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1 e backbone yields a sharp longest wavelength absorption edge.
2 ponses at 1064 and 532 nm and a short 180 nm absorption edge.
3 structure range beyond the onset of the iron absorption edge.
4 s diffraction (MAD) applied to the bromine K-absorption edge.
5 solution to distinguish individual elemental absorption edges.
6 fluorescence setup at certain energies near absorption edges.
7 has permitted XAS studies at both Cu and Se absorption edges.
8 ayer compounds exhibit a blue shift in their absorption edge (0.6-1.2 eV), due to the quantum confine
10 5 x KDP (600 x alpha-SiO2), and the shortest absorption edge (250 nm) of reported materials with a st
11 single pulse streaking reaching the carbon K-absorption edge (284 eV) by utilizing intense two-cycle
12 ond lengths and Debye-Waller factors at each absorption edge allowed us to rule out simple models for
13 Through the comparison by iron K-edge x-ray absorption edge and extended fine structure analyses of
14 with NC n-doping, including a bleach at the absorption edge, appearance of a new IR absorption band,
18 ese new devices include precisely adjustable absorption edges between 0.87 and 1.03 eV, low ideality
19 ccurring on the high-energy side of an X-ray absorption edge, can be used to identify interatomic dis
21 um efficiency data for wavelengths above the absorption edge, coupled with a strong sharp photolumine
22 We show that the shift of the main visible absorption edge does not constrain the point of band gap
24 ely distributed surface pigment with a sharp absorption edge in the red part of the visible spectrum,
25 ranging from 2.8 to 13.5 x KDP, and exhibit absorption edges in the mid- to deep-ultraviolet regime.
26 perimental UV/Vis measurements of the Tix Oy absorption edges in these species and reveal that molecu
29 osphorene at energies that closely match the absorption edge, indicating that they are direct bandgap
30 ng X-ray scattering differences at elemental absorption edges, is developed to quantitatively determi
32 n the photon energy is tuned to a core-level absorption edge of an atom neighboring the emitting atom
35 constructions at X-ray energies around the L absorption edge of iron demonstrates the advantages of t
37 collected at the X-ray wavelengths near the absorption edge of the K-shell alpha electrons of seleni
38 er visible-light irradiation by shifting the absorption edge of TiO2 nanocrystals to a shorter wavele
41 itional structure at the L(1), L(2) and L(3) absorption edges of gadolinium in gadolinium gallium gar
42 circular dichroism measurements at the N4,5 absorption edges of Gd to validate the high degree of ci
44 on energies corresponding to the fundamental absorption edges of matter, which lie in the soft X-ray
49 ieved through operating above the two-photon absorption edge, representing one of the largest optical
51 purified enzyme using X-rays tuned to the Fe absorption edge show Fe partitions primarily to the beta
52 near edge structure (XANES) around the Pb-L3 absorption edge showed that Pb pigments and Pb soaps can
54 efficient, good electron mobility, and sharp absorption edges that are defined by the twisted molecul
57 to the excitonic photoluminescence near the absorption edge, we find a red-shifted, broadband (full-
58 ng incident x-ray energies close to the Se K-absorption edge, we have collected quantitative, 100-mic
60 0 nm wavelength resides above the two-photon absorption edge, while still possessing large nonlineari
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