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1 n to a cubic phase with higher symmetry than tetragonal.
2 ate-Cu interaction and the site becomes less tetragonal.
3 onal block copolymer morphologies, including tetragonal and helical structures, from a combination of
4 rical transport studies reveal that both the tetragonal and hexagonal CoSe nanoplates show strong thi
5 of DAPAL from Escherichia coli (EcDAPAL) in tetragonal and monoclinic forms at 2.0 and 2.2 A resolut
7 to show that there is a coexistence of both tetragonal and orthorhombic phases through the low-tempe
8 the pure tetragonal phase into a mixture of tetragonal and orthorhombic phases), the electrical cond
9 n are calculated to be 50 and 27 meV for the tetragonal and orthorhombic phases, respectively, which
11 intermediate strain regime takes place, with tetragonal and orthorhombic structural phases coexisting
12 This material occurs in two crystal forms, tetragonal and orthorhombic, both with a band gap much s
15 rent occurrence of structural (monoclinic to tetragonal) and electrical (insulator to the conductor)
16 nic compounds (3-D Pm3n cubic, 3-D P4(2)/mnm tetragonal, and a crystallographically forbidden 12-fold
17 s are found, and three phases (orthorhombic, tetragonal, and collapsed tetragonal) coexist between TS
18 nd AB13 stoichiometry with cubic, hexagonal, tetragonal, and orthorhombic symmetries have been identi
19 ns result from moving the boundaries between tetragonal- and rhombohedral-like phases, which changes
26 ze and consist of a mixture of body centered tetragonal (bct) and body centered cubic (bcc) structure
27 ork, we report the presence of body-centered tetragonal (bct) and body-centered orthorhombic (bco) ph
30 es--body-centered cubic (bcc), body-centered tetragonal (bct), and face-centered cubic (fcc)--as conf
32 rom the cubic alpha-phase (Pm3 m, #221) to a tetragonal beta-phase (P4/mbm, #127) at around 285 K, fo
35 or superconductivity in U compounds with the tetragonal body-centered [Formula: see text] structure.
36 embly of single-crystal FeGe2 nanowires with tetragonal C16 crystal structure shows anisotropic magne
37 measurements demonstrate the presence of the tetragonal Cd(3)As(2) crystal phase in studied films.
39 The structure is monoclinic, with a pseudo-tetragonal cell that favors multiple twinning on a scale
41 structural differences between digenite and tetragonal chalcocite are believed to influence the acce
42 es undergo a spontaneous phase transition to tetragonal chalcocite in situ, prior to the onset of cat
45 lloidal superstructures, including cubic and tetragonal colloidal crystals, with no known atomic anal
46 We show that Cu(2+)-Abeta(11-40) forms a tetragonal complex with a 34 +/- 5 fm dissociation const
47 the growth temperature, ultrathin 2D layered tetragonal CoSe nanoplates and nonlayered hexagonal CoSe
48 ction of external dopants, and therefore the tetragonal crystal structure and carrier mobility of CuB
49 ay diffraction patterns yielded good fits to tetragonal crystal structures, with the BaTiO3 formed in
51 we show that common garnet with a non-cubic (tetragonal) crystal structure is much more widespread th
53 nt pressure: PI with a nonmagnetic collapsed tetragonal (cT) phase at low temperature and PII with an
54 onal (T), orthorhombic (O) and the collapsed-tetragonal (cT) phases in the structural phase diagram o
55 /Ala analogues suggest a dynamic view of the tetragonal Cu(2+) complex, with axial as well as equator
58 mantle discontinuities can be explained by a tetragonal-cubic phase transition in Ti-bearing CaSiO(3)
60 ing in a CuMnAs/Fe bilayer, we conclude that tetragonal CuMnAs films are suitable candidate materials
63 mine the spin axis and magnetic structure in tetragonal CuMnAs, and reveal the presence of an interfa
64 high-temperature antiferromagnetic material, tetragonal CuMnAs, which exhibits excellent crystal qual
66 pair of Cr(III) ions occupying edge-sharing tetragonal distorted octahedral sites generated by forma
67 ure (TC) and the substrate induced (pseudo-) tetragonal distortion (ratio of out-of-plane to in-plane
71 minishes the energy gain associated with the tetragonal distortion, allowing the cubic phase to be st
72 terface to be comparable to that of a single tetragonal domain of STO, the anisotropy of interfacial
75 systems are shown to correlate well with the tetragonal elongation of the coordination environment.
78 generated in solution (ESI-MS, m/z = 565.15; tetragonal EPR) by reacting *NO(g) with superoxo complex
79 tructure to chemically ordered face-centered tetragonal (fct) structure, and further promotes formic
83 FDMFT) scheme to comprehensively explain why tetragonal FeS shows both semiconducting and metallic re
84 he superconducting transition temperature of tetragonal FeS was gradually depressed by pressure, diff
85 S3-like complex associated with mackinawite (tetragonal FeS) rather than as a discrete As2S3 phase.
86 hypothesis that nanocrystalline mackinawite (tetragonal FeS), which is abundant in sediments where Hg
87 ucting and metallic responses in contrast to tetragonal FeSe which is a pseudogaped metal above the s
94 the sodium disorder and showing that a local tetragonal framework more accurately describes the struc
95 ust phenazine linkage into a two-dimensional tetragonal framework that is stable under boiling water,
96 K, followed by a first-order transition to a tetragonal gamma-phase (retaining P4/mbm, #127) at 140 K
98 ities and the second-order elastic moduli of tetragonal hen egg-white lysozyme crystals were determin
100 a solid oxide reaction method resulting in a tetragonal hollandite structure (space group I4/m).
101 accompanied by a structural distortion from tetragonal I4/m symmetry to monoclinic I2/m symmetry, wh
102 temperature, with the symmetry lowered from tetragonal I4/mmm to orthorhombic Immm and the size of t
104 dopts a non-centrosymmetric structure in the tetragonal I42m space group with unit cell parameters a=
107 d as face centered cubic (fcc)] structure to tetragonal intermetallic [denoted as face centered tetra
110 dd excitons of the Fe(2+) sites arise from a tetragonal Jahn-Teller active polaronic distortion of th
111 n the out-of-plane thermal conductivities of tetragonal L10 FePt (001) easy-axis and cubic A1 FePt th
112 ar phase transformed first to a new phase of tetragonal lattice (T-phase) over a narrow range of rela
120 y giving local structures that are cubic and tetragonal like from the point of view of the PbI(3) fra
122 Electric field-dependent studies show that a tetragonal-like phase can be reversibly converted into a
124 Further in-depth analyses suggested that tetragonal low spin iron(V)-nitrido and -oxo complexes f
125 ment with experiments on the growth rates of tetragonal lysozyme crystals as a function of pH, salt c
126 ctive self-assembly could be used to prepare tetragonal (M8L12), pentagonal (M10L15), and hexagonal (
127 nm diameter skyrmions in the centrosymmetric tetragonal magnet GdRu(2)Si(2) without a geometrically f
129 e mechanism that leads to the sudden drop of tetragonal magnetostriction at x ~ 19, a long-standing p
131 at around 338 K between a high-temperature, tetragonal, metallic state (T) and a low-temperature, mo
134 we develop three-dimensional silicon-coated tetragonal microlattices that transform into sinusoidal
136 the large geometric misfit between adjacent tetragonal Mn(3)O(4) grains results in tilt boundaries a
139 discovery and synthesis of a novel Cl-doped tetragonal Na3PS4 (t-Na3-xPS4-xClx) solid electrolyte wi
141 induce the rapid formation of ferroelectric (tetragonal) nanocrystalline BaTiO3 at room temperature f
144 p to 3.9 x 10(7) A cm(-2) , while the square tetragonal nanoplates show considerably lower conductivi
145 on temperature (Tc) and unit cell metrics of tetragonal (NH3)yCs0.4FeSe were investigated in high pre
147 yz)(5)](SbF(6))(2) (2) crystallize in either tetragonal or orthorhombic space groups; their structure
148 ed polycrystals of materials that are either tetragonal or rhombohedral cannot switch; yet polycrysta
150 ni-axial phase transformation mechanism, the tetragonal/orthorhombic-to-collapsed-tetragonal phase tr
151 lly cubic transition occurs from the ambient tetragonal P4 mm structure in pure PbTiO(3); whereas the
152 12(1)) is nonsuperconducting and undergoes a tetragonal (P4/nmm) to monoclinic (P2(1)/m) structural t
154 e average structure is orthorhombic Amm2 and tetragonal P4mm, was best described by the rhombohedral
155 tely 12 times larger than the stoichiometric tetragonal parent phase of CeNbO4 as a result of the hel
158 t the nanoscale ferroelectric switching of a tetragonal PbZr(0.2)Ti(0.8)O(3) thin film under an appli
160 ic change in the BCP morphology, and uniform tetragonal perforations were observed at f(PMPCS) approx
161 chiral spheres self-organize into cubic and tetragonal periodic arrays and into a quasiperiodic 12-f
162 ith the inversion-asymmetry parameter in the tetragonal perovskites, evaluate anisotropic g-factors f
164 ilms on NSTO100 coexist a commensurate [001]-tetragonal phase and two incommensurate [010]-monoclinic
165 ion of approximately 1/8, where a new pseudo-tetragonal phase appears and the electric modulation of
170 por transport and found to maintain the same tetragonal phase in ambient air for at least 197 d.
171 res from the initial monoclinic to the final tetragonal phase in crystalline vanadium dioxide; the ch
174 n the crystal structure (i.e., from the pure tetragonal phase into a mixture of tetragonal and orthor
176 e is recoverable to ambient pressure and the tetragonal phase is at least partially recoverable.
177 isothermal bulk modulus of the high-pressure tetragonal phase is calculated to be 209(2) GPa and V(0)
178 Here we report that a stable body-centred tetragonal phase is observed in silver nanoparticles wit
179 tric cubic phase, although the ferroelectric tetragonal phase is partly retained even in ca. 7 nm nan
182 rystals, while successful in stabilizing the tetragonal phase of isomorphous ZrO2, has produced nanor
186 resulting from recrystallizing the original tetragonal phase reported by Lis in acetonitrile and tol
187 s widely accepted that in a classic cubic-to-tetragonal phase transformation, with only three tetrago
190 nt mobility confirm that the orthorhombic-to-tetragonal phase transition is a first-order phase trans
192 dynamics of a tip bias-induced rhombohedral-tetragonal phase transition of strained (001)-BiFeO3 (rh
193 gation of the size-dependent orthorhombic-to-tetragonal phase transition using a combined temperature
196 as-synthesized nanomaterials possess a pure tetragonal phase with variable morphologies from shuttle
197 calculations identify softer bonding in the tetragonal phase, relative to the monoclinic phase, as t
198 r scattering, and gamma = 0.5 +/- 0.1 in the tetragonal phase, suggesting another dominant mechanism,
199 rystals at low temperature (still within the tetragonal phase, which is stable at room temperature).
203 hase, Si-VIII and two of our other predicted tetragonal phases are highly likely within laser-affecte
204 e also observed coexistence of the cubic and tetragonal phases over a range of temperature in all cas
206 n two slightly different non-superconducting tetragonal phases, PI and PII, through thermal treatment
207 ound to be similar to bulk yttria-stabilized tetragonal polycrystals of the same relative density but
209 a grain of stishovite (from the interior), a tetragonal polymorph of silica that only occurs at ultra
211 an emissive poly(ethylene glycol)-decorated tetragonal prismatic platinum(II) cage was prepared and
214 been tested on the assembly of trigonal and tetragonal prisms from the biphenyl rod, [Ph2P(CH2)3PPh2
215 ynthesis of stable 3-D metallosupramolecular tetragonal prisms in which multicomponent coordination-d
216 he giant strain originates from rhombohedral-tetragonal (R-T) phase transition under electric-filed,
218 nder electric-filed, and is recoverable from tetragonal-rhombohedral (T-R) phase transition by compre
219 complex non-centrosymmetric structure in the tetragonal space group I4 2m was solved by means of sing
220 Im network (alpha-phase) crystallizes in the tetragonal space group I4(1)cd (a = 23.5028(4) A, c = 12
221 e of Sr(3)Co(2)O(4)Cl(2) is described in the tetragonal space group I4/mmm [a = 4.007(1) A, c = 22.28
224 stals, the gammaN308K crystals belonged to a tetragonal space group with an unusually long unit cell
226 tion below 155 K, changing the symmetry from tetragonal (space group P4/nmm) to monoclinic (space gro
227 2)-Ac), which also crystallizes in an axial (tetragonal) space group but which now is recognized to c
228 ermined by single-crystal X-ray diffraction: tetragonal, space group I4(1)/acd, a = 19.102(2), b = 19
231 , in this paper, for the first time a unique tetragonal star-like morphology of polyaniline was appli
232 he transformation from twinned-monoclinic to tetragonal, starting at a twin boundary and propagating
233 strained BiFeO3 films transition into a true tetragonal state at 430 degrees C but remain polar to mu
234 lar to neat AB, that is, the orthorhombic-to-tetragonal structural phase transition is observed at 22
235 ed on thermal cycling above the STO cubic-to-tetragonal structural transition temperature, implying t
236 n orthorhombic structure (Pnma, no. 62) to a tetragonal structure (P4/mbm, no. 127) is found around 2
238 matrix by 2.35%, forcing it to maintain its tetragonal structure and resulting in the highest BaTiO(
240 nium into CaSiO(3) perovskite stabilizes the tetragonal structure at higher temperatures, and that th
241 k-like orthorhombically distorted phase to a tetragonal structure by shifting the oxygen octahedra ro
244 rystalline domains with the long axis of the tetragonal structure oriented perpendicular to the subst
245 ansformation of the cubic Mg(2)TiO(4) to the tetragonal structure was complete by 29.2 GPa, ~5 GPa hi
246 structural measurements reveal a persistent tetragonal structure with smooth changes in the atomic d
251 , the Bi2Se3 crystallizes into body-centered tetragonal structures rather than the recently reported
252 uperlattices, simple-cubic and body-centered-tetragonal structures, has been achieved using a home-bu
253 to growth of BiFeO3 thin films on cubic and tetragonal substrates involving high levels of tensile s
255 is a superstructure of the infinite-layered tetragonal superconducting phase of SrCuO2 and is not st
257 es the superlattice symmetry, leading to the tetragonal superlattice that becomes energetically favor
261 till higher levels of lithium intercalation, tetragonal symmetry is regained: Li(1.52(5))Y(2)Ti(2)O(5
263 um intercalation into Y(2)Ti(2)O(5)S(2), the tetragonal symmetry of the host is retained: Li(0.30(5))
264 Rather, cation inversion creates a local tetragonal symmetry that extends over sub-nanometer doma
266 ment, and B = boron) exhibit orthorhombic or tetragonal symmetry, with the only exception being hexag
270 piezoelectric d33 coefficient appears at the tetragonal (T) - orthorhombic (O) phase boundary rather
271 that Ca122 can be stabilized in two distinct tetragonal (T) phases at room temperature and ambient pr
272 perature range of 300 K-1.5 K, but induces a tetragonal (T) to an orthorhombic (OR) phase transition
273 tified the phase transition curves among the tetragonal (T), orthorhombic (O) and the collapsed-tetra
276 very thin and epitaxially constrained to be tetragonal (that is, with four-fold symmetry), so one ex
277 We report a liquid crystal (LC) phase with a tetragonal three-dimensional unit cell containing 30 glo
280 factor causing the phase transition from the tetragonal to cubic phase near T(C) is a change in the s
282 I) induced a change of crystal symmetry from tetragonal to monlclinic, which could lead to an increas
284 ion of paramagnetic to antiferromagnetic and tetragonal to orthorhombic structural transitions of "12
285 gap exists close to the transition from the tetragonal to orthorhombic structures (0.6 < x < 0.8).
286 ell parameters upon K content as well as the tetragonal to orthorhombic transition at low temperature
288 BaTiO(3) to at least 330 degrees C, and the tetragonal-to-cubic structural transition temperature to
289 llic compound [Formula: see text] exhibits a tetragonal-to-orthorhombic phase transition consistent w
290 in-domains without uniaxial strain below the tetragonal-to-orthorhombic structural (nematic) transiti
291 ides, these competing phases are marked by a tetragonal-to-orthorhombic structural transition and a c
292 n equilibrium phase characterized by a large tetragonal unit cell containing 30 microphase-separated
293 complex phase is characterized by a gigantic tetragonal unit cell, in which 30 sub-2-nm quasispherica
294 n a and a 5% decrease in c parameters of the tetragonal unit cells, which results in disintegration o
295 agonal phase transformation, with only three tetragonal variants having only six twin systems, tuning
296 mation of an HfO2 nanorod from monoclinic to tetragonal, with a transformation temperature suppressed
297 ther compressed, undergoes a transition to a tetragonal Xe(N2)2-II phase at 14 GPa; this phase appear
299 thacrylate-based resins to yttria-stabilized tetragonal zirconia polycrystals (Y-TZP) and further inv
300 etic semiconductor (Ba,K)F(Zn,Mn)As with the tetragonal ZrCuSiAs-type structure which is identical to