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1 al of the indicator tripropylamine by cyclic voltammetry.
2 trochemical impedance spectroscopy (EIS) and voltammetry.
3 ron transfer rates, were probed using cyclic voltammetry.
4 d at carbon nanotubes modified GCE by cyclic voltammetry.
5 posited on glassy carbon electrode by cyclic voltammetry.
6 tection of G, A, T, and C, using square-wave voltammetry.
7  before and after hybridization using cyclic voltammetry.
8 ng for bulk Ni that modulate the observed Ni voltammetry.
9 ase in vivo, measured using fast-scan cyclic voltammetry.
10  increase in DA inflow as observed by cyclic voltammetry.
11 hat is typically monitored using square-wave voltammetry.
12 ation-exchange capacity read out with cyclic voltammetry.
13 rochemical impedance spectroscopy and cyclic voltammetry.
14 tioxidants SO2 and ascorbic acid), by cyclic voltammetry.
15 idation using flow injection amperometry and voltammetry.
16 f silver (Ag) nanoparticles by direct-impact voltammetry.
17 on is accomplished potentiodynamically using voltammetry.
18 vity of 0.07muA/log(g/mL)/cm(2) using cyclic voltammetry.
19 f caffeine and paracetamol using square-wave voltammetry.
20 -vis-NIR reflectance spectroscopy and cyclic voltammetry.
21  spectroscopy, cyclic and differential pulse voltammetry.
22 g in intact rat brain using fast-scan cyclic voltammetry.
23  the peak current as measured by square wave voltammetry.
24 mical impedance spectroscopy and square wave voltammetry.
25 e to determine brucine employing square wave voltammetry.
26 t different thin-layer thicknesses by cyclic voltammetry.
27  yellow and tartrazine by differential pulse voltammetry.
28 single-crystal X-ray diffraction, and cyclic voltammetry.
29 in (RIF) by square wave adsorptive stripping voltammetry.
30 lic silver is determined by anodic stripping voltammetry.
31 uorescence, and IR spectroscopies and cyclic voltammetry.
32 previous detection limit for mediated-impact voltammetry (83 fM).
33 e previous detection limit for direct-impact voltammetry (900 fM), and is more than 30 times smaller
34                            In direct current voltammetry, a difference in k(0) of >3 orders of magnit
35 ticancer prodrug, using adsorptive stripping voltammetry (AdSV) was described for the first time.
36 e, electroanalytical methods (potentiometry, voltammetry, amperometry and electrochemical impedance s
37 ction of NO was investigated by linear sweep voltammetry analysis, utilising the G-Au modified GCE in
38                                       Cyclic voltammetry and amperometry demonstrate excellent electr
39                                       Cyclic voltammetry and amperometry studies confirmed the electr
40 he selectivity of CO2 reduction using cyclic voltammetry and chronoamperometric methods, a large sele
41 n increasing magnitude of response in cyclic voltammetry and chronoamperometry correlates with increa
42  differential pulse voltammetry, square wave voltammetry and chronoamperometry).
43 c glucose sensing in ionic liquids by cyclic voltammetry and chronoamperometry.
44 se of large amplitude Fourier transformed ac voltammetry and comprehensive analysis of the higher har
45  bi-enzyme biosensor was evaluated by cyclic voltammetry and constant potential amperometry using hyd
46  bi-enzyme biosensor as determined by cyclic voltammetry and constant potential amperometry were 112.
47                                       Cyclic voltammetry and controlled potential electrolysis studie
48  provided by the use of a.c. instead of d.c. voltammetry and data optimization methods over heuristic
49                           Differential pulse voltammetry and EIS were used for the quantitative LPS d
50             The results obtained from cyclic voltammetry and electrochemical impedance spectroscopy s
51  studied by cyclic voltammetry, linear sweep voltammetry and electrochemical impedance spectroscopy.
52 area (0.29+/-0.13cm(2)), confirmed by cyclic voltammetry and electrochemical impedance spectroscopy.
53 mission scanning electron microscope, cyclic voltammetry and electrochemical impedance spectroscopy.
54 -cholera toxin were investigated with cyclic voltammetry and Electrochemical Impedance Spectroscopy.
55 ectrochemical impedance spectroscopy, cyclic voltammetry and Fourier transform infrared spectroscopy.
56  aqueous H2SO4 solutions that employs cyclic voltammetry and frequency variation measurements.
57                           After linear sweep voltammetry and impedance spectroscopy, copper electrode
58 for various catalysts were established using voltammetry and impedance spectroscopy.
59                                       Cyclic voltammetry and in situ infrared spectroscopy were close
60                                       Cyclic voltammetry and optical spectroscopy reveal long-distanc
61 cular release of DA we used fast-scan cyclic voltammetry and pharmacological blockade of COMT.
62  reduction reaction was studied using cyclic voltammetry and rotating ring-disk electrode method.
63       The sensor was characterized by cyclic voltammetry and showed well defined and reversible Fe(+)
64 orane amino ester was investigated by cyclic voltammetry and spectroelectrochemistry after controlled
65 absorption spectroscopy, supported by cyclic voltammetry and spectroelectrochemistry.
66                                       Cyclic voltammetry and spectroscopy techniques confirmed the co
67 in 1,2-difluorobenzene solution using cyclic voltammetry and subsequently using the ferrocenium catio
68 tein was studied by protein film square wave voltammetry and transient absorption spectroscopy to obt
69                                       Cyclic voltammetry and UV-vis studies confirm very interesting
70 heir electrocatalytic activity (linear sweep voltammetry) and stability (cyclic voltammetry) with res
71 the sensors performance (evaluated by cyclic voltammetry), and chronoamperometry.
72 ne release as determined by fast-scan cyclic voltammetry, and cognitive deficits.
73      UV/Vis spectroscopy, differential pulse voltammetry, and density functional theory reveal that t
74 rties studied by UV-vis spectroscopy, cyclic voltammetry, and DFT calculations.
75 y-state and transient spectroscopies, cyclic voltammetry, and electron paramagnetic resonance spectro
76  impedance, double layer capacitance, cyclic voltammetry, and galvanostatic polarization measurements
77                                 Amperometry, voltammetry, and impedance spectroscopy represent electr
78 cal properties of the Ni cations measured by voltammetry, and instead emphasize the role of the local
79 tructure characterization via UV-PES, cyclic voltammetry, and UV-vis spectroscopy in direct compariso
80                   A protein film square-wave voltammetry approach was developed to successfully obtai
81 y out slow, high-resolution anodic stripping voltammetry approaches and imaging in concentrated solut
82                          The confined volume voltammetry ( approximately tens of attoliters) yields i
83        We perform in situ and ex situ cyclic voltammetry as well as density functional theory calcula
84 ll-defined quasi-reversible system in cyclic voltammetry associated with the Cu(II)/Cu(I) redox proce
85                         For anodic stripping voltammetry (ASV) of Pb, our sensor shows 21 nM (4.4 ppb
86 vels of heavy metal ions by anodic stripping voltammetry (ASV).
87  I2, and ICl has been investigated by cyclic voltammetry at a platinum macrodisk electrode in a binar
88 en the sensors are interrogated using cyclic voltammetry at a slow scan rate.
89                             Fast scan cyclic voltammetry at carbon fiber microelectrodes (CFEs) is an
90 he displaced triamcinolone using square wave voltammetry at patterned graphene-modified electrodes in
91 wine, respectively, using differential pulse voltammetry at pH 4.0.
92 intermittent titration technique, and cyclic voltammetry at varied scan rates, the NVPF-NTP shows lon
93  on the limiting conditions for ion-transfer voltammetry between an ion-exchanger doped and plasticiz
94                                 Steady-state voltammetry can be performed on such nanoparticle electr
95                   By use of fast-scan cyclic voltammetry, CNT-coated niobium (CNT-Nb) microelectrodes
96                                       Cyclic voltammetry coupled with synthetic and structural studie
97 these exports, adsorptive cathodic stripping voltammetry (CSV) was used to characterize the metal bin
98 d TNF alpha antigen were monitored by cyclic voltammetry (CV) and by electrochemical impedance spectr
99 etry (CC); and (iii) a combination of cyclic voltammetry (CV) and CA.
100                                       Cyclic voltammetry (CV) and differential pulse voltammetry (DPV
101  free DA and the drug was measured by cyclic voltammetry (CV) and differential pulse voltammetry (DPV
102 hemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and differential pulse voltammetry (DPV
103  and electrochemistry methods such as cyclic voltammetry (CV) and differential pulse voltammetry (DPV
104  modified electrode was studied using cyclic voltammetry (CV) and electrochemical impedance spectrosc
105  resulting biosensor were assessed by Cyclic Voltammetry (CV) and Electrochemical Impedance Spectrosc
106 mM) sodium dodecylsulfate (SDS) using cyclic voltammetry (CV) and electrochemical impedance spectrosc
107                                       Cyclic voltammetry (CV) and electrochemical impedance spectrosc
108 morphous manganese dioxide layers via cyclic voltammetry (CV) and electroless deposition (ED).
109 osensor was evaluated in each step by cyclic voltammetry (CV) and impedance spectroscopy (EIS).
110 ent terminations was determined using cyclic voltammetry (CV) and scanning electrochemical microscopy
111 The powerful combination of SECM with cyclic voltammetry (CV) at a gold substrate reveals that the el
112 OA was used as a working electrode in cyclic voltammetry (CV) for the detection of H2O2.
113                                       Cyclic voltammetry (CV) measurements confirmed the efficiency o
114 ical impedance spectroscopy (EIS) and cyclic voltammetry (CV) methods.
115 /bacteria film was characterized with cyclic voltammetry (CV) technique to provide quantitative index
116 he modified electrode was assessed by cyclic voltammetry (CV) to determine the surface coverage (Gamm
117                                       Cyclic voltammetry (CV) was applied during the WE functionaliza
118                                       Cyclic voltammetry (CV) was employed to assess the six MnOx nan
119 es but constant applied potential and cyclic voltammetry (CV) were also investigated.
120 ), Fourier transform infrared (FTIR), cyclic voltammetry (CV), and electrochemical impedance spectros
121 lidated as Amitriptyline sensor using cyclic voltammetry (CV), chronoamperometry (CA) and differentia
122 dified electrode was characterized by cyclic voltammetry (CV), differential pulse voltammetry (DPV) a
123 roperties of the layer, making use of cyclic voltammetry (CV), electrochemical impedance spectroscopy
124 s (AuNPs-PCWEs) were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy
125     A variety of techniques including cyclic voltammetry (CV), electrochemical impedance spectroscopy
126 ctrochemical characterization such as cyclic voltammetry (CV), electrochemical impedance spectroscopy
127 M) imaging, UV-vis spectrophotometry, cyclic voltammetry (CV), field emission scanning electron micro
128  electrochemical techniques including cyclic voltammetry (CV), impedance spectroscopy (EIS) and squar
129 e techniques used to do this work are cyclic voltammetry (CV), linear sweep voltammetry (LSV), chrono
130              Electrochemical methods (cyclic voltammetry (CV), potential steps, and electrochemical i
131 ical impedance spectroscopy (EIS) and cyclic voltammetry (CV).
132 ical impedance spectroscopy (EIS) and cyclic voltammetry (CV).
133 munosensor was characterized by using cyclic voltammetry (CV).
134 ical impedance spectroscopy (EIS) and cyclic voltammetry (CV).
135  behavior of rGO-PGEs was examined by cyclic voltammetry (CV).
136 ferential pulse voltammetry (DPV) and cyclic voltammetry (CV).
137 PR and UV/vis spectroscopy as well as cyclic voltammetry data are provided, and the radicals are show
138 were found to directly correlate with cyclic voltammetry data in aqueous solution.
139 electron microscopy, rotating disk electrode voltammetry, demonstrate that Li2O2 electrochemically fo
140 S subsetm-CBPQT](4(+*)) was probed by cyclic voltammetry, demonstrating that the radical states of th
141 only used electrochemical techniques (cyclic voltammetry, differential pulse voltammetry, square wave
142 studied by steady-state spectroscopy, cyclic voltammetry, differential scanning calorimetry, single-c
143           On the basis of differential pulse voltammetry (DPV) and amperometric techniques, the obtai
144 electrode was explored by differential pulse voltammetry (DPV) and cyclic voltammetry (CV).
145 d and characterized using differential pulse voltammetry (DPV) and electrochemical impedance spectros
146  cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectros
147 riminate it from Tyr with Differential Pulse Voltammetry (DPV) as it is a very important biomarker.
148 sfer resistance (Rct) and differential pulse voltammetry (DPV) current were relevant to the formation
149 electroanalysis that used differential pulse voltammetry (DPV) in NaOH (0.1M, pH 13) was conducted su
150 hronoamperometry (CA) and differential pulse voltammetry (DPV) methods.
151                       The differential pulse voltammetry (DPV) parameters, such as a maximum amplitud
152 clic voltammetry (CV) and differential pulse voltammetry (DPV) studies were carried out to measure th
153 (NTMCP) was detected using diffrential pulse voltammetry (DPV) technique and it was found between 2x1
154 electrochemical probe and differential pulse voltammetry (DPV) technique, two linear concentration ra
155 between DNR and DNA using differential pulse voltammetry (DPV) technique.
156                           Differential pulse voltammetry (DPV) was also performed for the estimation
157 clic voltammetry (CV) and differential pulse voltammetry (DPV) were used to analyze the surface chara
158  by using electrochemical differential pulse voltammetry (DPV) whose lowest detection limit was calcu
159                     Using differential pulse voltammetry (DPV), the prepared sensor showed good sensi
160 clic voltammetry (CV) and differential pulse voltammetry (DPV).
161 wave voltammetry (SWV) or differential pulse voltammetry (DPV).
162 rode surface, by means of differential pulse voltammetry (DPV).
163 vents were assessed using differential pulse voltammetry (DPV).
164 competitive aptasensor by differential pulse voltammetry (DPV).
165 clic voltammetry (CV) and differential pulse voltammetry (DPV).
166                           Differential pulse voltammetry (DPVs) exhibited two expanded linear dynamic
167    The sensor was characterized using cyclic voltammetry, electrochemical impedance spectroscopy (EIS
168 tion of retrograde tracing, fast-scan cyclic voltammetry, electrophysiology, and in vivo optogenetics
169 igand Exchange Adsorptive Cathodic Stripping Voltammetry enabled the prediction of the free metal ion
170                                       Cyclic voltammetry established the electron withdrawing influen
171 tuin in PBS samples, obtained by square wave voltammetry, exhibited a linear range from 0.5 to 25micr
172    This theory is applied to the analysis of voltammetry experiments involving ultramicroelectrodes m
173                                  Our ex vivo voltammetry experiments showed that the inhibitory effec
174                                    By cyclic voltammetry, fast turnover frequencies of 3.2 and 4.8 s(
175 rate here the use of liposome rupture impact voltammetry for the qualitative detection of model amphi
176 bserved drug-specific changes in square wave voltammetry from these chips at therapeutic ss-lap conce
177 icle, we use fast-scan controlled adsorption voltammetry (FSCAV), to measure serotonin's steady-state
178  spatiotemporal resolution, fast-scan cyclic voltammetry (FSCV) at carbon-fiber microelectrodes enabl
179                             Fast-scan cyclic voltammetry (FSCV) can measure rapid serotonin release a
180 onitored in real time using fast-scan cyclic voltammetry (FSCV) coupled with carbon-fiber microelectr
181  demonstrate the utility of fast-scan cyclic voltammetry (FSCV) for providing speciation information
182 y on Fourier-transformed alternating current voltammetry (FTACV) has been investigated theoretically
183 tude Fourier transformed alternating current voltammetry (FTacV) we have measured previously uncharac
184                     The limiting currents in voltammetry gave the size and number of atoms of the clu
185 lectroanalytical methods such as square wave voltammetry has not been declared.
186 elopment of electrochemical fast-scan cyclic voltammetry implementing microsized carbon fiber probe i
187 ics, electrophysiology, and fast-scan cyclic voltammetry in a TH-cre mouse line, we demonstrated that
188 se oxidation was then investigated by cyclic voltammetry in alkaline medium.
189                     We used fast-scan cyclic voltammetry in freely moving rats to measure real-time c
190 ine self-administration and fast-scan cyclic voltammetry in male rats, we show that low-dose, continu
191                                 Using cyclic voltammetry in mouse brain slices, nAChR-dependent spont
192 unting results (single-molecule fluorescence voltammetry) indicated a surface-controlled electrochemi
193 ained by using variable concentration cyclic voltammetry, infrared spectroelectrochemistry, and bulk
194 ing behavior observed in alternating current voltammetry; instead it enables simultaneous "signal-on"
195  were also compared with the standard cyclic voltammetry instrument and found in agreement with each
196                                       Cyclic voltammetry is a well-fitted experimental technique to u
197                                       Cyclic voltammetry is a widely used and powerful tool for sensi
198                                       Cyclic voltammetry is demonstrated without significant shifts i
199 a Aspergillus and Fusarium using solid-state voltammetry is described.
200 ed through computational studies, and cyclic voltammetry is used to better understand the effect of m
201 4@SiO2/DABCO/SPE have been studied by cyclic voltammetry, linear sweep voltammetry and electrochemica
202                                 Linear sweep voltammetry (LSV) and potential-step chronoamperometry (
203 rk are cyclic voltammetry (CV), linear sweep voltammetry (LSV), chronoamperometry (CA) and electroche
204 ated by UV-visible spectrophotometry, cyclic voltammetry, mass spectrometry, and products assessment
205           Absorption spectroscopy and cyclic voltammetry measurements provide experimental estimation
206                                       Cyclic voltammetry measurements showed that the electrode chip
207                                       In the voltammetry measurements, W32 oxidation-reduction occurs
208 s of Fourier transformed alternating current voltammetry measurements, we relate these changes in cat
209                                 Using cyclic voltammetry method, in this work, we demonstrated a rela
210                                   The cyclic voltammetry of 3 shows irreversible reduction and oxidat
211 validated using chronoamperometry and cyclic voltammetry of an ideal outer-sphere redox probe, revers
212                                       Cyclic voltammetry of CtCDH immobilized onto the AuNPs/BPDT/AuE
213                                       Cyclic voltammetry of H2B-Q shows two reversible, 1-electron re
214 yl radical is a principal contributor to the voltammetry of H2O2, as signal is attenuated when this s
215                                       Cyclic voltammetry of phosphate cobalt oxide (CoPi) films catal
216                            Additionally, the voltammetry of the first reduction peak of TNT in [P14,6
217 for electrochemical detection by square-wave voltammetry on commercial screen-printed electrodes.
218 ich is directly measured by difference pulse voltammetry on disposable screen-printed electrodes.
219             They were investigated by cyclic voltammetry, optical absorption, EPR spectroscopy, X-ray
220 ction, are explored through a combination of voltammetry, preparative electrolysis, thiol-electrode m
221 fferent individuals using differential pulse voltammetry, presenting limits of detection and quantifi
222 amage to the SECM probe, we implement cyclic voltammetry probe approach surfaces (CV-PASs), consistin
223 ss changes (deltaDeltam) for complete cyclic voltammetry profiles covering the 0.05-1.40 V range.
224                                              Voltammetry provides a tool for the prescreening of synt
225                     Alternating current (ac) voltammetry provides access to faster electrode kinetics
226 sal striatum as measured by fast-scan cyclic voltammetry, reduced striatal dopamine content, disrupte
227                                       Cyclic voltammetry responses are derived for two-electron, two-
228                                       Cyclic voltammetry results show that the as-prepared biosensor
229  of OH(*) probe compounds, which agreed with voltammetry results.
230                      Rotating disc electrode voltammetry revealed that initial rates of uptake and AM
231       Preliminary characterization by cyclic voltammetry revealed the effect of Fe(3+) on the electro
232 zed by UV-vis absorption/emission and cyclic voltammetry, revealing strong effects from both external
233                           Differential pulse voltammetry reveals detection limits of 100 muM for GSH
234                                       Cyclic voltammetry reveals that both isosceles triangles can ac
235  estimated using peak currents formed during voltammetry scanning.
236                                       Cyclic voltammetry showed that the response of the SPCE-G-COOH
237                                       Cyclic voltammetry shows the apparent onset of catalysis at the
238 0-fold enhancement in the differential pulse voltammetry signal carried out at pH 11.0 in a 0.1M bora
239 y measuring the change in differential pulse voltammetry signal of a redox probe ([Fe(CN)6](3-)/[Fe(C
240 ing events were studied by monitoring cyclic voltammetry signals and the developed nanosensor exhibit
241                                  Square wave voltammetry signals of MB provided quantitative measurem
242                     Three-dimensional cyclic voltammetry simulations using COMSOL were performed on 6
243               This was achieved using pulsed voltammetry, since the pulse sequence can be programmed
244 ditions, as determined by differential pulse voltammetry, solution-state spectroelectrochemistry, and
245 ques (cyclic voltammetry, differential pulse voltammetry, square wave voltammetry and chronoamperomet
246                                 Linear sweep voltammetry studies show that both phenol and trifluoroe
247                              Based on cyclic voltammetry studies, it was determined that alpha,alpha-
248 consistent with the spectroscopic and cyclic voltammetry studies, show decreased HOMO-LUMO energy gap
249 ese experiments combined with in situ cyclic voltammetry suggest that the doped CPE facilitates elect
250 s undergo reversible redox events (by cyclic voltammetry), suggesting that a cycloaddition pathway in
251 mination of HOMO-LUMO levels by linear sweep voltammetry suggests that the sensing mechanism likely i
252 cury in tuna of square wave anodic stripping voltammetry (SW-ASV) conducted at both solid gold electr
253 al detection by square wave anodic stripping voltammetry (SWASV) in 0.1M HNO3.
254 performed using square wave anodic stripping voltammetry (SWASV).
255  cadmium ions and lead ions with square wave voltammetry (SWV) after dissolution with acid.
256 impedance spectroscopy (EIS) and square wave voltammetry (SWV) confirmed the surface modification of
257 ctrocatalytic reduction of Mb by square wave voltammetry (SWV) or differential pulse voltammetry (DPV
258 d by following the change in the square wave voltammetry (SWV) reduction peak signal of ferrocyanide/
259 impedance spectroscopy (EIS) and square wave voltammetry (SWV), against a standard iron probe.
260 bsequently measured using differential pulse voltammetry technique by multi-walled carbon nanotubes m
261 antigen-125 was accomplished by differential voltammetry technique that demonstrated excellent sensit
262 r electrochemical characterization by cyclic voltammetry technique, the optimization of relevant para
263 in complex food samples using a linear sweep voltammetry technique.
264                 Differential pulse stripping voltammetry techniques were used to further enhance merc
265 escence (PL) spectroscopy, FT-IR, and cyclic voltammetry techniques.
266 tant-current charging/discharging and cyclic voltammetry tests, and from the frequency domain using n
267 absorption and emission spectroscopy, cyclic voltammetry, theoretical calculation, and fluoride titra
268 hore membranes can be interrogated by cyclic voltammetry to detect the ion activity of multiple speci
269               Here, we used fast-scan cyclic voltammetry to measure DA dynamics and explore such mech
270 l. reported a broad oxidation peak in cyclic voltammetry upon the binding between NGAL with its antib
271 aracterized by cyclic and differential pulse voltammetries using the ferrocyanide/ferricyanide as red
272                                      Nanogap voltammetry using scanning electrochemical microscopy (S
273 ologens have been characterized using cyclic voltammetry, UV-visible absorbance and fluorescence spec
274                                       Cyclic voltammetry, UV/Vis spectroscopy, spin density, and DFT
275                                      Herein, voltammetry was combined with electron paramagnetic reso
276                                       Cyclic voltammetry was implemented to activate the oxidation an
277                                  Square wave voltammetry was performed on the first reduction peak of
278                  A carbone paste method with voltammetry was used in the fabrication of the sensor fr
279     In this study, in vitro fast-scan cyclic voltammetry was used to examine the modulation of DA tra
280                                       Cyclic voltammetry was used to initially probe the electrochemi
281                           Differential pulse voltammetry was used to investigate the detection of Fe(
282                                  Square-wave voltammetry was used to quantify pyocyanin concentration
283                                  Square wave voltammetry was used to quantify the NO(*) concentration
284                       Using fast-scan cyclic voltammetry, we determined that the concentration of acc
285 ranial self-stimulation and fast scan cyclic voltammetry, we found that cocaine-induced increases in
286                                        Using voltammetry, we found that real-time DA signals in cocai
287                       Using fast-scan cyclic voltammetry, we show that METH-enhancement of evoked dop
288 lysis, fluorescence spectroscopy, and cyclic voltammetry were employed to study the properties of the
289 rochemical impedance spectroscopy and cyclic voltammetry were used as an analytical methods to optimi
290 namics were monitored using fast-scan cyclic voltammetry, whereas motivation was assessed using a pro
291  fluorescence spectroscopy as well as cyclic voltammetry, which allowed the establishment of structur
292 eed for a preconcentration step in stripping voltammetry, which requires optimization of the paramete
293 sing Fourier transformed alternating current voltammetry, which revealed that the 2-methylimidazolate
294  been quantified by undertaking linear sweep voltammetry with a silver nanoparticle-modified glassy c
295  mixed solution is an important advantage of voltammetry with an ionophore-based polymeric membrane a
296 avioral effect by combining fast-scan cyclic voltammetry with local pharmacological acetylcholine rec
297 ere studied by cyclic and differential pulse voltammetry with potassium ferrocyanide as a common redo
298 ruses by nonfaradaic liposome rupture impact voltammetry with the aid of 1,2-dioleoyl-sn-glycero-3-ph
299   The ultraflat eC surface permitted nanogap voltammetry with very thin electrode-to-substrate gaps,
300 ear sweep voltammetry) and stability (cyclic voltammetry) with respect to the HER in acidic condition

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