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1 uced membrane fluidity (measured by infrared ellipsometry).
2 were evaluated by total internal reflection ellipsometry.
3 olipid bilayers using neutron reflection and ellipsometry.
4 n microscopy, epifluorescence microscopy and ellipsometry.
5 (2) as determined via infrared spectroscopic ellipsometry.
6 c force microscopy, UV-vis spectroscopy, and ellipsometry.
7 ion, as well as Raman, IR, and spectroscopic ellipsometry.
8 s environments by employing in situ infrared ellipsometry.
9 elength range 190-850 nm using spectroscopic ellipsometry.
10 ymers, as confirmed by FTIR spectroscopy and ellipsometry.
11 ures up to 800 degrees C using spectroscopic ellipsometry.
12 osphatidylserine monolayers was estimated by ellipsometry.
13 dielectric function (<epsiloni>) obtained in ellipsometry.
14 properties are evaluated with spectroscopic ellipsometry.
15 er transform spectroscopy, and spectroscopic ellipsometry.
16 nied change in bilayer thickness detected by ellipsometry.
17 immunoreactions in total internal reflection ellipsometry.
18 ntal data from microslit electrokinetics and ellipsometry.
19 total reflection infrared spectroscopy, and ellipsometry.
20 plasmon resonance (SPR) imaging and imaging ellipsometry.
21 electrochemical impedance spectroscopy, and ellipsometry.
22 lled carbon nanotubes (CNT) by spectroscopic ellipsometry.
23 is differentiable from the background using ellipsometry.
24 om IR absorbance values are substantiated by ellipsometry.
25 events on the grating were also confirmed by ellipsometry.
27 sonance energy through in situ spectroscopic ellipsometry allowed the nanoparticles to be easily cont
28 le Mass spectrometry (QMS) and spectroscopic ellipsometry analyses to evaluate the residence time of
30 ness was evaluated by using a combination of ellipsometry and AFM height profiling, accompanied by se
33 iodooctane directly after spin-coating using ellipsometry and ion beam analysis, while using small an
35 (GSH), has been developed by combination of ellipsometry and Kretschmann surface plasmon resonance (
39 angle measurements, atomic force microscopy, ellipsometry and scanning electron microscopy were used
40 of the multilayer structure was verified by ellipsometry and sensor function characterized electroch
42 on these surfaces was characterized by using ellipsometry and the orientational behavior of liquid cr
43 knesses of the membranes were measured using ellipsometry and were in good agreement with the values
45 Reflection-absorption infrared spectroscopy, ellipsometry and X-ray photoelectron spectroscopy were u
46 the optical layer thickness (determined with ellipsometry) and the acoustic layer thickness (determin
48 c voltammetry, scanning electron microscopy, ellipsometry, and atomic force microscopy were used to c
49 using atomic force microscopy, spectroscopic ellipsometry, and reflection-absorption infrared spectro
50 cular dichroism spectroscopy, Mueller matrix ellipsometry, and simulation using theoretical scatterin
52 ansform infrared spectroscopy, spectroscopic ellipsometry, and X-ray photoemission spectroscopy shows
56 h modification step was monitored by imaging ellipsometry as the thickness increased with each modifi
58 ilized SAv is quantified using spectroscopic ellipsometry by monitoring binding of biotinylated probe
59 ere characterized by ultraviolet absorption, ellipsometry, circular dichroism, and polarized Fourier
60 py, X-ray and UV photoelectron spectroscopy, ellipsometry, contact angle goniometry, differential pul
62 s characterized using infrared spectroscopy, ellipsometry, contact angle measurements, and atomic for
63 n spectroscopy, quartz crystal microbalance, ellipsometry, contact angle measurements, atomic force m
64 of the OTMS SAMs and characterization using ellipsometry, contact angle, atomic force microscopy (AF
66 ped a unique technique, wet-surface enhanced ellipsometry contrast (Wet-SEEC), which magnifies the co
67 urface characterization techniques including ellipsometry, cyclic voltammetry (CV), and X-ray photoel
68 model for analysis of in-situ spectroscopic ellipsometry data in the photon energy range of 0.7-3.4
69 sufficient to explain in-situ spectroscopic ellipsometry data measured within and across multiple cy
70 data linearly correlated with spectroscopic ellipsometry data on the same samples with a scatter of
71 The use of the limited Lifshitz theory and ellipsometry data would seem to provide a suitable best
74 ncluding: UV-vis spectroscopy, spectroscopic ellipsometry, electrochemistry, synchrotron X-ray reflec
75 uartz Crystal Microbalance with Dissipation, Ellipsometry, Force Spectroscopy and Neutron Reflectomet
76 GSL and antibody films were confirmed using ellipsometry, Fourier transform infrared spectroscopy (F
77 (XPS), electron microprobe microscopy (EMP), ellipsometry, Fourier transform infrared spectroscopy (F
78 nd dry polymer brushes were analyzed by AFM, ellipsometry, FT-IRRAS, and surface plasmon resonance (S
79 s carried out by sessile drop contact angle, ellipsometry, grazing angle FT-IR spectroscopy, and elec
80 ntages make the technique of optical imaging ellipsometry (IE) highly suitable for quantitative chara
81 plasmon resonance imaging (SPRI) and imaging ellipsometry (IE) measurements are realized with a singl
82 bly, both X-ray scattering and spectroscopic ellipsometry indicate that the substrate exerts a neglig
83 ntial grafting of initiator and polymer, and ellipsometry indicated the formation of polymer coatings
84 ained by atomic force microscopy and imaging ellipsometry indicating continuous transport and deposit
85 for the validation of the porosity results, ellipsometry, interference fringes method (IFM), and foc
87 crystal microbalance (QCM) measurements and ellipsometry measurements have been performed simultaneo
88 during electrodeposition with spectroscopic ellipsometry measurements in order to ensure accurate in
89 quartz crystal microbalance-dissipation and ellipsometry measurements in order to investigate how a
91 troscopy, Raman microscopy and spectroscopic ellipsometry measurements on hBN confirm the formation o
92 rrent-voltage and simultaneous spectroscopic ellipsometry measurements on structures of the kind Al/M
99 nabled simultaneous nonlinear optical Stokes ellipsometry (NOSE) and polarized laser transmittance im
100 The application of nonlinear optical Stokes ellipsometry (NOSE) coupled with principal component ana
102 e absolute thicknesses determined by XPS and ellipsometry on dried films and quartz crystal microbala
103 eatures were characterized by contact angle, ellipsometry, optical, and atomic force microscopies.
104 ron and X-ray reflectivity and spectroscopic ellipsometry over a wide range of relative humidity (RH)
106 In this work, we demonstrate how operando ellipsometry provides detailed insights into charge stor
107 was confirmed by corroborating evidence from ellipsometry, reflectance FTIR, XPS, cyclic voltammetry,
108 udied by contact angle measurements, optical ellipsometry, reflection absorption infrared spectroscop
109 ay photoelectron spectroscopy, spectroscopic ellipsometry, reflection-absorption infrared spectroscop
112 lectrochemical impedance spectroscopy (EIS), ellipsometry, scanning electron microscopy (SEM), atomic
113 toelectron spectroscopy (XPS), spectroscopic ellipsometry (SE), and high-resolution electron energy l
114 lipsometric parameter, Psi, of spectroscopic ellipsometry (SE), for the rapid, simultaneous identific
115 ) as well as physFN ones using spectroscopic ellipsometry (SE), Fourier transform infrared spectrosco
116 Infrared spectroscopy (IRS), spectroscopic ellipsometry (SE), water contact angle (CA), and X-ray p
117 hin films are characterized by spectroscopic ellipsometry (SE), X-ray photoelectron spectroscopy, tra
118 results strongly indicate that PAS1-modified ellipsometry sensor can provide a high fidelity system f
120 teristics with applications in spectroscopic ellipsometry, spectropolarimetry, communications, imagin
121 tion, for surface plasmon resonance enhanced ellipsometry (SPREE) studies and assess the reactive coa
128 tron scattering rates measured with infrared ellipsometry to infrared ultrafast pump-probe measuremen
129 erot enhanced terahertz (THz) Mueller matrix ellipsometry to measure an electromagnon excitation in m
130 with ice between 243 and 186 K by using (i) ellipsometry to monitor the ice surface and (ii) coated-
131 tical conductivity measured by spectroscopic ellipsometry to prior predictions from dynamical mean-fi
133 photoelectron spectroscopy and spectroscopic ellipsometry to show that the metallic phase produced by
134 situ combination of QCM-D with spectroscopic ellipsometry unambiguously demonstrates that the conform
135 wavelength dispersion measured by reflection ellipsometry (using a Teng-Man apparatus) and attenuated
136 ce microscopy, scanning electron microscopy, ellipsometry, UV, and laser desorption ionization MS (LD
137 combination of variable angle spectroscopic ellipsometry (VASE), quartz crystal microbalance with di
144 anning electron microscopy and spectroscopic ellipsometry were used to characterize the surface morph
145 Kerr spectroscopies along with spectroscopic ellipsometry were used to deduce the complete permittivi
147 u pyroelectric calorimetry and spectroscopic ellipsometry were used to investigate surface reactions