ライフサイエンスコーパス: voltammogram

1 rate without appreciable perturbation of the voltammogram.

2 r scan rates and on the reverse sweep of the voltammogram.

3 the spacing the more sigmoidal the recorded voltammogram.

4 the temporal delay prior to acquisition of a voltammogram.

5 al modeling and quantitative analysis of the voltammogram.

6 rograms are sampled once to produce a single voltammogram.

7 otential curve akin to a pseudo steady state voltammogram.

8 lso by SECM but is not obvious from a cyclic voltammogram.

9 d from symmetric pairs of reversible nanogap voltammograms.

10 being supported by simulations of the cyclic voltammograms.

11 the effect of V and d on the shape of cyclic voltammograms.

12 s of rapid IT processes extracted from pipet voltammograms.

13 ed and used for analysis of steady-state tip voltammograms.

14 requires a single effort of simulating many voltammograms.

15 n of substances that give overlapping cyclic voltammograms.

16 to construct hydrodynamic current-potential voltammograms.

17 mallest electrodes producing strongly peaked voltammograms.

18 ent plateau analysis of the catalytic cyclic voltammograms.

19 ity ratios has been found when analysing the voltammograms.

20 surface stress closely resembles the cyclic voltammograms.

21 In each voltammogram a single point of zero net current denotes

22 NCO) displays two redox events in the cyclic voltammogram: a quasireversible event -0.11 V vs Fc/Fc(+

23 Catecholamine voltammograms acquired with platinum electrodes exhibite

24 able sigmoidal shape of a quasi-steady-state voltammogram although a transient voltammogram is obtain

25 The observed double-transfer voltammogram, although it has been largely neglected in

26 This leads to a broader voltammogram and a decreased wave slope, which can be so

27 Electrochemical detections as cyclic voltammogram and rotating ring-disk electrode tests show

28 The shape of the cyclic voltammogram and the magnitude of the steady-state limit

29 n this area involve the comparison of cyclic voltammograms and (near-infrared) optical absorption spe

30 Reversible voltammograms and a voltammetry half-wave potential vers

31 of electrochemical methods including cyclic voltammograms and amperometric images of high spatial an

32 developed to successfully obtain reversible voltammograms and E degrees 's of the very high-potentia

33 tion of the effects of the parameters on the voltammograms and for rapid simultaneous estimation of m

34 obust, surviving up to 50 consecutive cyclic voltammograms and sonication.

35 the basis of numerical simulations of cyclic voltammograms and voltabsorptograms and within the frame

36 best fits of simulations to the experimental voltammograms and voltabsorptograms, the partition coeff

37 ble repeatability over 20 cycles in a cyclic voltammogram, and reproducibility with root mean square

38 We apply this model to ensure that stripping voltammograms are based on desorption of all protamine m

39 ochemical parameters extracted from snapshot voltammograms are in good agreement with those obtained

40 The cyclic voltammograms are numerically analyzed to determine form

41 In fact, symmetric pairs of nanogap voltammograms are obtained with the cleaner HOPG surface

42 sweep, square-wave, and adsorptive-stripping voltammograms are recorded while electrokinetically "pum

43 st, the asymmetric shape and peak current of voltammograms are used to demonstrate that a Ca(2+)-sele

44 imited steady-state current and steady-state voltammogram at an UME-NEE.

45 It was shown that the cathodic peak in voltammograms at about -250 mV vs. Ag/AgCl can be associ

46 eversible square-wave and differential pulse voltammograms at acidic pH.

47 eversible square-wave and differential pulse voltammograms at alkaline pH.

48 The cyclic voltammograms at microdisk electrode arrays are grouped

49 By comparison, the well-defined cyclic voltammograms at Nafion gel-modified electrodes exhibit

50 d to be -595 mV from quasi-reversible cyclic voltammograms at pH = 10.8, and the pH-dependent E(1/2)

51 a) sizable potential splitting in the cyclic voltammogram, (b) quinonoidal distortion of T(*)(+)/T ce

52 rucial to obtaining reliable sampled-current voltammograms below 100 ms.

53 current and peak potential of the thin-layer voltammogram, but also the symmetry of the peak shape wi

54 Analysis of FT-ac voltammograms by theory based on stationary microband or

55 mpact look-up tables, from which approximate voltammograms can be calculated rapidly by interpolation

56 ted electrochemical array data (hydrodynamic voltammograms) can be used to identify carotenoids as we

57 arly useful for microelectrodes where cyclic voltammograms change shape as the mass transport regime

58 The resulting steady-state IT voltammogram comprises two waves corresponding to the in

59 Cyclic voltammograms, confirmed by in vitro testing, revealed t

60 reaction results in a characteristic cyclic voltammogram containing a pre-peak to the reduction curr

61 Cyclic voltammogram (CV) and amperometry were employed to study

62 e analysis of the resulting transient cyclic voltammogram (CV) with a sigmoidal forward wave followed

63 Cyclic voltammograms (CV) showed an irreversible oxidation peak

64 r extracting kinetic information from cyclic voltammograms (CVs) obtained in conditions under which t

65 ation and to manipulate the shapes of cyclic voltammograms (CVs) of analytes which oxidize at the swi

66 The cyclic voltammograms (CVs) of the modified GC electrode showed

67 Cyclic voltammograms (CVs) of the native Au/Ag(UPD) electrode i

68 Cyclic voltammogram data and simulations, together with computa

69 Multiple linear regression analysis of voltammograms demonstrated that the hydroxyl radical is

70 nalysis of the kinetically controlled cyclic voltammograms demonstrates for the first time that forma

71 idization is monitored by differential pulse voltammogram (DPV).

72 roelectrode, the molten salts exhibit cyclic voltammograms due to the physical diffusion (D(PHYS)) of

73 y satisfactorily reproduced the experimental voltammograms during the forward and backward potential

74 ulated SECM approach curves, images, and tip voltammograms enabled the fraction of active area and di

75 Experimentally, a symmetric voltammogram ensures the formation of a 1:1 complex for

76 Cp linkages; Cp = cyclopentadienyl) solution voltammograms exhibit well-resolved, separated 1e(-) wav

77 Analysis of commercial white wines gave voltammograms featuring two unresolved anodic waves corr

78 A chemically reversible cyclic voltammogram for HIBA was observed on this modified carb

79 asi-reversible, irreversible, and reversible voltammograms for a simple electron transfer reaction at

80 nt between experimental and simulated cyclic voltammograms for electrochemical oxidation of LiNO2 in

81 provide the electrochemical signature cyclic voltammograms for molecular identification.

82 he potential dependent current in the cyclic voltammograms for pH changes recorded in vivo was unclea

83 Cyclic voltammograms for reduction of 1-5 exhibit two irreversi

84 Cyclic voltammograms for the gel-entrapped ferrocene methanol (

85 Well-defined voltammograms for the redox reactions of ferrocene and t

86 Cyclic voltammograms for these ultramicroelectrodes obtained in

87 trodes (Glass/ITO), obtaining a linear sweep voltammogram from 0.1 V, where Ag(0) is stable, up to 1.

88 The peak current of cyclic voltammograms from a PAPP solution incubated inside the

89 The peak current of cyclic voltammograms from a PAPP solution, in which gold-coated

90 Cyclic voltammograms from the biofluid exhibit responses that a

91 eveloped to describe the features of the tip voltammograms generated under tpf, ts, or pf-ps conditio

92 CL) to provide a means for recording optical voltammograms in a single micrograph.

93 Simulations of the cyclic voltammograms in combination with DFT (density functiona

94 Hydrodynamic voltammograms in dual-electrode (generator-collector) ex

95 nt between simulated and experimental cyclic voltammograms in weak and strong acid and by the detecti

96 od utilizes training sets to separate cyclic voltammograms into contributions from multiple electroac

97 ze and compare the microdisk sampled-current voltammograms irrespective of sampling time.

98 In essence, the information in a snapshot voltammogram is contained in the spatial domain rather t

99 eady-state voltammogram although a transient voltammogram is obtained at the macroscopic substrate.

100 ubstrate within about a tip radius and a tip voltammogram is recorded as its potential is slowly scan

101 itions), a total positive feedback (tpf) tip voltammogram is recorded.

102 rather simple expression for proton transfer voltammograms is derived.

103 ception that the asymmetry of paired nanogap voltammograms is due to electron exchange mediated by Fc

104 Advantageously, a pair of quasi-steady-state voltammograms is obtained by employing both operation mo

105 Based on the cyclic and pulse voltammograms, it was observed that hop extract EI conta

106 ydrogen binding energy, obtained from cyclic voltammograms, linearly increases with the pH.

107 Linear sweep voltammograms (LSVs) obtained on the glass/ITO/Au NP (4

108 The voltammogram obtained from the experiment on polyaniline

109 either side of the membrane and supported by voltammograms obtained for a series of ions of varied li

110 Interpreting voltammograms obtained in the attoliter volume affected

111 Comparison between cyclic voltammograms obtained of this compound as well as of th

112 ity = 866 cP at 20 degrees C) from transient voltammograms obtained using a 1.6 mm diameter Pt electr

113 ransfer rate from the series of steady-state voltammograms obtained using Pt NP-deposited TUMEs.

114 Quantitative fits of experimental voltammograms obtained with an Au(111) electrode modifie

115 This set was used to evaluate cyclic voltammograms obtained with one or two compounds present

116 also resolved from a set of fast-scan cyclic voltammograms obtained with the electrode implanted in a

117 As expected, acquisition of the cyclic voltammogram of 1 in the presence of DNA produced cataly

118 In the presence of triflic acid, the cyclic voltammogram of 1 showed an increase in current at the f

119 The cyclic voltammogram of 2 exhibits both one-electron oxidation a

120 The cyclic voltammogram of 3 reveals two clean, reversible one-elec

121 The cyclic voltammogram of [((H)L)(2)Fe(6)](n+) in acetonitrile rev

122 The cyclic voltammogram of a SAM of 10 showed two well-resolved rev

123 earance of a catalytic current in the cyclic voltammogram of a solution containing the tris(aryl)amin

124 current intensity of the differential pulse voltammogram of adsorbed MB was monitored and found to b

125 of an effective, dynamically recorded cyclic voltammogram of an individual particle.

126 The cyclic voltammogram of I in THF, the EPR spectrum of I(+)PF(6)

127 Peaks in the cyclic voltammogram of PB on Au(110) are sharper than those on

128 o a higher current enhancement in the cyclic voltammogram of Ru(bpy)3(3)+/2+ (bpy = 2,2'-bipyridine)

129 observing current enhancement in the cyclic voltammogram of Ru(dmb)3(3)+/2+ (dmb = 4,4'-dimethyl-2,2

130 A cyclic voltammogram of Spiro-BTA in 1:2 MeCN:benzene/0.1 M Bu(4

131 The well-defined cyclic voltammogram of standard ferri/ferrocyanide is achieved

132 ted in a well-defined and stable square-wave voltammogram of the ferrocene moiety.

133 When M = Co(II), the cyclic voltammogram of the melt shows an oxidative wave due to

134 The voltammogram of the O2(-) anion transfer to the organic

135 The cyclic voltammogram of trigonal bipyramidal 2 displays successi

136 High quality steady-state voltammograms of > or = 1 molecules were obtained for di

137 ses the nonideal asymmetry of paired nanogap voltammograms of (ferrocenylmethyl)trimethylammonium (Fc

138 Cyclic voltammograms of 1 and 2 displayed quasi-reversible redo

139 Simulations of the electrocatalytic cyclic voltammograms of 2 suggest rate-limiting protonation of

140 The cyclic voltammograms of 3-5 reveal significantly larger DeltaE(

141 Specifically, cyclic voltammograms of Ag(+), K(+), Ca(2+), Ba(2+), and Pb(2+)

142 Cyclic voltammograms of CYP79A1 and CYP71E1 revealed reversible

143 o analysis of nearly reversible steady-state voltammograms of either IT at pipet-supported ITIES or e

144 vity coefficients are determined from cyclic voltammograms of excess amounts of analyte and interferi

145 Two signals were observed in voltammograms of HMP adsorbed on Gr, at -477 and -171 mV

146 nt differences were noted between the cyclic voltammograms of housanes bearing a CH2OR substituent ra

147 imaging technique allows us to obtain cyclic voltammograms of multiple droplets on a gold electrode s

148 The cyclic voltammograms of NiCo2O4 electrode using alkaline aqueou

149 Reductive hydrodynamic voltammograms of nitrobenzene, 2,4,6-trinitrotoluene, an

150 Cyclic and square-wave voltammograms of photolyase deposited on these electrode

151 approach to kinetic analysis of steady-state voltammograms of rapid IT reactions.

152 Compared to other nanomaterials, cyclic voltammograms of short GONRs show higher anodic oxidatio

153 ytic reaction current and measure the cyclic voltammograms of single nanoparticles.

154 electron anodic waves observed in the cyclic voltammograms of the bimetallic complexes 4a and 4b is l

155 Cyclic voltammograms of the clusters in acetonitrile display re

156 dence of quasi-reversible features in cyclic voltammograms of the CoO(x)(cf)s provides the basis for

157 The absorption spectra and cyclic voltammograms of the dyads show that the spectroscopic a

158 The cyclic voltammograms of the enzyme electrode after appearance o

159 Cyclic voltammograms of the immobilized hydrogenase films revea

160 hroughout the simulations to generate cyclic voltammograms of the model system.

161 The ion-transfer cyclic voltammograms of the perfluoroalkyl oxoanions are obtain

162 e of double layer charging current in cyclic voltammograms of the resulting 3D nanoelectrode ensemble

163 Cyclic voltammograms of the Ru and Os compounds are not affecte

164 The voltammograms of the samples were then deposited in an a

165 Cyclic voltammograms of the series of triiron clusters presente

166 The cyclic voltammograms of these heterobimetallic complexes show m

167 dependence of the shape of the steady-state voltammogram on kinetic parameters becomes weak when the

168 The nonlinear dependencies of the simulated voltammograms on multiple model parameters are represent

169 ent times yields a family of sampled-current voltammograms, one for each time scale.

170 Acquisition of cyclic voltammograms or chronoamperomograms of Ru(bpy)3(2+) at

171 e is changed, the series of steady-state tip voltammograms provide information about the reactants an

172 ntermediate for Co(II)(dmgBF2)2(CH3CN)2 from voltammograms recorded at 1000 psi of H2.

173 that high-pass filtering (200 Hz) of cyclic voltammograms recorded at 300 V/s decreases the backgrou

174 t various distances into channels and cyclic voltammograms recorded at 300 V/s were repeated at 0.1-s

175 his work, we evaluated the ability of cyclic voltammograms recorded at fast-scan rates to resolve neu

176 Cyclic voltammograms recorded on CpRe(PPh3)(NO)(CMeO), CpRe(PPh

177 It was demonstrated that voltammograms recorded on glassy carbon electrode in Bri

178 isk electrode were remarkably similar to the voltammograms regardless of the position of the microref

179 e generation of background subtracted cyclic voltammograms remarkably free from all but faradaic cont

180 These voltammograms represent the Y32 species at the upper edg

181 on of the optical spectrum and of the cyclic voltammogram, respectively).

182 Experimental tip voltammograms resulting from the reversible reduction of

183 The voltammogram reveals the critical redox features of CFX

184 Es exhibited less deterioration (in terms of voltammogram shapes, stability of peak currents, and app

185 Their cyclic voltammograms show a quasi-reversible process in the cat

186 Advantageously, the resultant thin-layer voltammogram shows no diffusional effect, which simplifi

187 polar electrodes to obtain numerous snapshot voltammograms simultaneously.

188 nce of other molecules that generate similar voltammograms, such as adenosine and histamine.

189 plored, and two of them yielded high-quality voltammograms suitable for kinetic experiments.

190 The peaks current of square wave voltammograms (SWV) of BPA and Sudan I increased linearl

191 Background subtracted square wave voltammograms (SWV) showed the appearance of two peaks a

192 tact ds-DNA to provide catalytic square wave voltammograms (SWV).

193 Cyclic voltammograms taken at 1-s intervals (scan rate 150 V/s)

194 A simulated pulse voltammogram that accounts for the TEM nanoparticle disp

195 ty to 5-HT, yielding a characteristic cyclic voltammogram that is easily distinguishable from other c

196 al, this can cause total shielding (ts) or a voltammogram that is the result of partial feedback/part

197 The result is a series of tip voltammograms that are characterized by tpf, pf-ps, or t

198 er electron transport to give rise to cyclic voltammograms that are distinctively different from thos

199 s are highly redox active and exhibit cyclic voltammograms that are more than just the sum of the met

200 gram, one can predict the type of the cyclic voltammograms that can be expected for different microel

201 nt potential while intermittently collecting voltammograms that indicated that over half of the Ru wa

202 rately simulate subsequently observed cyclic voltammograms (that is, generated current versus potenti

203 By analyzing the entire shapes of catalytic voltammograms, the energetics of the catalytic cycles (r

204 both complexes are determined from a single voltammogram to reveal that the preceding formation of a

205 quasireversible oxidation wave in the cyclic voltammogram to yield the dication species at E(ox)(pa)

206 d experimental (reduction of trans-stilbene) voltammograms to assess the capabilities of parameter re

207 tion that Y32 gives rise to fully reversible voltammograms translates into an estimated lifetime of >

208 ough the simulation of the respective cyclic voltammograms under the same experimental conditions.

209 ace causes only the small hysteresis of each voltammogram upon forward and reverse sweeps of the HOPG

210 The possibility to fit the same experimental voltammogram using different combinations of the standar

211 A calibration set of 30 cyclic voltammograms was constructed from 9 different substance

212 To facilitate qualitative analysis of the voltammograms, we convert the current-potential data rec

213 rameters, the electrochemically irreversible voltammograms were analyzed by assuming a one-step trans

214 Voltammograms were analyzed to extract the electron tran

215 Hydrodynamic voltammograms were constructed for DA and Ado, and the o

216 fits between the experimental and simulated voltammograms were found for scan rates up to 50 V/s.

217 Well-defined sigmoidal voltammograms were observed on the nanopipet electrodes

218 Square-wave voltammograms were obtained in the presence of redox med

219 Well-defined stripping voltammograms were obtained when Pb(2+) and Cd(2+) were

220 Voltammograms were obtained with the tip inside a single

221 First, voltammograms were recorded at a Pt ultramicroelectrode

222 age was applied (i.e., when the hydrodynamic voltammograms were recorded under flow injection conditi

223 for design and experiment with MEAs, cyclic voltammograms were simulated for coplanar and shallow re

224 Cyclic voltammograms were simulated using DigiSim software for

225 Cyclic voltammograms were taken with glassy carbon electrode or

226 incipal Component Analysis (PCA), derivative voltammograms were used to discriminate among wines of d

227 SCV) with a conditioning waveform to produce voltammograms where each data point is recorded with the

228 on scheme for digital simulation of a cyclic voltammogram which was subsequently fitted to the experi

229 tatively by the recording of numerous cyclic voltammograms which point, along with the use of redox-a

230 the micro NEEs resulted in sigmoidal-shaped voltammograms which were reproducible across the ANEMA.

231 e-electron reduction process in their cyclic voltammogram, which leads to the formation of the semiqu

232 s is established by recording real-time mass voltammograms, which allows one to identify the drug met

233 an be created from the obtained steady state voltammograms, which is analogous to the traditional Kou

234 probe and provide a distinct four-potential voltammogram, whose peak potentials reflect the identity

235 f the ladder systems consists of a multiwave voltammogram with a relatively low first oxidation poten

236 It exhibits a stable quasi-reversible cyclic voltammogram with nearly Nernstian dependency of midpeak

237 abricated array illustrated sigmoidal cyclic voltammogram with steady state current dominated by radi

238 lysis was improved by obtaining steady-state voltammograms with both oxidized and reduced forms of re

239 Voltammograms with multiple peaks are observed with each

240 The analysis of such voltammograms yields information about mass transfer, ad