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1 entrations of H(2)O(2) upon adsorption on an electrode.
2 ode disk, leading to transport away from the electrode.
3 IMI sensing performance of the as-fabricated electrode.
4 material over SiO(2) layer and Au as a metal electrode.
5 ctrode is 4.3 times greater than the bare Au electrode.
6 tial of -0.536 V vs. the reversible hydrogen electrode.
7  ions, a high DC field, and a wide exit ring electrode.
8 electrical double layer (EDL) of the working electrode.
9 c STM tip electrode and the metallic surface electrode.
10 ired with an ideal non-polarizable reference electrode.
11 y even at <-0.2 V versus reversible hydrogen electrode.
12 lytically active particle impacting an inert electrode.
13  from a ferromagnetic La(0.67)Sr(0.33)MnO(3) electrode.
14 ltrafast charger diffusion across the entire electrode.
15 ns, enabled by ionic screening of the carbon electrode.
16 hrough the presence of an internal reference electrode.
17 le cellular-size light sources and recording electrodes.
18 th 19 dry electrodes and another with 19 wet electrodes.
19 l communication with implanted neuromuscular electrodes.
20 urgical patients implanted with intracranial electrodes.
21 Hyalu/l-Cys and A-MWCNT/Hyalu/l-Ser modified electrodes.
22 nitored by potentiometric ammonium-selective electrodes.
23 its external location over parieto-occipital electrodes.
24 f a diazonium salt on glassy carbon and gold electrodes.
25 to develop pure or hybrid nanomaterial-based electrodes.
26 ible with simultaneous stimulation of paired electrodes.
27 um group metal-free (PGM-free) catalysts and electrodes.
28 ble fields and forces in the vicinity of the electrodes.
29 o ensure reproducible characteristics of the electrodes.
30 ns suffered signal loss due to intracortical electrodes.
31 ifference of >=20 ms between paired endo-epi electrodes.
32 suring the capacitances between the array of electrodes.
33 gh ionic resistance of the macropores in the electrodes.
34 M), which is about 312 folds that of silicon electrode (0.025 muA/muM) and excellent flexibility.
35 ble and breathable composite of nanomembrane electrodes (16 electrodes in a four by four array), elas
36 2 component for shape over lateral-occipital electrodes (250-400 ms), which also increased with highe
37 rticles to create working surfaces makes the electrode a reusable SPE which can be reutilized after t
38 al structure of laser-induced graphene based electrode, a single micro-supercapacitor exhibits an ult
39 locyanine-based cathode catalyst, the hybrid electrode achieves a CO Faradaic efficiency of 71 % with
40 2,2'-bipyridine) chromophore on nanoparticle electrodes, addition of the molecular catalysts, Ru(bda)
41                                          The electrode also allows coculturing with Shewanella for sy
42 ventional interphase between a typical solid electrode and a liquid electrolyte, the interphase betwe
43 e a controlled functionalisation of the gate electrode and avoid contamination or physisorption on th
44                             Breakthroughs in electrode and battery designs, stimulation paradigms, cl
45 five components: thermally reversible porous electrode and electrolyte gels; conductive polymer and c
46 i.e., catalysis at the interface between the electrode and electrolyte to facilitate charge transfer
47 stabilized the potential of the Ag reference electrode and enabled the selective detection in spiked
48 vo neuronal sensing requires a post-synaptic electrode and its reference electrode and the tissue bec
49  arising from interfacial issues between the electrode and solid electrolyte.
50 olecular bridge between the metallic STM tip electrode and the metallic surface electrode.
51  a post-synaptic electrode and its reference electrode and the tissue becomes the pre-synaptic signal
52 zed on the surface of the ammonium-selective electrode and with the AEM on top.
53 atially limited to cells in contact with the electrode and within a near-electrode zone (<30 mum) whe
54 hing electronics, consisting of viscoplastic electrodes and a strain sensor that eliminate the stress
55 ctor manufacturing technology (SMT)-produced electrodes and a streptavidin biomediator currently disp
56 roaches such as potentiometric ion selective electrodes and amperometric enzymatic sensors.
57 ecordings on different days, one with 19 dry electrodes and another with 19 wet electrodes.
58 ed: nisin molecules were immobilised on gold electrodes and Electrochemical Impedance Spectroscopy wa
59 rGO) within 3D-printed polylactic acid (PLA) electrodes and their potential applications for sensing
60 mmercial graphene oxide-based screen-printed electrodes and varying enzyme producing strains, encapsu
61 e (at 1.5 volts versus a reversible hydrogen electrode) and a cathodic-side (half-cell) ethylene powe
62 unds) serve as conductive traces and sensing electrodes, and office-copy papers work as flexible supp
63                            Ion intercalation electrodes are being investigated for use in mixed capac
64                               Li(5) B(4) /Li electrodes are coupled with a garnet-type ceramic electr
65 -term recordings in preclinical studies, the electrodes are foreign objects and might therefore be ex
66                                The harvester electrodes are made by biscrolling ferritin (40 wt%) in
67 aptured across scales by different recording electrodes are regularly used for Brain Machine Interfac
68    Our study shows that thin-film-coated ITO electrodes are simple to make and can be useful electrod
69                            Carbon fiber (CF) electrodes are thinner and more flexible than typical me
70                        A Prussian blue-based electrode array (PBEA) constituted by eight stencil-prin
71  of generated data, and manufacturing of the electrode array itself.
72  the fabrication of a 16-channel intraneural electrode array with ultramicro-dimensioned electrodes t
73                                              Electrode array-retina gap distances were measured at ea
74                 Using novel high-density EEG electrode arrays in the mouse model of CSR where mice un
75                   Here, we use silicon multi-electrode arrays to record respiratory local field poten
76  for the on-demand prototyping of customized electrode arrays well adjusted to specific anatomical en
77 n metal film modified Indium Tin Oxide (ITO) electrode as a highly conductive, transparent, and elect
78 mpact electrochemical cytometry (VIEC) at an electrode as the vesicle exits the nanopore.
79 ual distance between the fusion pore and the electrode as well as fusion pore size, which leads to di
80  catalyst loading is decreased in a membrane electrode assembly (MEA)-the power generation unit of a
81 vity by using a coaxial guide tube and sharp electrode assembly, which allows researchers to repeated
82 anide ions relative to conventional, mm-size electrodes at 25 degrees C.
83          The performance of pseudocapacitive electrodes at fast charging rates are typically limited
84 ive film was coated successfully on the gold electrode (Au).
85 charge density (over 4.0 mC m(-2)) in a TENG electrode based on quantified surface micro-contact effi
86 between copper (Cu) nanoparticles and the Cu-electrode beneath.
87 yl chloride) (PVC) membranes mounted into an electrode body are immersed into an aqueous solution con
88 to the stimulated hand over central-parietal electrodes but relative to its external location over pa
89  more flexible than typical metal or silicon electrodes, but the arrays described in previous reports
90 of three-dimensional electrodes, coating the electrodes by nanoflakes of reduced-graphene-oxide (rGO)
91 th the probe at a constant distance from the electrode (ca. 75 mum), while the electrode potential wa
92  and maintain its porous architecture during electrode calendering.
93                                          The electrode can still produce CO at an O(2) /CO(2) ratio a
94   These results strongly indicate that these electrodes can be used directly to determine the unbound
95  conditions, we demonstrate that planar CuAg electrodes can reduce CO to acetaldehyde with over 50% F
96        Fast-charging batteries typically use electrodes capable of accommodating lithium continuously
97 approaches to elucidate such impacts in flow-electrode capacitive deionization (FCDI) cells.
98 ncy were highly electrode dependent: On some electrodes, changes in frequency were perceptually disti
99 iew, we aim to highlight recent instances of electrode choice where rationale is offered, which shoul
100 ated by 3D nanoprinting of three-dimensional electrodes, coating the electrodes by nanoflakes of redu
101 ith a stable reference electrode, this three-electrode configuration will be critical in achieving re
102                                The biohybrid electrode containing Geobacter can also catalyze the red
103   In vivo, in the rat parietal cortex, these electrodes could detect brain NO released by local micro
104 hods and strategies to mitigate catalyst and electrode degradation, which is fundamentally essential
105 ed capacitive deionization (CDI) and battery electrode deionization (BDI) systems because they can ac
106 espite limited electronic coupling to the Au electrode, demonstrating the potential of this approach.
107                         The combination of n electrodes, demonstrating individually a Nernstian slope
108  sensory correlates of frequency were highly electrode dependent: On some electrodes, changes in freq
109                Herein, single-atom catalytic electrodes design for advanced battery systems is addres
110                        While, the TC-GQD/GCE electrode detected DA in the range of 1-500 muM DA, with
111                        The fouling effect on electrodes discourages the possibility of continuous onl
112 f electrophoresis at locations radial to the electrode disk, leading to transport away from the elect
113                    Thicker 10-layer graphene electrodes displayed only a small kinetic difference wit
114 yperpolarization decays with increasing cell-electrode distance.
115 urrent upon the formation of the microscopic electrode-electrolyte interface is used to determine the
116 ge and conversion processes occurring at the electrode-electrolyte interface.
117        The artificial receptor with a simple electrode-electrolyte-electrode structure simultaneously
118                  In this work, an artificial electrode/electrolyte (E/E) interface, made by coating t
119 ging), an electric double layer forms at the electrode/electrolyte interface due to the self-assembly
120 ight into the rate of charge transfer on the electrode/electrolyte interface.
121 ities of the electrolytes and the compatible electrode/electrolyte interfaces are highlighted.
122 nterfaces in fuel cells and ion insertion at electrode/electrolyte interfaces in solid-state batterie
123 through the design of in situ formed, stable electrode/electrolyte interphases on both the Li anode a
124       The combination of a pipette tip, wire electrodes, enzyme, and cotton wool filter, allows the f
125 c method using edge plane pyrolytic graphite electrode (EPPGE) as a novel sensor is presented for the
126  the hybrid system immobilized on the carbon electrode exhibits outstanding stability after electroly
127 ray of alternating current (AC) field-effect electrodes, experimentally demonstrate the separation of
128                        However, the scalable electrode fabrication based on this type of material usu
129 pid evaporation of mixed solvents during the electrode fabrication process.
130 dditionally, FDTO served as an excellent top electrode for ferroelectric switching in BiFeO(3) with n
131  dopamine (DA) was employed to modify a gold electrode for immobilization of DNA probes through the S
132 he high stability observed with the modified electrode for prolonging period indicated that the sensi
133 d carbon microspot boron doped diamond (BDD) electrode for voltammetric measurement of both pH and an
134 ge of 1.58 V at 30 mA cm(-2) as bifunctional electrode for water splitting, which is much better than
135 ioreceptor to validate the employment of DLC electrodes for bioelectrochemical sensing.
136 nzyme-modified carbon paste (CP) microneedle electrodes for square wave voltammetric (SWV) detection
137                               Composite PANI electrodes for the detection of ammonium (NH(4)(+)) have
138 ensors behaved almost identically to Au disk electrodes for the oxidation of an outer-sphere redox co
139 er and faster protocol (~1 h) and disposable electrodes for the transduction.
140 electrochemical impedance spectroscopy after electrode functionalization with specific anti-PARK7/DJ-
141                           Each ion-selective electrode functions in an equilibrium mode, hence, ensur
142 ctrochemical sensor based on a glassy carbon electrode (GC) modified with graphene quantum dots (GQDs
143 rticles (PtNPs) decorated on a glassy carbon electrode (GCE) modified with Fe-based metal-organic fra
144                                    Using two electrodes gives rise to an unequal distance between the
145                                   POC/MWCNTs electrode has shown a linear range for the detection of
146       The pre-eminence of EPPGE over mercury electrodes has been proved in terms of sensitivity and i
147 reveals the influence that charge-collecting electrodes have on the electronic noise at low frequency
148 r(2)O(3) on isostructural V(2)O(3) thin film electrodes helps eliminate the existence of twin domains
149  composed of several identical ion-selective electrodes immersed into separate sample solutions of eq
150 cal responses from 96 epilepsy patients with electrode implantation in left or right primary, seconda
151                 We applied this procedure to electrodes implanted in human epilepsy patients (both ma
152    We obtained direct neural recordings from electrodes implanted in human subjects and showed that a
153 d for application of the sensor as a working electrode in an EC setup.
154 ble composite of nanomembrane electrodes (16 electrodes in a four by four array), elastomer, and fabr
155 above 240 degrees C to maintain the metallic electrodes in a molten state.
156                           The stabilities of electrodes in different LHCEs indicate the intrinsic syn
157 electron acceptors such as graphene oxide or electrodes in microbial electrolysis cells.
158 es not require invasive procedures to impale electrodes in nerves and thus has advantages over micron
159 ications of these binder-free nanostructured electrodes in practical full-cell-configuration LIBs, in
160  structural and functional properties of the electrodes in sensing.
161  simultaneously in the positive and negative electrodes in the full electrochemical cell.
162 table passivation interphases formed on both electrodes in the novel IL electrolyte are the key to hi
163 cus on the fabrication of carbon black-based electrodes in the realisation of sensors and biosensors
164 owever, the added setup complexity caused by electrodes in the system impedes efficient screening of
165 he NMR experiments monitor processes in both electrodes individually, including Li-ion mobility and i
166 nger muscle activity using bipolar fine-wire electrodes inserted into the extrinsic finger muscles of
167                                   The 3DP GC electrode integrated with a NiFeP nanosheets array exhib
168 m at high potentials in conventional layered electrodes involving both cationic and anionic reactions
169 peak current of VAN obtained with the T3T-Au electrode is 4.3 times greater than the bare Au electrod
170 moval process, efficient regeneration of the electrode is achieved at -1.2 V wherein Fc(+) is reduced
171 III) removal can be achieved at 0 V once the electrode is activated via anodic polarization.
172 l performance of PANI-intercalated V(2) O(5) electrode is remarkable improved, exhibiting excellent h
173 : The self-corrosion of bR integrated Cu(2)O electrodes is delayed for about 36 times; The photocurre
174 mes; The photocurrent of bR integrated CuSCN electrodes is enhanced by about 400%, which is attribute
175 esult, the dynamic potential response of the electrodes is entirely ascribed to the stoichiometric fo
176 citive deionization (CDI) with porous carbon electrodes is limited by the high ionic resistance of th
177 g RGO on three-dimensional (3D) carbon paper electrodes is one strategy towards overcoming this chall
178                                Ion-selective electrodes (ISEs) are widely used analytical devices to
179                 Calibration of ion-selective electrodes (ISEs) is cumbersome, time-consuming, and con
180 transparent, and electrocatalytically active electrode material for studying nanobubbles generated at
181 w, but their energy densities are limited by electrode materials and conventional liquid electrolytes
182 rous carbons, as the most commonly used EDLC electrode materials in the field of capacitive energy st
183 developing rational frameworks for selecting electrode materials used to harvest salinity gradient en
184 the diverse set of electrolyte compositions, electrode materials, and operating parameters, a clear u
185 mprehensive and rigorous evaluation of novel electrode materials, application of scalable proof-of-co
186 ce of such batteries is limited by available electrode materials, especially for sodium-ion layered o
187 e the potential to further explore alternate electrode materials, use of ion exchange membranes, and
188 ces, including electrocatalytic reactions at electrode/membrane interfaces in fuel cells and ion inse
189 vice configuration comprises a glassy carbon electrode modified with a film of conductive MOF (M(3)HX
190 ection analysis (FIA) mode via the use of an electrode modified with TiO(2) impregnated with HRP.
191 Reduction of mediators on biocompatible gold electrodes modified with carbon ink or fumed silica can
192                                          The electrode modifier, PDA-Au, provided a functionalizable
193 mined that the electrochemical window of BDD electrodes narrows as temperature increases; activation
194 dependent on the trajectory of the implanted electrode nor on first surgery pneumocephalus (0.07%: %D
195                                     By using electrodes of low surface capacitance, we report for the
196    However, the fabrication of architectured electrodes often involves multiple laborious steps that
197  (PBEA) constituted by eight stencil-printed electrodes on a flexible PET (polyethylene terephthalate
198 prostheses have been limited either by large electrodes or small numbers of pixels.
199 ommonly observed in voltammograms of silicon electrodes originate from silica-silicon redox chemistry
200                             A screen-printed electrode pair coated by a membrane impregnated with a m
201 tein's orientation and binding nature to the electrodes play in determining the electron transport tu
202                                   Increasing electrode potential and associated EET current leads to
203 0% selectivity on a carbon basis at a modest electrode potential of -0.536 V vs. the reversible hydro
204 e from the electrode (ca. 75 mum), while the electrode potential was varied in time.
205 us electron transfer was not affected by the electrode potential.
206 binder-free and straightforward strategy for electrode preparation by silver nanoparticles may provid
207            The results demonstrate that gold electrodes prepared on polyolefin films exhibit a low ch
208 ances is addressed by the introduction of an electrode pretreatment and the integration of a tailor-m
209 nalizable interface for the sensitization of electrode probes; besides, a suitable hydrophilic interf
210   The device utilizes microfabricated planar electrodes projecting into one side of the microfluidic
211 ed (Nernstian) response slope, and reference electrodes provide sample-independent reference potentia
212 gnostic criteria of the stoichiometry of the electrode reaction.
213                          Based on individual electrode reconstructions, the volumes of tissue activat
214                                       Saline electrodes recorded unipolar and bipolar electrograms; m
215 period indicated that the sensitivity of the electrode remains active for several runs of the analysi
216  mA cm(-2) at 1.23 V vs. reversible hydrogen electrode (RHE) with an onset potential of 0.55 V vs. RH
217 ency (99% at -580 mV vs. Reversible Hydrogen Electrode (RHE)), small onset overpotential (<90 mV) and
218 1) at -0.95 V versus the reversible hydrogen electrode (RHE), with a FE for formate of 96 % and curre
219                                              Electrode's chronocoulometric responses at 0.3 V, in the
220 pping voltammetry (SW-ASV) with a solid gold electrode (SGE) and using a portable potentiostat.
221                                      Nanotip electrodes show a slightly higher and narrower spike tha
222  local field potentials (rLFPs) from 196-364 electrode sites within 8-10 mm(3) of brainstem tissue in
223 s, but the information content varies due to electrode size and location.
224 al for studying nanobubbles generated at the electrode/solution interface.
225 s are deposited on the screen printed carbon electrode (SPCE) using chitosan as cross-linked agent fo
226 onvenient assembly for screen printed carbon electrodes (SPCE) suitable for analyses in gaseous sampl
227 receptor with a simple electrode-electrolyte-electrode structure simultaneously detects temperature a
228 PS analysis are employed to characterize the electrodes' structure and composition and identify any s
229                                       Across electrodes, subadditivity correlated with visual respons
230 ctrodes are simple to make and can be useful electrode substrates for (single molecule) spectroelectr
231 ion spectra (XAS) on single particles of the electrode, such as the C and O K-edges to track the stab
232 ilters, separators, absorbents, and wearable electrodes, supercapacitors and cells.
233 trolyte (E/E) interface, made by coating the electrode surface with a quaternary ammonium cation (R(4
234  which isolates the dispersed phase from the electrode surface, is demonstrated as enabling such meas
235        When antibodies are introduced on the electrode surface, they selectively bind with the antige
236 dispersed phase is in close proximity to the electrode surface.
237 umber of antibodies (Abs) immobilized on the electrode surface.
238  thereby facilitating As desorption from the electrode surface.
239 cules at well-defined Pt(hkl) single-crystal electrode surfaces is a key step towards addressing cata
240 ng silicone pastes and in situ activation of electrode surfaces via cold-air plasma, we show that sof
241 ingle-cell-level dynamics of EET not only on electrode surfaces, but also during respiration of other
242 he salt and the solvent when they coexist on electrode surfaces.
243 oven challenging to fabricate suitable three-electrode systems on paper.
244 d that anisotropic corrosion of the platinum electrode takes place in different stages.
245 (2) ) MXene film with transparent conducting electrode (TCE) properties, including high electrical co
246 hod allows for an approach of the tip to the electrode that is electrolyte-free and consequently also
247 tion-based microfluidic sensor with embedded electrodes that can detect and enumerate cancer cells in
248  bath or blood pool directly in contact with electrodes that exhibit a pressure-induced reduction in
249 rganic frameworks (MOFs) as drop-casted film electrodes that facilitate voltammetric detection of red
250 ad (Pb)- and mercury (Hg)-based liquid metal electrodes, the nontoxic Ga alloys maintain high environ
251 work of Shewanella oneidensis MR-1 to a gold electrode, thereby increasing biocurrent ~150-fold over
252 low (ETF) in the electrolyte surrounding the electrode, thereby increasing the sensitivity of the SWV
253 ttachment points on the backbone to the gold electrodes, thereby giving rise to multiple conductance
254 ficant flaws related to metal/salt reference electrodes: they are bulky and difficult to miniaturize,
255       In conjunction with a stable reference electrode, this three-electrode configuration will be cr
256 al performance of the resultant NP-assembled electrodes through improved charge transfer efficiency.
257                     H(+)- and K(+)-selective electrodes thus prepared exhibit highly selective respon
258 BS devices undergoing MRI are heating at the electrode tips, induced currents, implantable pulse gene
259  electrode array with ultramicro-dimensioned electrodes to achieve improved functionally selective re
260 trapping, we employ two parallel sidewall 3D electrodes to produce a dielectrophoretic force which tr
261                             We used multiple electrodes to record BG spiking and field potentials dur
262 cose oxidase (GOD) enzyme onto an ultramicro electrode (UME) to measure the local glucose consumption
263 he near-surface region of polycrystalline Cu electrodes under in situ conditions through a combinatio
264 aviour of FNX was studied on a glassy carbon electrode using cyclic voltammetry, while glassy carbon
265 nces were measured at each of the array's 60 electrodes using the Cirrus HD-OCT software in both the
266 active volume fraction, thick, 3D-structured electrodes (V(2) O(5) cathode and Li metal anode) are re
267 tive cluster is connected to two macroscopic electrodes via anchoring ligands.
268            As proofs-of-concept, the rGO-PLA electrode was applied for serotonin determination in syn
269                                    The Pd/Au electrode was characterized by AFM and XPS as well as mu
270 lly detected by the DGTFT where the top gate electrode was connected to the extended MZO(nano) sensin
271 al sweep voltammetry on a glassy carbon (GC) electrode was developed to distinguish and quantify two
272       The whole surface of the microspot BDD electrode was found active toward the voltammetric oxida
273 yclic voltammetry, while glassy carbon paste electrode was selected for analytical purposes.
274                                 The modified electrode was then employed as an amperometric sensing e
275 he TEE for ion separation using flow-through electrodes was compared to a system using flow-by electr
276           A 16-well plate containing sensing electrodes was pre-coated with receptor binding domain (
277 explained by the observation that, on the Au electrode, water reduction improves with more alkaline p
278           Further, using a Clark-type oxygen electrode, we measured isolated rat liver mitochondrial
279  in the bR and p-type semiconductor combined electrodes, we reached several important conclusions: Th
280                      In this study, platinum electrodes were fabricated on the bio-based poly(ethylen
281      Furthermore, the biofilm microbiomes at electrodes were studied using the PacBio sequencing of f
282 chronically implanted electroencephalography electrodes were surrounded by lymphatic sprouts originat
283 zones each with shared reference and counter electrodes were used for SWASV and SWCSV, respectively.
284                         Intramuscular needle electrodes were used to sample individual motor unit pot
285 slightly higher and narrower spike than disk electrodes when measuring exocytosis.
286 rotect it during the deposition of the metal electrode which requires conditions under which organic
287  is the requirement for mass transfer to the electrode, which gives rise to the diffusional broadenin
288 e applied via two parallel three-dimensional electrodes, which interface the nanodroplets through pol
289 dorsal-lateral prefrontal cortex (dlPFC; 768 electrodes) while monkeys performed a two-armed bandit r
290 mmetric sensor based on a glassy carbon (GC) electrode with analysis following a short one-step extra
291                         Thus, nanostructured electrodes with binder-free designs are developed and ha
292 ed and fabricated Pd/Au bimetallic thin film electrodes with isolated Pd nanoparticles via underpoten
293   The array consists of 4,096 platinum-black electrodes with nanoscale roughness fabricated on top of
294 ef fish (bait) placed between the two Scuba7 electrodes with the deterrents randomly being turned on
295 rodes was compared to a system using flow-by electrodes with the same materials.
296 or with a fusion enzyme showed DET to a gold electrode, with a limited operational range less than 0.
297 gh comparison of polished and unpolished BDD electrodes, with hydrogen and oxygen surface termination
298 contrast, occurred first at medial occipital electrodes, with responses at later time-points being mo
299 ified via a pair of opposing planar titanium electrodes, within the cover (0.10 cm(2)) and base (0.50
300 contact with the electrode and within a near-electrode zone (<30 mum) where the hyperpolarization dec

 
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