition as demonstrated by thermogravimetry–mass spectrometry (TG–MS) measurements. The measured conductivities of the printed features on glass and polyethylene-terephthalate (PET) are 2.7 × 107 S m−1 and 1.1 × 107 S m−1, respectively, which correspond to 43% (glass) and 18% (PET) of the bulk silver conductivity. KW - Inkjet printing KW - Silver KW - Carboxylate KW - Ethyleneglycol KW - Flexible electronics Y1 - 2010 UR - http://www.sciencedirect.com/science/article/pii/S0040609010000866 U6 - https://doi.org/10.1016/j.tsf.2010.01.030 SN - 0040-6090 VL - 518 IS - 12 SP - 3218 EP - 3222 ER - TY - GEN A1 - Benndorf, Christopher A1 - Hohmann, Andrea A1 - Schmidt, Peer A1 - Eckert, Hellmut A1 - Johrendt, Dirk A1 - Schäfer, Konrad A1 - Pöttgen, Rainer T1 - 2D 31P Solid state NMR spectroscopy, electronic structure and thermochemistry of PbP7 T2 - Journal of Solid State Chemistry N2 - Phase pure polycrystalline PbP7 was prepared from the elements via a lead flux. Crystalline pieces with edge-lengths up to 1 mm were obtained. The assignment of the previously published 31P solid state NMR spectrum to the seven distinct crystallographic sites was accomplished by radio-frequency driven dipolar recoupling (RFDR) experiments. As commonly found in other solid polyphosphides there is no obvious correlation between the 31P chemical shift and structural parameters. PbP7 decomposes incongruently under release of phosphorus forming liquid lead as remainder. The thermal decomposition starts at T>550 K with a vapor pressure almost similar to that of red phosphorus. Electronic structure calculations reveal PbP7 as a semiconductor according to the Zintl description and clearly shows the stereo-active Pb-6s2 lone pairs in the electron localization function ELF. KW - Polyphosphide KW - Solid state NMR spectroscopy KW - Thermochemistry Y1 - 2016 UR - http://www.sciencedirect.com/science/article/pii/S0022459615302942 U6 - https://doi.org/10.1016/j.jssc.2015.12.028 VL - 235 SP - 139 EP - 144 ER - TY - GEN A1 - Schmidt, Peer A1 - Efimova, Anastasia T1 - Thermal Characterization of Ionic Liquids T2 - OnSet : News, Facts and Professional Solutions for Thermal Analysis N2 - Ionic liquids (ILs) are currently of high interest due to their high performance physicochemical properties over a wide tempera¬ture range of existence of the liquid state. Among the ionic liquids investigated, 1-alkyl- 3-methylimidazolium halides were found generally preferred for their low melting points and ease of handling and preparation. KW - Thermal Properties KW - Ionic Liquids Y1 - 2015 UR - https://dcyd0ggl1hia3.cloudfront.net/media/thermal-analysis/customer-magazine/OnSet_15_en_web.pdf?1454325612&Policy=eyJTdGF0ZW1lbnQiOlt7IlJlc291cmNlIjoiaHR0cHM6XC9cL2RjeWQwZ2dsMWhpYTMuY2xvdWRmcm9udC5uZXRcL21lZGlhXC90aGVybWFsLWFuYWx5c2lzXC9jdXN0b21lci1tYWdhemluZVwvT25TZXRfMTVfZW5fd2ViLnBkZj8xNDU0MzI1NjEyIiwiQ29uZGl0aW9uIjp7IkRhdGVMZXNzVGhhbiI6eyJBV1M6RXBvY2hUaW1lIjoxNTMzNzA4MDcwfX19XX0_&Signature=Q9l-r6mgKOmETHkMaU0IDzTKMH~FdduFunQKnxL6AmEhhrVMKNrbho6JK5pYF0NlM1GPkitI2SxlRwwdygr9m654DWkV5Ka4Qw0NA-BkcKczW4G0dX9WWiXbKk12lQGUe2Z1sMy6i9EJ2vW9wZtn8S-mCQHgrNV~hzE~I8BxV-Q_&Key-Pair-Id=APKAIBNUHYIJDHQEJVRQ VL - 15 SP - 14 EP - 17 ER - TY - CHAP A1 - Binnewies, Michael A1 - Glaum, Robert A1 - Schmidt, Marcus A1 - Schmidt, Peer ED - Dronskowski, Richard ED - Kikkawa, Shinichi ED - Stein, Andreas T1 - Crystal Growth Via the Gas Phase by Chemical Vapor Transport Reactions T2 - Handbook of Solid State Chemistry, Volume 2: Synthesis N2 - The term chemical vapor transport (CVT) summarizes a variety of reactions that show one common feature: a condensed phase, typically a metallic or salt like solid, is volatilized in the presence of a gaseous reactant, the so-called transport agent, and deposits elsewhere, usually in the form of crystals. The deposition will take place if the site of volatilization and the site of crystallization have different temperatures. In many cases, chemical vapor transport is associated with a purification effect. CVT-reactions of elements, oxides, sulfides, selenides, tellurides, phosphates, sulfates, halides, oxide halides, phosphides, arsenides, intermetallics, and so on, are known. KW - Crystal growth KW - Solid state chemistry Y1 - 2017 SN - 978-3-527-32587-0 PB - Wiley-VCH CY - Weinheim ER - TY - BOOK A1 - Binnewies, Michael A1 - Glaum, Robert A1 - Schmidt, Marcus A1 - Schmidt, Peer T1 - Chemical vapor transport reactions N2 - This comprehensive handbook covers the diverse aspects of chemical vapor transport reactions from basic research to important practical applications. The book begins with an overview of models for chemical vapor transport reactions and then proceeds to treat the specific chemical transport reactions for the elements, halides, oxides, sulfides, selenides, tellurides, pnictides, among others. Aspects of transport from intermetallic phases, the stability of gas particles, thermodynamic data, modeling software and laboratory techniques are also covered. Selected experiments using chemical vapor transport reactions round out the work, making this book a useful reference for researchers and instructors in solid state and inorganic chemistry. KW - Crystal growth Y1 - 2016 SN - 978-3-11-048349-9 PB - De Gruyter CY - Berlin ER - TY - GEN A1 - Heinemann, Robert A1 - Schmidt, Peer T1 - Thermodynamic analysis of crystal growth of zinc oxide T2 - Zeitschrift für Anorganische und Allgemeine Chemie N2 - Chemical vapor transport (CVT[1]) is a suitable method for production of single-crystals of high purity. In order to find proper strategies for CVT various tools of thermodynamic calculations and analysis of solid-gas equilibria are available. Those applications are demonstrated for vapor transport of zinc oxide under addition of phosphorous and water. KW - Crystal growth Y1 - 2016 UR - http://onlinelibrary.wiley.com/doi/10.1002/zaac.201690018/full U6 - https://doi.org/10.1002/zaac.201690018 SN - 1521-3749 VL - 642 IS - 18 SP - 1064 ER - TY - GEN A1 - Pfister, Daniela A1 - Schäfer, Konrad A1 - Ott, Claudia A1 - Gerke, Birgit A1 - Pöttgen, Rainer A1 - Janka, Oliver A1 - Baumgartner, Maximilian A1 - Efimova, Anastasia A1 - Hohmann, Andrea A1 - Schmidt, Peer A1 - Venkatachalam, Sabarinathan A1 - Wüllen, Leo van A1 - Schürmann, Ulrich A1 - Kienle, Lorenz A1 - Duppel, Viola A1 - Parzinger, Eric A1 - Miller, Bastian A1 - Becker, Jonathan A1 - Holleitner, Alexander A1 - Weihrich, Richard A1 - Nilges, Tom T1 - Inorganic double helices in semiconducting SnIP T2 - Advanced Materials N2 - SnIP is the first atomic-scale double helical semiconductor featuring a 1.86 eV bandgap, high structural and mechanical flexibility, and reasonable thermal stability up to 600 K. It is accessible on a gram scale and consists of a racemic mixture of right- and left-handed double helices composed by [SnI] and [P] helices. SnIP nanorods <20 nm in diameter can be accessed mechanically and chemically within minutes. KW - Helical semiconductor Y1 - 2016 UR - http://onlinelibrary.wiley.com/doi/10.1002/adma.201603135/full U6 - https://doi.org/10.1002/adma.201603135 SN - 1521-4095 VL - 28 IS - 44 SP - 9783 EP - 9791 ER - TY - BOOK A1 - Binnewies, Michael A1 - Glaum, Robert A1 - Schmidt, Marcus A1 - Schmidt, Peer T1 - Chemische Transportreaktionen N2 - Chemische Transportreaktionen weisen ein gemeinsames Merkmal auf: In Gegenwart eines gasförmigen Reaktionspartners, des Transportmittels, wird eine feste oder flüssige Komponente verflüchtigt. An anderer Stelle scheidet sie sich meist in Form gut ausgebildeter Kristalle wieder ab. So ist der Chemische Transport z. B. für den Festkörperchemiker ein unentbehrliches Verfahren zur Herstellung reiner, gut kristallisierter Feststoffe. Als umfassendes Handbuch behandelt dieses Werk die vielseitigen Aspekte von Chemischen Transportreaktionen: Von der Grundlagenforschung bis hin zur praktischen Bedeutung, beispielsweise für die Funktionsweise von Halogenlampen. KW - Kristallzüchtung Y1 - 2016 SN - 978-3-11-048350-5 PB - De Gruyter CY - Berlin ER - TY - GEN A1 - Schöneich, Michael A1 - Hohmann, Andrea A1 - Schmidt, Peer A1 - Pielnhofer, Florian A1 - Bachhuber, Frederik A1 - Weihrich, Richard A1 - Osters, Oliver A1 - Köpf, Marianne A1 - Nilges, Tom T1 - Element allotropes and polyanion compounds of pnicogenes and chalcogenes: stability, mechanisms of formation, controlled synthesis and characterization T2 - Zeitschrift für Kristallographie - Crystalline Materials N2 - The application of the EnPhaSyn (theoretical Energy diagrams, experimental Phase formation, Synthesis and characterisation) concept is reviewed with respect to prediction of structures and stability of element allotropes and compound polymorphs, their phase formation and transition processes, and their directed synthesis, respectively. Therein, the relative energetical stability (En) of target compounds and possible decomposition are determined from quantum chemical DFT calculations. Phase formation and transition (Pha) is probed by a gas balance method, developed as high temperature gas balance concept. It helped to study the synthesis and stability range of several compounds experimentally. Applications of the concept and synthesis principles (Syn) of non-equilibrium phases are presented for allotropes of P, As, P1-xAsx, as well as binary and ternary compounds including the Zintl and Laves like phases IrPTe, NiP2, CoSbS, NiBiSe, Li0.2CdP2, Cu3CdCuP10, and Cd4Cu7As. KW - Arsenic KW - Phosporus KW - DFT KW - energy diagram KW - polymorph structure Y1 - 2017 UR - https://www.degruyter.com/view/j/zkri.ahead-of-print/zkri-2016-1966/zkri-2016-1966.xml U6 - https://doi.org/10.1515/zkri-2016-1966 SN - 2194-4946 VL - 232 IS - 1-3 SP - 91 EP - 105 ER - TY - GEN A1 - Zeugner, Alexander A1 - Kaiser, Martin A1 - Schmidt, Peer A1 - Menshchikova, Tatiana V. A1 - Rusinov, Igor P. A1 - Markelov, Anton V. A1 - Van den Broek, Wouter A1 - Chulkov, Evgueni V. A1 - Doert, Thomas A1 - Ruck, Michael A1 - Isaeva, Anna T1 - Modular Design with 2D Topological-Insulator Building Blocks: Optimized Synthesis and Crystal Growth and Crystal and Electronic Structures of BiₓTeI (x = 2, 3) T2 - Chemistry of Materials N2 - Structural engineering of topological bulk materials is systematically explored with regard to the incorporation of the buckled bismuth layer [Bi₂], which is a 2D topological insulator per se, into the layered BiTeI host structure. The previously known bismuth telluride iodides, BiTeI and Bi₂TeI, offer physical properties relevant for spintronics. Herewith a new cousin, Bi₃TeI (sp.gr. R3m, a = 440.12(2) pm, c = 3223.1(2) pm), joins the ranks and expands this structural family. Bi₃TeI = [Bi₂][BiTeI] represents a stack with strictly alternating building blocks. Conditions for reproducible synthesis and crystal-growth of Bi₂TeI and Bi₃TeI are ascertained, thus yielding platelet-like crystals on the millimeter size scale and enabling direct measurements. The crystal structures of Bi₂TeI and Bi₃TeI are examined by X-ray diffraction and electron microscopy. DFT calculations predict metallic properties of Bi₃TeI and an unconventional surface state residing on various surface terminations. This state emerges as a result of complex hybridization of atomic states due to their strong intermixing. Our study does not support the existence of new stacking variants BiₓTeI with x > 3; instead, it indicates a possible homogeneity range of Bi₃TeI. The series BiTeI–Bi₂TeI–Bi₃TeI illustrates the influence of structural modifications on topological properties. KW - Crytal growth KW - Topological insulator KW - Crystal structure KW - Electronic structure KW - Bismuth layered compounds Y1 - 2017 UR - http://pubs.acs.org/doi/abs/10.1021/acs.chemmater.6b05038 U6 - https://doi.org/10.1021/acs.chemmater.6b05038 SN - 0897-4756 SN - 1520-5002 VL - 29 IS - 3 SP - 1321 EP - 1337 ER - TY - RPRT A1 - Schmidt, Peer A1 - Efimova, Anastasia T1 - Thermal Characterization of Ionic Liquids N2 - Ionic liquids (ILs) are currently of high interest due to their high performance physicochemical properties over a wide temperature range of existence of the liquid state. Among the ionic liquids investigated, 1-alkyl-3-methylimidazolium halides were found generally preferred for their low melting points and ease of handling and preparation. KW - Thermal analysis KW - Ionic liquid Y1 - 2015 UR - https://www.netzsch-thermal-analysis.com/en/service-support/customer-magazine-onset/ SP - 14 EP - 17 PB - NETZSCH-Gerätebau GmbH CY - Selb ER - TY - GEN A1 - Wels, Martin A1 - Schmidt, Peer T1 - Crystal growth of ternary phases with homogeneity range: Modeling and experiments T2 - Zeitschrift für Anorganische und Allgemeine Chemie N2 - Synthesizing crystals of ternary solid solutions M2Q3 (M=Bi, Q=Se, Te) with definite composition requires advanced knowledge on the phase relations in the system. By chemical vapor transport [1] the request of homogeneous crystallization can be fulfilled. The experimental scope gets supported by modeling. A phase diagram of the pseudobinary system generated with FactSage [2] (Fig. 1) provides the thermodynamic parameters of the miscibility gap respectively the solid solution. Additionally, these parameters are used to optimize the processes while chemical vapor transport with iodine [3]. The optimum transport conditions of ϑsource = 500 °C and ϑsink = 450 °C has been applied as for the synthesis of the binary compounds [4]. Both by modeling and experiments the congruent transport can be demonstrated, Fig. 2. KW - Crystal growth KW - Chemical vapor transport KW - Chalogenides KW - Solid solution KW - Phase diagram Y1 - 2016 UR - http://onlinelibrary.wiley.com/doi/10.1002/zaac.201690018/full U6 - https://doi.org/10.1002/zaac.201690018 SN - 1521-3749 VL - 642 IS - 18 SP - 1066 ER - TY - BOOK A1 - Schmidt, Peer T1 - Allgemeine Chemie, Teil 1: Atombau und Periodensystem N2 - Aufbau der Atome und die Ordnung der chemischen Elemente im Periodensystem KW - Allgemeine Chemie KW - Atombau KW - Periodensystem der Elemente Y1 - 2015 SN - 978-3-662-47347-4 PB - Springer Spektrum CY - Heidelberg [u.a.] ER - TY - BOOK A1 - Schmidt, Peer A1 - Binnewies, Michael A1 - Finze, Maik T1 - Anorganische Chemie, Band 2: Gruppe 2, Gruppe 13 N2 - Elemente der Gruppe 2 (Erdalkalimetalle); Elemente der Gruppe 13 KW - Anorganische Chemie KW - Periodensystem der Elemente KW - Erdalkalimetalle KW - Gruppe 13 Y1 - 2016 SN - 978-3-662-47549-2 PB - Springer CY - Heidelberg ET - 1. Auflage ER - TY - BOOK A1 - Schmidt, Peer A1 - Binnewies, Michael A1 - Finze, Maik T1 - Anorganische Chemie, Band 3: Gruppe 14, Ressourceneffizienz N2 - Elemente der Gruppe 14 (Tetrele); Strategien der Ressourceneffizienz KW - Anorganische Chemie KW - Periodensystem der Elemente KW - Tetrele KW - Gruppe 14 KW - Ressourceneffizienz Y1 - 2016 SN - 978-3-662-47561-4 PB - Springer CY - Heidelberg ET - 1. Auflage ER -