ライフサイエンスコーパス: XRD

1 XRD analysis of the aged powders showed no occurrence of

2 XRD analysis showed that a peak corresponding to 4.7 A i

3 XRD analysis showed that annealing of THNS at 400 degree

4 XRD assays showed that the overall molecular packing of

5 XRD indicated that PAA/QU/beta-CD-IC-NF were amorphous i

6 XRD pattern of native starch (C-type) did not change on

7 XRD revealed that soil clay aluminosilicates were hydrox

8 XRD showed an additional peak at 13 degrees and increase

9 XRD showed that the Cd(2+) was precipitated as pure otav

10 XRD study reveals that the cationic [Ta6Br12(H2O)6](2+)

11 XRD, contact angle, SEM, AFM and SECM studies revealed t

12 XRD, Raman, TPO, and TEM analysis confirmed that the dea

13 XRD, XPS, and ESR suggested the Na2Mo4O13/alpha-MoO3 hyb

14 ) from pure components and multiple (N = 10) XRD patterns were collected for each mixture.

15 The observation of a 4.7-A XRD spacing confirms the presence of beta-sheets and ill

16 roperties were studied by N2 gas adsorption, XRD, FTIR, Fe EXAFS, and STXM-NEXAFS techniques.

17 ized by means of X-ray diffraction analysis (XRD), field emission scanning electron microscopy (FE-SE

18 ization techniques (N2/Ar sorption analysis, XRD, (29)Si and (13)C NMR, TEM).

19 Notably, the FT-IR peak at 947cm(-1) and XRD peaks at 2theta approximately 13 degrees and 20 degr

20 layers were investigated by UV-vis, AFM, and XRD experiments.

21 (1)H, (13)C NMR, FT-IR spectral analyses and XRD data.

22 ighlight the presence of a Cu-Scys bond, and XRD analysis provides structural evidence.

23 stablished between RS formation in bread and XRD patterns, having a 96.7% fit indicating the potentia

24 DSC and XRD studies indicated that the addition of oil to the li

25 s of starch were studied by means of DSC and XRD.

26 electrode are characterized by SEM, EDX and XRD analyses.

27 catalysts are characterized by SEM, EDX, and XRD techniques.

28 FTIR and XRD analyses suggested that precipitation (formation of

29 er of surface pores; shown by SEM images and XRD data.

30 f CPCMs were characterized by SEM, FT-IR and XRD.

31 Microstructural and XRD analysis were carried out in detail to show the infl

32 The SEM and XRD results testified a slightly increase of the grain s

33 bricated and characterized with TEM, SEM and XRD.

34 catalyst was characterized by FT-IR, SEM and XRD.

35 determined by 1D and 2D NMR spectroscopy and XRD.

36 N NEXAFS, Fe K-edge EXAFS spectroscopy, and XRD were applied to provide additional information.

37 o Au) prepared were characterized by TEM and XRD.

38 rized with different methods such as TEM and XRD.

39 ologies are characterized with AFM, TEM, and XRD and are found to be virtually indistinguishable.

40 g FT-IR, UV/vis., FESEM, XEDS, XPS, TEM, and XRD techniques.

41 With use of TGA and XRD the volatilization behavior of Mo was studied.

42 The high-resolution TEM, SEM/EDX, UV-vis and XRD studies confirmed the homogeneous distribution of cr

43 like X-ray absorption spectroscopy (XAS) and XRD, demonstrating the potential of multimodal in situ X

44 aryl-Co(III) compounds (NMR, HRMS, XAS, and XRD) prepared through a C(sp(2))-H activation, using a m

45 Ex situ XPS and XRD both show significant oxidation of the irradiated Ta

46 and characterized with TEM, TGA, small-angle XRD, and nitrogen adsorption/desorption measurements.

47 ivity of the material and the absence of any XRD signature of FeO, it is very likely that FeO is form

48 SEM and TEM to study morphology, as well as XRD and EDS to study composition.

49 1D and 2D solid-state NMR, as well as XRD data on lithiated sample (after discharge) show that

50 eacted final solid phase samples analyzed by XRD.

51 The modified nanoclays were characterised by XRD, N2-physisorption, SEM and FT-IR spectroscopy.

52 rogenation of glycerol, was characterized by XRD, DFT calculations, HRMS, FTIR spectroscopy, and NMR

53 sized dendritic monomer was characterized by XRD, FT-IR, VSM, FE-SEM, and TEM analyses.

54 ures of the nanosheets were characterized by XRD, FTIR and Raman spectroscopy, FESEM and TEM.

55 uantum dots were thoroughly characterized by XRD, high-resolution transmission electron microscopy (H

56 id solutions were have been characterized by XRD, SEM, diffuse reflectance UV-Vis spectroscopy, BET a

57 thesized nanoparticles were characterized by XRD, SEM, TEM, FTIR, TGA, DSC and UV-visible spectroscop

58 rs with red phosphorus, and characterized by XRD, SEM, XPS, XRF, SAED and TEM measurements.

59 via a solution process and characterized by XRD, TEM, EDS, and XPS.

60 f as-prepared products were characterized by XRD, TEM, HRTEM, SEM and fluorescence spectrophotometer.

61 The phase purity has been confirmed by XRD and NMR.

62 line Ne inside hollow NPs is not detected by XRD, indicating that the oxide shell is impenetrable.

63 on of the anatase unit cell as determined by XRD.

64 istics of the adsorbent were investigated by XRD, EDX, FE-SEM, and VSM techniques.

65 pulsed cathodic arc had been investigated by XRD, SEM and Raman spectroscopy.

66 eversible polymorphs for TT were observed by XRD and grazing-incidence wide-angle X-ray scattering (G

67 This random distribution was supported by XRD data displaying Vegard's law.

68 motion at high temperature, unobservable by XRD but demonstrated by solid state NMR studies.

69 FTIR, CD, XRD, and ssNMR indicate the presence of cross-beta and p

70 Nanolayering and characteristic XRD peaks were rarely observed in specimens prepared fro

71 Single crystal XRD analysis indicated that unlike for 6, the hydride li

72 of spectroscopic evidence and single crystal XRD results, indicates that the detection pathway procee

73 s characterized by 2D NMR and single crystal XRD.

74 C-5 position was confirmed by single crystal XRD.

75 Single-crystal XRD analyses revealed that alpha to beta transition occu

76 ocarbazoles were confirmed by single-crystal XRD analyses.

77 Single-crystal XRD analysis of the dipeptide 1 showed parallel beta-she

78 Single-crystal XRD analysis reveals that POM:gamma-CD constitutes a hig

79 symmetry in 7 as confirmed by single-crystal XRD analysis, we established that the ground state UV-vi

80 been structurally solved via single-crystal XRD and analyzed by density functional theory calculatio

81 erivatives were determined by single-crystal XRD and NMR spectroscopy and confirmed that the solid-st

82 For instance, single-crystal XRD shows that at low temperatures, the methanol molecul

83 opic techniques as well as by single-crystal XRD study, and DFT calculations were performed to furthe

84 method were characterized by single-crystal XRD, giving two crystal structures, a trigonal (R-3c) an

85 troscopy (-155 degrees C) and single-crystal XRD.

86 from the decrease of material crystallinity (XRD) as well as sorption capacity (BET).

87 py (AFM), x-ray diffraction crystallography (XRD), and Fourier transform infrared spectroscopy (FTIR)

88 py (SEM), X-ray diffraction crystallography (XRD), differential scanning calorimetry (DSC), Fourier-t

89 ansition, as evidenced by pressure-dependent XRD.

90 rimetry, molecular simulations, and detailed XRD investigations of the changes in the crystal structu

91 bond is of similar length for the diamantyl [XRD, 1.642(2) A; GED, 1.630(5) A] and the oxadiamantyl d

92 nating synchrotron X-ray powder diffraction (XRD) with differential scanning calorimetry (DSC).

93 4 nm), morphology, X-ray Powder Diffraction (XRD), in vitro release profile, cytotoxicity and cell pr

94 In particular, x-ray diffraction (XRD) analyses show that carbonate minerals consist mainl

95 EM), UV-Vis spectroscopy, X-ray diffraction (XRD) analysis and Fourier transform infra-red (FTIR) spe

96 its were characterized by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM).

97 X-ray diffraction (XRD) analysis showed a type-C starch with a relative cry

98 tron microscopy (TEM) and x-ray diffraction (XRD) and also the results show that NiO nanoparticles we

99 c acid were determined by X-ray diffraction (XRD) and differential scanning calorimetry (DSC); and th

100 identified by synchrotron X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS

101 X-ray diffraction (XRD) and Fe K-edge X-ray absorption spectroscopy (XANES

102 ructure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments.

103 ta-phase was confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy.

104 lectron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR)

105 nanoribbon amelogenin by x-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR)

106 tip link is confirmed by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR).

107 oscopy and single-crystal X-ray diffraction (XRD) and in solution by (19)F NMR spectroscopy.

108 d state by single-crystal X-ray diffraction (XRD) and in solution using multinuclear NMR methods (inc

109 high-pressure synchrotron X-ray diffraction (XRD) and Raman spectroscopy study, and electrical transp

110 Powder X-ray Diffraction (XRD) and refinement were used to analyze the crystal str

111 dance spectroscopy (EIS), X-ray diffraction (XRD) and scanning electron microscopy (SEM) measurements

112 lasses were studied using X-ray diffraction (XRD) and scanning electron microscopy (SEM).

113 ctron microscopy (HRTEM), X-ray diffraction (XRD) and scanning electron microscopy (SEM).

114 In situ X-ray diffraction (XRD) and transmission electron microscopy (TEM) have bee

115 spersive X-ray (SEM-EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM).

116 lectron microscopy (TEM), X-ray diffraction (XRD) and ultraviolet-visible absorption spectroscopy (UV

117 ere used for simultaneous x-ray diffraction (XRD) and x-ray emission spectroscopy (XES) of microcryst

118 by a combined ESI MS and X-ray diffraction (XRD) approach.

119 basal spacing measured by X-ray diffraction (XRD) assay.

120 tron microscope (SEM) and X-ray diffraction (XRD) confirm the nanotube structure of composite polymer

121 sform infrared (FTIR) and X-ray diffraction (XRD) data supported.

122 sform infrared (FTIR) and X-ray diffraction (XRD) data].

123 along with supplementary X-ray diffraction (XRD) experiments and ab initio molecular dynamics (AIMD)

124 copy and angle dispersive X-ray diffraction (XRD) experiments of bismuth selenide (Bi2Se3) have been

125 tron diffraction (ND) and x-ray diffraction (XRD) experiments on magnetically-oriented fibers of Abet

126 erature and high pressure X-ray diffraction (XRD) measurement has identified the phase transition cur

127 amines the correlation of X-ray diffraction (XRD) measurements with the histopathological analysis of

128 X-ray diffraction (XRD) of the precipitates showed they were composed solel

129 The X-ray diffraction (XRD) pattern at 0.84 GPa suggests that the crystallized

130 e condition while in situ X-ray diffraction (XRD) probes the time-dependent atomic arrangement.

131 X-ray diffraction (XRD) results demonstrate phase-pure epitaxial growth of

132 Correlating with X-ray diffraction (XRD) results it is suggested that the strain relaxation

133 In-plane X-ray diffraction (XRD) revealed that the deposited nanosheets contract upo

134 Single-crystal X-ray diffraction (XRD) showed that the ZnCar framework adapts to MeOH and

135 -visible spectroscopy and X-ray diffraction (XRD) spectroscopy.

136 metric analysis (TGA) and X-ray diffraction (XRD) spectroscopy.

137 ctrocatalytic properties, X-ray diffraction (XRD) studies, and infrared spectroelectrochemistry (IR-S

138 was confirmed further by x-ray diffraction (XRD) study.

139 tron microscopy (TEM) and X-ray diffraction (XRD) to interpret the superstructure composing aqueous f

140 Thin-film glancing angle X-ray diffraction (XRD) was used to detect the characteristic peaks exhibit

141 RS determination and X-ray diffraction (XRD) were used to evaluate the influence of storage temp

142 microscopy (TEM), in situ X-ray diffraction (XRD), and in situ electrochemical Fourier transformed in

143 other techniques such as X-ray diffraction (XRD), and micro-Raman and infrared spectroscopies allowe

144 l cell (DAC), synchrotron X-ray diffraction (XRD), and small-angle X-ray scattering (SAXS) techniques

145 hroism (CD) spectroscopy, X-ray diffraction (XRD), and solid-state nuclear magnetic resonance (ssNMR)

146 ctron spectroscopy (XPS), X-ray diffraction (XRD), and UV-Vis diffuse reflectance spectroscopy (DRS),

147 frared (IR) spectroscopy, x-ray diffraction (XRD), and x-ray photoelectron spectroscopy (XPS) were em

148 ample magnetometer (VSM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS).

149 tron microscopy (FE-SEM), X-ray diffraction (XRD), atomic force microscopy (AFM), electrochemical imp

150 A combination of X-ray diffraction (XRD), chemical extraction, and X-ray absorption spectros

151 dance spectroscopy (EIS), X-ray diffraction (XRD), contact angle, scanning electron microscopy (SEM),

152 lectron microscopy (TEM), X-ray diffraction (XRD), dynamic laser scattering (DLS), and vibrating samp

153 e been accomplished using X-ray diffraction (XRD), electrochemical, transmission electron microscopy

154 ransform infrared (FTIR), X-ray diffraction (XRD), energy dispersive X-ray spectral analysis (EDS), s

155 al characterisation using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM

156 infrared spectra (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM

157 c force microscopy (AFM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), cyclic voltamme

158 The X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) an

159 mett-Teller method (BET), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), s

160 including single-crystal X-ray diffraction (XRD), gas-phase electron diffraction (GED), a combined G

161 rostructural analysis via X-ray diffraction (XRD), molecular modeling, molecular simulation, and soli

162 were characterized using X-ray diffraction (XRD), Mossbauer spectroscopy, and scanning electron micr

163 s constraints provided by X-ray diffraction (XRD), one- and two-dimensional solid-state nuclear magne

164 lectron microscopy (TEM), X-ray diffraction (XRD), Raman spectra and Brunauer-Emmett-Teller (BET) met

165 lectron microscopy (TEM), x-ray diffraction (XRD), Raman-spectroscopy, electrochemical impedance spec

166 investigated by means of X-Ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spect

167 X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmissio

168 X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dis

169 des were studied by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission e

170 tion techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission e

171 arefully characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission e

172 situ techniques including X-ray diffraction (XRD), scanning transmission electron microscopy (STEM),

173 etite was investigated by X-ray diffraction (XRD), solution chemistry, and X-ray absorption spectrosc

174 s proved by experimental (X-ray diffraction (XRD), thermal gravimetric analysis (TGA), (1)H NMR) and

175 -made nanocomposite using X-ray diffraction (XRD), transmission electron microscopy (TEM) and alterna

176 Ps were carried out using X-ray diffraction (XRD), transmission electron microscopy (TEM) and dynamic

177 X-ray spectroscopy (EDX), X-ray diffraction (XRD), UV-vis, photoluminescence (PL) spectroscopy, FT-IR

178 roscopy (SEM), and powder X-ray diffraction (XRD), were used to characterize the morphology and the s

179 XRF) spectrometry, powder X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS), and selective

180 as performed using powder X-ray diffraction (XRD), X-ray fluorescence mapping (mu-XRF), and X-ray abs

181 lectron microscopy (TEM), x-ray diffraction (XRD), x-ray photo-electron spectrum (XPS), electrochemic

182 The unique combination of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), in-field M

183 d spectroscopy (FTIR) and X-ray Diffraction (XRD).

184 tron microscopy (SEM) and X-ray diffraction (XRD).

185 ied out by single-crystal X-ray diffraction (XRD).

186 spectroscopy (FT-IR) and X-ray Diffraction (XRD).

187 n spectroscopy (XPS), and x-ray diffraction (XRD).

188 ing calorimetry (DSC) and X-ray diffraction (XRD).

189 oscopy (SEM), and in situ X-ray diffraction (XRD).

190 oscopy and single-crystal X-ray diffraction (XRD).

191 spectroscopy (FTIR) and X - ray diffraction (XRD).

192 x-ray diffraction(XRD) tests demonstrated the intermetallics were effectiv

193 copy (FT-IR) analysis, X-ray diffractometry (XRD) and gas chromatography-mass spectrometry (GC-MS).

194 Raman spectroscopy and X-ray diffractometry (XRD) to evaluate its morphology, crystallinity, composit

195 nalysis (DSC and TGA), X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FT-IR), s

196 pectroscopy (FTIR) and X-ray diffractometry (XRD).

197 ED, 1.630(5) A] and the oxadiamantyl dimers [XRD, 1.643(1) A; GED, 1.632(9) A; GED+MW, 1.632(5) A], d

198 of graphene oxide according to the SEM, EDS, XRD, XPS, Raman and TGA results.

199 rmal property were analyzed using FTIR, EDX, XRD, TGA, VSM, and TEM.

200 ing different tools such as FESEM, TEM, EDX, XRD, DLS and zeta potential measurements.

201 Electrochemical, XRD, and EELS experiments demonstrate that this effect s

202 ees (1.23 nm) were identified from thin-film XRD.

203 The d-spacing ratios estimated from XRD analysis of OXD derivatives possessing longer alkyl

204 by its experimental molecular structure from XRD analysis.

205 FTIR, XRD, XPS, and HRTEM measurements corroborate the formati

206 Solid state NMR, supported by FTIR, XRD, and electron microscopy, define the interactions of

207 material was characterized by means of FTIR, XRD, Raman spectra and TEM analyses.

208 ulations (RMC) guided by the experimental HE-XRD/PDF data.

209 led to atomic pair distribution function (HE-XRD/PDF) analysis to probe the atomic structure of PdNi

210 situ high-temperature X-ray diffraction (HT-XRD), ex-situ XRD and synchrotron X-ray absorption near

211 characterized by FTIR, magnetic hysteresis, XRD, SEM and N2-sorption measurements.

212 everal state of the art techniques including XRD, TEM, SEM and XPS.

213 -dentin interface along with lower intensity XRD peaks.

214 efully characterized by the SEM, TEM, FT-IR, XRD and so on.

215 amples were characterized by SEM-EDX, FT-IR, XRD and TGA-DSC techniques.

216 This material was characterised using FT-IR, XRD, SEM and VSM techniques.

217 s synthesized and characterized using FT-IR, XRD, SEM and VSM techniques.

218 peratures was studied by means of isothermal XRD experiments, in which the evolution of the solid is

219 ge cannot be gained from existing laboratory XRD instruments, since much longer collection times are

220 Meanwhile, XRD peaks of OEO-containing films were more intense, ind

221 First, mu-XRF-CT and mu-XRD-CT reveal the active state of Pt catalyst to be redu

222 ffraction computed tomography (mu-XRF-CT, mu-XRD-CT) in combination with X-ray absorption near-edge s

223 ocal probe synchrotron X-ray diffraction (mu-XRD) using a focused X-ray beam, X-ray Magnetic Circular

224 fluorescence (mu-XRF), X-ray diffraction (mu-XRD), and scanning transmission X-ray microscopy (STXM)

225 FTIR/muSR-FTIR), and X-ray diffraction (muSR-XRD) with synchrotron light.

226 bination of stimuli and were studied by NMR, XRD, EPR spectroscopy, and DFT calculations.

227 With the aid of XRD, XPS, and GC-MS analysis, we confirm DMTS could unde

228 The combination of XRD and DSC has further allowed us to identify mixtures

229 A combination of XRD, EXAFS, TEM, and CO chemisorption and TPD revealed t

230 ving a 96.7% fit indicating the potential of XRD to measure RS concentrations.

231 c Ni-Fe was elucidated by combining operando XRD and XAS analyses and energy-dispersive X-ray spectro

232 Evidenced by our XRD data up to 81.2 GPa, the Bi2Se3 crystallizes into bo

233 racterized using powder X-ray diffraction (p-XRD) and scanning electron microscopy (SEM).

234 The p-XRD spectra were used to evaluate the purity of the synt

235 lorimetry (DSC), X-ray diffraction patterns (XRD) and zeta potential.

236 oscopy (EDX) and X-ray diffraction patterns (XRD).

237 In-plane XRD experiments revealed the formation of a highly order

238 re was no contraction detectable by in-plane XRD, indicating well-intergrown MFI films that are stron

239 Powder XRD, HRTEM, and (23)Na NMR studies revealed that this co

240 semble-based electron diffraction and powder XRD data.

241 complex phase behavior as revealed by powder XRD and NMR spectroscopy.

242 Data from powder XRD, (1)H double-quantum solid-state magic-angle spinnin

243 s structure characterized by means of powder XRD and aberration corrected scanning transmission elect

244 SEM, EDS, UV/Vis., FTIR spectroscopy, powder XRD, and XPS techniques.

245 and OR phases, on basis of our high-pressure XRD data, indicate that the AFM order is robust in the p

246 Here we present in situ pump-probe XRD measurements on shock-compressed fused silica, revea

247 The structural properties (XRD, FTIR), morphology (TEM), hygroscopic properties (wa

248 High resolution XRD, XTEM, EDX, and RBS indicate that the resultant mono

249 The resulting XRD spectra were subjected to principal component analys

250 SC-XRD shows that anthraphane packs in layers irrespective

251 by single crystal X-ray crystallography (sc-XRD), Au279(SPh-tBu)84 named Faradaurate-279 (F-279) in

252 Single crystal X-ray diffraction (SC-XRD) is the principal method for determining the crystal

253 If SC-XRD is to retain its position as the definitive method o

254 established from a low-temperature 120 K sc-XRD study at 0.90 A resolution.

255 btained microparticles were analysed by SEM, XRD and DSC.

256 and several analytical techniques (ICP, SEM, XRD, etc.), which were used in order to investigate the

257 olubility, moisture content, structure (SEM, XRD), FT-IR and sensory properties.

258 These materials are characterized with SEM, XRD, TEM, SAED, EDX, XPS, UV-visible spectroscopy, and o

259 In total, 522 separate XRD measurements were made at different locations across

260 Simultaneously, XRD patterns of the soil suggest that crystallization of

261 Ex situ XRD studies confirm that KC36, KC24, and KC8 sequentiall

262 perature X-ray diffraction (HT-XRD), ex-situ XRD and synchrotron X-ray absorption near edge structure

263 A major limitation of in situ XRD and TEM is a compromise that has to be made between

264 riety of calorimetric techniques and in situ XRD at elevated temperatures has been used to evaluate t

265 Parallel in situ XRD measurements also confirm the transformation of beta

266 The in situ XRD showed that the new crystalline phase was still a mo

267 In situ XRD studies performed on pristine and chemically-delithi

268 r magnetic resonance (MAS NMR) spectroscopy, XRD, FT-IR spectroscopy, and N2 physisorption.

269 tion techniques (in situ Raman spectroscopy, XRD, SEM, and cryo-TEM) to investigate the formation and

270 ge Washington, by IR and Raman spectroscopy, XRD, X-ray photoelectron spectroscopy, and Mossbauer spe

271 udy by investigating the crystal structures (XRD, HRTEM), morphologies (SEM), porosities (BET), surfa

272 entary measurements by Raman and synchrotron XRD are in excellent agreement with the classifications

273 ways using in-situ STEM, in-situ synchrotron XRD, and DFT electronic structure calculations.

274 The nanocomposite was characterized by TEM, XRD, FTIR, XPS, TGA, BET, and CV using the redox couples

275 ation by FTIR, XPS, Raman Spectroscopy, TEM, XRD, TOC, collectively demonstrates that oxidized C60 de

276 the 11 hydrides revealed by low temperature XRD were supported by a density functional theory invest

277 everal techniques including: FTIR, XPS, TGA, XRD, and XANES to probe their integrity.

278 ough being significantly less sensitive than XRD, NIR, and also (35)Cl NQR, is still capable of provi

279 ese results are encouraging and suggest that XRD could be used for the intraoperative or postoperativ

280 The XRD and DSC results indicated that the amorphous TTO-bet

281 The XRD and Raman results show that the phase undergoes a pr

282 degrees and 43 degrees 2theta degrees in the XRD pattern, which indicated both crystalline and amorph

283 a low-level of crystallinity detected in the XRD, suggesting that long-range ordering is possible.

284 Shifting of the crystalline region of the XRD curve towards lower values of Bragg's angle was attr

285 rrelation between the shape/magnitude of the XRD spectra and the tissue type.

286 ults were correlated with the results of the XRD study.

287 d Molecular Sciences Laboratory in which the XRD measurements were performed.

288 solid solutions were calculated using their XRD patterns.

289 rando X-ray diffraction computed tomography (XRD-CT) to study specific components of an essentially u

290 Characterization of bioreduced solids via XRD indicate that this additional Fe(II) is incorporated

291 nt between low- and high-pressure states via XRD.

292 u nanocomposite was characterised by UV-vis, XRD, FTIR, TEM, XPS and Raman spectroscopy techniques.

293 ials were characterized by TEM, SEM, UV-Vis, XRD, XPS, EIS, fluorescence, and photoelectrochemical me

294 rized with FT-IR, SEM, EDX, TEM, UV-Visible, XRD and TG/DTA techniques.

295 zite structure of size ~24 nm by UV-visible, XRD, FTIR and TEM.

296 d minor change on the granule surface, while XRD profiles indicated slight loss of crystallinity.

297 resulting REE oxides were characterized with XRD, SEM-EDX, and ICP-OES, demonstrating that the membra

298 tu soft XAS measurements in combination with XRD.

299 f the end members was studied in detail with XRD and discussed with special regard to the oxygen posi

300 Experimental (NMR, IR, MS, EPR, XAS, XRD) and computational data (DFT) support an oxidation s