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1 strongly influences laser energy coupling to fast electrons.
2 d-density copper foil heated by laser-driven fast electrons.
3 opropylguanine (CPG) are used as kinetically fast electron and hole traps to probe the resulting elec
4 onic conductivity, structural stability, and fast electron and ion transport, are explored for boosti
5 w conformational changes mask the relatively fast electron and methyl transfer steps.
6                            Couplings between fast electrons and slow nuclei are ubiquitous across a r
7   Particle-in-Cell simulations indicate that fast electrons are emitted in different directions at di
8                                              Fast electrons are preferentially emitted along the lase
9 l cyst, and renal parenchymal volumes, using fast electron-beam computerized tomography scanning, and
10 , captured at 2.5 ms time resolution using a fast electron camera.
11 scopy alongside an angle-resolved pixellated fast-electron detector.
12                 Here, recent developments in fast electron detectors and data processing capability i
13 output beam distributions of the HiRES ultra-fast electron diffraction (UED) beam line at Lawrence Be
14  a part of the existing instrument for ultra-fast electron diffraction (UED) experiments at the Accel
15 ariable time interval, it was shown that the fast electron donating complex was reformed in about 60
16 ining cyt cy , however, was able to form the fast electron donating complex with the RC (half-time of
17 bance changes at 832 nm in the presence of a fast electron donor (phenazine methosulfate (PMS)).
18 cause the bound cytochrome is available as a fast electron donor in Chlorobium, it is not necessary t
19 rbance changes at 298 K in the presence of a fast electron donor indicate that two electron acceptors
20 n species in a pH as high as 11.5 when using fast electron donors such as ethanol.
21 fields of MV leads to anisotropic heating of fast electrons due to diffusion in the momentum space of
22 here is a regime change in the dependence of fast electron energy on incident laser energy that coinc
23 ficantly advances our understanding of rapid fast electron heating and energy relaxation in solid-den
24                          Using a kinetically fast electron hole trap, N(4)-cyclopropylcytosine ((CP)C
25 xamine the photooxidation of two kinetically fast electron hole traps, N4-cyclopropylcytosine (CPC) a
26 tocatalytic reactions remains low due to the fast electron-hole recombination and low light utilizati
27 y due to this electronic pairing benefitting fast electron-hole recombination.
28 tudy of transition metal clusters exhibiting fast electron hopping or delocalization remains challeng
29 e deltaG(ET) = 0.3-0.7 kcal mol(-1) for very fast electron hopping or peregrination around the hexago
30 ing electron beam damage, for example, using fast electron imaging and spectroscopy.
31 nd confirm the role of stochastic heating of fast electrons in the enhancement of the accelerating sh
32 nt interaction of electromagnetic waves with fast electrons in the relativistic plasma when the elect
33 tials increases the driving force and favors fast electron injection.
34 to substrates, high areal/specific capacity, fast electron/ion transfer, and free space for alleviati
35 shells and the polar Fe3 O4 cores facilitate fast electron/ion transport and promote continuous react
36 niform mesopores and ultrathin MnO(2) enable fast electron/ion transport comparable to electrical-dou
37              Such affinity together with the fast electron kinetics enables simultaneous and unambigu
38  the future development of single-shot ultra-fast electron microscope (UEM).
39 e X-ray free electron laser (XFEL) and ultra-fast electron microscopy.
40  many advantages such as cost-effectiveness, fast electron mobility, mask-free, green synthesis, good
41  solar cells, leading to the conclusion that fast electron motion is essential for efficient charge c
42 how to control signal transmission, i.e. how fast electrons or excitation energy could be transferred
43  enhancement of the energy and weight of the fast electron population and to play a major role in las
44 lated uric acid and adenosine and engaged in fast electron/proton transfer in the oxidation of both a
45 en transients largely governed by relatively fast electron relaxation.
46 tein, thereby eliminating the requirement of fast electron self-exchange, which is a condition that i
47 sorbing X-ray photons and converting them to fast electrons through the photoelectric effect.
48             Cu(H2 Tpy(NMes))Cl shows similar fast electron transfer ( approximately 10(5) m(-1) s(-1)
49 ol that enables quantitative measurements of fast electron transfer (ET) kinetics when coupled with m
50 organization free energies are necessary for fast electron transfer (ET) reactions.
51            The analytical response signified fast electron transfer and accessibility of several elec
52 lectrode surface in such a way that there is fast electron transfer and complete retention of the che
53 mV with enhanced peak currents, indicating a fast electron transfer at the modified electrode surface
54                                    Achieving fast electron transfer between a material and protein is
55     These structural features facilitate the fast electron transfer between the thin protein film and
56             The close packing contributes to fast electron transfer by increasing the rate of electro
57                               Because of the fast electron transfer by ruthenium (Ru) complex and int
58 (equivalent to H atom abstraction) following fast electron transfer from the catechols (QH(2)) to NO(
59 the absence of cyt c2 because it can mediate fast electron transfer from the cyt bc1 complex to the R
60 nd such rate acceleration is attributed to a fast electron transfer from the DA anion to dpph(*).
61 the MEG sensitization is based on an initial fast electron transfer from the pyrene ligands to the Pb
62  as a crosslinker and monomer leading to the fast electron transfer from the redox centre to the elec
63 eal the molecular driving force that ensures fast electron transfer in cryptochrome guaranteeing form
64                                              Fast electron transfer in less than 2 ps is observed for
65 duction by the imidazole bound complex under fast electron transfer is due to 1e(-)/1H(+) O2-reductio
66  guidance, a productive docking geometry for fast electron transfer is imposed by the guided trajecto
67 aligned HD-CNTf rods in the u-ES demonstrate fast electron transfer kinetics and offer excellent dete
68 chemical impedance spectroscopy (EIS) showed fast electron transfer kinetics of ZnO-rGO/ITO electrode
69 smitters because they are sensitive, exhibit fast electron transfer kinetics, and are more resistant
70 able devices show excellent conductivity and fast electron transfer kinetics.
71 iments and computation showing that the same fast electron transfer mechanism is operating in a diffe
72 ng photoexcitation of the electron acceptor, fast electron transfer occurs initially from the oligoqu
73 transfer on Pt, and catechol, which exhibits fast electron transfer on Au.
74 d two different species; l-dopa, which shows fast electron transfer on Pt, and catechol, which exhibi
75 three different electron transfer reactions, fast electron transfer outer sphere, metal electrodeposi
76 pports the hypothesis that the exceptionally fast electron transfer rate between Tvfd and the drug me
77 in the co-crystals, which is the same as the fast electron transfer rate in vivo and in solution.
78 scopy shows that this catalyst features very fast electron transfer rates, facile oxygen binding and
79 onductive part of the composite, facilitated fast electron transfer rates.
80 thanol, no regeneration is observed due to a fast electron transfer reaction from the tocopheryl radi
81             NADP(H) binding is essential for fast electron transfer through the flavoprotein domain o
82 se with bound NADP(H) is essential to ensure fast electron transfer through the two flavin cofactors.
83 oketyl radical, CH(3)C(*)(SH)NHCH(3) (1), by fast electron transfer to protonated thioacetamide in th
84 c interaction between the two, is crucial to fast electron transfer to the active sites and multi-ele
85 orescence of Trp68 and Trp156 is quenched by fast electron transfer to the amide backbone.
86 does the dopamine modified electrode yield a fast electron transfer with lower DeltaE(p) (30 mV) than
87 rent responses, and capable of demonstrating fast electron transfer) for outer sphere redox couples,
88                 The assembly is conducive to fast electron transfer, fast proton transfer, and a high
89 ns all the data needed to estimate the (very fast) electron transfer rates (both rate constants >/= 4
90 ced kinetics for electrooxidation of NA, and fast electron-transfer between electrode-electrolyte int
91 y oriented nano-graphitic-edges that exhibit fast electron-transfer kinetics and high electroactive s
92                                          The fast electron-transfer rate in TiO(2) single crystals an
93                                              Fast electron-transfer rates found in the two ruthenium
94 cise kinetic data may be obtained for a very fast electron-transfer reaction using this technique.
95 ommon use of xenon flashlamps to photoexcite fast electron-transfer reactions are discussed with rela
96 ve material-current collector connection for fast electron transport.
97 ol which combines strong optical pumping and fast electron tunneling.
98                              The emission of fast electrons with kinetic energies exceeding 3 keV is