Rational Synthesis of The Metastable Compounds BixCo4-xFexSb12

1998 ◽  
Vol 547 ◽  
Author(s):  
Joshua R. Williams ◽  
Joanna Hass ◽  
Heike Sellinschegg ◽  
David C. Johnson

AbstractThe synthesis of many targeted ternary compounds using conventional synthesis approaches has been unsuccessful because the ternary compounds are thermodynamically unstable with respect to disproportionation to a mixture of binary compounds. Typically these compounds have been synthetic targets based on predictions of enhanced properties. The ternary skutterudites with formula M'xM4Sbl2 (where M' = La, Lu, Y) are prime examples. Compounds with this structure have been found to be very promising thermoelectric materials having both good electrical properties and low thermal conductivities. Inserting heavy M' atoms into this crystal structure has been predicted to further decrease the thermal conductivity by increased phonon scattering. Attempts to make the title compound using conventional synthesis approaches failed due the formation of binary compounds as reaction products. Using modulated elemental reactants we were able to prepare the title compound at 160°C. Annealing at temperatures above 500°C resulted in exothermic decomposition into binary compounds. The Bi containing compounds are therefore thermodynamically unstable with respect to disproportionation at all temperatures. The amount of Bi can be varied by varying the composition of the starting modulated elemental reactant. Preliminary measurements to determine the variation of electrical conductivity and Seebeck coefficient as a function of bismuth content are presented.

1998 ◽  
Vol 545 ◽  
Author(s):  
Heike Sellinschegg ◽  
Joshua R. Williams ◽  
Steven P. Maxwell ◽  
Douglas Sillars ◽  
David C. Johnson

AbstractModulated elemental reactants have been used to synthesize metastable ternary compounds with the skutterudite crystal structure. The initial reactants are made up of multiple repeats of a unit containing elemental layers of a ternary metal, iron or cobalt (or a combination of these two) and antimony. The elemental layers interdiffuse upon low temperature annealing and form amorphous reaction intermediates. In this paper we target the compounds PbxFe4−yCoySb12. On annealing at temperatures between 12° and 150° C (depending on the composition) crystallization of the skutterudite structure occurs. The compounds are only kinetically stable, decomposing into a mixture of binary compounds upon annealing past a temperature of about 600°C. Preliminary data for the Seebeck coefficient and the electrical conductivity was collected The thermoelectric properties of the lead cobalt antimony skutterudite - films were measured as a function of lead occupancy.


1997 ◽  
Vol 478 ◽  
Author(s):  
Marc D. Hornbostel ◽  
Heike Sellinschegg ◽  
David C. Johnson

AbstractA series of new, metastable ternary crystalline compounds with the skutterudite crystal structure have been synthesized using modulated elemental reactants. The initial reactants are made up of multiple repeats of a ˜25Å thick unit containing elemental layers of the desired ternary metal, iron and antimony. Low temperature annealing (150°C) results in interdiffusion of the elemental layers to form amorphous reaction intermediates. Annealing these intermediates at temperatures between 200°C and 250°C results in exothermic crystallization of the desired skutterudite crystal structure. Most of the new compounds prepared are only kinetically stable, decomposing exothermically to form thermodynamically more stable mixtures of binary compounds and elements. Low angle x-ray diffraction studies show that the resulting films are exceedingly smooth. These films have an ideal geometry for measuring properties of importance for thermoelectric devices—the Seebeck coefficient and the electrical conductivity. Thermal conductivity can be measured using a modification of the 3ω technique of Cahill. Samples can be produced rapidly, allowing for systematic screening and subsequent optimization as a function of composition and doping levels.


1996 ◽  
Vol 453 ◽  
Author(s):  
Marc D. Hornbostel ◽  
Myungkeun Noh ◽  
Christopher D. Johnson ◽  
David C. Johnson

AbstractDiffusion distances within elementally modulated reactants can be controlled on an Angstrom length scale. Below a critical repeat thickness, elementally modulated reactants interdiffuse without nucleating crystalline compounds. Using this amorphous intermediate, we can prepare metastable compounds by controlling nucleation: Above this critical repeat thickness, crystalline compounds nucleate at the reacting interfaces. Using the architecture of the initial reactant to control the diffusion distances in the initial reactant, we have found that we can prepare crystalline superlattices. Crystalline superlattice compounds containing integral numbers of inter grown transition metal dichalcogenide layers and alternating layers of transition metal carbides have been prepared through controlled crystallization of superlattice reactants with designed compositional modulation. High quality c-axis oriented dichalcogenide crystalline superlattices result from extended annealing at relatively low temperatures. A large number of [00l] diffraction orders and off-axis [10l] diffraction peaks are observed indicating that these compounds are crystalline in three dimensions. Similar annealing conditions were used to prepare carbide superlattices, however the limited low temperature diffusion rates of the carbides limit the crystallite size to approximately 300Å. The rational synthesis of these intergrowth compounds from superlattice reactants permits the exploratory synthesis of a new class of compounds and the tailoring of physical properties as a function of compositional layer thicknesses and native properties of the parent compounds.


2000 ◽  
Vol 626 ◽  
Author(s):  
Heike Sellinschegg ◽  
David C. Johnson ◽  
Michael Kaeser ◽  
Terry M. Tritt ◽  
George S. Nolas ◽  
...  

ABSTRACTFilled skutterudite compounds possess very low thermal conductivities due to the scattering of a wide range of phonon modes caused by a loosely bound cation incorporated in a cavity of the structure. The inclusion of such a filler cation causes several synthetic difficulties since the desired compounds are thermodynamically unstable with respect to disproportionation. Modulated elemental reactants were used in this study to circumvent these difficulties. SnxCo4Sb12 samples with x=0.5 and nearly 1.0 were synthesized using this method. To prevent nucleation of unwanted binary compounds, the repeat unit made up of elemental layers was less than 20 angstroms 500mg of each sample were produced, allowing for the samples to be hot pressed into a pellet. Structural analysis as well as measurements of the physical properties are presented.


2015 ◽  
Vol 230 ◽  
pp. 254-265 ◽  
Author(s):  
Matthias Regus ◽  
Sergiy Mankovsky ◽  
Svitlana Polesya ◽  
Gerhard Kuhn ◽  
Jeffrey Ditto ◽  
...  

Author(s):  
Dae-Kyoung Kim ◽  
Seok-Bo Hong ◽  
Jonghoon Kim ◽  
Mann-Ho Cho

We investigate a high-quality Bi2Se3/black phosphorus (BP) heterostructure prepared through the modulated elemental reactants (MER, annealed in situ at 220 °C for 20 min under a vacuum of 10−9 Torr)...


2005 ◽  
Vol 886 ◽  
Author(s):  
Clay Mortensen ◽  
Ben Matelich ◽  
Benjamin Schmid ◽  
Raimar Rostek ◽  
David C. Johnson

AbstractDifficulty in preparing (Bi2Te3)x(Sb2Te3)y superlattices due to interdiffusion of Sb and Bi led to the study of interduffusion barriers. TiTe2 has been explored as an interdiffusion barrier to minimize the interdiffusion of Sb and Bi, as TiTe2 is not soluble in either Bi2Te3 or Sb2Te3. Preparation of (TiTe2)3(Sb2Te3)y(TiTe2)3(Bi2Te3)z superlattices has been achieved with varying x, y and z. The formation of the superlattices was studied as a function of annealing temperature and time. TOF-SIMS depth profiles were used to study the extent of interdiffusion in the samples. Unit cell control was achieved allowing for the preparation of an array of superlattices with varying periods with very good reproducibility.


1989 ◽  
Vol 42 (6) ◽  
pp. 959
Author(s):  
DE Clegg ◽  
PC Healy ◽  
GJ Patch ◽  
BW Skelton ◽  
AH White

Two dechlorinated products (B) and (D), formed in the reaction between endrin (C12H8Cl6O) and vanadium(II) for the purpose of confirmation of identity, are shown by single-crystal X-ray structure determination to be isomers of the title compound, C12H9Cl5O. Crystals of both are monoclinic, P21/c. For isomer (B), a 7.432(8), b 12.76(1), c 14.55(2) � , β 108.32(9)�, Z=4; R was 0.038 for 2594 observed reflections. For isomer (D), a 9.037(4), b 12.004(4), c 14.436(6) � , β 124.91(2)°, Z= 4; R was 0.041 for 1826 reflections. The geometries of the two isomers are compared.


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