Intrinsically modified thermoelectric performance of alkaline-earth isovalently substituted [Bi2AE2O4][CoO2]y single crystals

2013 ◽  
Vol 114 (4) ◽  
pp. 043705 ◽  
Author(s):  
N. Sun ◽  
S. T. Dong ◽  
B. B. Zhang ◽  
Y. B. Chen ◽  
J. Zhou ◽  
...  
1995 ◽  
Vol 50 (4) ◽  
pp. 577-580 ◽  
Author(s):  
H. Szillat ◽  
Hk. Müller-Buschbaum

Single crystals of (Cu0.22Mg0.78)BaNd2Mo4O16 have been prepared by crystallization from melts and investigated by X-ray methods. The compound crystallizes monoclinically, space group C62h - C12/c1, Z = 4, a = 5.351(1), b = 12.891(2), c = 19.391(4) Å,β = 90.899(14)° and is isotypic to CuKHo2Mo4O16. The crystal structure is dominated by BaO10 and NdO8 polyhedra forming a three-dimensional polyhedra network, which is filled by axially distorted (Cu,Mg)O6 octahedra and MoO4 tetrahedra.


1994 ◽  
Vol 49 (3) ◽  
pp. 355-359 ◽  
Author(s):  
F.-D. Martin ◽  
H. Müller-Buschbaum

Abstract Single crystals of KBaCuV2O7Cl have been prepared by a flux technique and investigated by X-ray analysis. The compound crystallizes with tetragonal symmetry, space group C24v-P4 bm, a = 8.8581, c = 5.4711 Å, Z = 2. The crystal structure shows Cu2+ within a one sided strongly distorted CuO4Cl2 octahedron. The copper ion is shifted towards the nearer Cl- neighbour to form a CuO4Cl square pyramid. Two VO4 tetrahedra are connected to give stretched V2O7 double tetrahedra, and linked in planes via the oxygen corners of the CuO4Cl pyramids. The crystal structure and the structure of the complex BaO8Cl2 polyhedron are discussed.


2011 ◽  
Vol 109 (10) ◽  
pp. 103704 ◽  
Author(s):  
Shukang Deng ◽  
Yuta Saiga ◽  
Kousuke Kajisa ◽  
Toshiro Takabatake

2020 ◽  
Vol 32 (16) ◽  
pp. 1908218 ◽  
Author(s):  
Kazuki Imasato ◽  
Chenguang Fu ◽  
Yu Pan ◽  
Max Wood ◽  
Jimmy Jiahong Kuo ◽  
...  

1964 ◽  
Vol 111 (8) ◽  
pp. 1009 ◽  
Author(s):  
P. F. Weller ◽  
J. E. Scardefield

1997 ◽  
Vol 52 (11) ◽  
pp. 1349-1358 ◽  
Author(s):  
Peter Höhn ◽  
Matthias Ludwig ◽  
Rüdiger Kniep

Yellow single crystals of the isotypic phases Ca51[WN4]12N8O3 and Sr51[WN4] 12N8O3 (triclinic, P1̄ (#2 ); a= 1056.4(3) / 1113.1(5) pm, b = 1239.7(3) / 1304.4(5) pm, c= 1598.2(3) / 1679.4(9) pm, α = 102.78(1)/102.47(2)°, β= 95.15( 1)/95.43(3)°, γ = 109.89(1)/109.77(2)°; Z = 1) were grown in a Tl-flux (Ca:Tl, molar ratio 5:1, W-crucible; Tmax = 1273K; reaction with N2, 1 atm, 36 h) or from pellets (Sr2N + W, molar ratio 6:1; Tmax = 1023K; reaction with N2, 1 atm, 36 h). The crystal structures contain tetrahedral anions [WN4]6- in addition to isolated nitride and isolated oxide ions, which are octahedrally coordinated by Ca and Sr, respectively.


1995 ◽  
Vol 50 (4) ◽  
pp. 581-584 ◽  
Author(s):  
S. Frenzen ◽  
Hk. Müller-Buschbaum

Single crystals of NaSr3RuO6 have been prepared in closed silver tubes and investigated by X-ray techniques. This compound crystallizes with trigonal (rhombohedral) symmetry, space group D63d - R3̅c , a = 9.6069(8), c = 11.513(2) Å, Z = 6, and is isotypic to compounds of the Sr4PtO6 type. The crystal structure is discussed with respect to related compounds with partial replacement of alkaline earth elem ents by sodium and copper.


2020 ◽  
Vol 8 (27) ◽  
pp. 9345-9351
Author(s):  
Kunling Peng ◽  
Bo Zhang ◽  
Hong Wu ◽  
Hailiang Che ◽  
Xuefeng Sun ◽  
...  

The unique evolution of transport bands with the occurrence of two bands above 600 K and the extending low-symmetry phase regime synergistically enhance thermoelectric performance in SnSe based single crystals.


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