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1 minant active catalyst and not Co(2+)(aq) or cobalt oxide.
2 d on Au is 40 times higher than that of bulk cobalt oxide.
3 and provides a molecular model for Mn-doped cobalt oxides.
4 LT-LiCoO2 is higher than that of both spinel cobalt oxide and layered lithium cobalt oxide synthesize
6 xed oxide catalyst composed of copper oxide, cobalt oxide, and ceria (dubbed CCC) that outperforms sy
7 is coupled with a water oxidation phosphate cobalt oxide anode in a home-made electrolyzer by means
9 the surface energies of the layered lithium cobalt oxide can be significantly lowered as a consequen
10 used a simple two-step method to synthesize cobalt oxide/carbon nanotube (CNT) strongly coupled hybr
11 er with good cyclability of a 4-volt lithium cobalt oxide cathode and operation as low as -60 degrees
13 ork, we have developed a simple and reliable cobalt oxide (Co(3)O(4)) based amperometric sensor for t
14 e use of engineered viruses as templates for cobalt oxide (Co(3)O(4)) particles, superparamagnetic co
17 anges with the transition between cobalt and cobalt oxide controlled by a voltage applied to the top
18 nged by studies suggesting that formation of cobalt oxide (CoOx) or other byproducts are responsible
20 the OER exhibited by approximately 0.4 ML of cobalt oxide deposited on Au is 40 times higher than tha
22 rnover frequency for approximately 0.4 ML of cobalt oxide deposited on Au is nearly three times highe
26 mical properties for a manganese center in a cobalt oxide environment, and provides a molecular model
29 oxygen evolution reaction (OER) occurring on cobalt oxide films deposited on Au and other metal subst
33 stalline platinum and manganese, nickel, and cobalt oxides, illustrating the catalytic potential of p
34 spectroscopy revealed that the as-deposited cobalt oxide is present as Co(3)O(4) but undergoes progr
35 study the active surfaces of layered lithium cobalt oxide (LCO) for the oxygen evolution reaction (OE
37 calation of nanosized stoichiometric lithium cobalt oxide LiCo(III)O(2) from low-spin to intermediate
38 capability, considerably better than lithium cobalt oxide (LiCoO2), the current battery electrode mat
40 that obtained from the electrodeposition of cobalt oxide materials from phosphate-buffered electroly
41 el the oxygen evolution reaction activity of cobalt oxide nanoislands and show that the nanoparticle
44 tic cobalt-platinum alloy nanowires and gold-cobalt oxide nanowires for photovoltaic and battery-rela
45 A self-assembled layer of virus-templated cobalt oxide nanowires serving as the active anode mater
46 n of preorganized NPs to form interconnected cobalt oxide nanowires via the nanoscale Kirkendall effe
48 Plasma-enhanced atomic layer deposition of cobalt oxide onto nanotextured p(+)n-Si devices enables
50 icle modified electrode, this nanosheet form cobalt oxide possesses a rapid background subsiding char
51 cathode layers based on graphite and lithium cobalt oxide, respectively, on thin flexible current col
54 mpression and tension induced by the lithium cobalt oxide substrate of ~5% were directly observed in
55 the existence of an active interface between cobalt oxide surface layers and manganese oxide nanopart
56 segregation of a thin platinum, rather than cobalt oxide, surface layer occurs concurrently with ord
57 both spinel cobalt oxide and layered lithium cobalt oxide synthesized at 800 degrees C (designated as
59 issues by employing a homogeneous model for cobalt oxide, the [Co(III)4] cubane (Co4O4(OAc)4py4, py
61 plied for structural characterization of the cobalt oxide water-splitting catalyst films using high e
62 be applied to study the structure of in situ cobalt oxide water-splitting film under functional catal
63 nanoparticles supported on mesoporous spinel cobalt oxide, which catalyses the conversion of carbon d
65 aching process, resulting in a highly porous cobalt oxide with a significant amount of defects in the
67 le extension of the process yielded platinum-cobalt oxide yolk-shell nanostructures, which may serve
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