Characterization of Milled High-Pressure High-Temperature NV-Center Nanodiamonds for Single-Photon Source Applications

2021 ◽  
Author(s):  
N. S. Kurochkin ◽  
S. A. Savinov ◽  
Dongxue Bi ◽  
V. V. Sychev ◽  
S. P. Eliseev ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Single Photon ◽  
Single Photon Source ◽  
High Pressure High Temperature ◽  
Nv Center ◽  
Photon Source

scholarly journals Multianvil High-Pressure/High-Temperature Synthesis and Characterization of multiferroic HP-Co3TeO6

2021 ◽  
Author(s):  
Gunter Heymann ◽  
Elisabeth Selb ◽  
Toni Buttlar ◽  
Oliver Janka ◽  
Martina Tribus ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Type Structure ◽  
Synthesis And Characterization ◽  
Temperature Synthesis ◽  
Space Group ◽  
Crystal System ◽  
High Temperature Synthesis ◽  
High Pressure High Temperature

By high-pressure/high-temperature multianvil synthesis a new high-pressure (HP) phase of Co3TeO6 was obtained. The compound crystallizes in the acentric trigonal crystal system of the Ni3TeO6-type structure with space group R3...

scholarly journals High-pressure synthesis and characterization of the non-centrosymmetric scandium borate ScB6O9(OH)3

2020 ◽  
Vol 75 (6-7) ◽  
pp. 597-603
Author(s):  
Birgit Fuchs ◽  
Hubert Huppertz
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Structure Solution ◽  
Temperature Experiment ◽  
Pressure Synthesis

AbstractThe non-centrosymmetric scandium borate ScB6O9(OH)3 was obtained through a high-pressure/high-temperature experiment at 6 GPa and 1473 K. Single-crystal X-ray diffraction revealed that the structure is isotypic to InB6O9(OH)3 containing borate triple layers separated by scandium layers. The compound crystallizes in the space group Fdd2 with the lattice parameters a = 38.935(4), b = 4.4136(4), and c = 7.6342(6) Å. Powder X-ray diffraction and vibrational spectroscopy were used to further characterize the compound and verify the proposed structure solution.

scholarly journals High-Pressure, High-Temperature Synthesis and Characterization of Polar and Magnetic LuCrWO6

2020 ◽  
Vol 59 (6) ◽  
pp. 3579-3584
Author(s):  
Sun Woo Kim ◽  
Xiaoyan Tan ◽  
Corey E. Frank ◽  
Zheng Deng ◽  
Huaiyu Wang ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Synthesis And Characterization ◽  
Temperature Synthesis ◽  
High Temperature Synthesis ◽  
High Pressure High Temperature

High Pressure High Temperature (HPHT) Synthesis and Physical Characterization of Magneto-Superconducting RuSr2Tb1.5Ce0.5Cu2O10 Ceramic Compound

2006 ◽  
Vol 47 ◽  
pp. 31-36
Author(s):  
Alberto Ubaldini ◽  
V.P.S. Awana ◽  
S. Balamurugan ◽  
E. Takayama-Muromachi
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Magnetic Transition ◽  
Magnetic Ordering ◽  
Superconducting Transition ◽  
Synthesis Conditions ◽  
High Pressure High Temperature ◽  
Interesting Class ◽  
Ceramic Compound

The ruthenocuprates family is a very interesting class of materials, because of the coexistence of superconductivity and magnetic ordering. Ruthenocuprates include RuSr2RECu2O8 and RuSr2(RE,Ce)2Cu2O10- (RE = rare earth elements or Y). It is possible to synthesize samples of these phases with Gd, Eu or Sm with normal synthesis conditions. For the others high-pressure high-temperature (HPHT) synthesis is required. We had successfully synthesized the RuSr2Tb1.5Ce0.5Cu2O10 by HPHT technique, starting from RuO2, SrO2, Tb4O7, CeO2, CuO and Cu. Around 300 mg of the mixture was allowed to react in a flat-belt-typehigh- pressure apparatus at 6GPa and 1200 °C – 1550 °C. The optimised temperature of synthesis was found to be in the range between 1350 °C – 1450 °C. The as-synthesized compound crystallized with a structure belonging to the space group I4/mmm. DC magnetic susceptibility versus temperature plot for RuSr2Tb1.5Ce0.5Cu2O10 in an applied field of 10 Oe demonstrated magnetic transition at 150 K but the superconducting transition was not clearly observed. To our knowledge this is the first successful synthesis of the Tb based Ru-1222 phase.

Ni6B22O39·H2O – extending the field of nickel borates

2017 ◽  
Vol 72 (12) ◽  
pp. 967-975 ◽  
Author(s):  
Martin K. Schmitt ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Temperature Reaction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
High Temperature Reaction ◽  
High Pressure High Temperature ◽  
Related Phase

AbstractNi6B22O39·H2O was synthesized in a high-pressure/high-temperature reaction at 5 GPa/900°C. It crystallizes in the orthorhombic space group Pmn21 (no. 31) with the lattice parameters a=7.664(2), b=8.121(2) and c=17.402(2) Å. The crystal structure is discussed with regard to the isotypic compounds M6B22O39·H2O (M=Fe, Co) and the structurally related phase Cd6B22O39·H2O. Furthermore, the characterization of Ni6B22O39·H2O via X-ray powder diffraction and vibrational spectroscopy is reported.

Electrically driven single photon source at high temperature

2016 ◽  
Vol 28 (8) ◽  
pp. 085303
Author(s):  
Ahmed El Halawany ◽  
Michael N Leuenberger
Keyword(s):  
High Temperature ◽  
Single Photon ◽  
Single Photon Source ◽  
Photon Source

scholarly journals Photon statistics characterization of a single-photon source

2004 ◽  
Vol 6 ◽  
pp. 85-85 ◽  
Author(s):  
R Alléaume ◽  
F Treussart ◽  
J-M Courty ◽  
J-F Roch
Keyword(s):  
Single Photon ◽  
Photon Statistics ◽  
Single Photon Source ◽  
Photon Source

Synthesis and Characterization of a Cubic Iron Hydroxy Boracite

2011 ◽  
Vol 66 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Stephanie C. Neumair ◽  
Johanna S. Knyrim ◽  
Oliver Oeckler ◽  
Reinhard Kaindl ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Single Crystals ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature

The cubic iron hydroxy boracite Fe3B7O13OH・1.5H2O was synthesized from Fe2O3 and B2O3 under high-pressure/high-temperature conditions of 3 GPa and 960 °C in a modified Walker-type multianvil apparatus. The crystal structure was determined at room temperature by X-ray diffraction on single crystals. It crystallizes in the cubic space group F4̄3c (Z = 8) with the parameters a = 1222.4(2) pm, V = 1.826(4) nm3, R1 = 0.0362, and wR2 = 0.0726 (all data). The B-O network is similar to that of other cubic boracites.

Sign in / Sign up

Export Citation Format

Share Document