PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 34927885-7 2021 Interestingly, the oxygen electrode activity (DeltaE) for (Fe,Co)-SA/CS and commercial Pt/C-RuO2 is calculated to be 0.73 V, exhibiting the bifunctional catalytic activity of (Fe,Co)-SA/CS. ruthenium dioxide 92-96 citrate synthase Homo sapiens 69-71 34913578-3 2022 The as-fabricated electrode of CoP@CF-900, when used as both the cathode and anode for overall water splitting, is able to deliver 200 mA cm-2 at a cell voltage of 1.89 V, significantly outshining the Pt/C RuO2 couple; when used as the air cathode for a zinc-air battery, is able to operate more than 150 h at 10 mA cm-2 with a nearly constant round-trip energy efficiency of 60%, also outperforming the Pt/C+RuO2 benchmark. ruthenium dioxide 207-211 caspase recruitment domain family member 16 Homo sapiens 31-34 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 6-10 spindlin 1 Homo sapiens 70-74 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 6-10 spindlin 1 Homo sapiens 135-139 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 6-10 spindlin 1 Homo sapiens 223-227 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 178-182 spindlin 1 Homo sapiens 70-74 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 178-182 spindlin 1 Homo sapiens 135-139 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 178-182 spindlin 1 Homo sapiens 223-227 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 188-192 spindlin 1 Homo sapiens 70-74 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 188-192 spindlin 1 Homo sapiens 135-139 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 188-192 spindlin 1 Homo sapiens 223-227 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 324-328 spindlin 1 Homo sapiens 70-74 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 324-328 spindlin 1 Homo sapiens 135-139 34862380-4 2021 Using RuO2 as a representative compensated antiferromagnet exhibiting spin-independent conductance along the (001) direction but a non-spin-degenerate Fermi surface, we design a RuO2/TiO2/RuO2 (001) AFMTJ, where a globally spin-neutral charge current is controlled by the relative orientation of the Neel vectors of the two RuO2 electrodes, resulting in the TMR effect as large as ~500%. ruthenium dioxide 324-328 spindlin 1 Homo sapiens 223-227 34475400-2 2021 Herein, we synthesize atomically dispersed platinum on ruthenium oxide (Pt1/RuO2) using a simple impregnation-adsorption method. ruthenium dioxide 55-70 zinc finger protein 77 Homo sapiens 72-75 34475400-2 2021 Herein, we synthesize atomically dispersed platinum on ruthenium oxide (Pt1/RuO2) using a simple impregnation-adsorption method. ruthenium dioxide 76-80 zinc finger protein 77 Homo sapiens 72-75 34927885-7 2021 Interestingly, the oxygen electrode activity (DeltaE) for (Fe,Co)-SA/CS and commercial Pt/C-RuO2 is calculated to be 0.73 V, exhibiting the bifunctional catalytic activity of (Fe,Co)-SA/CS. ruthenium dioxide 92-96 citrate synthase Homo sapiens 186-188 33983707-4 2021 From the series of MPX3, CoPS3 yields the best results with an overpotential within the range of values usually obtained for IrO2 or RuO2 catalysts. ruthenium dioxide 133-137 COP9 signalosome subunit 3 Homo sapiens 25-30 35231478-0 2022 Electrocatalytic oxidation of low concentration cefotaxime sodium wastewater using Ti/SnO2-RuO2 electrode: Feasibility analysis and degradation mechanism. ruthenium dioxide 91-95 strawberry notch homolog 1 Homo sapiens 86-89 35231478-7 2022 Therefore, the electrocatalytic oxidation of Ti/SnO2-RuO2 electrode was a clean and efficient technology, which could be widely used in the treatment of CFX wastewater. ruthenium dioxide 53-57 strawberry notch homolog 1 Homo sapiens 48-51 35512266-5 2022 The electrochemical tests manifest that CoS-5 show an overpotential of 290 mV at 10 mA cm-2 and a Tafel slope of 65.6 mV dec-1 in the OER in an alkaline solution, superior to those for other thicknesses of CoS, bulk CoS, and RuO2. ruthenium dioxide 225-229 zinc finger protein 69 Homo sapiens 40-45 32830455-5 2020 As a result of this OER-conditioned surface reconstruction, the optimized catalyst requires an overpotential of only 285 mV at a current density of 10 mA cm-2 with a Tafel slope of 34 mV dec-1 , outperforming commercial RuO2 catalysts. ruthenium dioxide 220-224 deleted in esophageal cancer 1 Homo sapiens 187-192 33977662-5 2021 Specially, PA2-Fe-MoS2 grown on nickel foam (PA2-Fe-MoS2/NF) exhibits excellent OER activity (218 mV@20 mA cm-2) and durability, even superior to RuO2 and many other previously reported OER catalysts. ruthenium dioxide 146-150 neurofascin Homo sapiens 57-59 32916576-6 2021 Consequently, the 10% Fe-Co2(OH)3Cl exhibits a superior OER activity with a lower overpotential of 273 mV at 10 mA cm-2 (after 500 CV cycles) along with an excellent stability as compared with commercial RuO2. ruthenium dioxide 204-208 complement C2 Homo sapiens 25-28 33113663-0 2020 Thermal decomposition based fabrication of dimensionally stable Ti/SnO2-RuO2 anode for highly efficient electrocatalytic degradation of alizarin cyanin green. ruthenium dioxide 72-76 strawberry notch homolog 1 Homo sapiens 67-70 33113663-2 2020 The morphology, crystal structure and composition of Ti/SnO2-RuO2 electrode are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray fluorescence spectroscopy (XRF), respectively. ruthenium dioxide 61-65 strawberry notch homolog 1 Homo sapiens 56-59 33570389-3 2021 Due to the abundant catalytically active sites, promoting electron conduction/mass transmission from the specific micro-nano structure, as well as the ultrasmall thickness of ~3.0 nm, the optimized alpha-Ni(OH)2/NF self-supporting electrode exhibits excellent electrocatalytic performance for OER, merely requiring low overpotentials of 192 and 240 mV to yield current densities of 10 and 100 mA cm-2 in 1.0 M KOH, respectively, which surpassed those of all of the reported nickel hydroxide/oxides and the benchmark RuO2. ruthenium dioxide 516-520 neurofascin Homo sapiens 212-214 32558533-3 2020 The NiS/Fe3O4 HNPs@CNT hybrid delivers superior OER activity in al-kaline medium: it delivers a current density of 10 mA cm-2 at ultralow low overpotential of 243 mV with a small Tafel slope of 44.2 mV dec-1, which outperforms the benchmark RuO2 electrocatalyst; moreover, it exhibits terrific long-term stability over 36 h without any noticeable performance decay. ruthenium dioxide 241-245 solute carrier family 5 member 5 Homo sapiens 4-7 32558533-3 2020 The NiS/Fe3O4 HNPs@CNT hybrid delivers superior OER activity in al-kaline medium: it delivers a current density of 10 mA cm-2 at ultralow low overpotential of 243 mV with a small Tafel slope of 44.2 mV dec-1, which outperforms the benchmark RuO2 electrocatalyst; moreover, it exhibits terrific long-term stability over 36 h without any noticeable performance decay. ruthenium dioxide 241-245 deleted in esophageal cancer 1 Homo sapiens 202-207 32311236-5 2020 Furthermore, O-Co0.5 Mo0.5 Se2 air cathode-based zinc-air batteries exhibit an excellent power density of 120.28 mW cm-2 and exceptional cycling stability for 60 h, superior to those of state-of-art Pt/C+RuO2 pair-based zinc-air batteries. ruthenium dioxide 204-208 fucosyltransferase 2 Homo sapiens 27-30 32509491-4 2020 Ni/CTF-1-600 requires 374 mV overpotential in OER to reach 10 mA/cm2, which outperforms the benchmark RuO2 catalyst, which requires 403 mV under the same conditions. ruthenium dioxide 102-106 cardiotrophin 1 Homo sapiens 3-8 30684751-3 2019 Electrochemical measurements indicate that as-obtained NOC-800 sample has satisfactory multifunctional oxygen-involving electrocatalytic properties in alkaline media, showing an onset and half-wave potential of -0.141 and -0.249 V vs. Ag/AgCl for oxygen reduction and an overpotential of 377 and 448 mV at 10 and 50 mA cm-2 for electrocatalytic oxygen evolution, respectively, even comparable to commercial RuO2 catalyst and majority of present mainstream metal-free catalysts. ruthenium dioxide 407-411 nocturnin Homo sapiens 55-58 32296963-2 2020 The electrocatalytic performance evaluations show that the as-prepared electrocatalyst exhibits an overpotential of 342 mV at current density of 10 mA cm-2 and the Tafel slope of 74 mV dec-1 for oxygen evolution reaction (OER), which is superior to the most advanced ruthenium oxide electrocatalyst. ruthenium dioxide 267-282 deleted in esophageal cancer 1 Homo sapiens 185-190 31215575-5 2019 Moreover, the MOF shows higher durability with >70% performance retention after 25 hours of reaction and tolerance towards methanol; this demonstrates its potential for application in direct methanol fuel cells (DMFCs); furthermore, due to the availability of more active sites and accessible surface area, the Co-MOF performs well towards the OER with lower onset potential and small Tafel slope as compared to the commercial RuO2 nanoparticles. ruthenium dioxide 430-434 lysine acetyltransferase 8 Homo sapiens 14-17 31215575-7 2019 It shows the high TOF value of 93.21 s-1 at the overpotential of 350 mV as compared to the reported MOF/nanoparticle-based electrocatalysts and the state-of-the-art RuO2. ruthenium dioxide 165-169 lysine acetyltransferase 8 Homo sapiens 100-103 31140732-7 2019 More importantly, the Co/Cox My +Pt/C achieves higher voltaic efficiency and several times longer cycle life than conventional RuO2 +Pt/C catalysts in rechargeable Zn-air batteries. ruthenium dioxide 127-131 cytochrome c oxidase subunit 8A Homo sapiens 25-28 32280875-3 2020 The synthesized codoped RuO2 with a Mn/Fe molar ratio of 1 reflected a Tafel slope of only 41 mV dec-1, which is appreciably lower than 64 mV dec-1 for pure RuO2. ruthenium dioxide 24-28 deleted in esophageal cancer 1 Homo sapiens 97-102 32280875-3 2020 The synthesized codoped RuO2 with a Mn/Fe molar ratio of 1 reflected a Tafel slope of only 41 mV dec-1, which is appreciably lower than 64 mV dec-1 for pure RuO2. ruthenium dioxide 24-28 deleted in esophageal cancer 1 Homo sapiens 142-147 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 63-66 32254471-3 2018 The quantitative detection of matrix metalloproteinase-2 (MMP-2) (bio-marker for stroke and vascular diseases) was demonstrated by tracking the spectral shift of the characteristic G band of graphene caused by the adsorption of RuO2 NPs. ruthenium dioxide 228-232 matrix metallopeptidase 2 Homo sapiens 30-56 30043787-4 2018 Based on CP 1, a device FTO/CP 1/RuO2 was constructed, which showed a much enhanced photoresponse with a much larger specific capacity (120.7 C g-1) than the individual CP 1 (<1 C g-1) and RuO2 (10.5 C g-1) when irradiated by visible light in the presence of methanol. ruthenium dioxide 33-37 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 24-27 30043787-4 2018 Based on CP 1, a device FTO/CP 1/RuO2 was constructed, which showed a much enhanced photoresponse with a much larger specific capacity (120.7 C g-1) than the individual CP 1 (<1 C g-1) and RuO2 (10.5 C g-1) when irradiated by visible light in the presence of methanol. ruthenium dioxide 192-196 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 24-27 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 43-47 lysine acetyltransferase 8 Homo sapiens 30-33 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 43-47 lysine acetyltransferase 8 Homo sapiens 63-66 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 30-33 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 63-66 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 30-33 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 63-66 30902984-4 2019 Specifically we demonstrate a MOF-confined RuO2 catalyst (RuO2@MOF-808-P) with exceptionally high catalytic CO oxidation below 150 C as compared to the conventionally made SiO2-supported RuO2 (RuO2/SiO2). ruthenium dioxide 58-62 lysine acetyltransferase 8 Homo sapiens 30-33 30902984-5 2019 This can be caused by weaker interactions between CO/O and the MOF-encapsulated RuO2 surface thus avoiding adsorption-induced catalytic surface passivation. ruthenium dioxide 80-84 lysine acetyltransferase 8 Homo sapiens 63-66 30398084-1 2018 AIM: To study of the interactions of two new ruthenium(II) complexes (C1 and C2) with calf thymus (CT)-DNA; production of RuO2 nanoparticles using the complexes precursor. ruthenium dioxide 122-126 complement C2 Bos taurus 70-79 32254471-3 2018 The quantitative detection of matrix metalloproteinase-2 (MMP-2) (bio-marker for stroke and vascular diseases) was demonstrated by tracking the spectral shift of the characteristic G band of graphene caused by the adsorption of RuO2 NPs. ruthenium dioxide 228-232 matrix metallopeptidase 2 Homo sapiens 58-63 28868759-4 2017 The iron oxide nanocarbon electrocatalyst performances are highlighted by the overall overpotential of approximately 1 V needed to reach the benchmark threshold of 10 mA cm-2 for the oxygen reduction reaction and the particular activity towards oxygen evolution reaction (eta 0.4 V at 10 mA cm-2 ), comparable to that of the precious RuO2 and IrO2 catalysts. ruthenium dioxide 334-338 endothelin receptor type A Homo sapiens 272-275 29215259-4 2018 As for the chemical/aging stability, the hybrid TCF of Ag NW and TiO2 NS reveals a retained initial conductivity (DeltaRs/Rs < 1%) under ambient oxidant gas over a month, superior to that of bare Ag NW (DeltaRs/Rs > 4000%) or RuO2 NS-Ag NW hybrid (DeltaRs/Rs > 200%). ruthenium dioxide 232-236 hepatocyte nuclear factor 4 alpha Homo sapiens 48-51 29201620-4 2017 By integrating the catalytically active CoFe2O4 nanoparticles with the N-doped carbon nanofibers, the as-synthesized CoFe2O4@N-CNF nanohybrid manifests superior OER performance with a low overpotential, a large current density, a small Tafel slope, and long-term durability in alkaline solution, outperforming the single component counterparts (pure CoFe2O4 and N-doped carbon nanofibers) and the commercial RuO2 catalyst. ruthenium dioxide 408-412 NPHS1 adhesion molecule, nephrin Homo sapiens 127-130 28006096-2 2017 When an electrically contiguous ~9 nm thick RuO2 nanoskin is expressed on commercially available, insulating SiO2 fiber paper, the RuO2@SiO2 electrode exhibits high current density at low overpotential (10 mA cm-2 @ eta = 280 mV), courtesy of a catalyst amplified in 3D; however, the mass-normalized activity falls short of that achieved for films deposited on planar, metallic substrates (Ti foil). ruthenium dioxide 44-48 endothelin receptor type A Homo sapiens 216-219 28006096-2 2017 When an electrically contiguous ~9 nm thick RuO2 nanoskin is expressed on commercially available, insulating SiO2 fiber paper, the RuO2@SiO2 electrode exhibits high current density at low overpotential (10 mA cm-2 @ eta = 280 mV), courtesy of a catalyst amplified in 3D; however, the mass-normalized activity falls short of that achieved for films deposited on planar, metallic substrates (Ti foil). ruthenium dioxide 131-135 endothelin receptor type A Homo sapiens 216-219 28006096-3 2017 By wrapping the fibers with a <100 nm thick graphitic carbon layer prior to RuO2 deposition (RuO2@C@SiO2), we retain the high mass activity of the RuO2 (40-60 mA mg-1 @ eta = 330 mV) and preserve the desirable macroscale properties of the 3D scaffold: porous, lightweight, flexible, and inexpensive. ruthenium dioxide 79-83 endothelin receptor type A Homo sapiens 114-117 28006096-3 2017 By wrapping the fibers with a <100 nm thick graphitic carbon layer prior to RuO2 deposition (RuO2@C@SiO2), we retain the high mass activity of the RuO2 (40-60 mA mg-1 @ eta = 330 mV) and preserve the desirable macroscale properties of the 3D scaffold: porous, lightweight, flexible, and inexpensive. ruthenium dioxide 96-100 endothelin receptor type A Homo sapiens 114-117 28006096-3 2017 By wrapping the fibers with a <100 nm thick graphitic carbon layer prior to RuO2 deposition (RuO2@C@SiO2), we retain the high mass activity of the RuO2 (40-60 mA mg-1 @ eta = 330 mV) and preserve the desirable macroscale properties of the 3D scaffold: porous, lightweight, flexible, and inexpensive. ruthenium dioxide 96-100 endothelin receptor type A Homo sapiens 114-117 24663242-3 2014 Here, we report a simple and scalable way of preparing a three-dimensional (3D) sub-5 nm hydrous ruthenium oxide (RuO2) anchored graphene and CNT hybrid foam (RGM) architecture for high-performance supercapacitor electrodes. ruthenium dioxide 97-112 repulsive guidance molecule BMP co-receptor a Homo sapiens 159-162 27700048-3 2016 Herein, we report growth of one-dimensional highly crystalline RuO2 nanowires on carbon nitride (1D-RuO2-CNx) for their applications in HER and OER at all pH values. ruthenium dioxide 63-67 calnexin Homo sapiens 105-108 27700048-6 2016 The mass activity of 1D-RuO2-CNx catalyst is 352 mA mg-1, which is ~14 times higher than that of commercial RuO2. ruthenium dioxide 24-28 calnexin Homo sapiens 29-32 27700048-7 2016 Most importantly, the 1D-RuO2-CNx catalyst has remarkably higher stability compared to commercial RuO2. ruthenium dioxide 25-29 calnexin Homo sapiens 30-33 27700048-12 2016 This superior catalytic activity of 1D-RuO2-CNx composite can be attributed to catalyst-support interaction, enhanced mass and electron transport, one-dimensional morphology, and highly crystalline rutile RuO2 structure. ruthenium dioxide 39-43 calnexin Homo sapiens 44-47 27440473-2 2016 Impressively, this noble-metal-free 3 D Cu(OH)2 -NWAs/Cu foil electrode shows the highest catalytic activity with a Tafel slope of 86 mV dec(-1) , an overpotential (eta) of about 530 mV at ~10 mA cm(-2) (controlled-potential electrolysis method without iR correction) and almost 100 % Faradic efficiency, paralleling the performance of the state-of-the-art RuO2 OER catalyst in 0.1 m NaOH solution (pH 12.8). ruthenium dioxide 357-361 deleted in esophageal cancer 1 Homo sapiens 137-143 27440473-2 2016 Impressively, this noble-metal-free 3 D Cu(OH)2 -NWAs/Cu foil electrode shows the highest catalytic activity with a Tafel slope of 86 mV dec(-1) , an overpotential (eta) of about 530 mV at ~10 mA cm(-2) (controlled-potential electrolysis method without iR correction) and almost 100 % Faradic efficiency, paralleling the performance of the state-of-the-art RuO2 OER catalyst in 0.1 m NaOH solution (pH 12.8). ruthenium dioxide 357-361 endothelin receptor type A Homo sapiens 26-29 24663242-3 2014 Here, we report a simple and scalable way of preparing a three-dimensional (3D) sub-5 nm hydrous ruthenium oxide (RuO2) anchored graphene and CNT hybrid foam (RGM) architecture for high-performance supercapacitor electrodes. ruthenium dioxide 114-118 repulsive guidance molecule BMP co-receptor a Homo sapiens 159-162 24663242-4 2014 This RGM architecture demonstrates a novel graphene foam conformally covered with hybrid networks of RuO2 nanoparticles and anchored CNTs. ruthenium dioxide 101-105 repulsive guidance molecule BMP co-receptor a Homo sapiens 5-8 22742810-1 2012 A non-enzymatic glucose sensor of multi-walled carbon nanotube-ruthenium oxide/composite paste electrode (MWCNT-RuO(2)/CPE) was developed. ruthenium dioxide 63-78 carboxypeptidase E Homo sapiens 119-122 17386417-1 2007 A bilayer surface coating, prepared by electrodepositing ruthenium oxide (RuOx) onto a carbon nanotube (CNT) layer, offers dramatic improvements in the stability and sensitivity of voltammetric and amperometric measurements of insulin compared to the individual (CNT or RuOx) coated electrodes. ruthenium dioxide 57-72 insulin Homo sapiens 227-234 17386417-1 2007 A bilayer surface coating, prepared by electrodepositing ruthenium oxide (RuOx) onto a carbon nanotube (CNT) layer, offers dramatic improvements in the stability and sensitivity of voltammetric and amperometric measurements of insulin compared to the individual (CNT or RuOx) coated electrodes. ruthenium dioxide 74-78 insulin Homo sapiens 227-234 16910042-0 2006 Determination of catalase-like activity in plants based on the amperometric monitoring of hydrogen peroxide consumption using a carbon paste electrode modified with ruthenium(IV) Oxide. ruthenium dioxide 165-184 catalase Homo sapiens 17-25 16491497-3 2006 Oxidation of PEG-1 by m-CPBA in CH(2)Cl(2), dioxane, or water afforded a water-soluble PEG-supported dioxoruthenium(VI) porphyrin (PEG-2), which could react with hydrocarbons to give oxidation products in up to 80 % yield. ruthenium dioxide 101-115 mesoderm specific transcript Homo sapiens 13-18 11248902-3 2001 The glucose probe is based on the biocatalytic action of glucose oxidase, and the insulin one relies on the electrocatalytic activity of ruthenium oxide. ruthenium dioxide 137-152 insulin Homo sapiens 82-89 15038276-6 2004 In contrast to the RuO2(110) surface, the RuO2(100) surface stabilizes also a catalytically inactive c(2 x 2) surface phase onto which CO is not able to adsorb above 100 K. We argue that this inactive RuO2(100)-c(2 x 2) phase may play an important role in the deactivation of RuO2 catalysts in the electrochemical Cl2 evolution and other heterogeneous reactions. ruthenium dioxide 42-46 endogenous retrovirus group W member 5 Homo sapiens 314-317 15038276-6 2004 In contrast to the RuO2(110) surface, the RuO2(100) surface stabilizes also a catalytically inactive c(2 x 2) surface phase onto which CO is not able to adsorb above 100 K. We argue that this inactive RuO2(100)-c(2 x 2) phase may play an important role in the deactivation of RuO2 catalysts in the electrochemical Cl2 evolution and other heterogeneous reactions. ruthenium dioxide 42-46 endogenous retrovirus group W member 5 Homo sapiens 314-317 15038276-6 2004 In contrast to the RuO2(110) surface, the RuO2(100) surface stabilizes also a catalytically inactive c(2 x 2) surface phase onto which CO is not able to adsorb above 100 K. We argue that this inactive RuO2(100)-c(2 x 2) phase may play an important role in the deactivation of RuO2 catalysts in the electrochemical Cl2 evolution and other heterogeneous reactions. ruthenium dioxide 42-46 endogenous retrovirus group W member 5 Homo sapiens 314-317