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1 the algal growth medium (which was also the catholyte).
2 atively stable pH values in both anolyte and catholyte.
3 notube cathode and a liquid-type polysulfide catholyte.
4 een achieved when coupled with a I3(-) /I(-) catholyte.
7 oped a dual-redox EC consisting of a bromide catholyte and an ethyl viologen anolyte with the additio
8 sing hydroquinone (H2BQ) aqueous solution as catholyte and graphite in aprotic electrolyte as anode.
9 ion of this approach with the use of bromide catholyte and tetrabutylammonium cation that induces rev
10 ium sulfide cathodes and lithium polysulfide catholytes, as well as recent burgeoning efforts in the
11 but not the salinity ratio, indicating high catholyte conductivity was essential for maximizing hydr
14 nt of anolytes has lagged far behind that of catholytes due to the major limitations of the redox spe
15 lso been extended to the use of a Br2 -based catholyte, exhibiting a higher cell voltage with a theor
18 w battery via linkage of an I3(-)/I(-) based catholyte, for the simultaneous conversion and storage o
19 MFCs were designed to harvest the generated catholyte in the internal chamber, which showed that liq
20 ilibrium at cation exchange membrane-anolyte/catholyte interfaces, the Na(+) ion in the anolyte actua
21 en demonstrated that uses this molecule as a catholyte material and operated stably for 100 charge/di
23 4-trimethylammonium-TEMPO (N(Me) -TEMPO) as catholyte, [(NPr)2 TTz]Cl4 enables a 1.44 V AORFB with a
25 liquid-to-solid phase transition of oxidized catholyte (or reduced anolyte) with confinement in the p
26 go redox events at as low (anolyte) or high (catholyte) potentials as possible while exhibiting the s
28 l-solid-state Li/LiFePO4 cell with a polymer catholyte shows good cyclability and a long cycle life.
29 e cathode overpotential was dependent on the catholyte (sodium bicarbonate) concentration, but not th
30 g derivatized fullerenes as both anolyte and catholyte species in a series of battery cells, includin
32 tends to acidify (or basify) the anolyte (or catholyte), their effects are buffered by a cascade of c
33 g the strength of ammonia diffusion from the catholyte toward the anolyte, will help effective design
36 ack of electroactive compounds (anolytes and catholytes) with the necessary combination of (1) redox
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