ライフサイエンスコーパス: photoelectron spectroscopy

1 d by means of diffraction, optical and X-ray photoelectron spectroscopy.

2 including XRD, electron microscopy and X-ray photoelectron spectroscopy.

3 silicon substrate, as demonstrated by X-ray photoelectron spectroscopy.

4 croscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy.

5 spin resonance, UV-vis-NIR, and ultraviolet photoelectron spectroscopy.

6 s decrease of Mn valence measured from X-ray photoelectron spectroscopy.

7 ing synchrotron-based ambient pressure X-ray photoelectron spectroscopy.

8 have been investigated by using negative ion photoelectron spectroscopy.

9 elative to more traditional methods based on photoelectron spectroscopy.

10 haracterized by Raman spectroscopy and X-ray photoelectron spectroscopy.

11 r transform infrared spectroscopy, and X-ray photoelectron spectroscopy.

12 the tethered catalysts, determined by X-ray photoelectron spectroscopy.

13 confirmed using elemental analysis and X-ray photoelectron spectroscopy.

14 potential of -0.75 V, as observed from X-ray photoelectron spectroscopy.

15 ements, optical/solvent exposures, and X-ray photoelectron spectroscopy.

16 n between Au and ZnO was manifested by X-ray photoelectron spectroscopy.

17 namely X-ray magnetic circular dichroism and photoelectron spectroscopy.

18 lk water, using either optical absorption or photoelectron spectroscopy.

19 determined using X-ray diffraction and X-ray photoelectron spectroscopy.

20 ized by contact angle measurements and X-ray photoelectron spectroscopy.

21 temperature-programmed desorption, and X-ray photoelectron spectroscopy.

22 red by quite different methods such as X-ray photoelectron spectroscopy.

23 NiO(x) membrane, which is confirmed by X-ray photoelectron spectroscopy.

24 ns, and synchrotron-based near ambient X-ray photoelectron spectroscopy.

25 l strain microscopy and sputter-etched X-ray photoelectron spectroscopy.

26 spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy.

27 n iron-deficient sulfide, according to X-ray photoelectron spectroscopy.

28 lms using photoluminescence, Raman and x-ray photoelectron spectroscopies.

29 crystal arrays is confirmed via infrared and photoelectron spectroscopies.

30 Nuclear magnetic resonance(11), X-ray photoelectron spectroscopy(12) and cryogenic transmissio

31 Angle-resolved X-ray photoelectron spectroscopy analyses indicate that GNSs c

32 Evidence from high resolution X-ray photoelectron spectroscopy analyses indicated that the u

33 X-ray photoelectron spectroscopy analysis confirmed the presen

34 The X-ray photoelectron spectroscopy analysis confirms the presenc

35 X-ray photoelectron spectroscopy analysis of ABP and ACP confi

36 probable adsorption mechanism based on X-ray photoelectron spectroscopy analysis was also proposed in

37 calculations and further confirmed by X-ray photoelectron spectroscopy analysis.

38 d the reduction of Cr(VI) according to X-ray photoelectron spectroscopy analysis.

39 Here, using time-resolved photoelectron spectroscopy and ab initio calculations, w

40 of a mixed B/Bi target and characterized by photoelectron spectroscopy and ab initio calculations.

41 we report the results obtained via combined photoelectron spectroscopy and ab initio studies of the

42 egradation mechanism of GaS(0.87) with X-ray photoelectron spectroscopy and annular dark-field scanni

43 ating voltage regions, as confirmed by X-ray photoelectron spectroscopy and atomic force microscopy e

44 urier transform infrared spectroscopy, X-ray photoelectron spectroscopy and atomic force microscopy.

45 is hydrophobic ligand was confirmed by X-ray photoelectron spectroscopy and contact angle goniometry

46 Here, a combined anion photoelectron spectroscopy and density functional theory

47 and 8-hydroxyquinoline molecules using anion photoelectron spectroscopy and density functional theory

48 X-ray photoelectron spectroscopy and electrochemistry confirm

49 fides has been evaluated by conducting X-ray photoelectron spectroscopy and electron microscopy studi

50 ion of oxygen defects as determined by X-ray photoelectron spectroscopy and electron paramagnetic res

51 ion, and characterized by a synergy of anion photoelectron spectroscopy and electronic structure calc

52 Using X-ray photoelectron spectroscopy and Fourier transform infrare

53 In the present study, we employed X-ray photoelectron spectroscopy and Fourier-transform infrare

54 Using operando ambient pressure X-ray photoelectron spectroscopy and high pressure scanning tu

55 With the aid of experimental photoelectron spectroscopy and highly correlated ab init

56 itial CO loss as determined by in situ X-ray photoelectron spectroscopy and mass spectrometry.

57 Furthermore, valence band analysis by X-ray photoelectron spectroscopy and photoluminescence spectro

58 C-Pt-H(CO(2))](-) by a synergy between anion photoelectron spectroscopy and quantum chemical calculat

59 be H-Pt-CH(3) (-) by a synergy between anion photoelectron spectroscopy and quantum chemical calculat

60 The CoB18 (-) cluster was characterized by photoelectron spectroscopy and quantum chemistry calcula

61 Here, we use photoelectron spectroscopy and quantum chemistry calcula

62 on cluster (PrB7(-) ) are investigated using photoelectron spectroscopy and quantum chemistry.

63 ased on a combination of detailed core-level photoelectron spectroscopy and quantum-chemical calculat

64 (-) and ReB(2) O(-) and investigated them by photoelectron spectroscopy and quantum-chemical calculat

65 y infrared, electronic absorption, and X-ray photoelectron spectroscopy and revealed formation of a s

66 olled electron-impact irradiation with X-ray photoelectron spectroscopy and scanning electron microsc

67 X-ray photoelectron spectroscopy and scanning electron microsc

68 haracterized using Raman spectroscopy, X-ray photoelectron spectroscopy and scanning tunneling micros

69 ulating films of WO3 Here, we use hard X-ray photoelectron spectroscopy and spectroscopic ellipsometr

70 nd probed their structures and bonding using photoelectron spectroscopy and theoretical calculations.

71 rk, where temperature-dependent negative ion photoelectron spectroscopy and theoretical studies demon

72 r anions (Bn-) have allowed systematic joint photoelectron spectroscopy and theoretical studies, reve

73 roscopy, scanning electron microscopy, X-ray photoelectron spectroscopy and transmission electron mic

74 troscopy, powdered X-ray spectroscopy, X-ray photoelectron spectroscopy and UV-Vis diffused reflectan

75 ristics were assessed by TEM, SEM-EDX, X-ray photoelectron spectroscopy and vibrating sample magnetom

76 to bind with mercury as determined by X-ray photoelectron spectroscopy and X-ray absorption fine str

77 structural and transport measurements, X-ray photoelectron spectroscopy, and ab initio calculations a

78 ed by scanning tunneling spectroscopy, X-ray photoelectron spectroscopy, and complementary density fu

79 ere investigated by mass spectrometry, anion photoelectron spectroscopy, and computations.

80 rature scanning tunnelling microscopy, X-ray photoelectron spectroscopy, and density functional theor

81 y, grazing incident X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier transform infrar

82 d using a quartz crystal microbalance, X-ray photoelectron spectroscopy, and infrared spectroscopy, s

83 urier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and ion-exchange measurement

84 on, by IR and Raman spectroscopy, XRD, X-ray photoelectron spectroscopy, and Mossbauer spectroscopy c

85 X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and nitrogen adsorption-deso

86 O-poor environment, in agreement with X-ray photoelectron spectroscopy, and O-H bond formation of H

87 ectron microscopy and energy-dependent X-ray photoelectron spectroscopy, and prove the existence of v

88 heir intermediate phases of borophene; X-ray photoelectron spectroscopy, and scanning tunneling micro

89 ed reflection/absorption spectroscopy, X-ray photoelectron spectroscopy, and surface plasmon resonanc

90 uded size, surface charge, morphology, X-ray photoelectron spectroscopy, and transmission Fourier tra

91 nance spectroscopy, mass spectrometry, X-ray photoelectron spectroscopy, and X-ray absorption spectro

92 scopic images before and after growth, x-ray photoelectron spectroscopy, and x-ray diffraction invest

93 n microscopy, ultra violet-visible and X-ray photoelectron spectroscopy, and Zeta-potential.

94 Using ambient-pressure X-ray photoelectron spectroscopy (AP-XPS), we studied the adso

95 IF) spectrometry, and ambient-pressure X-ray photoelectron spectroscopy (AP-XPS).

96 Ambient-pressure X-ray photoelectron spectroscopy (APXPS) and high-pressure sca

97 um mechanics (QM) and ambient-pressure X-ray photoelectron spectroscopy (APXPS) experiments.

98 Here, we show that ambient pressure X-ray photoelectron spectroscopy (APXPS) with a conventional X

99 s was performed using ambient pressure X-ray photoelectron spectroscopy (APXPS), Fourier transform in

100 vanced in situ electron microscopy and X-ray photoelectron spectroscopy are used to demonstrate that

101 (23)Na solid-state NMR, Mossbauer, and X-ray photoelectron spectroscopies, are employed as probes of

102 Angle-resolved photoelectron spectroscopy (ARPES) is used to study thes

103 icrographs, x-ray diffraction spectra, x-ray photoelectron spectroscopy, as well as TFT output and tr

104 al organic films was analyzed by ultraviolet photoelectron spectroscopy at room temperature.

105 immobilization, which was confirmed by X-ray Photoelectron Spectroscopy, Atomic Force Microscopy and

106 ound molecules through high-resolution X-ray photoelectron spectroscopy, atomic force microscopy, and

107 Photoelectron spectroscopy confirms that Ag acts as a p-

108 ay diffraction, magnetic measurements, X-ray photoelectron spectroscopy, cyclic voltammetry, and dens

109 Temperature-programmed desorption and X-ray photoelectron spectroscopy data provide information abou

110 We employed microwave conductivity, X-ray photoelectron spectroscopy, diffuse reflectance spectros

111 eparation was directly proved by ultraviolet photoelectron spectroscopy, electrochemical impedance sp

112 mbining inelastic tunneling spectroscopy, UV photoelectron spectroscopy, electronic structure calcula

113 X-ray photoelectron spectroscopy, EPR, and magnetometry suppor

114 UV-Vis, far-IR, and X-ray photoelectron spectroscopies evidence the reduction of H

115 xposed samples were investigated using X-ray photoelectron spectroscopy, Fourier transform infrared s

116 r at surfaces and interfaces, angle-resolved photoelectron spectroscopy has become a core technique i

117 Negative-ion photoelectron spectroscopy has shown the adiabatic detac

118 m interface, performed using liquid microjet photoelectron spectroscopy, has been interpreted to sugg

119 he trade include near-ambient-pressure X-ray photoelectron spectroscopy, high-pressure scanning tunne

120 ully studied by X-ray crystallography, X-ray photoelectron spectroscopy, hydrogen evolution experimen

121 reduced and characterized by Raman and X-ray photoelectron spectroscopies in addition to microscopies

122 y forming the Mo Se bond, confirmed by X-ray photoelectron spectroscopy, in which the formed MoSe(2)

123 Experiments using ambient pressure X-ray photoelectron spectroscopy indicate that methane dissoci

124 X-ray photoelectron spectroscopy indicated that the predominan

125 d by transmission electron microscopy, X-ray photoelectron spectroscopy, infrared spectra, ultraviole

126 Using ambient pressure X-ray photoelectron spectroscopy interpreted with quantum mech

127 X-ray photoelectron spectroscopy invariably detected elemental

128 s of the foam were characterized using X-ray photoelectron spectroscopy, inverse gas chromatography,

129 Recent angle-resolved photoelectron spectroscopy investigations provided insig

130 Combined with in situ ambient-pressure X-ray photoelectron spectroscopy, IR, and Raman spectroscopic

131 Hard-x-ray photoelectron spectroscopy is a valuable source of infor

132 Finally, X-ray photoelectron spectroscopy is used to characterize the P

133 Here we report liquid jet X-ray photoelectron spectroscopy measurements that provide dir

134 A combination of near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and CO temperature-

135 Using near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) we show that a time

136 ctroscopy and by near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS).

137 lectrochemistry, synchrotron radiation-X-ray photoelectron spectroscopy, near edge X-ray absorption f

138 (-) anions were investigated by negative ion photoelectron spectroscopy (NIPES) along with high-resol

139 nvestigated in the gas phase by negative-ion photoelectron spectroscopy (NIPES), velocity-map imaging

140 in the AuNP suspensions, as judged by X-ray photoelectron spectroscopy, nuclear magnetic resonance e

141 X-ray photoelectron spectroscopy of C 1s and Br 3d core levels

142 Photoelectron spectroscopy of microjets expanded into va

143 quantum state specificity by high-resolution photoelectron spectroscopy of the vinylidene anions H2CC

144 X-ray photoelectron spectroscopy of these electrochemically tr

145 In situ, depth-resolved X-ray photoelectron spectroscopy of various graphene-coated tr

146 Raman and X-ray photoelectron spectroscopy on BN films show no significa

147 by means of operando ambient-pressure X-ray photoelectron spectroscopy performed at the solid/liquid

148 ro charge by means of ambient pressure X-ray photoelectron spectroscopy performed under polarization

149 troscopy, scanning tunneling microscopy, and photoelectron spectroscopy provide unique information ab

150 X-ray photoelectron spectroscopy, Raman microscopy and spectro

151 X-ray photoelectron spectroscopy, Raman spectroscopy, together

152 DFT calculations, X-ray photoelectron spectroscopy, Raman, and FTIR show that th

153 X-ray photoelectron spectroscopy recommends the chemical inter

154 The X-ray photoelectron spectroscopy results indicated that Fe(0)

155 Moreover, the X-ray photoelectron spectroscopy results show that the valence

156 g and predominated the powder surface (X-ray photoelectron spectroscopy results) in both camel and bo

157 ay absorption spectroscopy and ex situ X-ray photoelectron spectroscopy reveal that PbO(2) is unpertu

158 nctional theory calculations and ultraviolet photoelectron spectroscopy reveal that the effective wor

159 oscopy together with ex situ Raman and X-ray photoelectron spectroscopy reveal the reversibility of m

160 X-ray photoelectron spectroscopy revealed significant core-lev

161 X-ray photoelectron spectroscopy revealed that an effective mo

162 X-ray photoelectron spectroscopy revealed that the hydroxyl gr

163 Angle-resolved photoelectron spectroscopy reveals a quasi-1D valence ba

164 X-ray photoelectron spectroscopy reveals that, at pH </= 3.5,

165 upled with atomic force microscopy and X-ray photoelectron spectroscopy reveals the architectures to

166 In situ ambient pressure X-ray photoelectron spectroscopy reveals up to a fourfold enha

167 formation of the SAM was confirmed by X-ray photoelectron spectroscopy, scanning electron microscopy

168 urier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy

169 s formation are elucidated by means of X-Ray photoelectron spectroscopy, scanning transmission electr

170 samples on SiC(000) combining angle-resolved photoelectron spectroscopy, scanning tunneling microscop

171 yst during the reaction, quasi in situ X-ray photoelectron spectroscopy showed that the surface is me

172 Ambient-pressure x-ray photoelectron spectroscopy showed that water added to me

173 scopy (AFM), and synchrotron radiation-X-ray photoelectron spectroscopy (SR-XPS) were used to elucida

174 razing incidence x-ray diffraction and x-ray photoelectron spectroscopy studies indicating that the f

175 X-ray absorption spectroscopy and X-ray photoelectron spectroscopy studies of SNNO/LSMO heterost

176 aramagnetic resonance spectroscopy and X-ray photoelectron spectroscopy studies suggest that the chem

177 aramagnetic resonance spectroscopy and X-ray photoelectron spectroscopy studies suggested that the ch

178 UV-vis spectroscopy and X-ray photoelectron spectroscopy suggest that a substituent's

179 X-ray photoelectron spectroscopy suggests that NaCu(4)Se(4) is

180 mined using a novel approach combining X-ray photoelectron spectroscopy, surface tension measurements

181 Through X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(VI) su

182 trospray ionization mass spectrometry, X-ray photoelectron spectroscopy, thermogravimetric analysis a

183 rcame this limitation by applying soft x-ray photoelectron spectroscopy to characterize excess electr

184 nization aerosol mass spectrometry and X-ray photoelectron spectroscopy to confirm these predictions.

185 We employed ambient pressure X-ray photoelectron spectroscopy to investigate the electronic

186 d X-ray diffraction, and Mossbauer and X-ray photoelectron spectroscopy to investigate their morpholo

187 8H8I2) produces m-C8H8 in gas phase; we used photoelectron spectroscopy to probe the first two electr

188 hanges in the physical properties of SAMs to photoelectron spectroscopy to unambiguously assign bindi

189 th temperature, temperature-programmed X-ray photoelectron spectroscopy (TP-XPS) experiments are perf

190 Scanning electron microscopy, X-ray photoelectron spectroscopy, transmission electron micros

191 e scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy, transmission infrared spectr

192 onal spectroscopy and ambient pressure X-ray photoelectron spectroscopy under catalytically relevant

193 mbient conditions and (ii) contactless X-ray photoelectron spectroscopy under ultrahigh vacuum.

194 evel offset (epsilon(h)(UPS)) by ultraviolet photoelectron spectroscopy (UPS) for CnT and CnDT SAMs a

195 asurements of epsilon(h)(UPS) by ultraviolet photoelectron spectroscopy (UPS) for OPT n and OPD n SAM

196 lectrical conductors and exhibit ultraviolet-photoelectron spectroscopy (UPS) signatures expected of

197 soft X-ray scattering (R-SoXS); ultraviolet photoelectron spectroscopy (UPS); Fourier transform-infr

198 X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, UV-vis absorption spectra, a

199 X-ray photoelectron spectroscopy was used to characterize the

200 properties with degree of functionalization, photoelectron spectroscopy was used to map the occupied

201 r the metallic glasses, measured using X-ray photoelectron spectroscopy, was higher by 0.2 eV to 0.4

202 ering beyond the dipole limit and hard X-ray photoelectron spectroscopy we establish the dual nature

203 circular dichroism, combined with hard X-ray photoelectron spectroscopy, we derived a complete pictur

204 Using femtosecond time-resolved two-photon photoelectron spectroscopy, we determine (i) the vertica

205 LTS reaction, as well as complementary X-ray photoelectron spectroscopy, we observed the activation a

206 using ambient-pressure X-ray absorption and photoelectron spectroscopy, we proved that the dominant

207 Applying angle-resolved photoelectron spectroscopy, we show that the silicon sur

208 croscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy were employed to characterize

209 transmission electron microscopy, and X-ray photoelectron spectroscopy were used to understand the n

210 A powerful approach is angle-resolved photoelectron spectroscopy, whereby the kinetic energy a

211 method and showed good agreement with X-ray photoelectron spectroscopy (which is surface sensitive).

212 layer on the surface, as determined by X-ray photoelectron spectroscopy, which likely prevented furth

213 Here we apply time-resolved photoelectron spectroscopy with a seeded extreme ultravi

214 Here we combine ambient pressure X-ray photoelectron spectroscopy with quantum mechanics to exa

215 In situ techniques (X-ray photoelectron spectroscopy, X-ray absorption spectroscop

216 mbination of powder X-ray diffraction, X-ray photoelectron spectroscopy, X-ray fluorescence spectrosc

217 ilms before and after the treatment by X-ray photoelectron spectroscopy (XPS) also evidencing the cor

218 y ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS) analyses indicated bind

219 X-ray photoelectron spectroscopy (XPS) analysis results showed

220 X-ray photoelectron spectroscopy (XPS) analysis revealed that

221 Report, Nakamura et al argue that our x-ray photoelectron spectroscopy (XPS) analysis was affected b

222 as a valuable tool when combined with X-ray photoelectron spectroscopy (XPS) analysis.

223 t X-ray absorption spectroscopy (XAS), X-ray photoelectron spectroscopy (XPS) and atomic multiplet cl

224 X-ray photoelectron spectroscopy (XPS) and attenuated total re

225 X-ray photoelectron spectroscopy (XPS) and electrochemical imp

226 isms are also investigated in terms of X-ray photoelectron spectroscopy (XPS) and electrochemical mea

227 s of CMP are proposed according to the X-ray photoelectron spectroscopy (XPS) and electrochemical mea

228 X-ray photoelectron spectroscopy (XPS) and electron microprobe

229 led plasma-mass spectrometry (ICP-MS), X-ray photoelectron spectroscopy (XPS) and Fourier-transform i

230 cterization of the prepared samples by X-ray photoelectron spectroscopy (XPS) and optimization of the

231 substrate electrode surfaces based on X-ray photoelectron spectroscopy (XPS) and synchrotron radiati

232 ystem performance is validated through X-ray photoelectron spectroscopy (XPS) and the spatial distrib

233 iosensor surfaces were optimized using X-ray photoelectron spectroscopy (XPS) and the ultra-high freq

234 ution interface, and observe with both X-ray photoelectron spectroscopy (XPS) and XUV-RA the existenc

235 scopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and zeta potential meas

236 entified by fitting of high-resolution X-ray photoelectron spectroscopy (XPS) C 1s and O 1s spectra.

237 nning electron microscopy (FE-SEM) and X-ray photoelectron spectroscopy (XPS) characterization result

238 X-ray photoelectron spectroscopy (XPS) characterized a transie

239 dded within the polymer matrix, whilst X-ray Photoelectron Spectroscopy (XPS) confirmed that they exi

240 Infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) confirmed the role of p

241 Nuclear magnetic resonance (NMR) and X-ray photoelectron spectroscopy (XPS) demonstrate formation o

242 Nuclear magnetic resonance (NMR) and X-ray photoelectron spectroscopy (XPS) demonstrate the covalen

243 during the biosensor construction and X-ray photoelectron spectroscopy (XPS) experiments confirmed c

244 ure published data obtained by in situ X-ray photoelectron spectroscopy (XPS) for the concentration o

245 studied for their HER activity and by X-ray photoelectron spectroscopy (XPS) for the first time; MoB

246 g Microscopy (STM) in combination with X-ray Photoelectron spectroscopy (XPS) has been utilized to ch

247 electron microscopy (PEEM) and imaging X-ray photoelectron spectroscopy (XPS) have over the years bee

248 X-ray photoelectron spectroscopy (XPS) is one of the most used

249 IPY-type fluorescence, photometry, and X-ray photoelectron spectroscopy (XPS) label allows estimation

250 X-ray photoelectron spectroscopy (XPS) measurements confirms n

251 asma-Mass Spectrometry (LA-ICP-MS) and X-ray photoelectron spectroscopy (XPS) measurements, which wer

252 sy carbon electrode (GCE), as shown by X-ray photoelectron spectroscopy (XPS) measurements.

253 ed here using a combination of SPR and X-ray photoelectron spectroscopy (XPS) measurements.

254 Ex situ X-ray photoelectron spectroscopy (XPS) of the 2-ABT modified e

255 Raman and X-Ray photoelectron spectroscopy (XPS) revealed that the synth

256 ) While surface characterization using X-ray photoelectron spectroscopy (XPS) showed the presence of

257 Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS) spectroscopy confirmed

258 cterizations by Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) support the presence of

259 study were to evaluate the ability of X-ray photoelectron spectroscopy (XPS) to differentiate rice m

260 troscopy, x-ray diffraction (XRD), and x-ray photoelectron spectroscopy (XPS) were employed for ligni

261 Zeta potential measurements and X-ray photoelectron spectroscopy (XPS) were used to analyse th

262 ray absorption spectroscopy (XAS), and X-ray photoelectron spectroscopy (XPS) were used to determine

263 y-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and (10)B and (11)B so

264 ransmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS), and Nanoparticle Size

265 -ray spectroscopy (EDS), quasi in situ X-ray photoelectron spectroscopy (XPS), and operando X-ray abs

266 sion electron microscopy (HAADF-STEM), X-ray photoelectron spectroscopy (XPS), and powder X-ray diffr

267 , X-ray absorption spectroscopy (XAS), X-ray photoelectron spectroscopy (XPS), and Raman microscopy.

268 ysis, UV-vis, energy-dispersive X-ray, X-ray photoelectron spectroscopy (XPS), attenuated total refle

269 Various techniques, such as X-ray photoelectron spectroscopy (XPS), confirmed the occurren

270 spectroscopy, photoluminescence (PL), x-ray photoelectron spectroscopy (XPS), Fourier transform infr

271 ombination of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), in-field Mossbauer spe

272 Fluorescence detection, X-ray photoelectron spectroscopy (XPS), infrared spectra (FT-I

273 es have been determined by synchrotron X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorp

274 ional theory (DFT), ion chromatograph, X-ray photoelectron spectroscopy (XPS), particle size analysis

275 d triclosan in batch experiments using X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, an

276 ochemical exposure in combination with X-ray photoelectron spectroscopy (XPS), scanning electron micr

277 odified surfaces were characterized by X-ray photoelectron spectroscopy (XPS), scanning electron micr

278 riate MOFs (MTV-MOFs) were examined by X-ray photoelectron spectroscopy (XPS), ultraviolet-visible di

279 opy, X-ray diffraction analysis (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis-NIR spectroscop

280 ure characterization methods including X-ray photoelectron spectroscopy (XPS), V and S X-ray absorpti

281 erometry, cyclic voltammetry (CV), and X-ray photoelectron spectroscopy (XPS), we demonstrate that hi

282 ransmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD

283 ng was observed based on quasi in situ X-ray photoelectron spectroscopy (XPS).

284 ed by UV, circular dichroism (CD), and X-ray photoelectron spectroscopy (XPS).

285 ng electron microscopy (SEM) and Fe 2p X-ray photoelectron spectroscopy (XPS).

286 er (VSM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS).

287 ), surface plasmon resonance (SPR) and X-ray photoelectron spectroscopy (XPS).

288 mission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS).

289 iO2 powder using near-ambient-pressure X-ray photoelectron spectroscopy (XPS).

290 smission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS).

291 mly modified columns were assessed via X-ray photoelectron spectroscopy (XPS).

292 aracterized by electrochemistry and by X-ray photoelectron spectroscopy (XPS).

293 -ray absorption spectroscopy (XAS) and X-ray photoelectron spectroscopy (XPS).

294 neling microscopy and spectroscopy and X-ray photoelectron spectroscopy (XPS).

295 flection X-ray fluorescence (TXRF) and X-ray photoelectron spectroscopy (XPS).

296 n and Brunauer Emmett-Teller (BET) and X-ray Photoelectron Spectroscopy (XPS).

297 sform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS).

298 ), powder X-ray diffraction (PXRD) and X-ray photoelectron spectroscopy (XPS).

299 ochemical mass spectrometry (OEMS) and X-ray photoelectron spectroscopy (XPS).

300 hment on the compacts was confirmed by X-ray photoelectron spectroscopy (XPS).