ライフサイエンスコーパス: crystal growth

1 y revealing routes for ex situ synthesis and crystal growth.

2 res form mesocrystals by oriented attachment crystal growth.

3 e used to teach the basics of nucleation and crystal growth.

4 y as potential additives for controlling MDM crystal growth.

5 crystallization may differ from traditional crystal growth.

6 f lateral contacts leading to nucleation and crystal growth.

7 ective surface modification, and anisotropic crystal growth.

8 ate phase (i.e., a solvent) that promotes Si crystal growth.

9 emplate for the subsequent quasiepitaxial 3D crystal growth.

10 materials were used as scaffolds for calcite crystal growth.

11 set of ice-binding proteins that control ice crystal growth.

12 ntly affect nucleation but slightly retarded crystal growth.

13 nd play a marginal sterical hindrance of the crystal growth.

14 n oligomerize as a prelude to nucleation and crystal growth.

15 "how to" guide for those interested in oxide crystal growth.

16 evelop biotechnological approaches to single-crystal growth.

17 , blocking surface sites for more productive crystal growth.

18 so relevant information on the inhibition of crystal growth.

19 ation, the kinetics of which depends only on crystal growth.

20 irus capsids for uses from bioconjugation to crystal growth.

21 e classical polynuclear theory developed for crystal growth.

22 the acidic amino acids to aid in controlling crystal growth.

23 conditions and optimize diffraction-quality crystal growth.

24 nsion, which are advantageous for beta-Ga2O3 crystal growth.

25 ibly related to altered amelogenin-modulated crystal growth.

26 in conjunction with the vectorial control of crystal growth.

27 ystal structures in phasing and high-quality crystal growth.

28 lation of hydroxylapatite (HA) formation and crystal growth.

29 This stablization appears necessary for crystal growth.

30 erials, in addition to their pivotal role in crystal growth.

31 icles may provide alternative mechanisms for crystal growth.

32 n switching and molecular recognition during crystal growth.

33 f solutions noncolligatively and inhibit ice crystal growth.

34 ionally confined liquids and the dynamics of crystal growth.

35 ctionalities found to promote matrix/analyte crystal growth.

36 ment for new and improved methodology to aid crystal growth.

37 interaction with the crystal surfaces during crystal growth.

38 state may play a role in inhibiting the ice crystal growth.

39 olecular level the processes responsible for crystal growth.

40 transport resulted in additional substantial crystal growth.

41 s is one of the most important challenges in crystal growth.

42 they also increase the tolerance toward ice-crystal growth.

43 e of the fundamental puzzles in the field of crystal growth.

44 ted layer, created at the {010} faces during crystal growth.

45 on by X-ray crystallographic methods-that of crystal growth.

46 teins that promote or inhibit hydroxyapatite crystal growth.

47 e and act as modifiers during nucleation and crystal growth.

48 from G(T) using the Wilson-Frenkel model of crystal growth.

49 boundary, which is widely known to catalyze crystal growth.

50 ominated impedance, occurring as a result of crystal growth.

51 es a better fundamental understanding of the crystal growth.

52 enamel, taken to regulate crystal shape and crystal growth.

53 enges that are unprecedented in the field of crystal growth.

54 ization of the prism structure and deficient crystal growth.

55 lter results in phosphorus precipitation and crystal growth, (3) crystal retention takes place by fil

56 , inorganic materials via protein-influenced crystal growth--a process known as biomineralization.

57 ased dopants, which were used to control the crystal growth, adsorbed to the surfaces of the boron-ri

58 be valuable systems for detailed studies of crystal growth, allowing testing of theoretical concepts

59 r which there already exist industrial-scale crystal growth and advanced microfabrication techniques.

60 lated to its functionality in inhibiting HAP crystal growth and can explain how oral pathogens select

61 associated with a nonclassical mechanism of crystal growth and can trigger a self-purifying cascade

62 We term the phenomenon Plateau-Rayleigh crystal growth and demonstrate that it can be used to gr

63 ted to overcome the stochastic nature of the crystal growth and dissolution processes.

64 f important chemical transformations such as crystal growth and dissolution.

65 Such forces can be used to control crystal growth and enable surface-confinement of these m

66 critically depends on the fine tuning of the crystal growth and error correction rates within large D

67 n implicated in modulating calcium carbonate crystal growth and has been reported to possess an EF-ha

68 Understanding crystal growth and improving material quality is importa

69 most likely by preventing calcium phosphate crystal growth and inducing cellular mineral resorption.

70 lution by physically blocking hydroxyapatite crystal growth and inducing expression of carbonic anhyd

71 on, these additives face-selectively inhibit crystal growth and lead to overall slower crystal appear

72 f high-temperature solutions for exploratory crystal growth and materials discovery of novel complex

73 e that the energetic barriers to interfacial crystal growth and organization can be overcome by targe

74 can then provide important information about crystal growth and particle size distributions.

75 tween nanoparticle assembly and atomic scale crystal growth and providing confidence that many more s

76 s on ice growth, the AF(G)Ps can inhibit MDM crystal growth and recrystallization, and more significa

77 Here we describe how a different mechanism, crystal growth and scission, can accurately replicate ch

78 nd drug molecules to the inorganic surfaces, crystal growth and shape development, catalyst performan

79 enamel matrix proteins in the regulation of crystal growth and the structural organization of the re

80 ds of science (hydrodynamics, combustion and crystal growth) and this has led to a search for a unifi

81 eously as an electrode, a solvent/medium for crystal growth, and a coreactant for the synthesis of a

82 nduce recirculation in the ink for enhancing crystal growth, and engineered the curvature of the ink

83 ly in the nucleation of new chemical phases, crystal growth, and other materials' transformations.

84 Here, we report synthesis, crystal growth, and structural characterization of the f

85 This lateral confinement causes aligned crystal growth, and the smallest patterns of 0.5 mum wid

86 In addition to limiting calcite crystal growth, AP7 is also observed to induce aggregate

87 s, and the implications for the mechanism of crystal growth are discussed.

88 Nucleation and crystal growth are important in material synthesis, clim

89 growth on biomineralization and spherulitic crystal growth are noted.

90 Although the effects of kinetics on crystal growth are well understood, the role of substrat

91 Additionally, the rate of crystal growth as a function of increased DNA linker len

92 nstrate the principal effect of As doping on crystal growth as reflected by considerably reduced aver

93 l six peptides dramatically affected calcite crystal growth (as observed by scanning electron microsc

94 ant-composition, hydroxyapatite (HA)-seeded, crystal growth assays.

95 behavior can be attributed to inhibition of crystal growth at microscopic length scale, as revealed

96 e gel particles were consumed during further crystal growth at room temperature, forming a colloidal

97 Studying nucleation and crystal growth at surfaces with submolecular-resolution

98 from freezing temperatures by inhibiting ice crystal growth at temperatures below the colligative fre

99 mpetent to self-assemble and control apatite crystal growth at the nanometer scale.

100 reactor, which draws from ideas of step-flow crystal growth augmented by detailed first-principles ca

101 tural-ordering processes, by which ultrafast crystal growth becomes possible.

102 probably because of the intrinsic isotropic crystal growth behavior of Pt.

103 Many fundamental questions in crystal-growth behavior remain unanswered because of the

104 So far, the factors preventing crystal growth beyond the favorable thickness of ca. 3 n

105 discovered that under certain conditions new crystal growth (branch) can be induced on specific cryst

106 ding to kink sites, which is consistent with crystal growth by a classical mechanism.

107 ral and synthetic aragonite spherulites that crystal growth by attachment of ACC particles is more th

108 Although inhibition of crystal growth by L-cystine "imposters" at L-cystine cry

109 d form ordered aragonitic structures through crystal growth by particle attachment.

110 We review progress toward understanding crystal growth by particle-attachment processes and show

111 Crystal growth can be observed, quantified and controlle

112 e growth front is slow and the corresponding crystal growth can suitably be followed in time.

113 -mediated stress relaxation during epitaxial crystal growth comes from the study of inorganic heteros

114 ut screening to find suitable nucleation and crystal growth conditions.

115 Nanoscale crystal growth control is crucial for tailoring two-dime

116 thought to influence processes as diverse as crystal growth, corrosion, charge trapping, luminescence

117 his entropic component of lattice mismatched crystal growth could be used to develop unique methods f

118 es involves four critical steps: nucleation, crystal growth, crystal aggregation, and crystal adhesio

119 The method allows control of the pentacene crystal growth direction and domain-size distribution.

120 In contrast to crystal growth, dissolution is a process of size reducti

121 zeolite analcime and zeolite A implies that crystal growth does not always follow the classic theory

122 developing a comprehensive understanding of crystal growth dynamics.

123 hnique is demonstrated for the Bridgman-type crystal growth enabling remote and direct measurements o

124 ace-bound AFPs are sufficient to inhibit ice crystal growth even in solutions depleted of AFPs.

125 inuous jump in crystal growth rate or "shock crystal growth" eventually produces 2D carpet-type fract

126 Crystal growth experiments were performed on fluoroapati

127 Here, we show that the crystal growth faces of methyl alpha-D-mannopyranoside (

128 ) fix a bisignate tensor with respect to the crystal growth faces.

129 During crystal growth, faceted interfaces may be perturbed by d

130 solution and their influence upon perovskite crystal growth, film formation and device performance.

131 articles may dominate in the early stages of crystal growth, followed by surface crystallization, and

132 y be possible by trapping of melt by cumulus crystal growth following melt drainage from an anomalous

133 Part of the challenge of macromolecular crystal growth for structure determination is obtaining

134 nnealing promoted oriented aggregation-based crystal growth, forming individual crystalline nanowires

135 large mobility-lifetime product, and simple crystal growth from solution.

136 or stiffening of the melt can be induced by crystal growth from the melt or variation in oxygen fuga

137 position of the growing polymer chain on the crystal growth front as the chain is formed by the catal

138 Microporous zincophosphate sodalite crystal growth has been studied in situ by atomic force

139 ess natural and industrial processes such as crystal growth, heterogeneous catalysis, electrochemistr

140 Thus crystal growth, honeycomb manufacture and floret evoluti

141 The theory of dislocation-controlled crystal growth identifies a continuous spiral step with

142 e amelogenins on octacalcium phosphate (OCP) crystal growth in a gelatin gel.

143 either d- and l-crystals can be achieved by crystal growth in agarose gel, a naturally occurring chi

144 eing capable of catalyzing ice formation and crystal growth in clouds at temperatures near 0 degrees

145 ystal hotel" microfluidic device that allows crystal growth in confined volumes to be studied in situ

146 rent crystal systems, attempts to understand crystal growth in detail have so far relied on developin

147 Antifreeze proteins prevent ice crystal growth in extracellular fluids, allowing fish to

148 A detailed study of carbamazepine crystal growth in four different bis(urea) gelators, inc

149 now recognized as an important mechanism of crystal growth in many materials, yet the alignment proc

150 Recent studies have found that crystal growth in organic glasses can be orders of magni

151 The kinetics of crystal growth in porous media controls a variety of nat

152 y be of value in probing parallel systems of crystal growth in solid inclusion compounds, crystal gro

153 e of research on the chemistry of doping and crystal growth in solution.

154 ilms form through homogeneous nucleation and crystal growth in the bulk to form equal-sized disk-shap

155 Although the theory describing crystal growth in the geological environment is well est

156 ril mineralization by selectively inhibiting crystal growth in the solution outside of the fibril.

157 own to form as inclusions during peritectoid crystal growth in the ternary CrZnSe solid-state compoun

158 Confinement of crystal growth in this manner provides a snapshot of the

159 that the presence of CCH can inhibit the ice crystals growth in NAM to reduce protein freeze-denatura

160 perpetuating steps to enable one-dimensional crystal growth, in contrast to mechanisms that require m

161 ent explanations differ for surface-enhanced crystal growth, including released tension and enhanced

162 of synthetic compounds for the regulation of crystal growth, including the freezing of water and grow

163 film is structurally confined by directional crystal growth, inducing intense anisotropy in charge tr

164 n" antifreeze activity as exemplified by ice crystal growth inhibition concomitant with melting tempe

165 Crystal growth inhibition, as measured by the slope of l

166 with classical mechanisms of layer-by-layer crystal growth inhibition.

167 ations of the crystal habit and polymorph by crystal growth inhibitors may not affect crystal aggrega

168 on of L-cystine stones by rational design of crystal growth inhibitors.

169 ing temperature, the ordered layer initiates crystal growth into the bulk, leading to an oriented, ho

170 range of applications, including catalysis, crystal growth, ion sensing, drug delivery, data storage

171 completes alignment and enables coalescence.Crystal growth is a fundamental process, important in a

172 Ice crystal growth is a major problem in cell/tissue cryopre

173 Crystal growth is accomplished by eliminating water mole

174 The Sb-assisted crystal growth is associated with the formation of a Sb-

175 gantic molecules formed by self-assembly and crystal growth is challenging as it combines two conting

176 A molecular-scale understanding of crystal growth is critical to the development of importa

177 s that can diffuse into the fibril to affect crystal growth is critical to understanding the mechanis

178 , a novel collision-based approach to seeded crystal growth is described in which seed crystals are d

179 irst example of biomacromolecular core-shell crystal growth is described, by showing that these cryst

180 During the entire experiment, no crystal growth is detected, and rigid grain rotation is

181 Self-organized dendritic crystal growth is explored to assemble uniform semicondu

182 Understanding and predicting crystal growth is fundamental to the control of function

183 d of lead chloride or iodide, the perovskite crystal growth is much faster, which allows us to obtain

184 ber of crystals increases with time, but the crystal growth is slowed down by the surrounding dense i

185 trates that ordering in nacre is a result of crystal growth kinetics and competition either in additi

186 Our work paves the way to tune the crystal growth kinetics by simple chemistry.

187 ice of the lead salt will aid in controlling crystal growth, leading to superior films and better per

188 e that electrostatic interactions in aqueous crystal growth may be systematically manipulated to synt

189 The process of surface crystal growth, meanwhile, is unperturbed by eliminating

190 nciled by invoking a three-step nonclassical crystal growth mechanism comprising (i) docking of clust

191 hollow crystals is attributed to a reversed crystal growth mechanism heretofore described only in th

192 show that, at high temperature, the observed crystal growth mechanisms and crystallization speed are

193 Crystal growth mechanisms are crucial to understanding t

194 ered, providing new insight into constricted crystal growth mechanisms underlying confined synthesis.

195 by a hydrophobic interface confined lateral crystal growth method.

196 Indeed, traditional crystal growth models emphasize the inhibiting effect of

197 Classical crystal growth models posit that crystallization outcome

198 crystal growth in solid inclusion compounds, crystal growth modifiers, emulsion stabilization, and re

199 terfacial phenomena such as charge transfer, crystal growth, nanoscale self-assembly and colloidal st

200 rge amount of new information, new rules for crystal growth need to be developed and tested.

201 nables simultaneous monitoring of individual crystal growth, nucleation rate, and macroscopic crystal

202 Collectively, these results demonstrate that crystal growth occurs such that the fast-growing directi

203 Lattice rotation in this new mode of crystal growth occurs upon crystallization through a wel

204 e demonstrate our approach by predicting the crystal growth of a diverse set of crystal types, includ

205 port where AF(G)Ps have been used to control crystal growth of carbohydrates and on AFGPs controlling

206 The synthesis and single crystal growth of clathrate-II Na(24)Si(136) is performe

207 t provides an overview of the method of flux crystal growth of complex oxides and can function as a "

208 oxidative decomposition of PB microcubes and crystal growth of iron oxide shells, we have demonstrate

209 istence of In(3+) and Cr(3+) induces a rapid crystal growth of large single crystals of heterometalli

210 While crystal growth of NaClO3 from pure aqueous solutions yie

211 nvestigation of some of the axioms governing crystal growth of nanoporous framework solids in general

212 We exploited this feature to separate the crystal growth of otherwise concomitant polymorphs from

213 e crucial in the manufacturing of chemicals, crystal growth of semiconductors, waste recovery of biol

214 a novel preparatory method for synthesis and crystal growth of solid state materials.

215 Here, we report new insights on the crystal growth of the perovskite materials, especially c

216 Single crystal growth of the rare earth hexaboride, SmB6, has b

217 oved understanding and better control of the crystal growth of these perovskites could further boost

218 e critical in the surface nucleation for the crystal growth of this material.

219 We infer that crystal growth of wurtzite is kinetically controlled by

220 Crystal growth of wurtzite stops when the diameter of th

221 ledges that could serve as nucleation sites, crystal growth of YN occurs on only (101)(PA).

222 d understanding of the dynamics of colloidal crystal growth on curved interfaces.

223 tor defects and thus can be harnessed during crystal growth or annealing to suppress defect populatio

224 s in solution at concentrations required for crystal growth or liquid state NMR measurements, high-re

225 iate occurs with a switch from bidirectional crystal growth parallel to the calcite c axis to growth

226 rol the reaction rate and, consequently, the crystal growth pathway and morphology of final products.

227 Dendritic crystal growth patterns have fascinated scientists for s

228 ngle-unit-cell level reveals novel nanoscale crystal-growth phenomena associated with the lateral siz

229 Evidence of such a novel crystal growth phenomenon can be also found in many othe

230 d this assembly was likely to be governed by crystal growth principles.

231 nciple the approach could be adapted to many crystal growth problems.

232 he starting materials is the first step of a crystal growth procedure.

233 F and the micelles, making self-assembly and crystal growth proceed under the direction of the cooper

234 ty were systematically varied to control the crystal growth process and determine the optimal conditi

235 Biomineralization in sea urchin embryos is a crystal growth process that results in oriented single-c

236 Here we present a rapid crystal growth process to obtain MAPbX3 single crystals,

237 roturbulent transport, must be active in the crystal growth process.

238 The current understanding of crystal growth processes in the presence of macromolecul

239 ements and observations of phase changes and crystal growth processes relevant to atmospheric science

240 e is widely applicable and is not limited to crystal growth processes.

241 es than those that are possible by classical crystal growth processes.

242 ors grown by sophisticated, high-temperature crystal growth processes.

243 Crystal growth propagates a sequence of bits while mecha

244 This rapid crystal growth rate (approximately 1 m/s) suggests that,

245 imated in the model included dissolution and crystal growth rate constants, as well as the dissolutio

246 compression rate, this discontinuous jump in crystal growth rate or "shock crystal growth" eventually

247 ee of fivefold symmetry has little effect on crystal growth rate, suggesting that growth may be only

248 ng the net charge on a protein increases the crystal growth rate.

249 uffer conditions, and generally had a faster crystal growth rate.

250 efect concentration could be correlated with crystal growth rate.

251 on microscopy indicate lateral size-limiting crystal growth related to amyloid fiber formation.

252 Crystal growth required the assistance of an anti-A3 nan

253 that PGEmix-8 is a nucleation enhancing and crystal growth retarding additive in palm oil crystalliz

254 The discovery of reversed crystal growth routes in zeolite analcime and zeolite A

255 To accomplish these ends, crystal growth should be fast and adaptable to rate fluc

256 ein self-interaction is important in protein crystal growth, solubilization, and aggregation, both in

257 In this paper we report the crystal growth, structure determination, and magnetic pr

258 Crystal growth studies in the presence and absence of a

259 reported along with detailed solubility and crystal growth studies of the alpha-Kappa(2)Hg(3)Ge(2)S(

260 and l-enantiomers on pairs of mirror-related crystal-growth surfaces.

261 New hydrothermal crystal growth technique enabled isolation of environmen

262 hemical vapor transport (CVT), an old single-crystal growth technique, has been extended from growing

263 The process utilizes templated liquid-phase crystal growth that results in user-tunable, patterned m

264 A requirement for crystal growth, the additive n-heptyl-beta-d-glucopyrano

265 Despite its ability to direct crystal growth, the interaction of the amelogenin protei

266 In an exactly analogous mechanism to crystal growth, the participation of critical conditions

267 tructure is one of the primary objectives in crystal growth, the present lack of predictive understan

268 example, during phase separation) or faceted crystal growth, their surfaces tend to have minimum-area

269 inetics and those predicted from fundamental crystal growth theories confirms that the growth of thes

270 indings not only expand the current scope of crystal growth theory, but may also lead to a broader sc

271 imental findings in the context of classical crystal growth theory, the former is suggested to create

272 During the crystal growth, these dopant-based surface complexions b

273 t for antifreeze proteins (AFPs) to stop ice crystal growth, they must irreversibly bind to the ice s

274 idation is only to sulfenic acid despite the crystal growth time period of 2 weeks.

275 extends the possibility of mesoporous single-crystal growth to a range of functional ceramics and sem

276 om phase transitions, chemical reactions and crystal growth to grain boundary dynamics.

277 itive branching during one-step hydrothermal crystal growth to synthesize a new hierarchical zeolite

278 Crystal growth under methanol diffusion favored depositi

279 utually soluble in a solvent that encourages crystal growth upon evaporation.

280 Crystal growth upon firing of hydrous transition metal o

281 lling the initiation and kinetics of polymer crystal growth using dip-pen nanolithography and an atom

282 Here we systematically study secondary ZnO crystal growth using organic diamine additives with a ra

283 ation due to dislocations at surfaces during crystal growth, very little is known about the effects o

284 highly direction-specific interactions drive crystal growth via oriented attachment.

285 extraneous nucleation is avoided relative to crystal growth via spatially localized laser heating and

286 The intra-ER crystal growth was accompanied by cell enlargement and m

287 Crystal growth was also greatly reduced when using 0.7%

288 ystallinity, preferred orientation, and cage crystal growth was obtained by experimental and computat

289 centrations, the rate-limiting factor of the crystal growth was the adsorption of the precursor ions,

290 iting the amount of metal ion present during crystal growth, we have now obtained a crystal structure

291 allows for proper initiation of algorithmic crystal growth, which could lead to the high-yield synth

292 sent observations of pressure-induced ice VI crystal growth, which have been predicted theoretically,

293 n appear to be determined by the kinetics of crystal growth with a statistical bias, but the diversit

294 Crystal growth with addition of trehalose resulted in a

295 wed increased inhibitory effects on palm oil crystal growth with increasing concentration of PGEmix-8

296 However, methods to control zeolite crystal growth with nanometer precision are still in the

297 odification can significantly facilitate the crystal growth with respect to the corresponding native

298 rovides a snapshot of the earliest stages of crystal growth, with insights into nucleation, size-depe

299 Confined crystal growth within these templates leads to size-tuna

300 sited, DPT's pendant phenyl groups frustrate crystal growth, yielding amorphous films.