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1                                              EELS analysis and iron mapping suggest controlled stoich
2                                              EELS, obtained at high spatial resolution, confirmed tha
3 d a large library of experimentally acquired EELS core edges.
4 materials phenomena during rapid acquisition EELS, trustworthy analysis of noisy spectra must be demo
5                                           An EELS spectral database is synthesized by using our forwa
6 ng transmission electron microscopy, EDX and EELS to discover how closely-packed Ti/Mn/Fe cations of
7  analytical spectroscopy techniques (EDX and EELS), we demonstrate that Fe in APC is present as iron
8 demonstrated by XRD, HRTEM, SAED, EFTEM, and EELS).
9                    Electrochemical, XRD, and EELS experiments demonstrate that this effect stems from
10                                       Atomic EELS element mappings reveal that the Ruddlesden-Popper
11                                     For both EELS and XAS, 2+, 3+, and 4+ reference spectra need to b
12 he oxidation state of Mn L2,3 edges for both EELS and XAS.
13  a sufficient variety of data including both EELS and XAS spectra.
14 es of the mean Mn valence can be acquired by EELS if proper care is taken.
15 rders of magnitude over that of conventional EELS methods.
16 cal structure was studied by PXRD, TEM, EDX, EELS, AFM, and solid-state NMR spectroscopy, revealing a
17 thin both elastic (HAADF) and inelastic (EDX/EELS) signals.
18 rce of the functionalization reaction, EFTEM EELS mapping shows a striking lack of spatial correlatio
19 automation of core-loss edge recognition for EELS spectra with high accuracy.
20 ization of in operando EELS Spectrum Images (EELS-SI).
21 l imaging mode, which is extremely useful in EELS and CL experiments.
22 s the need for complementary techniques like EELS when evaluating the magnetic and electronic propert
23 lysis and confirmed by electron energy loss (EELS) spectroscopy.
24  a three-dimensional solid and establishes M-EELS as a versatile technique sensitive to valence band
25 esolved electron energy-loss spectroscopy (M-EELS), we studied electronic collective modes in the tra
26   Furthermore, spatially selective nanoscale EELS spectroscopy provides additional evidence for chang
27 nally, the specific range of applications of EELS and CL with respect to other nano-optic techniques
28                               The results of EELS experiments do not provide evidence for an ultrarap
29 ve greatly improved the acquisition speed of EELS spectra.
30 , as well as the strengths and weaknesses of EELS as compared with CL.
31 sessment and characterization of in operando EELS Spectrum Images (EELS-SI).
32 +) was measured using time-resolved parallel EELS.
33              The development of the parallel EELS instrument and fast, sensitive detectors have great
34 jump ratio of the core-loss edges on the raw EELS spectra have been challenging for the automation of
35 ultrathin Li-ion cells, we acquire reference EELS spectra for the various constituents of the solid-e
36  make a link between optical cross-sections, EELS and CL probabilities, and the surface plasmons' phy
37 ed during electron energy loss spectroscopy (EELS) acquisition.
38 scopy and electron energy-loss spectroscopy (EELS) and are in agreement with theoretical calculations
39 he use of electron energy loss spectroscopy (EELS) and cathodoluminescence (CL) spectroscopy for surf
40 y in situ electron energy loss spectroscopy (EELS) and density functional theory (DFT) simulations.
41 vealed by electron energy loss spectroscopy (EELS) and diffuse reflectance infrared Fourier transform
42 pled with electron energy loss spectroscopy (EELS) and energy-filtered transmission electron microsco
43 estingly, electron energy loss spectroscopy (EELS) and soft X-ray absorption spectroscopy (sXAS) resu
44           Electron energy loss spectroscopy (EELS) and soft X-ray absorption spectroscopy (XAS) measu
45 les using electron energy loss spectroscopy (EELS) at the oxygen (O) K-edge with a spatial resolution
46   In situ Electron Energy Loss Spectroscopy (EELS) combined with Transmission Electron Microscopy (TE
47     While electron energy loss spectroscopy (EELS) data acquisition speeds with electron counting are
48 mtosecond electron energy loss spectroscopy (EELS) for mapping electronic structural changes in the c
49 les using electron energy-loss spectroscopy (EELS) in a scanning transmission electron microscope (ST
50 ging with electron energy loss spectroscopy (EELS) in scanning transmission electron microscopy (STEM
51 ge during electron energy-loss spectroscopy (EELS) in the transmission electron microscope have been
52 red using electron energy-loss spectroscopy (EELS) of individual carbon fibers and MWNTs as a charact
53 oupled to electron energy loss spectroscopy (EELS) points to the redox processing of Fe-bearing meteo
54 (PES) and electron energy-loss spectroscopy (EELS) probe different regions of the anionic potential e
55 AES), and electron energy loss spectroscopy (EELS) reveal a composition close to the nominal ones.
56           Electron energy loss spectroscopy (EELS) reveals the existence of water ice under cryogenic
57           Electron energy loss spectroscopy (EELS) showed that the smallest and largest samples were
58 ysis from electron energy loss spectroscopy (EELS) showed the stoichiometry of the nominal 15 nm NbO2
59 ed in the electron energy loss spectroscopy (EELS) spectra enable advanced material analysis includin
60           Electron energy loss spectroscopy (EELS) studies coupled with first-principles calculations
61 d in situ electron energy-loss spectroscopy (EELS) to identify an intermetallic example of a dominant
62 aphy, and electron energy loss spectroscopy (EELS) to investigate the B atom positions, properties, a
63 is study, electron energy loss spectroscopy (EELS) was used to evaluate a model encapsulated solution
64 (TEM) and electron energy-loss spectroscopy (EELS) were used to measure the atomic-level structure of
65  (HRTEM), electron energy loss spectroscopy (EELS), and X-ray absorption spectroscopy (XAS) in conjun
66 including electron energy loss spectroscopy (EELS), cathodoluminescence (CL), and electron energy gai
67 probe and electron energy loss spectroscopy (EELS), it is also discovered that the electronic conduct
68 (EDS) and electron energy loss spectroscopy (EELS), the distribution of the metals Mn and Fe was inve
69 copy with electron energy loss spectroscopy (EELS), we show organo-organic interfaces in contrast to
70 scopy and electron energy loss spectroscopy (EELS), we show that the graphene layer redshifts the ene
71 pping and electron energy loss spectroscopy (EELS).
72 TEM), and electron energy loss spectroscopy (EELS).
73 nning TEM electron energy-loss spectroscopy (EELS).
74 (TEM) and electron energy loss spectroscopy (EELS).
75 alytical STEM techniques, including 4D-STEM, EELS, and EDS.
76                                         STEM-EELS reveals mixed interfacial stoichiometry, subtle lat
77 electron energy loss spectroscopy (cryo-STEM-EELS).
78 enhances the efficiency and accuracy of STEM-EELS by autonomously identifying and targeting only area
79 d by electron energy loss spectroscopy (STEM-EELS) and hypothesized to be the mechanism for reduction
80  and electron energy loss spectroscopy (STEM-EELS), and density functional theory (DFT) is employed t
81 copy/electron energy loss spectroscopy (STEM/EELS).
82 S, quantitative NMR, operando NMR, cryo-TEM, EELS, and EDS.
83                 XRD, He-ion imaging, HR-TEM, EELS, PL, fluorescence lifetime imaging, Raman, FTIR, TG
84 TGA), transmission electron microscopy (TEM, EELS), and X-ray photoelectron spectroscopy (XPS).
85  with electron energy-loss spectroscopy (TEM-EELS).
86 scopy/electron energy loss spectroscopy (TEM/EELS) to investigate the evolution of transition metals
87                                          The EELS analysis of cross-sectional samples revealed the th
88                                          The EELS data show that Te doping introduced a high density
89  nanocarrots show a clear red shift, and the EELS maps show an asymmetric distribution of the resonan
90         This is confirmed by our vibrational EELS spectrum.
91 afast transient changes, now achievable with EELS and TEM, necessitates innovative analytical framewo
92 ools (e.g., ICP-MS, electron microscopy with EELS) and functional reactivity assays applied to enviro
93             The in situ studies (HERFD-XAS & EELS) indicated the key role of oxygen vacancies of defe