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

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

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

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

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

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

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

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

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

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

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

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

12 ce, which was probed by angle-resolved X-ray photoelectron spectroscopy.

13 OCCO) was observed and investigated by anion photoelectron spectroscopy.

14 y transmission electron microscopy and X-ray photoelectron spectroscopy.

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

16 s-pyridinyltetrazine, as determined by X-ray photoelectron spectroscopy.

17 spectroscopy, fluorescence imaging and X-ray photoelectron spectroscopy.

18 clic voltammetry as well as UV/Vis and X-ray photoelectron spectroscopy.

19 bamates, with Cu(+) ions elucidated by X-ray photoelectron spectroscopy.

20 was probed in situ by ambient-pressure X-ray photoelectron spectroscopy.

21 lus energy dispersive spectroscopy and X-ray photoelectron spectroscopy.

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

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

24 have been investigated by using negative ion photoelectron spectroscopy.

25 elative to more traditional methods based on photoelectron spectroscopy.

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

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

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

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

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

31 According to X-ray photoelectron spectroscopy analysis, the Pd clusters exh

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

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

34 Both x-ray photoelectron spectroscopy and (1)H NMR data confirmed t

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

36 Using time-resolved photoelectron spectroscopy and ab initio calculations, w

37 ike structures of CoB16(-), characterized by photoelectron spectroscopy and ab initio calculations.

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

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

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

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

42 a measurements in DMSO and H2O, negative ion photoelectron spectroscopy and binding constant determin

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

44 X-ray photoelectron spectroscopy and electrochemistry confirm

45 X-ray photoelectron spectroscopy and electrochemistry confirm

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

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

48 High-resolution X-ray photoelectron spectroscopy and in-field (57)Fe Mossbauer

49 PhOH, and Me2NOH or Et2NOH) are examined by photoelectron spectroscopy and M06-2X and CCSD(T) comput

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

51 We have used X-ray photoelectron spectroscopy and polarization-resolved O K

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

53 Here, we use photoelectron spectroscopy and quantum chemistry calcula

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

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

56 X-ray photoelectron spectroscopy and Raman spectroscopy show t

57 X-ray photoelectron spectroscopy and scanning electron microsc

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

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

60 tal dichalcogenides by using microbeam X-ray photoelectron spectroscopy and scanning tunnelling micro

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

62 atite) that combining ambient-pressure X-ray photoelectron spectroscopy and standing-wave photoemissi

63 n bonding in gold(I)-alkynyl complexes using photoelectron spectroscopy and theoretical calculations.

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

65 chiral boron cluster of [B30](-) in a joint photoelectron spectroscopy and theoretical study.

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

67 We applied cryogenic X-ray Photoelectron Spectroscopy and wet chemical analysis to

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

69 orption mechanisms were assessed using X-ray photoelectron spectroscopy and X-ray absorption spectros

70 sing in situ, time- and depth-resolved X-ray photoelectron spectroscopy, and complementary grand cano

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

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

73 IR reflection absorption spectroscopy, X-ray photoelectron spectroscopy, and electrochemical impedanc

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

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

76 and acetonitrile electrolytes, UV and X-ray photoelectron spectroscopy, and Kelvin force microscopy

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

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

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

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

81 ron X-ray reflectivity, angle-resolved X-ray photoelectron spectroscopy, and spectroelectrochemistry.

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

83 ransform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy, and time-of-flight secondary

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

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

86 report electrochemical, in situ electrical, photoelectron spectroscopy, and X-ray diffraction measur

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

88 In situ atmospheric-pressure X-ray photoelectron spectroscopy (AP-XPS) experiments demonstr

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

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

91 Through the use of ambient pressure X-ray photoelectron spectroscopy (APXPS) and a single-sided so

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

93 tructure (NEXAFS) and ambient-pressure X-ray photoelectron spectroscopy (APXPS) under catalytically r

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

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

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

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

98 g the PbS(111) facets, consistent with x-ray photoelectron spectroscopy as well as other spectroscopi

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

100 From near-ambient pressure X-ray photoelectron spectroscopy at 0.9 mbar CO2, the amount o

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

102 Liquid-jet photoelectron spectroscopy can be used to directly study

103 ear-edge X-ray absorption fine structure and photoelectron spectroscopy complemented by theoretical m

104 Photoelectron spectroscopy confirms that Ag acts as a p-

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

106 er transform infrared spectroscopy and X-ray photoelectron spectroscopy data reveal that carboxylic a

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

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

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

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

111 X-ray diffraction and X-ray photoelectron spectroscopy experiments were used to exam

112 y coupled plasma mass spectrometry and X-ray photoelectron spectroscopy for quantitative analysis of

113 Negative-ion photoelectron spectroscopy has shown the adiabatic detac

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

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

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

117 X-ray photoelectron spectroscopy indicated that the predominan

118 Cyclic voltammetry and angle resolved X-ray photoelectron spectroscopy indicated that the SAMs deriv

119 altered N-CNT surface chemistry, with X-ray photoelectron spectroscopy indicating addition of Cl, lo

120 ed by low-energy electron diffraction, X-ray photoelectron spectroscopy, infrared reflection-absorpti

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

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

123 X-ray photoelectron spectroscopy invariably detected elemental

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

125 Recent angle-resolved photoelectron spectroscopy investigations provided insig

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

127 Time-resolved photoelectron spectroscopy is performed on thymine and t

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

129 Photoelectron spectroscopy measurements confirmed that t

130 X-ray photoelectron spectroscopy measurements demonstrate the

131 Here we report angle-resolved photoelectron spectroscopy measurements of the supercond

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

133 Near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) is a promising meth

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

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

136 (57)Fe Mossbauer spectroscopy, X-ray photoelectron spectroscopy, neutron activation analysis,

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

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

139 Photoelectron spectroscopy of B36(-) reveals a relativel

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

141 X-ray photoelectron spectroscopy of Cu 2p3/2 and Os 4f signals

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

143 X-ray photoelectron spectroscopy of these electrochemically tr

144 ared spectroscopy, and high resolution X-ray photoelectron spectroscopy of TPI-carbons to elucidate t

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

146 Here we report the observation, by photoelectron spectroscopy, of an all-boron fullerene-li

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 Anion photoelectron spectroscopy (PES) and electron energy-los

150 X-ray photoelectron spectroscopy, Raman microscopy and spectro

151 X-ray photoelectron spectroscopy, Raman spectroscopy, together

152 The SAMs were characterized using X-ray photoelectron spectroscopy, reflection-absorption infrar

153 C16)2DDP SAMs were characterized using X-ray photoelectron spectroscopy, reflection-absorption infrar

154 d binding energy shifts as observed by X-ray photoelectron spectroscopy, respectively.

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

156 X-ray photoelectron spectroscopy results show ferrate resultan

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

158 X-ray photoelectron spectroscopy revealed significant core-lev

159 X-ray photoelectron spectroscopy revealed that an effective mo

160 X-ray photoelectron spectroscopy revealed that the hydroxyl gr

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

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

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

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

165 in detail by X-ray powder diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy

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

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

168 X-ray diffraction and ambient-pressure X-ray photoelectron spectroscopy showed that the crystal struc

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

170 X-ray spectroscopy (SXS) techniques such as photoelectron spectroscopy, soft X-ray absorption spectr

171 utherford backscattering spectrometry, X-ray photoelectron spectroscopy, spectroscopic ellipsometry,

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

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

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

175 UV photoelectron spectroscopy studies were performed with t

176 ve characterization techniques such as X-ray photoelectron spectroscopy suffer from sensitivity and q

177 hy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy suggest that reduction of 1 a

178 and surface oxygen concentrations from X-ray photoelectron spectroscopy suggests that surface sites g

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

180 troscopy, X-ray emission spectroscopy, X-ray photoelectron spectroscopy, synchrotron radiation circul

181 trochemical impedance spectroscopy and X-ray photoelectron spectroscopy techniques.

182 trochemical impedance spectroscopy and X-ray photoelectron spectroscopy techniques.

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

184 cause of a P-based coating detected by X-ray photoelectron spectroscopy, the zeta potential of the fo

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

186 ation of the new phase is presented by X-ray photoelectron spectroscopy, thermogravimetry, zeta poten

187 tammetry, UV-vis absorption, and ultraviolet photoelectron spectroscopy to characterize hole energy l

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

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

190 8H8I2) produces m-C8H8 in gas phase; we used photoelectron spectroscopy to probe the first two electr

191 We use gas-phase negative ion photoelectron spectroscopy to study the quasilinear carb

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

193 ngle measurements, X-ray reflectivity, X-ray photoelectron spectroscopy, ultraviolet photoelectron sp

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

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

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

197 -ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy (UPS), cyclic voltammetry, an

198 o BN isosteres of indole using a combined UV-photoelectron spectroscopy (UV-PES)/computational chemis

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

200 Ultraviolet photoelectron spectroscopy was employed to determine the

201 X-ray photoelectron spectroscopy was used to analyze sorbent s

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

203 X-ray photoelectron spectroscopy was utilized to determine the

204 Chemical derivatization coupled to X-ray photoelectron spectroscopy was utilized to quantify spec

205 By using infrared spectroscopy and X-ray photoelectron spectroscopy we demonstrate that airborne

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

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

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

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

210 nsient absorption spectroscopy and gas-phase photoelectron spectroscopy, we show that hexane, a commo

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

212 nfrared spectroscopy, ellipsometry and X-ray photoelectron spectroscopy were used to follow the stepw

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

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

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 Infrared (IR) and X-ray photoelectron spectroscopy (XPS) analyses indicate citra

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

220 The electrochemical and X-ray photoelectron spectroscopy (XPS) analyses of the reduced

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

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

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

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

225 py, atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS) and compared with a pro

226 nt and aggregate size, as confirmed by X-ray photoelectron spectroscopy (XPS) and dynamic light scatt

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

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

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

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

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

232 nd adsorption spectroscopy techniques [X-ray photoelectron spectroscopy (XPS) and near edge X-ray ads

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

234 The results of X-ray photoelectron spectroscopy (XPS) and reflection-absorpti

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

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

237 X-ray photoelectron spectroscopy (XPS) and valence band studie

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

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

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

241 X-ray photoelectron spectroscopy (XPS) confirmed the formation

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

243 We use X-ray photoelectron spectroscopy (XPS) for characterization of

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 and fibronectin (FN) were measured by X-ray photoelectron spectroscopy (XPS) in ultrahigh vacuum at

247 Our X-ray photoelectron spectroscopy (XPS) investigation revealed

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

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

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

251 orm infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS) showed that the nanowir

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

253 X-ray photoelectron spectroscopy (XPS) studies confirm that at

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

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

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

257 m infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) were used to characteri

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

259 Comparing elemental depth-profiling by X-ray photoelectron spectroscopy (XPS) with detailed modeling

260 Experimental methods (TOF-SIMS, X-ray photoelectron spectroscopy (XPS)) were used in combinati

261 ction absorption spectroscopy (IRRAS), X-ray photoelectron spectroscopy (XPS), and contact angles of

262 opy-energy dispersive X-ray (SEM-EDX), X-ray photoelectron spectroscopy (XPS), and Fourier transform

263 IAXRD), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and scanning transmiss

264 ectron microscopy (TEM), Raman spectroscopy, photoelectron spectroscopy (XPS), and SQUID magnetometry

265 ansform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and x-ray diffraction

266 by the MIP cavities was monitored with X-ray photoelectron spectroscopy (XPS), as manifested by a neg

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

268 new nanoparticle was characterized by X-ray photoelectron spectroscopy (XPS), dynamic light scatteri

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

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

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

272 ransmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Re K-edge X-ray absorp

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

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

275 ansform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), thermogravimetric anal

276 irrors and AgNPs was confirmed through X-ray photoelectron spectroscopy (XPS), transmission electron

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

278 ransmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflect

279 copolymer layer were characterized by X-ray photoelectron spectroscopy (XPS), water contact angle, e

280 dispersive spectroscopy (SEM-EDS) and X-ray photoelectron spectroscopy (XPS), whereas the precise qu

281 the sensor surface was monitored using X-ray photoelectron spectroscopy (XPS), while the binding of c

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

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

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

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

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

287 ction (GA-ATR) FT-IR spectroscopy, and X-ray photoelectron spectroscopy (XPS).

288 in the presence of liquids by means of X-ray photoelectron spectroscopy (XPS).

289 ation (LDI) mass spectrometry (MS) and X-ray photoelectron spectroscopy (XPS).

290 erlayer is independently determined by X-ray photoelectron spectroscopy (XPS).

291 Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS).

292 , secondary ion mass spectrometry, and X-ray photoelectron spectroscopy (XPS).

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

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

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

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

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

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

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

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