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1 is designed to modulate the properties of an electrolyte solution.
2 ing the electric field within the contacting electrolyte solution.
3 opy (SEM), and resistance measurements in an electrolyte solution.
4 with a contact (reference) electrode and an electrolyte solution.
5 provided for high-resolution STM imaging in electrolyte solution.
6 ate perfusion of the jejunum with a balanced electrolyte solution.
7 above by immersing them in a TPrA-containing electrolyte solution.
8 dium or water during perfusion of a balanced electrolyte solution.
9 ss polar medium than that of the surrounding electrolyte solution.
10 adhered on the tape during experiments in an electrolyte solution.
11 od cells, and cancer cells from a suspending electrolyte solution.
12 fabrication until dissolved by an ultrapure electrolyte solution.
13 aphy imaging of single nanostructures in the electrolyte solution.
14 tact method was found to leak Ag(+) into the electrolyte solution.
15 K(a) of a proton relay matches the pH of the electrolyte solution.
16 and LiNi(0.5)Mn(1.5)O4 (LNMO)) into the same electrolyte solution.
17 face between porous carbon electrodes and an electrolyte solution.
18 trode (NiO-RuRe) was confirmed in an aqueous electrolyte solution.
19 limited if the surface is in contact with an electrolyte solution.
20 rce by simple modification of the sustaining electrolyte solution.
21 ppropriately selecting the salt anion in the electrolyte solution.
22 urrent signals of a redox probe taken in the electrolyte solution.
23 ional reference electrode with its reference electrolyte solution.
24 ated for the first time in the absence of an electrolyte solution.
25 on on unpatterned substrates in an isotropic electrolyte solution.
26 in the whole membrane was influenced by the electrolyte solution.
27 nanopores can transiently localize DNA in an electrolyte solution.
28 balt oxide materials from phosphate-buffered electrolyte solutions.
29 ons, followed by flushing with particle-free electrolyte solutions.
30 ion increases dramatically on > 30-muM inert electrolyte solutions.
31 enzoyl peroxide as a coreactant in the above electrolyte solutions.
32 (-)] = 0.15 M, [Ca(2+)] = 0 - 75 mM) aqueous electrolyte solutions.
33 ty measurements of the interface between two electrolyte solutions.
34 ater at the Ag-water interface in NaF and KF electrolyte solutions.
35 te the photophysics and chemistry of aqueous electrolyte solutions.
36 sisted anion transfer between two immiscible electrolyte solutions.
37 ubstituted tetraphenylborate in both aqueous electrolyte solutions.
38 edefined upon hydration owing to swelling in electrolyte solutions.
39 e nanoscale interface between two immiscible electrolyte solutions.
40 n batteries with standard non-aqueous liquid electrolyte solutions.
41 estimate the solubility of gypsum in aqueous electrolyte solutions.
42 cles at the interface between two immiscible electrolyte solutions.
43 ode in chloride-containing and chloride-free electrolyte solutions.
44 s" based on their impact on the viscosity of electrolyte solutions.
45 f Li2O2 in low-polarity and weakly solvating electrolyte solutions.
46 , perchlorate-, sulfate-, and chloride-based electrolyte solutions.
47 trends in mean activity coefficients of the electrolyte solutions.
48 ke on the role of ions in traditional dilute electrolyte solutions.
49 charged redox species as expected for dilute electrolyte solutions.
50 -supported interfaces between two immiscible electrolyte solutions.
51 liquid-junction potentials between miscible electrolyte solutions.
52 ase (SCD) lyse in deoxygenated isosmotic non-electrolyte solutions.
53 whereas the water uptake was lower in 0.1 M electrolyte solutions.
54 t surface layers transferrable to fresh base electrolyte solutions.
56 included: split-dose 6-L polyethylene glycol-electrolyte solution, a gastroenterology electronic note
58 efficiency of the calcium pump in background electrolyte solutions, a complexometric titration with k
59 rted ITIES (interface between two immiscible electrolyte solutions, also called a liquid/liquid (L/L)
60 SICM employs a nanopipette tip that contains electrolyte solution and a quasi-reference counter elect
61 serted inside a nanopipette probe containing electrolyte solution and a second electrode placed in a
64 ccelerated the redox couple diffusion in the electrolyte solution and improved charge transfer at the
65 region between the electrode surface and the electrolyte solution and is often characterized by numer
66 ion of uncompensated ohmic resistance of the electrolyte solution and of the adsorbed film, as distin
68 M]O(2) cells cycled with a low amount of the electrolyte solution and practical cycling parameters.
69 s a dual-barrel theta pipet probe containing electrolyte solution and quasi-reference counter electro
70 ollowing their first contact with an aqueous electrolyte solution and used these transients to determ
71 ertion was evaluated in concentrated aqueous electrolyte solutions and aprotic electrolytes as well.
72 do not simply form coils in acidic or strong electrolyte solutions and elongated structures in dilute
73 se nanoparticles can be transferred to fresh electrolyte solutions and there exhibit stable ferrocene
74 NMs by allowing the membrane to separate two electrolyte solutions and using an electrode in each sol
77 endence of the applied potentials within the electrolyte solution, and most importantly the shift of
78 led pipet and filling the open channels with electrolyte solution, and quasi-reference counter electr
79 ally, conditioning creates free Cl(-) in the electrolyte solution, and we suggest the free Cl(-) adso
80 ation of Li metal anodes, consumption of the electrolyte solutions, and limited cycle life of full Li
81 by placing the nanotube membrane between two electrolyte solutions, applying a transmembrane potentia
82 an electrochemically inactive monolayer and electrolyte solution are also simulated as a function of
83 ractions of Mn(3+) in the aprotic nonaqueous electrolyte solution are constant over the duration of o
84 s, in particular the transference number, of electrolyte solutions are important design parameters fo
88 t-supported interface between two immiscible electrolyte solutions as an SECM probe not only to image
89 tion potential between two mutually miscible electrolyte solutions, as commonly described with the He
90 ntaining good ionic conductivity for aqueous electrolyte solution at pH 9, where the redox-active org
91 olutions in the pH range of 3-14, in <250 mM electrolyte solutions, at high and low temperatures (95
93 tions of poor reductive stability of aqueous electrolyte solutions, broadening their electrochemical
94 ive to electric double layer interactions in electrolyte solutions, but provides only a qualitative v
95 out electron transfer between two immiscible electrolyte solutions, but to the best of our knowledge,
96 vironment enabled simple manipulation of the electrolyte solution by adjusting the bulk pH and buffer
98 d Au(100) and Au(111) electrodes immersed in electrolyte solution by implementing finite-field method
99 mum in the surface tension of dilute aqueous electrolyte solutions by Jones and Ray in the 1930s is c
100 ween the nanochannel surface and the aqueous electrolyte solution, causing significant changes in mea
102 Understanding how applied potentials and electrolyte solution conditions affect interfacial proto
103 +/- 0.02, which exceeds that of the bathing electrolyte solution conductivity, Q(10) = 1.17 +/- 0.01
104 cycling between 3.5 and 4.5 V vs Li/Li(+) in electrolyte solution containing 1 M LiPF6 or LiClO4 in 1
105 re experimentally characterized in different electrolyte solutions containing a range of mono-, di-,
106 ractive force between identical macroions in electrolyte solutions containing divalent counterions.
108 ane (100-nm-diam pore size) hydrated with an electrolyte solution, containing a redox-active probe mo
110 ectrode in contact with a non-aqueous liquid electrolyte solution could provide useful insights that
111 In pH 2 citrate buffer with added NaClO4 electrolyte, solution cyclic voltammetry of these nanopa
112 se molecules to muscovite mica in an aqueous electrolyte solution demonstrates that direct intramolec
116 se of conventional organic-based non-aqueous electrolyte solutions enables the formation of interphas
117 Laplace's equation has been solved for the electrolyte solution for a range of tip geometries, enab
118 ygen-carrying blood substitute, colloid, and electrolyte solution for limited fluid resuscitation wit
119 isms for ethylene carbonate (EC) molecule in electrolyte solutions for lithium-ion batteries are comp
120 , which is contacted at its edges by aqueous electrolyte solution, has been characterized electrochem
121 Previous NO gas sensors that employ internal electrolyte solutions have been assembled using acidic i
124 e electrochemical instability of ether-based electrolyte solutions hinders their practical applicatio
125 e range of current densities in contact with electrolyte solutions, IEDEM behave as ideally non-polar
126 ic polymer semiconductors interfaced with an electrolyte solution in a closed sandwich architecture i
127 a hydrophilic sorbent supporting an aqueous electrolyte solution in a four-phase electric-field-assi
128 t Prussian blue (PB) film in contact with an electrolyte solution in a separate detection compartment
129 metal anode and a non-aqueous NaClO(4)-based electrolyte solution in coin cell configuration, the CuM
130 t interaction and use the dilute non-aqueous electrolyte solution in high-voltage lithium metal batte
131 ode using additional non-aqueous fluorinated electrolyte solution in lab-scale pouch cell configurati
132 electrode with an ionic liquid-based liquid electrolyte solution in pouch cell configuration, we rep
133 ly, when sufficient voltage is applied to an electrolyte solution in which a BPE is immersed, the pot
134 simultaneously by applying a voltage to the electrolyte solution in which the BPE array is immersed.
135 y detect (13)C signals on formulated battery electrolyte solutions in different degradation stages on
136 The use of aqueous/non-aqueous biphasic electrolyte solutions in Li-based battery systems circum
138 ace identifies six fast-charging non-aqueous electrolyte solutions in two work-days and forty-two exp
140 from the sensor surface and the salinity of electrolyte solution, in the framework of both linear an
141 a liquid/liquid interface between immiscible electrolyte solutions, in which the ion transfer approac
142 ene and the electrochemical potential of the electrolyte solution, indicating that the n-Si/Graphene
144 crom) containing an electroactive species in electrolyte solution is brought to a sample electrode su
147 approach for positioning the UME in aqueous electrolyte solution is presented using either changes o
148 o promote solution-phase discharge in stable electrolyte solutions is a central challenge for develop
149 escribe structure and dynamics of nonaqueous electrolyte solutions is challenging, and experimental o
150 ctions between proteins and nanoparticles in electrolyte solutions is crucial for advancing biologica
151 nts of natural gas in pure water and aqueous electrolyte solutions is important in terms of engineeri
153 composition reactions of lithium-ion battery electrolyte solutions is of critical importance in contr
154 t across an interface between two immiscible electrolyte solutions (ITIES) and its diffusion into the
155 dies at the interface between two immiscible electrolyte solutions (ITIES) are often performed to det
156 sfer at the interface between two immiscible electrolyte solutions (ITIES) as a platform to study pro
158 Unlike the interface between two immiscible electrolyte solutions (ITIES) formed between water and p
162 A nanoscale interface between two immiscible electrolyte solutions (ITIES) provides a unique analytic
163 de based on interface between two immiscible electrolyte solutions (ITIES) to achieve in vivo measure
164 stry at the interface between two immiscible electrolyte solutions (ITIES) to investigate changes in
165 try with an interface between two immiscible electrolyte solutions (ITIES) to mimic the NE interface,
166 -supported interfaces between two immiscible electrolyte solutions (ITIES) to quantitatively study tr
167 t-supported interface between two immiscible electrolyte solutions (ITIES) to reveal the important io
168 t-supported interface between two immiscible electrolyte solutions (ITIES) were carried out, and the
169 e polarized interface between two immiscible electrolyte solutions (ITIES) with ion transfer voltamme
173 arboxylate) followed by soaking in a typical electrolyte solution leads to the new solid lithium elec
174 on (IGL-1) is an emerging extracellular-type electrolyte solution, low in viscosity, containing polye
175 ion that fluid resuscitation with unbuffered electrolyte solutions may cause harm and their use shoul
176 to humidity prior to their first contact to electrolyte solution minimizes the initial (reproducible
177 tinum UME remains unchanged from the aqueous electrolyte solution mixed potential until approximately
179 microscale interfaces between two immiscible electrolyte solutions (muITIES) were formed using glass
182 across nanointerfaces between two immiscible electrolyte solutions (nanoITIES); (2) combined atomic f
183 iguration of this hybrid power cell, aqueous electrolyte solution of PVA-MnO(2)-Eosin Y has been util
184 rine at a ratio of 5:1 are simulated in NaCl electrolyte solutions of different concentration using t
185 nt dissolved manganese cation in LiPF6-based electrolyte solutions of Li-ion batteries with lithium m
186 emical behaviour of caffeine was examined in electrolyte solutions of phosphate buffer saline, sodium
187 on-bridged cations in the ion atmosphere for electrolyte solutions of salts with reduced activity.
188 ing pipet electrodes filled with the organic electrolyte solutions of their tetrakis(4-chlorophenyl)b
189 ance (e.g., due to solubility in the battery electrolyte solution or low internal surface area).
190 s a highly active electrocatalyst in aqueous electrolyte solution (overpotential of approximately 200
191 This novel design is based on the flow of electrolyte solution past a microwire electrode situated
193 rents of around -10 muA cm(-2) in an aqueous electrolyte solution (pH 5.5) with a photocurrent onset
194 including charged molecules, ionic liquids, electrolyte solutions, polar dipeptides, surface adsorpt
195 tients received either a polyethylene glycol electrolyte solution preparation or a phospho-soda prepa
198 anodic polarization using an inner alkaline electrolyte solution provides the basis for improved sel
199 pH 7 and under conditions of flowing aqueous electrolyte solutions ranging in NaCl concentrations fro
200 OM carbon, filling of the 3DOM pores with an electrolyte solution results in a nanostructured materia
201 baseline experiment that uses a non-aqueous electrolyte solution selected a priori from the design s
202 tal electrodes, we demonstrate that KFSI:DME electrolyte solutions show higher salt diffusion coeffic
203 The prepared 0.5 M NaFSI in PreTFSI (SIPS5) electrolyte solution shows an electrochemical stability
204 how solubility can be tuned by modifying the electrolyte solution structure or by tailoring the molec
205 rgo sol-gel transition in the presence of an electrolyte solution such as biological fluids and salts
206 ons of the liquid-vapor interface of aqueous electrolyte solutions suggest that ions little larger th
207 The electrical energy generates heat in an electrolyte solution surrounding the electrode, and the
208 amic properties of a model non-aqueous K-ion electrolyte solution system comprising potassium bis(flu
209 (often of the brand named Vycor) contain the electrolyte solution that forms a salt bridge between th
210 s glass plugs are widely used to contain the electrolyte solution that forms a salt bridge between th
211 ses the resistive heating of the surrounding electrolyte solution that leads also to the electrotherm
212 d poly(vinyl chloride) (PVC) membrane and an electrolyte solution that was triggered via the oxidatio
213 y on Pt electrodes from CH(3)CN/Bu(4)NClO(4) electrolyte solutions that films comprised of 1-2 monola
214 opipette is positioned close to a surface in electrolyte solution, the direct ion current (DC), drive
215 al expectations, for charged macroions in an electrolyte solution, the entropic force is repulsive at
218 vours the ion-transport properties in liquid electrolyte solutions, thus, making KIBs potentially cap
219 n order to transfer analytes from a volatile electrolyte solution to the gas-phase as a single-charge
220 nsfer of charge-compensating anions from the electrolyte solution to the monolayer nanoparticle "phas
221 ported interface between aqueous and organic electrolyte solutions to confirm that larger GR(n) among
222 eposited MWNTs were then rinsed at different electrolyte solutions to induce the release of MWNTs fro
224 cts on characteristic time scale in a binary electrolyte solution using parallel plate electrode conf
225 lavage with warmed polyethylene glycol 3350/electrolyte solution via the ileostomy and postoperative
227 ition from gas-phase clusters to behavior of electrolyte solutions was clearly revealed, and the larg
229 a generator-collector device submerged in an electrolyte solution, were carried out to calibrate the
231 AA7075-T73 aluminum alloy in a 3.5 wt % NaCl electrolyte solution, which is typically challenging in
232 The 2D crystalline systems form in aqueous electrolyte solution, which provides a high dielectric e
233 at in a non-polar dipropyl ether (DPE)-based electrolyte solution with lithium bis(fluorosulfonyl) im
234 noise in baseline conductance upon mixing an electrolyte solution with water, and dispersion/relative
235 ting the onset potential of *CO formation in electrolyte solutions with a lower carbonate concentrati
238 uantification of supported lipid bilayers in electrolyte solutions with nanoscale spatial resolution.
239 s and concomitant solvent molecules from the electrolyte solution, with gaseous propylene molecules t
240 iquids are expected to behave as dilute weak electrolyte solutions, with typical effective dissociate
241 cles can be transferred to nanoparticle-free electrolyte solutions without desorption and ferrocene v