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1 generated as gas-phase templates by methanol electrooxidation.
2 t improved energy generation through deep EG electrooxidation.
3 ch relates with the pre-oxidation peak of CO electrooxidation.
4 m) Pd-Ni-P ternary nanoparticles for ethanol electrooxidation.
5 atalyst was designed and synthesized for DME electrooxidation.
6 ent change in the protein occurred following electrooxidation.
7 ivity over commercial catalysts for methanol electrooxidation after 10,000 cycles.
8 de fouling) of byproducts resulting from the electrooxidation and polymerization of tyramine.
9 a stable N2 nanobubble is determined by N2H4 electrooxidation at the three phase contact line.
10 anic matter (NOM) negatively affected the TC electrooxidation because of competition for CNT sorption
11 ingly, those two CO bands showed independent electrooxidation behavior with electrode potential chang
12 t and the charge transfer coefficient of ACh electrooxidation by the active nickel species, and the d
13                 The observed promotion in CO electrooxidation by the existence of a Ru island on Pt n
14  are much higher than reported for any water electrooxidation catalyst before.
15 , and economic sound electrocatalysts for CO electrooxidation (COE) are the emerging key for wide var
16                                Moreover, the electrooxidation conditions were harsh, involving an oxi
17                                        Using electrooxidation, crystals of cationic mixed-valence (MV
18          As a result, the ratio of the urate electrooxidation current to the O2 electroreduction curr
19 during cyclic voltammetry, while the glucose electrooxidation current was increased 3-fold to approxi
20 ynergistic combination of electrocoagulation-electrooxidation (EC-EO) process was used in the current
21                                              Electrooxidation experiments conducted with high initial
22                                      Ammonia electrooxidation has received considerable attention in
23 ger of Earth-abundant 3d metal catalysis and electrooxidation has recently been recognized as an incr
24 nd commercial Pt/C catalysts toward methanol electrooxidation, highlighting the importance of crystal
25                                    Hydrazine electrooxidation, hydroxylamine electrooxidation/reducti
26 hey were subsequently exploited for methanol electrooxidation in alkaline media.
27                                 For methanol electrooxidation in an acid electrolyte, due to the cont
28 stimation of hydrogen peroxide (H(2)O(2)) by electrooxidation in physiological conditions is reported
29 d into enhanced CO tolerance during hydrogen electrooxidation in the presence of CO.
30                Because an unidentified urate electrooxidation intermediate, formed in the presence of
31 dies confirm that the product of isopropanol electrooxidation is acetone, generated with a Faradaic e
32 cterized and their catalytic activity for CO electrooxidation is evaluated.
33  for determination of vanillin including the electrooxidation mechanism of vanillin and different par
34 holinobenzene thiols was carried out via the electrooxidation of 4-morpholinoaniline in the presence
35  in freely moving and anesthetized rats, the electrooxidation of 5-HT forms products that quickly pol
36    When water is present in an ionic liquid, electrooxidation of a gold electrode forms gold oxides.
37 tween base pairs of ds-DNA and catalyzes the electrooxidation of AA.
38           The third example investigates the electrooxidation of aniline by utilizing an EMLC column
39 hibits high electrocatalytic activity toward electrooxidation of AP, Ph, and NP to three well-separat
40                                              Electrooxidation of ascorbyl palmitate (AP) over gold sc
41 ncept, electrooxidative C-H/N-H coupling and electrooxidation of benzyl alcohol were shown to be acce
42                                          The electrooxidation of benzylic C(sp(3))-H bonds to produce
43 layed enhanced catalytic activity toward the electrooxidation of carbohydrates.
44  metal-oxide, and the catalytic activity for electrooxidation of carbon monoxide.
45 tically-underutilized strategy for selective electrooxidation of carboxylic acids in the presence of
46                        In this research, the electrooxidation of carotenoid astaxanthin was confirmed
47                                              Electrooxidation of CH3OH (1.23 M) in a buffered aqueous
48 es studied (1.5 nm) were the most active for electrooxidation of CO and had the largest fraction of o
49       The surface stress response during the electrooxidation of CO at Pt{111}, Ru{0001}, and Ru(thet
50                                          The electrooxidation of CO has been studied on reconstructed
51                           The adsorption and electrooxidation of CO molecules at well-defined Pt(hkl)
52                   Also, it is shown that the electrooxidation of CO on large Ru islands is less facil
53 at GO and PcCo have a synergic effect in the electrooxidation of CSH.
54 potential waveform was employed, causing the electrooxidation of either IC solely or IC and AR simult
55 litting the C-C bond is the main obstacle to electrooxidation of ethanol (EOR) to CO(2).
56                        However, the complete electrooxidation of ethanol to CO(2) involves 12 electro
57                           As test cases, the electrooxidation of formaldehyde and methanol on carbon
58 hedra show higher poisoning tolerance in the electrooxidation of formic acid than Pt cubes; the oxida
59                             The simultaneous electrooxidation of four alcohols (ethanol, 1-propanol,
60 tudies revealed that, on the hybrid material electrooxidation of glucose occurs at a lower potential
61 for the first time that laccase can catalyze electrooxidation of H2O to molecular oxygen.
62 sk electrodes (6-90 nm) via the irreversible electrooxidation of hydrazine (N2H4 --> N2 + 4H(+) + 4e(
63 l graphite electrode (PC-rGO/PGE) to provide electrooxidation of hydrazine.
64         Complexes 1 and 2 are active for the electrooxidation of isopropanol in the presence of stron
65 ully to fabrication of new biosensor for the electrooxidation of l-cysteine (CSH) in aqueous media.
66 onstrate here a strategy enabling the direct electrooxidation of liquefied NH(3) to NO(3)(-) and NO(2
67  studies in the hydrogen evolution reaction, electrooxidation of methanol and CO, and electroreductio
68 ocarbon conversion reactions for fuel cells (electrooxidation of methanol, ethanol, and formic acid).
69 f hydrogen ions, which were generated in the electrooxidation of methanol.
70 trocatalytic activity, enhanced kinetics for electrooxidation of NA, and fast electron-transfer betwe
71 idize the tyrosine residues have allowed the electrooxidation of NADH at low potentials due to the ca
72 CHIT-AZU matrix facilitated the AZU-mediated electrooxidation of NADH.
73 robust CNT-CHIT films, which facilitated the electrooxidation of NADH.
74 s review, we discuss the state-of-the-art on electrooxidation of PFASs in water, aiming at elucidatin
75 r the efficient and environmentally friendly electrooxidation of phenol to benzoquinone.
76                    The reaction occurring on electrooxidation of Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridin
77 oor kinetics in prior reports of the organic electrooxidation of small hydrocarbons, we explored the
78 onto the gate electrode of the transistor by electrooxidation of the primary amine of the glycine moi
79                                          The electrooxidation of thymine on screen-printed carbon ele
80                                              Electrooxidation of TPA generates a TPA*+ radical cation
81 ctron-two proton process was involved in the electrooxidation of vanillin, which takes place more rea
82 ts, we unveil an electrochemical process for electrooxidation of various benzylic C(sp(3))-H bonds in
83 mation of a similar diimine species from the electrooxidation of xanthine, which has not been previou
84                                         Urea electrooxidation offers a cost-effective alternative to
85              The glucose was detected by its electrooxidation on a stationary glassy carbon disk surr
86 igated the structure sensitivity of methanol electrooxidation on eight transition metals (Au, Ag, Cu,
87 opic labeling were employed to study ethanol electrooxidation on Pt under well-defined electrolyte fl
88 th theoretical calculation to investigate CO electrooxidation on Pt(hkl) surfaces in acidic solution.
89 stigate two separate mechanisms for methanol electrooxidation: one going through a CO* intermediate (
90        This work deepens knowledge of the CO electrooxidation process and provides new perspectives f
91 nd perchlorate (ClO(4)(-)) as by-products in electrooxidation process has raised concern.
92 T electrodes were used for investigating the electrooxidation process of insulin and amperometric det
93            The mechanism and kinetics of the electrooxidation process were investigated by cyclic vol
94 species plays a vital role in expediting the electrooxidation process, which relates with the pre-oxi
95  adsorbed CO* was detected during the entire electrooxidation process.
96 -SHINERS) is utilized to in situ monitor the electrooxidation processes at atomically flat Au(hkl) si
97 be acquired, which can help in understanding electrooxidation processes.
98                                  The ammonia electrooxidation reaction (AOR) has attracted significan
99                    However, current ethylene electrooxidation reaction (EOR) is limited to alkaline a
100 cellent catalytic activities in the methanol electrooxidation reaction (MEOR).
101 ate, which improved efficiency in an ethanol electrooxidation reaction compared with a conventional p
102 , platinum-based electrocatalysts for the CO electrooxidation reaction in CO(g)-saturated solution; t
103 function of particle composition for various electrooxidation reactions of liquid fuels (formic acid,
104 eved for the hydrogen evolution and methanol electrooxidation reactions.
105    Hydrazine electrooxidation, hydroxylamine electrooxidation/reduction, and nitrite electroreduction
106 er, higher active surface area, and improved electrooxidation response towards CBM than the unmodifie
107 00) surfaces explains the origin of methanol electrooxidation's experimentally-established structure
108  because of competition for CNT sorption and electrooxidation sites.
109 ation efficiency of halide ions prior to the electrooxidation step.
110 ectrocatalytic activity and stability for CO electrooxidation than commercial and other reported prec
111 ction to formate and 5-hydroxymethylfurfural electrooxidation to 2,5-furandicarboxylic acid with fara
112 f adsorbed CO* and OH* can describe methanol electrooxidation trends on various metal surfaces reason
113 of the inhibition on Cl(-) transformation by electrooxidation was explored.
114 sting that the formation of ClO(4)(-) during electrooxidation was largely mitigated or even eliminate
115 nderpotential deposition and carbon monoxide electrooxidation, which showed that nanoframe surfaces w
116  the tremendous progress of coupling organic electrooxidation with hydrogen generation in a hybrid el
117                                  Formic acid electrooxidation with this novel material shows 4 times

 
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