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1 e solvation of the partly positively charged adsorbate.
2 structural parameters of a model (n)Bu2DTPA adsorbate.
3 tion of bulkier groups on the Ch atom of the adsorbate.
4 detailed electronic structure of a resonant adsorbate.
5 oduce an effective drag on the motion of the adsorbate.
6 plet-excited-state lifetime of the molecular adsorbate.
7 on is bound, and the h is transferred to the adsorbate.
8 g the binding energy between the surface and adsorbates.
9 stigate electron-transfer processes of redox adsorbates.
10 solely based on covalent binding of organic adsorbates.
11 vealed distinct individual properties of the adsorbates.
12 gold(I) ion are surprisingly small for both adsorbates.
13 the difference in chelation between the two adsorbates.
14 ch can be occupied or blocked by some of the adsorbates.
15 used to achieve this goal for electroactive adsorbates.
16 roism by Au nanoparticles modified by chiral adsorbates.
17 n activation energy for a range of spherical adsorbates.
18 or detection and identification of molecular adsorbates.
19 entify the atomic-scale structure of unknown adsorbates.
20 ission lifetimes due to electron transfer to adsorbates.
21 redominantly to study aggregation of racemic adsorbates.
22 ed on graphene and bulk graphite in terms of adsorbates.
23 ites, and bonding and orientation of surface adsorbates.
24 and hence vanishes in regions accessible by adsorbates.
25 mi level exchanges electrons with the oxygen adsorbates.
26 atic atomic-scale interrogation of molecular adsorbates.
27 esponds to where the refractive index of the adsorbate achieves its largest value, which occurs at wa
29 id He cooling minimizes surface diffusion of adsorbates across the solid surface, allowing direct STM
31 state properties will provide information on adsorbate-adsorbate and adsorbate-substrate interactions
32 ividual pores have been extensively studied, adsorbate-adsorbate interactions across pore walls have
33 , can give rise to collective and long-range adsorbate-adsorbate interactions and the formation of ad
36 l to understand both adsorbent-adsorbate and adsorbate-adsorbate interactions, and also the energy re
37 he mean-field kinetic model includes lateral adsorbate-adsorbate interactions, and the BEEF-vdW error
38 ngmuirian Moreau isotherm due to significant adsorbate-adsorbate interactions, whereas the isotherms
42 s in the bc crystallographic plane where the adsorbate-adsorbent interactions are maximized by both t
45 lute from solution and/or because the tested adsorbate:adsorbent ratios are not varied sufficiently.
46 by our data, with clear evidence for initial adsorbate aggregation in distinct domains and ordering b
48 it is essential to understand both adsorbent-adsorbate and adsorbate-adsorbate interactions, and also
50 and desorption efficiency and showing stable adsorbate and adsorbent properties, this paper suggests
52 ion occurs is strongly dependent on both the adsorbate and the support, and this effect is general fo
54 ave revealed unexpected interactions between adsorbates and defects that influence macroscopic reacti
55 , well-developed and accessible porosity for adsorbates and reactants, and are non-toxic, biocompatib
56 gh understanding of the interactions between adsorbates and SWNTs is therefore critical to predicting
57 ometric and electronic structures of the two adsorbates and that the energetic difference between mon
58 By experimentally quantifying the number of adsorbates and the average amount of charge carried by e
63 ar chiral ensembles made out of small chiral adsorbates, and by adsorption of more complex chiral mol
64 ere V is McGowan's characteristic volume for adsorbates, and S reflects the adsorbate's polarity/pola
66 new mechanism for surface diffusion whereby adsorbates are carried by propagating ripples in a motio
68 d to redox chemistry of adventitious organic adsorbates are observed, indicating that air exposure re
70 erings of solid microparticles and molecular adsorbates are strongly coupled at the interfaces of LCs
73 urement capabilities to simultaneously probe adsorbates at multiple length scales will provide new in
74 by coadsorbed water in the photochemistry of adsorbates at solid interfaces and the roles that molecu
75 hannel and Schottky contact formation due to adsorbates at the interface between the gold contacts an
76 gle-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the select
81 demonstrate the ability to control the metal-adsorbate bond through external electronic modifications
84 oparticle size, it is generally assumed that adsorbates bond in an identical fashion as on a semiinfi
87 ion of zeolites and MOF-801 with water as an adsorbate by conducting desorption experiments with conv
88 f 10 by adding a mildly electron-withdrawing adsorbate, C60, which also modifies the step geometry.
90 ayers (SAMs) of dialkyldithiophosphinic acid adsorbates [CH3(CH2)n]2P(S)SH (R2DTPA) (n = 5, 9, 11, 13
92 ms formed by e-beam evaporation in which all adsorbates chelate to gold, in contrast to (C16)2DTPA SA
95 n, contact time, extent of modification, and adsorbate concentration on the biosorption capacity of C
96 ent removal in deionized water at low-target-adsorbate concentrations potentially suggests that DOM i
99 e calculate relative surface stabilities and adsorbate coverages of the most stable low-index surface
101 arge-scale 'before' and 'after' images of an adsorbate covered surface, the spatial extent of the non
103 reby preparing spatially inhomogeneous local adsorbate densities, could add a new design tool for MOF
104 alysis of the simulated heats of adsorption, adsorbate density distributions, and minimum energy 0 K
106 The structural dynamics-cluster size and adsorbate-dependent thermal behaviors of the metal-metal
108 of SAMs formed from the structurally similar adsorbate dihexadecyldithiophosphinic acid (C16)2DTPA.
109 on originates from a sizable cancellation of adsorbate dipole moments by mirror charges dynamically i
111 rafast charge separation in this quantum dot-adsorbate donor-acceptor complex provides a potential ap
113 res can be functionalized with many types of adsorbates, enabling the use of OWL-generated structures
114 but on surfaces with palladium particles the adsorbates exhibit relative disorder at low surface cove
115 -nitrophenyl-acetylacetonate or coumarin 343 adsorbates, exhibit hole injection into surface states w
117 d calculating the enthalpies of well-defined adsorbates, few measurements of the entropies of adsorba
119 we show that the chemical shift value of an adsorbate (formic acid) on metal colloid catalysts measu
121 Despite their importance, knowledge of how adsorbate frequencies scale across materials is lacking.
123 ar, the instrument has often been applied to adsorbates from a liquid phase and, also, to samples wit
125 erials for evaluating the effects of surface adsorbates from the initial state for application-orient
126 igurations of the LC droplets induced by the adsorbates generate distinct changes in light scattering
127 orimetric, and infrared studies of the probe adsorbates H2, CO, and CO2 reveal the presence of severa
128 as a function of particle size (1-3 nm) and adsorbate (H2, CO) using synchrotron radiation pair dist
130 is effect is characterized by strongly bound adsorbates (HCOx) on reducible oxide supports (TiO2 and
132 enter and the number of p electrons) and the adsorbates' highest occupied molecular orbital (HOMO) en
133 red spectroscopy to directly observe surface adsorbates, hydrogen atoms and methyl groups, chemisorbe
135 energetic projectile directly reacts with an adsorbate in a single-collision event to form a hyperthe
136 tional evidence for the integral role of the adsorbate in determining ASJ reorganization dynamics.
138 roved understanding of the role of ligand or adsorbates in colloidal catalysis and photocatalysis and
142 re less than 10(-5) Langmuir, are not due to adsorbate-induced changes in the interfacial energy of t
144 gion is nonemissive (dead layer), surfactant adsorbate-induced modulation of the depletion layer widt
145 n of chemical and biological assays based on adsorbate-induced ordering transitions within LC droplet
148 ing density functional theory predictions of adsorbate-induced surface reconstruction visually with a
149 clusters do exhibit, however, both size- and adsorbate-induced trends in bond strain that are similar
150 ter and stormwater was independent of target-adsorbate initial concentrations (C0) when C0s were belo
151 rption/desorption/reaction properties of the adsorbates inside such environments, screen and design n
152 e adsorption isotherms for a given adsorbent-adsorbate interaction at temperature/pressure conditions
155 P structure can be diminished in favor of NP/adsorbate interactions when NP catalysts are prepared by
156 exchange due to both metal-support and metal-adsorbate interactions--play in mediating the structural
159 hene but from self-assembly of environmental adsorbates into a highly regular superlattice of stripes
162 , XRD (X-ray diffraction), IR (infrared) and adsorbate-IR, N2 and CO2 physisorption at 77 and 273 K,
167 ation of the data obtained for heterogeneous adsorbate layers is not straightforward in particular if
168 s, organic films for polymer electronics and adsorbate layers) suffer degradation under the energetic
170 resonance (LSPR) of metal nanostructures to adsorbates lends itself to a powerful class of label-fre
171 d empirically from the observed response for adsorbate loading on gold surface plasmon resonance (SPR
173 significance of incorporating an additional adsorbate-metal bonding effect in the calculation is dem
174 space between graphene and metals, with the adsorbate-metal interaction being modified significantly
179 tive contributions of factors related to the adsorbate molecular structures that serve to strongly me
180 y transition at approximately 3 Al atoms per adsorbate molecule (3 EL) from formation of a buried app
181 s (up to 0.04 ML, where 1 ML is equal to one adsorbate molecule for every surface Pt atom) using sing
182 shows a significant mismatch of the average adsorbate molecule spacings with the spacings of an intr
183 e to states induced by the Fe-dopant and the adsorbate molecule, and crossing between excited states
185 text of hydrophobic interactions between the adsorbate molecules and the methylated surface in the pr
186 ack and map the distribution and ordering of adsorbate molecules in five members of the mesoporous MO
188 ctive energy migration pathways of monolayer adsorbate molecules on differently sized metal nanoparti
192 AS results reveal that nanoframes which bind adsorbates more strongly have a rougher Pt surface cause
193 ing on the temperature and the nature of the adsorbate, more than one type of organic radical was for
195 F) with and without post-treatments by (31)P adsorbate nuclear magnetic resonance, supported by a ran
197 ith four p-nitrophenyl acetylacetone (NPA-H) adsorbates, of which the atomic structure has been fully
199 or visualizing the distribution of molecular adsorbates on graphene semi-quantitatively using teraher
204 ise engineering of the position of molecular adsorbates on surfaces of 2D materials is key to their d
207 tionalized by the stronger binding energy of adsorbates on the (100) facet versus the (111) facet.
208 provided consistent results of the amount of adsorbates on the BAC after adsorption and/or regenerati
210 s work, we explore the influence of resonant adsorbates on the LSPR of bare Ag nanoparticles (lambda(
211 ion and chemical specificity of surfaces and adsorbates on the molecular scale at pressures of up to
212 quantum tunneling and hindered rotations of adsorbates on the rate of surface reactions have been in
213 EPFRs were produced by the chemisorption of adsorbates on the supported metal oxide surface and tran
217 or diffusion and show how it also applies to adsorbates other than water, thus opening up the prospec
218 the mineral surface (i.e., the adsorption of adsorbates past the point of electrostatic equilibrium)
220 The reaction between the titrant and the adsorbate provides a transient positive feedback loop un
221 the vibrational energy of a carbon monoxide adsorbate rapidly dissipates into the particle through e
222 by surface control using surface charges and adsorbates, reaching a low temperature value more than 2
223 investigated, which depends on the competing adsorbates' relative adsorbabilities and if they adsorb
224 known-competitor adsorbates decrease target-adsorbate removal in the presence of DOM is investigated
225 ch surfaces, apparently because surfaces and adsorbates restructure to balance CO surface binding and
226 ectrostatic field, and charged impurities or adsorbates, resulting in a tuneable photoresponsivity.
232 le that under-coordinated surface atoms bind adsorbates stronger, thereby providing the atomic-level
237 l stability is dependent on the interplay of adsorbate-substrate and ionic interactions and opens new
239 acroscopic observations assuming a separable adsorbate-substrate interaction and pairwise adsorbate-a
240 explained by a nonlocal modification of the adsorbate-substrate interaction, reflecting a many-body
241 ovide information on adsorbate-adsorbate and adsorbate-substrate interactions and may allow for inver
242 g approach for unraveling the intricacies of adsorbate-substrate interactions that are inaccessible b
244 PA self-organize within SAMs on TS gold: (i) adsorbate-substrate interactions; (ii) gold substrate mo
245 ation of nonequilibrium energy states in the adsorbate-substrate system are proposed and discussed.
246 : on a clean single-layer graphene membrane, adsorbates such as atomic hydrogen and carbon can be see
248 -adsorbate interactions and the formation of adsorbate superlattices that extend beyond an original M
258 tion/desorption processes of porous material-adsorbate systems, such as zeolites and metal-organic fr
259 ecursor for the bond-breaking step is a CHOC adsorbate that preferentially adsorbs on a square ensemb
260 in adsorption energies of a wide variety of adsorbates that attach to transition metal surfaces thro
261 patterning of platinum surfaces with cyanide adsorbates that can efficiently block the sites for adso
262 esults in vibrational energy migration among adsorbates that occurs on a twenty times slower timescal
263 By transferring electrons to or from the adsorbate, the process of bond weakening and/or cleavage
264 oiting the nonlinear optical response of the adsorbate, the temporal correlation of headgroup adsorpt
265 the nonzero intercept of a SPR shift versus adsorbate thickness calibration and incorporated into th
266 ion shows greater consistency over different adsorbate thicknesses and better agreement with theory d
267 ed from Maxwell's equation, particularly for adsorbate thicknesses that are much smaller (<5%) than t
270 tions can sensitively report the presence of adsorbates through their impact on ballistic electron tr
272 surface and transfer of an electron from the adsorbate to the metal center, resulting in reduction of
273 e-Frenkel conduction threshold can stimulate adsorbates to desorb without heating the sensor substant
274 uch as to study the molecular orientation of adsorbates to films or protein conformation upon adsorpt
275 ent-like character in the binding of surface adsorbates to GaP, which results in a more rigid hydroge
276 f mechanical strain on the binding energy of adsorbates to late transition metals is believed to be e
277 e of surface oxygen vacancies, electrons and adsorbates to the electrochemical polarization at the ce
279 ocess takes 13-36 h depending on the type of adsorbate used to functionalize the nanostructures.
281 rated through exposure of particles to three adsorbate vapors at 230 degrees C: phenol, 2-monochlorop
284 the average amount of charge carried by each adsorbate, we find that the PAH is associated with only
285 nyl chloride as a model electron-withdrawing adsorbate, we show that reversible adsorption sites can
286 ection of energized charge carriers into the adsorbate, which can result in chemical transformations.
287 he position and orientation of the molecular adsorbates, which in turn determine the origin, directio
288 heterostructures are devoid of wrinkles and adsorbates, which is critical for 2D nanoelectronics.
292 opy (TERS) provides chemical information for adsorbates with nanoscale spatial resolution, single-mol
293 covery system (GRS) using ACFC-ESA for three adsorbates with relative pressures between 8.3 x 10(-5)
294 alkyl chain crystallinity; SAMs formed from adsorbates with short alkyl chains (n = 5) are ordered a
297 e original characteristic energy (Eo), i.e., adsorbates with tendency to form stronger interactions w
298 tion, connecting binding energies of complex adsorbates with those of simpler ones (e.g., C, O), is u
299 ces reaction of both of the C-I bonds in the adsorbate, with an order-of-magnitude greater efficiency
300 oncentrations>5 muM, tetrahedral monodentate adsorbates (Zn-O 1.98 A) dominated, transitioning to a Z
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