Ion Induced Damage and their Annealing in LiTaO3 Single Crystal

1995 ◽  
Vol 396 ◽  
Author(s):  
Z Zhang ◽  
I.A. Rusakova ◽  
W.K. Chu

AbstractLiTaO3 single crystals have been implanted with 100 keV oxygen ions at room temperature with doses of 1×1014 /cm2,6xl014/cm2,1.2x1015/cm2, 6xl015/cm2, and 2xl016/cm2. Annealing temperatures ranged from 550 °C to 1075 °C. RBS-channeling and TEM were used for characterization. For partially damaged samples, complete recovery of the crystalline structure was achieved after annealing at 550 °C, which is below the Curie temperature. For totally amorphized samples, thermal annealing induced multidomain growth. These domains extend beyond the original amorphous/crystal interface deep into bulk (1 – 1.5 μm ).

2016 ◽  
Vol 843 ◽  
pp. 155-160 ◽  
Author(s):  
D.A. Vinnik ◽  
I.A. Zakharchuk ◽  
Erkki Lähderanta

This paper presents magnetic properties of manganese substituted barium hexaferrite BaFe12-xMnxO19 single crystals. Crystals of BaFe12–xMnxO19 with x up to 1.5 and sizes up to 8 mm were observed. The influence of Fe substitution by Mn on the magnetic properties was investigated. For the BaFe10.5Mn1.5O19 single crystal samples saturation magnetization reduced from 72 to 63.5 emu/g at room temperature, and Curie temperature decreased from 455 to 380 °C.


2006 ◽  
Vol 510-511 ◽  
pp. 842-845 ◽  
Author(s):  
Noriko Bamba ◽  
Kentaro Kato ◽  
Toshinori Taishi ◽  
Takayuki Hayashi ◽  
Keigo Hoshikawa ◽  
...  

Langasite (La3Ga5SiO14: denoted by LGS) single crystal is one of the lead free piezoelectric materials with high piezoelectricity that is maintained up to its melting point (1470°C). Although LGS single crystals have usually been grown by Czochralski (CZ) method in oxygen contained atmosphere to prevent evaporation of Ga, they were grown by the vertical Bridgman (VB) method in Ar atmosphere without oxygen, and their properties were evaluated in this work. Transparent and colorless LGS single crystals were successfully obtained without Ga evaporation by the VB method in Ar atmosphere, and their resistivity at room temperature was much higher than that grown by conventional CZ method. Piezoelectric constant d11 of the crystal grown by the VB method was 6 x 10-12 C/N, which was close to that of the crystal grown by CZ method. The colorless transparent LGS single crystal turned to orange and its resistivity decreased by annealing in air. Since an orange-colored transparent LGS single crystal has been grown by conventional CZ method, this indicates that color change and the resistivity decrease of LGS crystal is caused by extra interstitial oxygen atoms in the crystal.


2004 ◽  
Vol 449-452 ◽  
pp. 985-988
Author(s):  
S.M. Lee ◽  
J.W. Shur ◽  
T.I. Shin ◽  
W.S. Yang ◽  
G.Y. Kim ◽  
...  

[MnO2(1.0mol%) : Tb4O7(0.5mo%)] doped stoichiometric LiNbO3 (Mn:Tb:SLN) single crystals of 0.5~1.0 mm in diameter and 30~35 mm in length were grown by micro pulling down(µ-PD) method. We investigated the photoluminescence (PL) properties of Mn:Tb:SLN single crystal. The OH- absorption band of the single crystals observed infrared the absorption spectra by using an FT-IR spectrophotometer at room temperature. Homogeneous distributions of Mn and Tb concentration were confirmed by the EPMA and observed defects by optical microscopy.


1997 ◽  
Vol 478 ◽  
Author(s):  
T. M. Tritt ◽  
M. L. Wilson ◽  
R. L. Littleton ◽  
C. Feger ◽  
J. Kolis ◽  
...  

AbstractWe have measured the resistivity and thermopower of single crystals as well as polycrystalline pressed powders of the low-dimensional pentatelluride materials: HfTe5 and ZrTe5. We have performed these measurements as a function of temperature between 5K and 320K. In the single crystals there is a peak in the resistivity for both materials at a peak temperature, Tp where Tp ≈ 80K for HfTe5 and Tp ≈ 145K for ZrTe5. Both materials exhibit a large p-type thermopower around room temperature which undergoes a change to n-type below the peak. This data is similar to behavior observed previously in these materials. We have also synthesized pressed powders of polycrystalline pentatelluride materials, HfTe5 and ZrTe5. We have measured the resistivity and thermopower of these polycrystalline materials as a function of temperature between 5K and 320K. For the polycrystalline material, the room temperature thermopower for each of these materials is relatively high, +95 μV/K and +65 μV/K for HfTe5 and ZrTe5 respectively. These values compare closely to thermopower values for single crystals of these materials. At 77 K, the thermopower is +55 μV/K for HfTe5 and +35 μV/K for ZrTe5. In fact, the thermopower for the polycrystals decreases monotonically with temperature to T ≈ 5K, thus exhibiting p-type behavior over the entire range of temperature. As expected, the resistivity for the polycrystals is higher than the single crystal material, with values of 430 mΩ-cm and 24 mΩ-cm for Hfre5 and ZrTe5 respectively, compared to single crystal values of 0.35 mΩ-cm (HfTe5) and 1.0 mΩ-cm (ZrTe5). We have found that the peak in the resistivity evident in both single crystal materials is absent in these polycrystalline materials. We will discuss these materials in relation to their potential as candidates for thermoelectric applications.


2004 ◽  
Vol 82 (2) ◽  
pp. 301-305 ◽  
Author(s):  
Kenneth CW Chong ◽  
Brian O Patrick ◽  
John R Scheffer

When crystals of 9-tricyclo[4.4.1.0]undecalyl-4-(carbomethoxy)phenyl ketone (1) were allowed to stand in the dark for extended periods of time at room temperature, the compound underwent a thermal reaction — the enolene rearrangement — to afford enol 2. The crystals remained transparent and appeared unchanged in shape as the reaction proceeded. X-ray diffraction data were collected on single crystals containing 17%, 25%, 66%, and 100% of the enol. The crystal structure of a simple enol was obtained via this novel single-crystal-to-single-crystal enolene rearrangement.Key words: single crystal, thermal, rearrangement, enol, enolene.


2021 ◽  
Author(s):  
◽  
Michael Ng

<p>Energy consumption worldwide is constantly increasing, bringing with it the demand for low cost, environmentally friendly and efficient energy technologies. One of these promising technologies is thermoelectrics in which electric power is harvested from waste heat energy. The efficiency of a thermoelectric device is determined by the dimensionless figure of merit ZT = σS²T/k where σ is the electrical conductivity, S is the thermopower, k is the thermal conductivity, and T is the average temperature. In this thesis we investigate the use of nanostructuring, which has been known to lead to significant reduction in the lattice thermal conductivity to maximise the figure of merit.  One of the most successful bulk thermoelectric materials is Bi₂Te₃, with a ZT of unity at room temperature. Here we investigate the effects of nanostructuring on the thermoelectric properties of Bi₂Te₃. Sub-100 nm ₂Te₃ nanoparticles were successfully synthesized and the figure of merit was found to be ZT ~ 5X10⁻⁵ at room temperature. The effect of a ligand exchange treatment to replace the long chain organic ligand on the as-synthesized nanoparticles with a short chain alkyl ligand was explored. After ligand exchange treatment with hydrazine the figure of merit of sub-100 nm Bi₂Te₃ was found to increase by two fold to ZT ~ 1X10⁻⁴ at room temperature. Overall the figure of merit is low compared to other nanostructured Bi₂Te₃, this was attributed to the extremely low electrical conductivity. The thermopower and thermal conductivity were found to be ~96 μVK⁻¹ and ~0.38 Wm⁻¹ K⁻¹ at 300 K respectively, which show improvements over other nanostructured Bi₂Te₃.  Further optimisation of the figure of merit was also investigated by incorporating Cu, Ni and Co dopants. The most successful of these attempts was Co in which 14.5% Co relative to Bi was successfully incorporated into sub-100 nm Bi₂Te₃. The figure of merit of nanostructured Bi₁.₇₁Co₀.₂₉Te₁.₇₁ alloy was found to increase by 40% to a ZT ~ 1.4X10⁻⁴ at room temperature. Although overall the figure of merit is low, the effect of Co alloying and hydrazine treatment shows potential as a route to optimise the figure of merit.  A potential novel material for thermoelectrics applications is inorganicorganic perovskite single crystals. Here we report a synthetic strategy to successfully grow large millimetre scale single crystals of MAPbBr₃₋xClx, FAPbBr₃₋xClx, and MAPb₁-xSnxBr₃ (MA = methylammonium and FA = formamidinium) using inverse temperature crystallisation (ITC) in a matter of days. This is the first reported case of mixed Br/Cl single crystals with a FA cation and mixed Pb/Sn based perovskites grown using ITC. The bandgap of these single crystals was successfully tuned by altering the halide and metal site composition. It was found that single crystals of FAPbBr₃₋xClx were prone to surface degradation with increased synthesis time. This surface degradation was observed to be reversible by placing the single crystals in an antisolvent such as chloroform.  A tentative model was proposed to analyse the IV characteristics of the single crystal perovskites in order to extract mobilities and diffusion lengths. The MAPbBr₃ and MAPbBr₂.₅Cl₀.₅ single crystal mobilities were found to be between 30-390 cm² V⁻¹ s⁻¹ and 10-100 cm² V⁻¹ s⁻¹ respectively, the diffusion lengths were found to be between 2-8 μm and 1-4 μm respectively. This is an improvement over polycrystalline thin film perovskites and comparable to other single crystal perovskites. The conductance of MAPb₁-xSnxBr₃ based perovskites was found to increase by 2 orders of magnitude even with just 1% of Sn incorporated. The thermal conductivity of MAPbBr₃ single crystals was found to be ~1.12 Wm⁻¹ K⁻¹ at room temperature which is reasonable low for single crystals, however no other thermoelectric properties could be measured due to the self cleaving nature of the single crystals with decreasing temperature and the high resistivity of the material.</p>


1968 ◽  
Vol 46 (8) ◽  
pp. 949-958 ◽  
Author(s):  
R. A. Armstrong

The adsorption of CO on two large single crystals of tungsten exposing (100) and (211) surfaces has been studied by measuring changes in the work function [Formula: see text] at 300 °K and above, where some CO remained adsorbed. The results for the two surfaces were quite different.CO adsorbed on the clean W(100) surface at room temperature as β-CO causing [Formula: see text] to increase by 0.48 V. As β adsorption saturated, α-CO adsorption began and caused [Formula: see text] to decrease. The major effect of heating was desorption.CO adsorbed on the clean W(211) surface with a sticking probability near unity and increased [Formula: see text] by 0.68 V. Heating the crystal to temperatures below 1100 °K produced large irreversible changes in [Formula: see text]. These irreversible changes are attributed to the formation and dissociation on the surface of complexes consisting of two CO molecules.


Single crystal rods of gold, silver and nickel have been prepared from the melt by a modified cooling method. The three metals differ in that the gold is very pure and has no surface contamination; the silver is very pure and the surface normally shows contamination; the nickel is markedly less pure. These three features find expression in the results. The stress-glide relationship has been investigated over the whole range to fracture, special attention being paid to the region of small glide. At very small glides the results show certain variations attributed to metastable conditions. For pure metals at low temperatures a region of easy glide has been established, which is absent in nickel. Considerations of the variation of hardening with temperature at constant glide show that, at moderate glide, rise of temperature at low temperature promotes hardening, but rise of temperature at high temperature leads to decrease of hardening. From these results it is concluded that in metals without notable impurity glide is due to two distinct processes, first the initiation of glide planes, which temperature agitation tends to check, and secondly to glide proceeding on planes already initiated, which temperature agitation tends to promote. The surface contamination of silver single crystals which takes place by exposure to air at room temperature raises the critical shear stress somewhat, but has a much more marked effect on the hardening after some tens of per cent of glide has taken place, which is attributed to diffusion of the impurity atoms, probably oxygen, taking place during the travel of the dislocations. This is distinct from normal diffusion, which is negligible at room temperature. The results on the effect of surface contamination explain abnormalities previously noted with silver. The close connexion of asterism and hardening is exhibited in the results obtained with gold and silver. In particular, silver in the region of easy glide shows very small asterism, even at large glide. The cube root of the breaking stress of all metals in single-crystal form has been found to show a linear relationship with temperature.


MRS Advances ◽  
2020 ◽  
Vol 5 (1-2) ◽  
pp. 19-26
Author(s):  
S. BERTOLOTTO ◽  
S. SZENKNECT ◽  
S. LALLEMAN ◽  
R. PODOR ◽  
L. CLAPAREDE ◽  
...  

Abstract:Millimetre UO2 single crystals were cut and oriented at JRC Karlsruhe. The orientation of each face of the parallelepiped single crystals was determined with Laue diffraction and the corresponding surface area by geometric measurements. Then, the (111), (100), (110) faces of each single crystal were polished to optical grade and characterized by XRD in order to confirm the surface orientation. The dissolution of the three single crystals was achieved in nitric acid media under dynamic conditions, at room temperature. Two dissolution regimes were observed for all samples. The normalized dissolution rate measured in the first step was not influenced by the crystallographic orientation of the faces. However, during the second step, (110) oriented faces were found to dissolve 4 times faster than the (100) faces. One explanation could involve the atomic composition of each oriented surface in the fluorite-type structure


2008 ◽  
Vol 388 ◽  
pp. 217-220 ◽  
Author(s):  
Xin Yan Yue ◽  
Rong Tu ◽  
Takashi Goto

Poly- and single-crystalline BaTi2O5 co-substituted with SrO and ZrO2, Ba0.99Sr0.01(Ti1-xZrx)2O5 (BT2SZ) were prepared by arc-melting and floating-zone (FZ) melting, respectively. The specimens showed a significant (020) orientation. The highest permittivity of poly-crystalline BT2SZ was 3880 at x = 0.005 and that of single-crystal was 27000 at x = 0.005. The Curie temperature (Tc) of poly-crystals decreased from 750 to 640 K with increasing x from 0 to 0.026 and that of single-crystals decreased from 750 to 710 K with increasing x from 0 to 0.008. The highest remnant polarization of single crystalline BT2SZ was 7.8×10-2 Cm-2 at x = 0.008, higher than that of the poly-crystal.


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