ライフサイエンスコーパス: voltammogram

1 rograms are sampled once to produce a single voltammogram.

2 otential curve akin to a pseudo steady state voltammogram.

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

4 rate without appreciable perturbation of the voltammogram.

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

6 the spacing the more sigmoidal the recorded voltammogram.

7 the temporal delay prior to acquisition of a voltammogram.

8 al modeling and quantitative analysis of the voltammogram.

9 being supported by simulations of the cyclic voltammograms.

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

11 s of rapid IT processes extracted from pipet voltammograms.

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

13 requires a single effort of simulating many voltammograms.

14 n of substances that give overlapping cyclic voltammograms.

15 to construct hydrodynamic current-potential voltammograms.

16 mallest electrodes producing strongly peaked voltammograms.

17 waves in the cathodic regions of the cyclic voltammograms.

18 sessed from half-wave potentials of obtained voltammograms.

19 surface stress closely resembles the cyclic voltammograms.

20 d from symmetric pairs of reversible nanogap voltammograms.

21 ile was obtained by recording real-time mass voltammograms.

22 ent plateau analysis of the catalytic cyclic voltammograms.

23 ity ratios has been found when analysing the voltammograms.

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

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

26 Catecholamine voltammograms acquired with platinum electrodes exhibite

27 ing a linear fit from a selected region of a voltammogram after the switching potential (E(lambda)),

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

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

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

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

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

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

34 Reversible voltammograms and a voltammetry half-wave potential vers

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

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

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

38 80 h (66 days) by analyzing more than 43,800 voltammograms and quantifying approximately 730 kinetic

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

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

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

42 carried out by recording simultaneous cyclic voltammograms and voltfluorograms at the same electrode.

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

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

45 d square wave voltammetry since the required voltammograms are collected with a single sweep, which i

46 Experimental voltammograms are compared with each mechanism by employ

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

48 The cyclic voltammograms are numerically analyzed to determine form

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

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

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

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

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

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

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

56 The cyclic voltammograms at microdisk electrode arrays are grouped

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

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

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

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

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

62 focused on identifying dopamine from cyclic voltammograms, but it would be better to analyze all the

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

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

65 the source of non-ideal behaviour in cyclic voltammograms can be challenging as different types of d

66 Analysis of catalytic voltammograms can quickly furnish qualitative evidence o

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

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

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

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

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

72 es and wine OCRs from first order difference voltammogram curves.

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

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

75 Cyclic voltammograms (CV) showed an irreversible oxidation peak

76 anistic origin of each feature on the cyclic voltammograms (CVs) due to charge accumulated from Farad

77 Cyclic voltammograms (CVs) from 1.4 to 1.7 V(RHE) (RHE = revers

78 V vs Fc(+/0) (Fc = ferrocene) in the cyclic voltammograms (CVs) in DMF (0.1 M TBAPF(6)).

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

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

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

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

83 Cyclic voltammogram data and simulations, together with computa

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

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

86 as the counteranion in all the stages of the voltammogram, demonstrating the strategy to modulate the

87 The CV and DPV voltammograms display significant correlations with the

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

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

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

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

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

93 The latter produces an AC voltammogram equivalent to a "blank" measurement in the

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

95 the product yield under AC electrolysis from voltammogram features.

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

97 In this medium, a cyclic voltammogram for a reduction of 1 exhibits a reversible

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

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

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

101 provide the electrochemical signature cyclic voltammograms for molecular identification.

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

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

104 Cyclic voltammograms for the gel-entrapped ferrocene methanol (

105 re able to produce well-defined steady-state voltammograms for the oxygen evolution reaction (OER) in

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

107 Cyclic voltammograms for these ultramicroelectrodes obtained in

108 eural network trained to recognize dc cyclic voltammograms for three commonly encountered mechanisms

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

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

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

112 Cyclic voltammograms from the biofluid exhibit responses that a

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

114 aneous adenosine events, as adenosine cyclic voltammograms have a primary oxidation at 1.3 V and a se

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

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

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

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

119 Differential pulse voltammograms indicated that the linear range of the sen

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

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

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

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

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

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

126 rather simple expression for proton transfer voltammograms is derived.

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

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

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

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

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

132 The voltammogram obtained from the experiment on polyaniline

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

134 Interpreting voltammograms obtained in the attoliter volume affected

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

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

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

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

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

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

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

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

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

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

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

146 The voltammogram of a coffee extract (prepared as simulating

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

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

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

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

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

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

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

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

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

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

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

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

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

160 Cyclic voltammogram of the synthesised CH biosensor exhibited w

161 The cyclic voltammogram of trigonal bipyramidal 2 displays successi

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

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

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

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

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

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

168 revealed significant differences between the voltammograms of biofilm-forming and biofilm-deficient c

169 Cyclic voltammograms of CYP79A1 and CYP71E1 revealed reversible

170 t, both types of sensors yielded well-shaped voltammograms of dopamine down to ca. 1 nM concentration

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

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

173 Cyclic voltammograms of hangman chlorins exhibit a hangman effe

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

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

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

177 The cyclic voltammograms of NiCo2O4 electrode using alkaline aqueou

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

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

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

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

182 that parasitic signals commonly observed in voltammograms of silicon electrodes originate from silic

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

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

185 Cyclic voltammograms of the clusters in acetonitrile display re

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

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

188 The cyclic voltammograms of the enzyme electrode after appearance o

189 Cyclic voltammograms of the immobilized hydrogenase films revea

190 We simulated the voltammograms of the individual deposits, assuming the V

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

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

193 obtained through the investigation of cyclic voltammograms of the reactants.

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

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

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

197 Cyclic voltammograms of the series of triiron clusters presente

198 ct redox events being observed in the cyclic voltammograms of these compounds.

199 The cyclic voltammograms of these heterobimetallic complexes show m

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

201 A steady-state voltammogram on the single Pt deposits is observed by el

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

203 ntial deposited hydrogen (H(upd) ) in cyclic voltammograms on the Pt surface is of significance in te

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

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

206 rpart to study the effect of mesoporosity on voltammogram output signals.

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

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

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

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

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

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

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

214 t proton transfer rate constants from cyclic voltammograms recorded with acids ranging 22 pK(a) units

215 Cyclic voltammograms recorded with proton sources that span a w

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

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

218 These voltammograms represent the Y32 species at the upper edg

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

220 t and second wave of the first derivative of voltammograms, respectively.

221 Experimental tip voltammograms resulting from the reversible reduction of

222 work has been chosen according to the cyclic voltammogram results.

223 Differential pulse voltammograms revealed a detection limit of 8 pM, while

224 The voltammogram reveals the critical redox features of CFX

225 ion and is observed regardless of the cyclic voltammogram scan rate.

226 f electrochemical signals (e.g., square wave voltammogram shape) suggests that the large unbound nucl

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

228 Cyclic voltammograms show a Mn(0/-I) redox couple at -3.13 V vs

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

230 Digital simulations of cyclic voltammograms show ligand loss accompanying initial redu

231 simulations of electrostatic effects on CNP voltammograms show permselective ion transport in a sing

232 Cyclic voltammograms showed a reproducible nernstian behavior f

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

234 doxime reduction were determined from cyclic voltammograms simulated using Digisim.

235 polar electrodes to obtain numerous snapshot voltammograms simultaneously.

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

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

238 Cyclic voltammograms support the mechanism of this electro-oxid

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

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

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

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

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

244 a diffusion-limiting current plateau in the voltammogram that can be used to estimate the radius of

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

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

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

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

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

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

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

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

253 demonstrate that d(ELF)/dV acts as an "opto-voltammogram" that can be used to selectively probe and

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

255 mass transport with BV to analyze the entire voltammogram to infer transfer coefficients directly, so

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

257 Complex 2-Tb displays a similar voltammogram to the Ce(4+) analogue but with redox event

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

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

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

261 Changes to the voltammograms under illumination follow mechanistic pred

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

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

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

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

266 derivative counterparts, evident in the DPV voltammograms, was confirmed by molecular modeling.

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

268 The voltammograms were also evaluated for the quantitative d

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

270 Voltammograms were analyzed to extract the electron tran

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

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

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

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

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

276 Voltammograms were obtained with the tip inside a single

277 First, voltammograms were recorded at a Pt ultramicroelectrode

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

279 modes, for which approach curves and cyclic voltammograms were recorded.

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

281 Cyclic voltammograms were simulated using DigiSim software for

282 Cyclic voltammograms were taken with glassy carbon electrode or

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

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

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

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

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

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

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

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

291 veraged peak potential of nonturnover cyclic voltammograms, which is presumably the formal potential

292 Electrocatalytic voltammograms, which show the rate of electron flow at s

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

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

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

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

297 e electrochemical cell provides local cyclic voltammograms with a nanoscale spatial resolution for vi

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

299 Voltammograms with multiple peaks are observed with each

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