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1 us electron transfer was not affected by the electrode potential.
2 olecular dynamics simulations under constant electrode potential.
3 al-independent, the barrier reduces with the electrode potential.
4 olecule interaction can also be tuned by the electrode potential.
5 for the restructuring, itself induced by the electrode potential.
6  the oxidation states of Cu, and the applied electrode potential.
7 orbate configurations, and the effect of the electrode potential.
8  can be controlled externally by the working electrode potential.
9 passive layer evolution as a function of the electrode potential.
10 ransfer kinetics on the electrode at a given electrode potential.
11 small current-induced drift in the reference electrode potential.
12  (graphene oxide), producing a negative-rise electrode potential.
13  at a fixed energy while varying at will the electrode potential.
14 ution and a careful control of the reference electrode potential.
15 ctance of 1 is independent of the pH and the electrode potential.
16 adlayer structure was found to depend on the electrode potential.
17 s constantly held at the reversible hydrogen electrode potential.
18 rids is achieved by simple adjustment of the electrode potential.
19 crease in the absolute value of the negative electrode potential.
20  to the mediator and variations in reference electrode potential.
21 he electrochemical process to proceed at low electrode potentials.
22 trode surface and its behavior under varying electrode potentials.
23 ulations over a broad range of pressures and electrode potentials.
24 oenrichment and SERS screening for different electrode potentials.
25 rious side reactions in the presence of high electrode potentials.
26 t exhibited highly reproducible electrode-to-electrode potentials.
27 ented, based on surface charge densities and electrode potentials.
28  nitrogen and hydrogen over a broad range of electrode potentials.
29 ibit significantly different ferrocene-based electrode potentials.
30 n the substrate electronic properties and at electrode potentials 0.5-1.2 V lower than that of direct
31 c relationship between activation energy and electrode potential, a rather simple expression for prot
32  material is inactive, the application of an electrode potential activates the material by the format
33 or the high selectivity as a function of the electrode potential: aldehyde and ketone at low potentia
34 how how the continuous cyclic application of electrode potential allows Pt nanoparticles to electroox
35 ntal factors, including pressure and various electrode potentials along the ion path.
36 E(0)) for oxidation), where E is the applied electrode potential, alpha (~1/2) is the transfer coeffi
37                                   Increasing electrode potential and associated EET current leads to
38 f Pu(IV), which is produced by adjusting the electrode potential and can be released by electroreduct
39 dented ~100% Faradaic efficiency across wide electrode potential and reactant concentration ranges.
40  The features of ECL intensity responsive to electrode potential and solution pH under ambient condit
41                                          The electrode potential and the ellipsometric signal (corres
42 ealing because they provide a stable counter-electrode potential and typically avoid interference wit
43  to distinct changes in rates in response to electrode potential, and hence, disparate Tafel slopes.
44 ering the electronic band structure, varying electrode potential, and morphological diversity.
45 s (u(i)), determined by reactant activities, electrode potential, and temperature.
46                                      Maps of electrode potential as a function of current and frequen
47 c polarization conditions, using the applied electrode potential as a probe to form catalytically act
48  polymer recharging in order to maintain the electrode potential at a constant level when (i) ions ar
49                                   Reversible electrode potentials at 298 degrees K for the redox medi
50 ing bipolar electrochemistry with the actual electrode potentials being self-regulated by the redox p
51 ectrode, redox buffers were able to maintain electrode potentials below the onset of water electrolys
52 e of complementary DNA target influences the electrode potential, besides the current, owing to chang
53 es PFE allow control of redox states via the electrode potential but also the immobilized state of th
54 yield for H2 production as a function of the electrode potential, but the main finding is that CO2 re
55 nstrates the synthetic possibility of tuning electrode potentials by over a volt, with profound impli
56 e model evaluates the gating charges and the electrode potentials (c.f. measured voltage) upon charge
57 mulation also reveals that the diffusion and electrode potential cause the differences in signal cros
58 d independent electrooxidation behavior with electrode potential changes.
59 ynamic nature of water as a solvent, and the electrode potentials considered.
60          Therefore, we demonstrated that the electrode potential could effectively and reversibly mod
61                               The networked, electrode potential (current) spike generating electroch
62 ics and kinetics for the air cathode through electrode potential decoupling monitoring, oxygen bubble
63                  In the presence of DFP, the electrode potential decreases rapidly with time due to t
64 electroanalytical techniques reveal that the electrode potential depends on both current and frequenc
65  shown that under appropriate conditions the electrode potential determines the quasi-Fermi level thr
66 in end-tidal pH(2) indicate the variation of electrode potential during daily activities in healthy h
67 the potential sufficiently past the standard electrode potential, E degrees , of the pumping redox sp
68       This average i is reported against the electrode potential, E.
69   The dependence of TFTPA conductance on the electrode potential (electrode Fermi level) suggests a L
70  furfural reduction by rationally tuning the electrode potential, electrolyte pH, and furfural concen
71 nce intensities as a function of the applied electrode potential enables construction of an effective
72    In this way, an oxidation reaction at low electrode potentials enables homogeneous reduction of ar
73 e temperature dependencies of the reversible electrode potentials for a number of charge transfer rea
74 d from < 75 nm to > 15 microm by varying the electrode potential from -600 mV to more than -1000 mV,
75 ow unusual dependences of catalytic rates on electrode potential have stark similarities with electro
76 , to synchronously obtain spatially resolved electrode potential (i.e., electrochemical activity) and
77 experimental and simulation studies, and the electrode potential identified as the corresponding driv
78 arious approaches for maintaining a constant electrode potential in electronic structure calculations
79  hydrogen ion (H(+))/H(2) ratio suggests the electrode potential in the solution according to the Ner
80  changes in pH(2) indicated the variation of electrode potential in the solution and whether changes
81  O(2) and reduces O(2) at exceptionally high electrode potentials in the range of +700 to +540 mV vs
82 can be conveniently combined to maximize the electrode potential increase.
83                                          The electrode potential-induced electromagnetic enhancement
84 s via the combination of external stimuli of electrode potential, internal modulation of molecular st
85 c character of Ni(x)(Fe(1-x))O(y)H(z) as the electrode potential is cycled between the resting (here
86 not induced electrochemically if the imposed electrode potential is in the mid-physiological range.
87  cation-induced cathodic corrosion, when the electrode potential is more negative than an onset value
88                                       As the electrode potential is swept to positive potentials thro
89 o strongly bound water is monitored when the electrode potential is varied in the H(upd) range in bot
90  configuration and adjustment of the working electrode potential, it was found that reserpine oxidati
91 conduction band edge down at a given working electrode potential, leading to an increased surface ele
92 usion coefficient-also respond reversibly to electrode potential, likely as a result of Li(+)/EC inte
93 ddition, and breaking the universal standard electrode potential linear scaling relations.
94 t it exhibits linear responses to changes in electrode potential, making the ROMIAC suitable for mobi
95 king electrode, the solvent systems, and the electrode potentials necessary to accumulate and strip t
96 0% selectivity on a carbon basis at a modest electrode potential of -0.536 V vs. the reversible hydro
97                            While a sustained electrode potential of -0.85 V fails to reduce the disul
98 ated ATH434 exhibits a chemically reversible electrode potential of 328.5 mV, unique to all antioxida
99                          In this method, the electrode potential of a SC-ISE is reset by short-circui
100 nt interactions, which together decrease the electrode potential of the Np(VI)/Np(V) couple by up to
101 e amperometric EC detection circuit provides electrode potentials of +/-2 VDC and gains of 1, 10, and
102 e initial and final phases, and the standard electrode potentials of the active electrodes.
103     Thermogalvanic effect, the dependence of electrode potential on temperature, can construct such c
104 inciples dictating the impact of the applied electrode potential on the vibrational probe frequency i
105 s redox capacitive charging as a function of electrode potential one not only reproduces observations
106 ns were identified on-site by monitoring the electrode potential online.
107                           Modulations of the electrode potential or catalytic turnover result in the
108                                          For electrode potentials outside the redox-active region, th
109                 We assessed the impact of 11 electrode potentials ranging from -0.45V to +0.2V vs. Ag
110 EMPM are controlled by switching the working electrode potential, rather than via a switch in mobile-
111  model, such as solvation, electrolyte ions, electrode potential, reaction kinetics, and pH.
112  rate on CpFe concentration, film thickness, electrode potential relative to the CpFe formal potentia
113 of MXene oxidation and its dependence on the electrode potential remain poorly understood.
114               Here, we establish the minimum electrode potentials required for fast Cu oxidation (-0.
115 and adsorbate coverages as a function of the electrode potential, revealing the presence of hydrogen
116   This reaction is enabled by time-dependent electrode potential sequences, combined with monolayer-s
117 -terminated BDF can be tuned by changing the electrode potentials showing clearly an off/on/off singl
118   We propose an alternative method here, the electrode potential slope (EPS) analysis, to enable quan
119 bination of cyclic voltammetry analysis with electrode potential studies suggests that Ni(I) species
120 e catalyst reduction potential as well as an electrode potential study provides a convenient route fo
121                              Controlling the electrode potential such that the film mediates oxidatio
122 cal decomposition rate was controlled by the electrode potential, suggesting a rare example of a liqu
123  a result, we establish correlations between electrode potential TCs and Li-ion solvation structures
124 ore this phenomenon, we compare the Li/Li(+) electrode potential TCs in a series of electrolyte formu
125 ever, the fundamental significance of single electrode potential TCs is little known.
126        We show that measurements of Li/Li(+) electrode potential TCs provide valuable knowledge regar
127 icantly contributes to the measured Li/Li(+) electrode potential TCs.
128  driven in either direction depending on the electrode potential that is applied.
129 introducing molecular changes by the applied electrode potential, the highly effective SERS intensity
130       The data show that at a characteristic electrode potential, the low affinity of polyene chains
131 cope and a bipotentiostat for control of the electrode potential, the oxidation and reduction process
132                       At neutral or positive electrode potentials, this 'free-OD' peak disappears abr
133  be accelerated either by tuning the working electrode potential to a more negative value or by lower
134 cated single-molecule junctions by using the electrode potential to control the molecular orientation
135 hanical switch that controllably employs the electrode potential to orient the molecule in the juncti
136 ortantly, our approach allows us to vary the electrode potential to promote the fragmentation of etha
137                                Switching the electrode potential to reducing conditions reverses the
138                                Switching the electrode potential to temporarily favor either an anodi
139 is suggests the intriguing prospect of using electrode potential to tune surface interactions and to
140 ons required multiple HPLC runs at different electrode potentials to construct hydrodynamic current-p
141                             Depending on the electrode potential, two successive catalytic pathways h
142 2)H(4) conversion as function of the applied electrode potential using differentially pumped electroc
143 to TPB*+ radical cation as a function of the electrode potential was achieved via selective ion monit
144  the formation of TPB2+ as a function of the electrode potential was also monitored.
145 n, PdRox:NAD+ + 2e- --> PdRrd:NAD+, when the electrode potential was lowered.
146                             The variation of electrode potential was obtained by multiplying the pH(2
147 e from the electrode (ca. 75 mum), while the electrode potential was varied in time.
148 tion of Na(+) and OH(-) at the same absolute electrode potential, we demonstrate that higher concentr
149                               Changes in the electrode potential were proportional to ([Formula: see
150 presence of MnO2 also positively shifted the electrode potential window of sodium removal, reducing p
151 eal the origin of C-N coupling under a small electrode potential window with both the dynamic nature
152 eactions are avoided by maintaining the gold electrode potential within the ideally polarizable regio

 
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