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1 uced membrane fluidity (measured by infrared ellipsometry).
2 s environments by employing in situ infrared ellipsometry.
3 c force microscopy, UV-vis spectroscopy, and ellipsometry.
4 ion, as well as Raman, IR, and spectroscopic ellipsometry.
5 osphatidylserine monolayers was estimated by ellipsometry.
6 dielectric function (<epsiloni>) obtained in ellipsometry.
7 properties are evaluated with spectroscopic ellipsometry.
8 er transform spectroscopy, and spectroscopic ellipsometry.
9 nied change in bilayer thickness detected by ellipsometry.
10 immunoreactions in total internal reflection ellipsometry.
11 ymers, as confirmed by FTIR spectroscopy and ellipsometry.
12 ntal data from microslit electrokinetics and ellipsometry.
13 total reflection infrared spectroscopy, and ellipsometry.
14 plasmon resonance (SPR) imaging and imaging ellipsometry.
15 electrochemical impedance spectroscopy, and ellipsometry.
16 lled carbon nanotubes (CNT) by spectroscopic ellipsometry.
17 is differentiable from the background using ellipsometry.
18 om IR absorbance values are substantiated by ellipsometry.
19 events on the grating were also confirmed by ellipsometry.
20 olipid bilayers using neutron reflection and ellipsometry.
21 n microscopy, epifluorescence microscopy and ellipsometry.
22 sonance energy through in situ spectroscopic ellipsometry allowed the nanoparticles to be easily cont
24 ness was evaluated by using a combination of ellipsometry and AFM height profiling, accompanied by se
27 iodooctane directly after spin-coating using ellipsometry and ion beam analysis, while using small an
29 (GSH), has been developed by combination of ellipsometry and Kretschmann surface plasmon resonance (
32 of the multilayer structure was verified by ellipsometry and sensor function characterized electroch
34 on these surfaces was characterized by using ellipsometry and the orientational behavior of liquid cr
36 Reflection-absorption infrared spectroscopy, ellipsometry and X-ray photoelectron spectroscopy were u
37 the optical layer thickness (determined with ellipsometry) and the acoustic layer thickness (determin
39 c voltammetry, scanning electron microscopy, ellipsometry, and atomic force microscopy were used to c
40 using atomic force microscopy, spectroscopic ellipsometry, and reflection-absorption infrared spectro
42 ansform infrared spectroscopy, spectroscopic ellipsometry, and X-ray photoemission spectroscopy shows
45 h modification step was monitored by imaging ellipsometry as the thickness increased with each modifi
46 ilized SAv is quantified using spectroscopic ellipsometry by monitoring binding of biotinylated probe
47 ere characterized by ultraviolet absorption, ellipsometry, circular dichroism, and polarized Fourier
48 py, X-ray and UV photoelectron spectroscopy, ellipsometry, contact angle goniometry, differential pul
50 s characterized using infrared spectroscopy, ellipsometry, contact angle measurements, and atomic for
51 n spectroscopy, quartz crystal microbalance, ellipsometry, contact angle measurements, atomic force m
52 of the OTMS SAMs and characterization using ellipsometry, contact angle, atomic force microscopy (AF
54 ped a unique technique, wet-surface enhanced ellipsometry contrast (Wet-SEEC), which magnifies the co
55 urface characterization techniques including ellipsometry, cyclic voltammetry (CV), and X-ray photoel
56 data linearly correlated with spectroscopic ellipsometry data on the same samples with a scatter of
59 ncluding: UV-vis spectroscopy, spectroscopic ellipsometry, electrochemistry, synchrotron X-ray reflec
60 GSL and antibody films were confirmed using ellipsometry, Fourier transform infrared spectroscopy (F
61 nd dry polymer brushes were analyzed by AFM, ellipsometry, FT-IRRAS, and surface plasmon resonance (S
62 s carried out by sessile drop contact angle, ellipsometry, grazing angle FT-IR spectroscopy, and elec
63 ntages make the technique of optical imaging ellipsometry (IE) highly suitable for quantitative chara
64 plasmon resonance imaging (SPRI) and imaging ellipsometry (IE) measurements are realized with a singl
65 ntial grafting of initiator and polymer, and ellipsometry indicated the formation of polymer coatings
66 ained by atomic force microscopy and imaging ellipsometry indicating continuous transport and deposit
67 for the validation of the porosity results, ellipsometry, interference fringes method (IFM), and foc
68 crystal microbalance (QCM) measurements and ellipsometry measurements have been performed simultaneo
69 during electrodeposition with spectroscopic ellipsometry measurements in order to ensure accurate in
70 quartz crystal microbalance-dissipation and ellipsometry measurements in order to investigate how a
71 troscopy, Raman microscopy and spectroscopic ellipsometry measurements on hBN confirm the formation o
78 nabled simultaneous nonlinear optical Stokes ellipsometry (NOSE) and polarized laser transmittance im
79 The application of nonlinear optical Stokes ellipsometry (NOSE) coupled with principal component ana
80 e absolute thicknesses determined by XPS and ellipsometry on dried films and quartz crystal microbala
81 eatures were characterized by contact angle, ellipsometry, optical, and atomic force microscopies.
82 ron and X-ray reflectivity and spectroscopic ellipsometry over a wide range of relative humidity (RH)
84 was confirmed by corroborating evidence from ellipsometry, reflectance FTIR, XPS, cyclic voltammetry,
85 udied by contact angle measurements, optical ellipsometry, reflection absorption infrared spectroscop
86 ay photoelectron spectroscopy, spectroscopic ellipsometry, reflection-absorption infrared spectroscop
88 lectrochemical impedance spectroscopy (EIS), ellipsometry, scanning electron microscopy (SEM), atomic
89 toelectron spectroscopy (XPS), spectroscopic ellipsometry (SE), and high-resolution electron energy l
90 lipsometric parameter, Psi, of spectroscopic ellipsometry (SE), for the rapid, simultaneous identific
91 ) as well as physFN ones using spectroscopic ellipsometry (SE), Fourier transform infrared spectrosco
92 Infrared spectroscopy (IRS), spectroscopic ellipsometry (SE), water contact angle (CA), and X-ray p
94 teristics with applications in spectroscopic ellipsometry, spectropolarimetry, communications, imagin
95 tion, for surface plasmon resonance enhanced ellipsometry (SPREE) studies and assess the reactive coa
102 with ice between 243 and 186 K by using (i) ellipsometry to monitor the ice surface and (ii) coated-
104 photoelectron spectroscopy and spectroscopic ellipsometry to show that the metallic phase produced by
105 situ combination of QCM-D with spectroscopic ellipsometry unambiguously demonstrates that the conform
106 wavelength dispersion measured by reflection ellipsometry (using a Teng-Man apparatus) and attenuated
107 ce microscopy, scanning electron microscopy, ellipsometry, UV, and laser desorption ionization MS (LD
112 anning electron microscopy and spectroscopic ellipsometry were used to characterize the surface morph
113 Kerr spectroscopies along with spectroscopic ellipsometry were used to deduce the complete permittivi
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