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1 pitaxial growth and ion erosion in ultrahigh vacuum.
2       However, we do not operate in a social vacuum.
3 y photoelectron spectroscopy under ultrahigh vacuum.
4 levitation from atmospheric pressure to high vacuum.
5 s of high- and low-vapor pressure liquids in vacuum.
6 eft vast areas of health care in an evidence vacuum.
7 thout generating oxygen defects even in high vacuum.
8 ity gases and introduce the analyte into the vacuum.
9 in control of its built-in NV centres in low vacuum.
10 than 60 at the interface of copper metal and vacuum.
11  and reactions at the surfaces of liquids in vacuum.
12 eter decreases chatter, up to 400 mm Hg with vacuum.
13 ignificant amounts of water, even under high vacuum.
14 d layer that is stable within the microscope vacuum.
15 t, they were not subjected to degassing into vacuum.
16 nclassical states of light like the squeezed vacuum.
17 sure is reduced or the sample is annealed in vacuum.
18 dies at temperatures of finite difference in vacuum.
19 bly of two-dimensional building blocks under vacuum.
20 dynamics of a levitated nanoparticle in high vacuum.
21 create atmospheric plasma without an applied vacuum.
22 vironment is changed from atmosphere to high vacuum.
23 lativistic or near-relativistic electrons in vacuum.
24  stepwise SPD process in a UIC KDL 5 system (vacuum 10(-3)mbar, feeding flow 1.0 mL/min) was proceede
25  vaginal delivery with the use of forceps or vacuum (115 of 304 women [38%] and 104 of 314 women [33%
26                     Samples were fried under vacuum (6.5 kPa, Twater-boiling-point=38 degrees C) or a
27 gestibility can be reduced when frying under vacuum (9.9kPa), after feeding Sprague-Dawley rats, whil
28 ymmetric double tunnel junctions with both a vacuum and a MgO tunnel barrier.
29 ency on the examples of alanine dipeptide in vacuum and C-terminal beta-hairpin of protein G in expli
30               Sensory characteristics of the vacuum and conventionally fried potato crisps were evalu
31 y-Assisted Vapor Deposition (ESAVD) is a non-vacuum and cost-effective method to deposit metal oxide,
32 ecular probe is not restricted to ultra-high vacuum and cryogenic settings.
33  nano/atomic scale from ambient to ultrahigh-vacuum and electrochemical environments.
34 oviding stabilization to proteins during the vacuum and electron-beam irradiation steps.
35                 Chatter correlated with both vacuum and flow such that increasing either parameter de
36               In our work, eco-friendly, non-vacuum and low cost Electrostatic Spray Assisted Vapour
37                                              Vacuum and low temperature drying without osmotic pretre
38 h 15% of maltodextrin were dried by freeze-, vacuum and spray drying methods.
39                     Samples were dried under vacuum, and carbonyl groups were protected with methoxyl
40 ions were successfully electrosprayed into a vacuum, and these three ECX(-) anions were investigated
41 x nanosheet colloidal solutions, followed by vacuum annealing at 200 degrees C.
42 tic adaptation utilizing liquid rubidium and vacuum annealing of the mixed elemental reagents in fuse
43                                      After a vacuum annealing process, a high gain in exceeding 10(7)
44            A total of 1509 MR imaging-guided vacuum-assisted biopsy procedures were performed in nine
45  ADH and DCIS diagnosed at MR imaging-guided vacuum-assisted biopsy were high, at around 25%, and wer
46    Both patients underwent ultrasound-guided vacuum-assisted biopsy.
47 S) at magnetic resonance (MR) imaging-guided vacuum-assisted breast biopsy and to explore the imaging
48 tato slices were fried in rapeseed oil under vacuum at 125 degrees C and atmospheric pressure at 165
49  sublime this high-spin diradical under high vacuum at 140 degrees C with no significant decompositio
50 ucting state is accomplished by annealing in vacuum at 400 degrees C.
51 recursor followed by thermal treatment under vacuum at 500 degrees C.
52 corated with iridium deposited in ultra-high vacuum at low temperature (7 K) as a function of Ir conc
53 minantly fabricated by complex and expensive vacuum-based integrated circuit (IC) processes.
54 hin films into organic solar cells through a vacuum-based polymer vapor printing technique.
55                                    MR-guided vacuum biopsy and MR-guided lesion bracketing were perfo
56 o acknowledge that they operate not within a vacuum but within a society in which diverse perspective
57  1 muC.cm(-2), and is preserved in ultrahigh vacuum, but disappears upon heating to 100 degrees C.
58 ty factors, such as cantilevers vibrating in vacuum, can show characteristic Fano asymmetric curves w
59             This material is prepared by the vacuum carbonization of a zinc-based metal-organic frame
60 idual gas analyzer (RGA) coupled with a high-vacuum chamber has been explored to measure atmospheric
61 a capillary pressure reduction system into a vacuum chamber, where they are analyzed using a quadrupo
62 ctor approach, i.e. minimizing the number of vacuum chambers and sample transferences.
63 tional microelectronic devices with a gas or vacuum channel may scale their speed, wavelength and pow
64 m pipette-dispensed PDMS microdroplets using vacuum-chucked microspheres.
65  and POP levels in dust from their household vacuum cleaners.
66 re more predictive of serum PBDE levels than vacuum-collected dust.
67 erties of three resulting products (an under-vacuum concentrate, a dilute-to-taste syrup and a ready-
68  why they overwhelmingly preferred the under-vacuum concentrate, regardless of their age, gender or f
69  components in the last stage of processing (vacuum concentration).
70 to 5 nm gap sizes, performed under ultrahigh vacuum conditions between a Au-coated probe featuring em
71 es at well-defined surfaces under ultra-high vacuum conditions represents an unconventional synthesis
72 cally-heated chemical vapor deposition under vacuum conditions were relatively thick and short.
73  on the known surface dynamic behavior under vacuum conditions, indicating that the same dynamics als
74  at room temperature so as to preserve ideal vacuum conditions, represent concrete alternatives, inde
75 r high oxygen conditions for 15 or 22days in vacuum conditions.
76 a turbomolecular pump-by 2% compared to high-vacuum conditions.
77  within water's "no man's land" in ultrahigh-vacuum conditions.
78 f molecular building blocks under ultra-high-vacuum conditions.
79 by calculations under crystal, solution, and vacuum conditions.
80 orophene) on silver surfaces under ultrahigh-vacuum conditions.
81 em appreciated potato-like fresh flavour of 'vacuum crisps' and classified this product as 'tasty'.
82                            We present a high-vacuum cryo-transfer system that streamlines the entire
83 mbrane contactor (MC) and distillation under vacuum (D).
84 the functions of the Na treatment in our non-vacuum deposited CIGS are mainly used for defect passiva
85 igh-resolution e-beam lithography, thin film vacuum deposition and reactive-ion etching processes eli
86 ng a domestic microwave oven equipped with a vacuum desiccator inside.
87                 For volatile DBPs, cryogenic vacuum distillation performed unsatisfactorily.
88  in the field, we found that a single PYP in vacuum does not provide an accurate description of the c
89 erence in the proximate composition; however vacuum dried CPI (VDCPI) had the highest bulk density an
90                 For this purpose, beads were vacuum-dried and stored under controlled conditions.
91 acquired blood viscosity was compared with a vacuum-driven capillary viscometer at high shear rates (
92 ying (VD), convective drying (CD), microwave-vacuum drying (MVD) and combination of convective pre-dr
93  hot air convective drying (HACD), microwave vacuum drying (MWVD) and their combination (HACD+MWVD) o
94            The effect of freeze-drying (FD), vacuum drying (VD), convective drying (CD), microwave-va
95            An industrially applicable 2-step vacuum drying and heating process was explored, which fi
96  study drying of pequi slices (convective or vacuum drying at 40 degrees C and 60 degrees C) preceded
97 converted to powders using spray, freeze and vacuum drying methods, to investigate the effect of dryi
98 ion with a PG aqueous solution followed with vacuum drying of the supernatant.
99 se in temperature up to 100 degrees C during vacuum drying of XAD extracts resulted in degradation of
100 investigate the effect of temperature in the vacuum drying process of Mentha piperita L.
101 investigate the effect of temperature in the vacuum drying process of Mentha piperita L. (50 to 90 de
102             Fresh red currants were dried by vacuum drying process under different drying conditions.
103                   It could be concluded that vacuum drying provides samples with good physico-chemica
104 ng with super critical CO2 drying, or simple vacuum drying up to 95 degrees C.
105         Mango slices were dried by microwave-vacuum drying using a domestic microwave oven equipped w
106 sses affect the quality of product, however, vacuum drying works under sub-atmospheric pressures.
107 r collected by passive sampler and in sieved vacuum dust (<150 mum).
108        Among all PFAAs, only PFNA in air and vacuum dust predicted serum PFNA.
109  illustrate the potential of engineering the vacuum electromagnetic environment to modify and to impr
110 riers into states that are hybridized to the vacuum electromagnetic field.
111 es benefit from the advantages of gas-plasma/vacuum electronic devices while preserving the integrabi
112 as many possible applications, such as novel vacuum electronic devices, particle detectors, accelerat
113 ibility of the liquid samples with ultrahigh vacuum environment of the electron optics and detector.
114 morphology, allows analysis in the ultrahigh vacuum environment, and reduces topographic artifacts, t
115 t oxygen stoichiometry, especially in a high vacuum environment, has been viewed as a challenge.
116  temperatures higher than 300 degrees C in a vacuum environment.
117 eutral, or low charged molecules into a high vacuum environment.
118 ives (2H-TPCN) with Co atoms in an ultrahigh vacuum environment.
119 lf-assembly on solid surface in an ultrahigh vacuum environment.
120 ize-selected supported clusters in ultrahigh-vacuum environments and under realistic reaction conditi
121                                To prevent in-vacuum evaporation of the liquid content of the small gl
122 rown on kenaf/lignin agar followed by either vacuum evaporation or acid precipitation.
123 n nanotube electrodes (ICE) were prepared by vacuum filtering a well-dispersed carbon nanotube-Nafion
124  carbon nanotubes can be prepared using slow vacuum filtration.
125 s and are prepared into transparent paper by vacuum filtration.
126 tion intermediate that was generated by high-vacuum flash pyrolysis (HVFP) of the corresponding p-tos
127                                 Fortunately, vacuum fluctuations are not immutable and can be 'squeez
128                                              Vacuum fluctuations are one of the most distinctive aspe
129 at enable the inhibition and manipulation of vacuum fluctuations have been key to our ability to cont
130      Here, we theoretically demonstrate that vacuum fluctuations may be naturally inhibited within bo
131  per cent below the fundamental limit set by vacuum fluctuations, while the photon statistics remain
132 ht into oxygen stoichiometry control in high vacuum for understanding the fundamental properties of S
133                                              Vacuum fried samples showed less starch gelatinization (
134                          Results showed that vacuum-fried dough has a lower degree of gelatinization
135  and higher unavailable glucose fractions in vacuum-fried dough.
136  f 1, Der p 1, Mus m 1, and Rat n 1) in dust vacuumed from nearly 7000 bedrooms were measured by usin
137 arch was focused on a critical assessment of vacuum frying as a technology enabling minimization of a
138             In vitro studies have shown that vacuum frying may be an effective process to reduce star
139            This study assessed the effect of vacuum frying on starch gelatinization and its in vitro
140                                              Vacuum frying reduced the formation of acrylamide by 98%
141 nal asymmetry between the polar Cu2N and the vacuum gap breaks inversion symmetry in the alkali halid
142 requency acoustic phonons tunnel through the vacuum gap by coupling to evanescent electric fields, pr
143                        We also find that the vacuum gap resulting from the widely used 300 nm-oxide s
144 nsfer between planar surfaces separated by a vacuum gap smaller than the thermal wavelength exceeds t
145 r, dominated by frustrated modes, only for a vacuum gap thickness of 10 nm and if both electrical and
146  upon 2D material type and number of layers, vacuum gap, oxide thickness, and detecting wavelength, t
147 cale planar surfaces separated by a nanosize vacuum gap.
148 ity 2 W/cm(2) with ~47% efficiency at 300 nm vacuum gap; at 2100 degrees K, 24 W/cm(2) with ~57% effi
149 e-based extraction method does not require a vacuum-gap, which is a significant reduction in the requ
150 d or even new models of heat transfer across vacuum gaps at nanometre distances.
151           Our measurements were performed in vacuum gaps between prototypical materials (SiO2-SiO2, A
152                 Using planar capacitors with vacuum gaps of 60 nm and spiral inductor coils of micron
153 y high efficiency and output power, at large vacuum gaps.
154 lied for the analysis of a basic fraction of vacuum gas oil.
155 ckaging materials (i.e. natural casing under vacuum, glass jar, aluminum tube and OVTENE(R)) during 1
156 ed with time (glass jar>natural casing under vacuum&gt;aluminum tube>OVTENE(R)).
157  zinc-oxide-based ultraviolet sensors in air/vacuum has long been an obstacle to developing such dete
158 ing Ru(bpy)3, emission is bipolar, occurs in vacuum, has rapid rise time (<5 ms), and persists for >1
159 ) centre in a nanodiamond, levitated in high vacuum, has recently been proposed as a probe for demons
160 s with nitrogen-vacancy (NV) centres in high vacuum have been proposed as a unique system for experim
161                                           By vacuum heating the hybrid materials at an intermediate t
162 u growth of graphene on flaky Cu powders and vacuum hot-press sintering.
163 e glycol (PEG) and RMS were prepared through vacuum impregnating method.
164                                              Vacuum improved efficiency up to 500 mm Hg independent o
165       However, liberating electrons into gas/vacuum in a practical microelectronic device is quite ch
166 s and layers and a post-annealing process in vacuum in order to remove the organic template.
167                                   Increasing vacuum increased efficiency regardless of aspiration rat
168 roduces the same high-quality images without vacuum-induced artifacts; it is also less invasive, whic
169 Put at 0, 1 and 2mM were applied to fruit by vacuum infiltration at 26.665kPa for 8min and then store
170 "interfacial" hydrated electron at the water/vacuum interface, performed using liquid microjet photoe
171  Au plasmon resonance is localized at the Au/vacuum interface, rather than presenting an isotropic di
172 tion microchannel", before entering the high-vacuum ion source.
173 effect on efficiency through 50 mL/min, when vacuum is at 400 mm Hg or higher, and only up to 35 mL/m
174 yer, a molecule whose HOMO energy level in a vacuum is close to the Fermi level of the gold bottom el
175 eak field gravitational waves propagating in vacuum is derived directly from the linearized general r
176 icate that oxygen vacancy generation in high vacuum is strongly influenced by the energetics of the l
177 thermal-activation (400-500 degrees C) under vacuum, is demonstrated.
178 /- 0.8)c, where c is the speed of light in a vacuum, is in the incipient stages of a collision with a
179 mm Hg or higher, and only up to 35 mL/min at vacuums less than 400 mm Hg.
180 (-)(aq) in bulk water lies too far below the vacuum level to induce such reactions.
181    A recent measurement of the energy (below vacuum level) of the putative "interfacial" hydrated ele
182 ndent already a few electron-Volts above the vacuum level.
183 pothetical Zn-based ZIFs with respect to the vacuum level.
184 from the Fermi level of the electrode to the vacuum level.
185  of MoTe2 flakes annealed via RTA at various vacuum levels are tuned between predominantly pristine n
186                                              Vacuum levels were tested at 200, 300, 400, and 500 mm H
187 onradioactive electron emitters require high vacuum (&lt;10(-6) hPa) to prevent electrical sparkovers.
188 ext to the ion trap mass analyzer inside the vacuum manifold.
189 ve optical heating of the nanodiamonds under vacuum may make the method impractical with currently av
190 ior development with cyanoacrylate fuming or Vacuum Metal Deposition, was also examined.
191 , for example, surface plasmon-polaritons at vacuum-metal interfaces.
192 lood from the micro-channel (4.17cP) and the vacuum method (4.22cP) at 500 s(-1) were closely correla
193  by a combined method (convective pre-drying+vacuum microwave finish drying).
194 onvective drying (CD: 50, 60, 70 degrees C), vacuum-microwave drying (VMD: 120, 480, 480-120 W), a co
195 , a combination of convective pre-drying and vacuum-microwave finish drying [(CPD (60 degrees C)-VMFD
196  machine was used in peristaltic and Venturi vacuum modes with transversal and micropulsed ultrasound
197 ed DPH is stable for at least 24 h under the vacuum of our MALDI mass spectrometer.
198 nto the substrate, and then deposit them (in vacuum-off mode) in the desired location.
199  which provides values of ca. -4.0 eV versus vacuum on both ITO and TiO2 electrodes.
200 ronic circuitry by using an empty nozzle (in vacuum-on mode) to pick up individual components, place
201 b:TiO2 conductors on glass (without breaking vacuum) only occurs within a narrow processing range and
202  scale using simple metal precursors without vacuum or heat.
203 ging conditions (MAP), in our case, aerobic, vacuum or high O2, to extend the shelf life of beef.
204  instability and the need to work under high-vacuum or high-temperature conditions have imposed strin
205 nly becoming relevant for structures held in vacuum or under extreme thermal isolation.
206 teviol glycosides (SGs) by spray, freeze and vacuum oven drying in order to minimise the bitter after
207 tracts, then spray drying, freeze drying, or vacuum oven drying to prepare dry, flour-like matrices.
208  polarization from ferroelectric material in vacuum (P 10(-6) torr).
209 rgent data were compared to those subject to vacuum packaging as well as conventional preservative me
210 concentration was higher under air than in a vacuum packaging atmosphere.
211 ical, microbiological and sensory quality in vacuum-packed fresh shibuta (Barbus grypus) fillets duri
212 egarding the total metabolites content, were vacuum packing and freezing for intermediary storage tim
213 t of freezing, freeze-drying, air drying and vacuum packing, was evaluated on these potential aroma m
214 TiO2 multishell nanotubes by a combined full vacuum-plasma approach at mild temperatures.
215                                 A three-step vacuum procedure for the fabrication of vertical TiO2 an
216 zed as near-infrared absorbing materials for vacuum processable organic solar cells.
217  any external chemical, high-temperature, or vacuum processes.
218                       These results show how vacuum processing may be used to control the degree of s
219  Quantum fluctuations of the electromagnetic vacuum produce measurable physical effects such as Casim
220 by e-beam to the eC surface without breaking vacuum protects the surface from the environment after f
221                                  When a 12 W vacuum pump was used for carrying the generated CO2 out
222 rbenes were generated by falling solid flash vacuum pyrolysis (FS-FVP).
223 y 2080 cm(-1) by a combination of mild flash vacuum pyrolysis (FVP) at 200-600 degrees C with low tem
224                                        Flash vacuum pyrolysis (FVP) of 1-(5-(13)C-5-tetrazolyl)isoqui
225                                        Flash vacuum pyrolysis (FVP) of azides is an extremely valuabl
226 iazolo[1,5-a]quinoline by conventional flash vacuum pyrolysis (FVP) were observed by IR spectroscopy.
227                                        Flash vacuum pyrolysis of 1,3-bis-iodomethyl-benzene (m-C8H8I2
228                                Through flash vacuum pyrolysis of CF3 S(O)NCO at ca. 1200 K, sulfinyl
229 e cascade (RDA/ICE) reaction under the flash-vacuum pyrolysis of maleic anhydride adducts is develope
230                                   Upon flash vacuum pyrolysis of sulfinyl azide CF3S(O)N3 at 350 degr
231 apors rapidly through a very hot oven (flash vacuum pyrolysis) promotes high-temperature thermal reac
232                                    Via flash vacuum pyrolysis, even metaparacyclophanes as small and
233 enzyne, 1,2-azaborine, is generated by flash vacuum pyrolysis, trapped under cryogenic conditions, an
234 kcal/mol and thus to be accessible via flash vacuum pyrolysis.
235 ew route harnessing a ring-contracting flash vacuum pyrolytic extrusion of sulfur dioxide from the re
236      For example, a direct modulation of the vacuum Rabi frequency is obtained by deforming the EMNZ
237                     We selectively stimulate vacuum Rabi oscillations between the transmon and indivi
238     We also observe quantum beats, so-called vacuum Rabi oscillations, between the upper and lower vi
239 asmons, polarons, and a phonon analog of the vacuum Rabi splitting in atomic systems.
240 owave cavity, as shown by the observation of vacuum Rabi splitting.
241  inner pressures of the device in the medium vacuum range (>10(-3) hPa).
242 nt coming from a nanoLC column into the high-vacuum region of an electron ionization source.
243   Cleaving a single crystal under ultra-high vacuum results in multiple terminations: an ordered Pt4A
244                       Annealing in ultrahigh vacuum revealed a thermal stability limit of approximate
245 erminated scanning probe is performed at the vacuum-solid interface often at a few Kelvin, but is not
246 dimensional bimolecular organizations at the vacuum-solid interface.
247 s become possible through the utilization of vacuum-stabilized imaging windows.
248                                  Compared to vacuum-stabilized windows, this window produces the same
249 linking atmospheric pressure and the initial vacuum stage of the mass spectrometer.
250 the operation time, each cavity remains in a vacuum state, thus decoherence caused by the cavity deca
251        Only the charged crystal structure in vacuum supports a LBHB if Arg52 is neutral in PYP at the
252 ion by infrared laser pumping, and ultrahigh vacuum surface analysis techniques make it possible to s
253                              While ultrahigh vacuum surface science techniques have provided useful i
254 ce of low-frequency nonlocal plasmons at the vacuum-surface interface of a superlattice of N graphene
255 ty used for frequency stabilisation with its vacuum system takes 30 x 30 x 30 cm(3).
256 d within a single superconducting magnet and vacuum system.
257  with O2, the nitrene was generated by flash vacuum thermolysis (FVT) of phenylazide and subsequently
258 uctive membrane to protect animal cells from vacuum, thus enabling high-resolution electron microscop
259                                    Ultrahigh vacuum tip-enhanced Raman spectroscopy (UHV-TERS) combin
260 e of Cot molecules and Eu vapor in ultrahigh vacuum to an inert substrate, such as graphene.
261 olarization from a ferroelectric material in vacuum to dramatically enhance the TENG output power.
262 ing and spectroscopy, from operation at high vacuum to in live cells.
263 spot for global biodiversity, we used a seed vacuum to increase dispersal at spatial scales varying f
264            These are collected by applying a vacuum to the top of the bottle and cryo-trapping the ex
265 ealistic model for parameter dispersion, and vacuum, to confirm the existence of one-way scatter-immu
266 of technological advances which took us from vacuum tubes to cell phones.
267 ht sources, such as free-electron lasers and vacuum tubes, rely on bunching of relativistic or near-r
268  decomposition of adsorbed 1 under ultrahigh vacuum (UHV) conditions proceeds through initial CO loss
269 (111) upon thermal annealing under ultrahigh vacuum (UHV) conditions.
270 d on a rutile TiO2(110) surface in ultrahigh vacuum (UHV) is studied with spin-polarized density func
271                                 In ultrahigh vacuum (UHV), TERS can be performed in pristine environm
272 as devised to integrate a gas chromatography-vacuum ultraviolet (GC-VUV) data set in order to provide
273                                         A GC-vacuum ultraviolet (UV) method to perform group-type sep
274                                        A new vacuum ultraviolet (VUV) detector for gas chromatography
275  are ionized by 10 eV photons generated by a vacuum ultraviolet (VUV) krypton discharge lamp.
276 aneous-detection spectrometer working in the vacuum ultraviolet (VUV) region of 125-240 nm overcomes
277                               Here we report vacuum ultraviolet absorption spectra for the lowest-lyi
278                                              Vacuum ultraviolet spectra emanating from krypton atoms,
279 via dispersive wave emission in the deep and vacuum ultraviolet, with a multitude of applications.
280  that uniquely reaches simultaneously to the vacuum ultraviolet, with up to 1.7 W of total average po
281 eration of high harmonics extending into the vacuum-ultraviolet and extreme-ultraviolet regions of th
282 on provides a potential approach to generate vacuum-ultraviolet frequency comb.
283 cs as a potential source of intense coherent vacuum-ultraviolet radiation has received considerable a
284 nization (by tunable low energy electrons or vacuum-ultraviolet synchrotron radiation) for product de
285             Chatter improved with increasing vacuum, up to 400 mm Hg (P = .003 for 200 vs 300 mm Hg a
286 chromatography, with selective detection via vacuum UV absorption spectroscopy.
287                                              Vacuum UV detection was necessary to solve a coelution b
288 e via various spectroscopic tools, including vacuum UV photoionization mass spectrometry, absorption
289                  The gas chromatography (GC)-vacuum UV results for the Synfuel samples were similar (
290 ancies were noted between SFC results and GC-vacuum UV results; however, these samples are known to b
291 namics (AIMD) simulations and molecular beam vacuum-UV (VUV) photoionization mass spectrometry experi
292                 Here, we implement ultrafast vacuum-UV (VUV)-driven electron-ion coincidence imaging
293                                      We used vacuum-UV photoionization aerosol mass spectrometry and
294 rowth substrates (Ni(C)/(B, N)-source/Ni) in vacuum, wafer-scale graphene/h-BN films can be directly
295 aspiration further increased efficiency when vacuum was at 400 and 500 mm Hg (P = .004 for 20 vs 35 m
296 -lived, metastable species does exist at the vacuum/water interface, it would be extremely difficult
297 cal-density-of-states which tunnels into the vacuum, when compared with the ferromagnetic background,
298 icant buckling and numerous polymorphs as in vacuum, whereas on more reactive Ag, Cu, and Ni, the pol
299 s the complete CO2 desorption at 328 K under vacuum with an associated moderate energy input of 54 kJ
300 ion factor values exceeding 10(8) A C(-1) in vacuum with undiminished responses in open air, and clea

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