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1 electrode and silver chloride as the counter/reference electrode).
2 plied to the working electrode (0.0 V vs. Ag reference electrode).
3 ectivity through the presence of an internal reference electrode.
4 uction with E(PEAK) at ca. +0.2 V vs Ag/AgCl reference electrode.
5 rms a salt bridge between the sample and the reference electrode.
6 voltage of about 0.6 volts versus a Li/Li(+) reference electrode.
7 (pH 6) was estimated to be -0.78 vs Ag/AgCl reference electrode.
8 ing a carbon working electrode and a Ag/AgCl reference electrode.
9 solvent ratio vs a nonaqueous Ag/AgCl/Cl(-) reference electrode.
10 onducting salt polarized at 0.15V vs Ag/AgCl reference electrode.
11 easily collide with a separately positioned reference electrode.
12 otential of 600 mV with respect to a Ag/AgCl reference electrode.
13 a 1 mm diameter platinum wire as the counter/reference electrode.
14 An Ag/AgCl electrode was used as the reference electrode.
15 and coated with Nafion to employ as a quasi-reference electrode.
16 le to the commercial porous-junction Ag/AgCl reference electrode.
17 g electrodes, a common counter, and a common reference electrode.
18 compared to the drift seen with a commercial reference electrode.
19 ial of +0.250 V versus an internal pseudo Ag reference electrode.
20 a similar behavior to a conventional Ag/AgCl reference electrode.
21 he conventional liquid-junction type Ag|AgCl reference electrode.
22 o 0.64V vs. the screen-printed carbon pseudo-reference electrode.
23 the microfluidic channel with respect to the reference electrode.
24 ctron reduction pathway at -0.6 V vs Ag/AgCl reference electrode.
25 ration, paired with an ideal non-polarizable reference electrode.
26 of up to 3000 V/cm, using a standard Ag/AgCl reference electrode.
27 ime of 5 s in batch mode) and a miniaturized reference electrode.
28 rent pulse operation of liquid junction free reference electrodes.
29 l, without the need of external conventional reference electrodes.
30 able from those of sensors made with Ag/AgCl reference electrodes.
31 potential of -200 mV between the working and reference electrodes.
32 reate a nanovial with "built-in" working and reference electrodes.
33 electrode, as well as peripheral counter and reference electrodes.
34 ese Ti/Ag/AgCl constructs in capillary-based reference electrodes.
35 Pt and Ag/AgCl depositions as auxiliary and reference electrodes.
36 r-based K(+) ISEs and hydrogel-based Ag/AgCl reference electrodes.
37 of magnitude smaller than that of commercial reference electrodes.
38 oduce both the indicator (pH nanosensor) and reference electrodes.
39 orking electrodes and silver/silver chloride reference electrodes.
40 g electrode and two bare pins as counter and reference electrodes.
41 e is no potential difference between the two reference electrodes.
42 icrosensor, 8-microm tip diameter, as a self-referencing electrode.
43 g, 100-nm thick) and a common central pseudo-reference electrode (60- microm wide, 500- microm long,
44 electrochemical potential measured versus a reference electrode acting as a gate electrode in a soli
45 cens biofilm on the tip and a pseudo Ag/AgCl reference electrode, all enclosed in a glass outer case
48 ntiometric cell composed of an Ag/AgCl-based reference electrode and a solid-contact indicating elect
49 ochemical impedance of both the Ag/AgCl-wire reference electrode and carbon-fiber working electrode.
50 n coating stabilized the potential of the Ag reference electrode and enabled the selective detection
51 om cathodic polarization of the Ag/AgCl-wire reference electrode and increased electrochemical impeda
52 otassium ion-selective electrode acts as the reference electrode and is placed in contact with the sa
53 using it as a working electrode, Ag/AgCl as reference electrode and Pt wire as auxiliary electrode c
54 ever, strong demands on the precision of the reference electrode and requires careful temperature con
55 g requires a post-synaptic electrode and its reference electrode and the tissue becomes the pre-synap
56 the assessment of the effects of an Au quasi-reference electrode and the use of shared reference/coun
59 The cell positions the working, counter, and reference electrodes and has an interior volume of appro
60 salt concentrations in terms of working and reference electrodes and the solutions in which they res
62 ric cell into paper, complete with an ISE, a reference electrode, and a paper-based microfluidic samp
63 u working/sensing electrode, on-chip Ag/AgCl reference electrode, and Poly(3,4-ethylenedioxythiophene
64 rolytes as it is usually required when using reference electrodes, and at the same time, it mitigates
65 e frit characteristics on the performance of reference electrodes, and show that the unwanted changes
66 rode and modified by Ag/AgCl to serve as the reference electrode; and the nonmodified gold fiber coul
67 this new methodology, working, counter, and reference electrodes are completely flat on the surface,
75 ring sensors made with CeO(2-x) nanoparticle reference electrodes are undistinguishable from those of
77 d to potential variations against an Ag/AgCl reference electrode as a function of Tn I-T-C complex co
78 ode holder for the working (WE), counter and reference electrode as mounted in the IR spectrometer ca
79 stepper motors to move the biosensor/counter/reference electrode assemblies sequentially between the
80 arbon working electrode and platinum counter/reference electrode at a potential of 0.3V and in the fr
82 A charged LiCoO2 or LiMn2O4 was used as the reference electrode, because of their insensitivity to a
84 strate the efficacy of the leakless, bipolar reference electrode (BPRE) and miniaturize it to the mic
85 Herein, we report the stability of Ag/AgCl reference electrodes built atop a titanium scaffold usin
86 e electrode is arguably the most widely used reference electrode, but it leaks silver and chloride io
87 n was accomplished at -0.20 V (vs. Ag pseudo-reference electrode) by measuring the catalytic current
88 for all-solid-state ISE and all-solid-state reference electrodes cancel each other in differential p
89 of wired glucose dehydrogenase and enzymatic reference electrode composed of wired laccase we have cr
90 ionic strength, the half-cell potentials of reference electrodes comprising nanoporous Vycor frits a
93 ial range of -0.50 to -0.90 V (vs an Ag/AgCl reference electrode), corresponding to the electrochemic
94 working electrode (WE) and a Ag/AgCl counter/reference electrode covered with an expanded poly(tetraf
95 t ca. -0.71 to -0.78 V vs. Ag printed pseudo reference electrode depending on the sample's matrix, an
96 ch membranes may be suitable with counter or reference electrode, depending on the adopted cell confi
97 pes with Pt counter, Pt working, and Ag/AgCl reference electrode disks were combined with silicone li
98 leakless BPREs behave the same as commercial reference electrodes during potentiometric measurements
100 an encased PPyQRE as a simple and practical reference electrode for electrochemical measurements in
101 eel metal shim counter electrode and Ag/AgCl reference electrode for electrochemiluminescent (ECL) me
102 odes and integrates them with a copper-based reference electrode for simple fabrication and compatibi
106 Additionally, this paper analyzes integrated reference electrodes from a new perspective, focusing ma
107 egrated architecture of working, counter and reference electrodes) grown by low pressure chemical vap
109 nted carbon and on sputtered gold constitute reference electrodes having a redox potential similar to
110 se electrode arrays with internal quasi-gold reference electrodes, higher resolution, and broader mel
111 lectrode for a specific reaction, metal/salt reference electrode (i.e., Ag/AgCl or Hg/Hg(2)Cl(2)) for
112 rodes (ISEs) are performed relative to these reference electrodes immediately after the current pulse
113 H variation of the medium, and a solid-state reference electrode implemented with PVC membranes doped
114 onsumed oxygen was monitored at -0.7 V vs Ag reference electrode in a phosphate buffer (50 mM, pH 7.0
117 owing oxygen consumption at -0.7V vs. the Ag reference electrode in phosphate buffer (50mM, pH 6.0).
118 t a scan rate of 100 mVs(-1) against Ag/AgCl reference electrode in phosphate buffer pH 4.0 within li
119 t a scan rate of 100 mVs(-1) against Ag/AgCl reference electrode in phosphate buffer pH 4.0 within li
121 l value of +160 mV vs. screen-printed pseudo-reference electrode, in the presence of alpha-, delta- a
122 ments were carried out with a platinum quasi-reference electrode instead of a Ag/AgCl reference elect
123 feasibility of the miniaturized working and reference electrodes integrated in the array were studie
126 integrate solid-contact ISEs and solid-state reference electrodes into compact, interconnected archit
131 evices (EPADs) in which a miniaturized paper reference electrode is integrated with a small ion-selec
132 ry, where the potential of the SC-ISE vs the reference electrode is kept constant using a potentiosta
135 sed in PVC membranes of liquid-junction-free reference electrodes (LJFREs) providing a stable potenti
137 cribes the development of a high temperature reference electrode material for gas phase electrochemis
138 tion with a Pt counter-electrode and Ag/AgCl reference electrode, moving sequentially through the 24
140 ly as porous frits in commercially available reference electrodes, namely frits made of Teflon, polye
141 commercially available and in-house-prepared reference electrodes, nanoporous glass frits (often of t
143 e both the potassium-selective electrode and reference electrode needed for the potentiometric readou
145 onse measured at -0.2 V vs the silver pseudo-reference electrode of the SPCE upon the addition of H(2
146 ses measured at -0.2 V vs. the silver pseudo-reference electrode of the SPdCE upon the addition of H2
147 tes used in the annual manufacture of ~10(9) reference electrodes of glucose monitoring strips for di
148 afion-coated NanoMEA platform with decoupled reference electrodes, offering enhanced sensitivity for
149 ble, electrodeposited silver/silver chloride reference electrode on-chip and a perm-selective membran
151 ge-neutral biomolecules, without requiring a reference electrode or any sophisticated instrumentation
152 indicator electrode inside the cell and the reference electrode outside of (but nearby) the studied
154 n at the Ti/Ag interface does not affect the reference electrode performance; in particular, over a w
156 n alternative, where the traditional Ag/AgCl reference electrode porous frit is replaced by a conduct
157 between the reference electrode and a second reference electrode positioned in bulk solution when the
161 lly expected (Nernstian) response slope, and reference electrodes provide sample-independent referenc
162 The Ag/AgCl/Nafion-coated HD-CNTf rod quasi-reference electrode provided a very stable potential com
164 tilizing a microfabricated solid-state quasi-reference electrode (QRE) paired with a pH-insensitive r
166 to the usual commercial reference and quasi-reference electrodes (QREs), we propose metal (Pt, stain
167 allic wire to a conventional Ag/AgCl/3 M KCl reference electrode (RE) in a solution containing primar
170 f alternatives to the commonly used Ag/Ag(+) reference electrode (RE), the introduction of junction p
178 Three-electrode experiments with a real reference electrode revealed the same size selective dep
179 these reactions, including the cell design, reference electrode selection, counter electrode concern
180 emonstrate that the incorporated low-leakage reference electrode shows similar voltammetry, potentiom
181 asi-reference electrode instead of a Ag/AgCl reference electrode, similar shifts in half-wave potenti
184 hod can be used to prepare more reproducible reference electrodes than Ag/AgCl prepared with alternat
185 ed polyvinyl butyral membrane finally gave a reference electrode that demonstrated an outstanding per
186 al with a bulky, difficult to microfabricate reference electrode that limits the potential for massiv
187 ed in epoxy while the other houses a Ag/AgCl reference electrode that makes electrical contact to the
189 t is found that when Au is used as the quasi-reference electrode, the arrays with shared reference an
192 rding electrode, due to the use of a distant reference electrode, they often reflect those of synapti
193 has significant flaws related to metal/salt reference electrodes: they are bulky and difficult to mi
195 sensor was coupled with a carbon fibre-based reference electrode to obtain a potentiometric device.
197 sponses measured at -0.10 V (vs an Ag pseudo-reference electrode) upon the addition of 3,3',5,5'-tetr
198 Amperometry at -200 mV (vs the Ag pseudo-reference electrode) upon the addition of hydroquinone (
199 ices, the prospect of miniaturization of the reference electrodes using printing techniques becomes p
200 nted device, of a fabricated on-chip Ag/AgCl reference electrode - vital in any electrochemical senso
201 l along the microfluidic channel for a given reference electrode voltage regardless of the flow veloc
202 rence between colonic lumen and a peripheral reference electrode was -14 mV (lumen side negative).
204 s the auxiliary electrode; and a micro quasi-reference electrode was fabricated by electroplating CNT
206 made of graphene by laser patterning and the reference electrode was handmade by casting a silver ink
208 stencil printed with graphite ink while the reference electrode was stencil printed with Ag|AgCl ink
210 ition, the position and configuration of the reference electrode were investigated in cell-based expe
214 h miniaturized potentiometric systems, these reference electrodes were integrated into paper-based po
215 easurements, in which both the indicator and reference electrodes were located inside the same cell,
220 SFET) pH sensing technologies both require a reference electrode which may suffer from leakage of ele
221 rbon fiber microdisk working electrode and a reference electrode with a miniature junction, both inse
222 ces, successfully replacing the conventional reference electrode with its reference electrolyte solut
224 e to the intrinsic properties of CIM carbon, reference electrodes with a CIM carbon solid contact exh
226 c membranes offer a promising alternative to reference electrodes with conventional salt bridges.
228 viability of producing low-cost miniaturized reference electrodes with interest in many electrochemic
229 strate the compatibility of CIM carbon-based reference electrodes with miniaturized potentiometric sy
230 wer than 100 mM, the half-cell potentials of reference electrodes with nanoporous glass plugs are not
233 The potential drift of CIM carbon-based reference electrodes without redox couple is as low as 1