ライフサイエンスコーパス: electrooxidation

1 atalyst was designed and synthesized for DME electrooxidation.

2 m) Pd-Ni-P ternary nanoparticles for ethanol electrooxidation.

3 ent change in the protein occurred following electrooxidation.

4 ivity over commercial catalysts for methanol electrooxidation after 10,000 cycles.

5 de fouling) of byproducts resulting from the electrooxidation and polymerization of tyramine.

6 a stable N2 nanobubble is determined by N2H4 electrooxidation at the three phase contact line.

7 anic matter (NOM) negatively affected the TC electrooxidation because of competition for CNT sorption

8 ingly, those two CO bands showed independent electrooxidation behavior with electrode potential chang

9 t and the charge transfer coefficient of ACh electrooxidation by the active nickel species, and the d

10 The observed promotion in CO electrooxidation by the existence of a Ru island on Pt n

11 are much higher than reported for any water electrooxidation catalyst before.

12 , and economic sound electrocatalysts for CO electrooxidation (COE) are the emerging key for wide var

13 Moreover, the electrooxidation conditions were harsh, involving an oxi

14 As a result, the ratio of the urate electrooxidation current to the O2 electroreduction curr

15 during cyclic voltammetry, while the glucose electrooxidation current was increased 3-fold to approxi

16 hey were subsequently exploited for methanol electrooxidation in alkaline media.

17 stimation of hydrogen peroxide (H(2)O(2)) by electrooxidation in physiological conditions is reported

18 d into enhanced CO tolerance during hydrogen electrooxidation in the presence of CO.

19 Because an unidentified urate electrooxidation intermediate, formed in the presence of

20 dies confirm that the product of isopropanol electrooxidation is acetone, generated with a Faradaic e

21 cterized and their catalytic activity for CO electrooxidation is evaluated.

22 holinobenzene thiols was carried out via the electrooxidation of 4-morpholinoaniline in the presence

23 in freely moving and anesthetized rats, the electrooxidation of 5-HT forms products that quickly pol

24 When water is present in an ionic liquid, electrooxidation of a gold electrode forms gold oxides.

25 tween base pairs of ds-DNA and catalyzes the electrooxidation of AA.

26 The third example investigates the electrooxidation of aniline by utilizing an EMLC column

27 hibits high electrocatalytic activity toward electrooxidation of AP, Ph, and NP to three well-separat

28 Electrooxidation of ascorbyl palmitate (AP) over gold sc

29 layed enhanced catalytic activity toward the electrooxidation of carbohydrates.

30 metal-oxide, and the catalytic activity for electrooxidation of carbon monoxide.

31 Electrooxidation of CH3OH (1.23 M) in a buffered aqueous

32 es studied (1.5 nm) were the most active for electrooxidation of CO and had the largest fraction of o

33 The surface stress response during the electrooxidation of CO at Pt{111}, Ru{0001}, and Ru(thet

34 The electrooxidation of CO has been studied on reconstructed

35 Also, it is shown that the electrooxidation of CO on large Ru islands is less facil

36 at GO and PcCo have a synergic effect in the electrooxidation of CSH.

37 potential waveform was employed, causing the electrooxidation of either IC solely or IC and AR simult

38 litting the C-C bond is the main obstacle to electrooxidation of ethanol (EOR) to CO(2).

39 As test cases, the electrooxidation of formaldehyde and methanol on carbon

40 hedra show higher poisoning tolerance in the electrooxidation of formic acid than Pt cubes; the oxida

41 The simultaneous electrooxidation of four alcohols (ethanol, 1-propanol,

42 tudies revealed that, on the hybrid material electrooxidation of glucose occurs at a lower potential

43 for the first time that laccase can catalyze electrooxidation of H2O to molecular oxygen.

44 sk electrodes (6-90 nm) via the irreversible electrooxidation of hydrazine (N2H4 --> N2 + 4H(+) + 4e(

45 Complexes 1 and 2 are active for the electrooxidation of isopropanol in the presence of stron

46 ully to fabrication of new biosensor for the electrooxidation of l-cysteine (CSH) in aqueous media.

47 studies in the hydrogen evolution reaction, electrooxidation of methanol and CO, and electroreductio

48 ocarbon conversion reactions for fuel cells (electrooxidation of methanol, ethanol, and formic acid).

49 f hydrogen ions, which were generated in the electrooxidation of methanol.

50 trocatalytic activity, enhanced kinetics for electrooxidation of NA, and fast electron-transfer betwe

51 idize the tyrosine residues have allowed the electrooxidation of NADH at low potentials due to the ca

52 CHIT-AZU matrix facilitated the AZU-mediated electrooxidation of NADH.

53 robust CNT-CHIT films, which facilitated the electrooxidation of NADH.

54 The reaction occurring on electrooxidation of Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridin

55 Electrooxidation of TPA generates a TPA*+ radical cation

56 mation of a similar diimine species from the electrooxidation of xanthine, which has not been previou

57 The glucose was detected by its electrooxidation on a stationary glassy carbon disk surr

58 igated the structure sensitivity of methanol electrooxidation on eight transition metals (Au, Ag, Cu,

59 stigate two separate mechanisms for methanol electrooxidation: one going through a CO* intermediate (

60 T electrodes were used for investigating the electrooxidation process of insulin and amperometric det

61 The mechanism and kinetics of the electrooxidation process were investigated by cyclic vol

62 -SHINERS) is utilized to in situ monitor the electrooxidation processes at atomically flat Au(hkl) si

63 ate, which improved efficiency in an ethanol electrooxidation reaction compared with a conventional p

64 , platinum-based electrocatalysts for the CO electrooxidation reaction in CO(g)-saturated solution; t

65 eved for the hydrogen evolution and methanol electrooxidation reactions.

66 00) surfaces explains the origin of methanol electrooxidation's experimentally-established structure

67 because of competition for CNT sorption and electrooxidation sites.

68 ation efficiency of halide ions prior to the electrooxidation step.

69 ectrocatalytic activity and stability for CO electrooxidation than commercial and other reported prec

70 f adsorbed CO* and OH* can describe methanol electrooxidation trends on various metal surfaces reason

71 nderpotential deposition and carbon monoxide electrooxidation, which showed that nanoframe surfaces w

72 Formic acid electrooxidation with this novel material shows 4 times