scholarly journals Erratum: Determination of Low Loss in Isotopically Pure Single Crystal 28Si at Low Temperatures and Single Microwave Photon Energy

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Nikita Kostylev ◽  
Maxim Goryachev ◽  
Andrey D. Bulanov ◽  
Vladimir A. Gavva ◽  
Michael E. Tobar
Keyword(s):  
Single Crystal ◽  
Photon Energy ◽  
Low Temperatures ◽  
Low Loss ◽  
Microwave Photon ◽  
Pure Single Crystal

scholarly journals Determination of Low Loss in Isotopically Pure Single Crystal 28Si at Low Temperatures and Single Microwave Photon Energy

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Nikita Kostylev ◽  
Maxim Goryachev ◽  
Andrey D. Bulanov ◽  
Vladimir A. Gavva ◽  
Michael E. Tobar
Keyword(s):  
Dielectric Loss ◽  
Single Crystal ◽  
Line Width ◽  
Photon Energy ◽  
Single Photon ◽  
Narrow Line ◽  
Low Loss ◽  
Low Dielectric ◽  
Narrow Line Width ◽  
Pure Single Crystal

Abstract The low dielectric losses of an isotopically pure single crystal 28Si sample were determined at a temperature of 20 mK and at powers equivalent to that of a single photon. Whispering Gallery Mode (WGM) analysis revealed large Quality Factors of order 2 × 106 (dielectric loss ~5 × 10−7) at high powers, degrading to 7 × 105 (dielectric loss ~1.4 × 10−6) at single photon energy. A very low-loss narrow line width paramagnetic spin flip transition was detected with extreme sensitivity in 28Si, with very small concentration below 1011 cm−3 (less than 10 parts per trillion) and g-factor of 1.995 ± 0.008. Such determination was only possible due to the low dielectric photonic losses combined with the long lifetime of the spin transition (low magnetic loss), which enhances the magnetic AC susceptibility. Such low photonic loss at single photon energy combined with the narrow line width of the spin ensemble, indicate that single crystal 28Si could be an important crystal for future cavity QED experiments.

AN INTERNAL FRICTION STUDY OF N-H AND O-H PAIRS IN SINGLE CRYSTAL OF NIOBIUM AT LOW TEMPERATURES

1981 ◽  
Vol 42 (C5) ◽  
pp. C5-757-C5-761 ◽  
Author(s):  
R. Hanada ◽  
M. Shinohara ◽  
Y. Sado ◽  
H. Kimura
Keyword(s):  
Internal Friction ◽  
Single Crystal ◽  
Low Temperatures ◽  
Friction Study

Single crystal neutron diffraction studies of antiferromagnets at low temperatures in applied magnetic fields

1959 ◽  
Vol 20 (2-3) ◽  
pp. 180-184 ◽  
Author(s):  
W.C. Koehler ◽  
M. K. Wilkinson ◽  
J.W. Cable ◽  
E.O. Wollan
Keyword(s):  
Magnetic Fields ◽  
Neutron Diffraction ◽  
Single Crystal ◽  
Low Temperatures

Single Crystal Growth of High-Pressure Phases of Ice and Salt Hydrate Far Below the Original Melting Point by Mixing Alcohol: Crystal Structure Determination of Magnesium Chloride Heptahydrate

2020 ◽  
Author(s):  
Keishiro Yamashita ◽  
Kazuki Komatsu ◽  
Hiroyuki Kagi
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
Crystal Growth ◽  
Single Crystal ◽  
Room Temperature ◽  
Growth Technique ◽  
Salt Hydrate ◽  
X Ray

An crystal-growth technique for single crystal x-ray structure analysis of high-pressure forms of hydrogen-bonded crystals is proposed. We used alcohol mixture (methanol: ethanol = 4:1 in volumetric ratio), which is a widely used pressure transmitting medium, inhibiting the nucleation and growth of unwanted crystals. In this paper, two kinds of single crystals which have not been obtained using a conventional experimental technique were obtained using this technique: ice VI at 1.99 GPa and MgCl<sub>2</sub>·7H<sub>2</sub>O at 2.50 GPa at room temperature. Here we first report the crystal structure of MgCl2·7H2O. This technique simultaneously meets the requirement of hydrostaticity for high-pressure experiments and has feasibility for further in-situ measurements.

Two lithium tricyanomethanide compounds: syntheses and single-crystal structure determination of LiK[C(CN)3]2 and Li[C(CN)3]·½ (H3C)2CO

2015 ◽  
Vol 70 (3) ◽  
pp. 191-196 ◽  
Author(s):  
Olaf Reckeweg ◽  
Francis J. DiSalvo
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Single Crystals ◽  
Structure Determination ◽  
Monoclinic Space Group ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
Cell Parameters ◽  
New Compounds

AbstractThe new compounds LiK[C(CN)3]2 and Li[C(CN)3]·½ (H3C)2CO were synthesized and their crystal structures were determined. Li[C(CN)3]·½ (H3C)2CO crystallizes in the orthorhombic space group Ima2 (no. 46) with the cell parameters a=794.97(14), b=1165.1(2) and c=1485.4(3) pm, while LiK[C(CN)3]2 adopts the monoclinic space group P21/c (no. 14) with the cell parameters a=1265.7(2), b=1068.0(2) and c=778.36(12) pm and the angle β=95.775(7)°. Single crystals of K[C(CN)3] were also acquired, and the crystal structure was refined more precisely than before corroborating earlier results.

Magnetic Quantum Oscillations from Surface States of Bi Nanowires

2011 ◽  
Vol 1350 ◽  
Author(s):  
L. A. Konopko ◽  
T. E. Huber ◽  
A. A. Nikolaeva
Keyword(s):  
Single Crystal ◽  
Low Temperatures ◽  
Surface States ◽  
Charge Carriers ◽  
Quantum Oscillations ◽  
Wide Range ◽  
Spin Orbit Interactions ◽  
Conducting Tube ◽  
Magnetic Quantum Oscillations ◽  
Strong Spin

ABSTRACTIn this work, we report the results of studies of the transverse magnetoresistance (MR) of single-crystal Bi nanowires with diameter d<80 nm. The single-crystal nanowire samples were prepared by the Taylor-Ulitovsky technique. Due to the semimetal-to-semiconductor transformation and high density of surface states with strong spin-orbit interactions, the charge carriers are confined to the conducting tube made of surface states. The non monotonic changes of transverse MR that are equidistant in a direct magnetic field were observed at low temperatures in a wide range of magnetic fields up to 14 T. The period of oscillations depends on the wire diameter d as for the case of longitudinal MR. An interpretation of transverse MR oscillations is presented.

Wechselwirkungen in Molekülkristallen, 160 [1,2]. Kristallzüchtung und Strukturbestimmung der verschiedenartigen Polyphenyl-Kontaktionenmultipel [p-Quaterphenylee⊖⊖][Na⊕(DME)3]2, [p-Quaterphenyl⊖⊖(Na⊕(THF)3)2] und [p-Terphenyl⊖⊖Na⊕(DME)2Na⊕(DME)]2 / Interaction in Molecular Crystals, 160 [1, 2]. Crystallization and Structure Determination of the Different Polyphenyl Contact Ion Multiples [p-Quaterphenylee⊖⊖][Na⊕(DME)3]2, [p-Quaterphenyl⊖⊖(Na⊕(THF)3)2] und [p-Terphenyl⊖⊖Na⊕(DME)2Na⊕(DME)]2

2000 ◽  
Vol 55 (12) ◽  
pp. 1103-1113 ◽  
Author(s):  
Hans Bock ◽  
K. Gharagozloo-Hubmann ◽  
M. Sievert
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Sodium Salt ◽  
Structure Determination ◽  
Metal Cation ◽  
Molecular Crystals ◽  
Sodium Salts ◽  
Structure Determinations ◽  
Cation Coordination

The π-hydrocarbons p-terphenyl and p-quaterphenyl are reduced to their dianions in aprotic solutions of different ethers at sodium metal mirrors. Single crystal structure determinations of the solvent-separated or solvens-shared contact ion multiples, [p-terphenyl⊖⊖ Na⊕(DME)2Na⊕DME]2, p-quaterphenyl⊖⊖ ][Na⊕(DME)3]2 and [p-quaterpheny⊖⊖( Na⊕(THF)3)2], prove the essential cation solvation by the chelating dimethoxyethane (DME) versus the bulky tetrahydrofuran (THF) ligands: The solution network of equilibria between solvent separated and solvent shared ion aggregates can be considerably and transparently modified by the ether solvent selected. In addition, the structures of the monomeric sodium salts reveal partly novel details of metal cation coordination by contacts Na⊕ ··· O as well as Na⊕ ··· Cπ such as in the dimeric sodium salt of p-terphenyl dianion, [(DME)2Na⊕ (terphenyl⊖⊖)(Na⊕ DME)(terphenyl⊖⊖)Na⊕ (DME)2].

Sign in / Sign up

Export Citation Format

Share Document