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1 media and over the potential range of an air cathode.
2 nd producing hydrogen peroxide (H2O2) at the cathode.
3 l pore diameter is near 60 nm in a practical cathode.
4 ty and excellent cycling stability in a Li2S cathode.
5 lline sodium superoxide (NaO2) on the carbon cathode.
6 erated along with byproduct reduction at the cathode.
7 directional response and migrated toward the cathode.
8 e anode and a previously described enzymatic cathode.
9 ed Na3 MnTi(PO4 )3 as both the anode and the cathode.
10 progenitor cells (fNPCs) migrated toward the cathode.
11 al ionic media to meet with electrons at the cathode.
12 2 battery by using a suitable graphene-based cathode.
13 DNA probe on the surface of an AuNP/graphite cathode.
14 ry with a Mg anode and Chevrel (Mo3S4)-phase cathode.
15 sheets (GNs) as anode and MnOx catalyzed air cathode.
16 tely 20 mA/cm(2)), using Fe as the anode and cathode.
17 h an activated carbon cloth/sulfur composite cathode.
18 voltage/current output than that with single cathode.
19 es while benefiting charge transfer with the cathode.
20 he anode side, while CO2 is generated at the cathode.
21 lymer composites, and a solid-state NPG/MnO2 cathode.
22 membrane fuel cell (PEMFC) using Pt/C at the cathode.
23 ve layer, and eutectic indium-gallium as the cathode.
24 combination of an enzymatic anode with a Pt cathode.
25 ode while Fe(3+) is reduced to Fe(2+) in the cathode.
26 rid microfluidic fuel cell using Pt/C as the cathode.
27 evice employing an unselective platinum (Pt) cathode.
28 and explains well pseudocapacitance of RuO2 cathodes.
29 ited by the low-capacity lithium metal oxide cathodes.
30 enables good compatibility with high-voltage cathodes.
31 designing high-power electrodes, especially cathodes.
32 ic cycling when paired with commercial-grade cathodes.
33 ance of batteries that use 4 V high-capacity cathodes.
34 es of each class of materials as multivalent cathodes.
35 r the oxygen reduction reaction in fuel cell cathodes.
36 ant contributors to long-term fouling of MFC cathodes.
37 al oxide anodes coupled with stainless steel cathodes.
38 applied to study common lithium ion battery cathodes.
39 ed for flexible, high-loading lithium-sulfur cathodes.
40 ersibility and cycling performance of sulfur cathodes.
41 electrochemical reduction pathway for sulfur cathodes.
42 Li4NiTeO6 and Li2MnO3 for the spinel LiMn2O4 cathodes.
43 w diffusion of divalent magnesium cations in cathodes.
44 e for industrial CO2-consuming gas diffusion cathodes.
45 able magnesium batteries using intercalation cathodes.
46 ing a maximum of 0.77 mmol-Na(+) per gram of cathode (2.29 mmol-Na(+) g-MnO2(-1)), and peak charge ef
47 electrolyte and La0.8Sr0.2FeO3-delta as the cathode achieved a power density of 423 mWcm(-2) at 700
50 alogue, (NH4 )1.47 Ni[Fe(CN)6 ]0.88 , as the cathode, an organic solid, 3,4,9,10-perylenetetracarboxy
52 power density of 6.4 kW kg(-1) (based on the cathode and 200% Zn anode), making it a promising candid
53 ric potential, being 87-90% lower on the ICE cathode and 59-93% lower on the ICE anode than that on t
54 atmosphere between a solid pin type tungsten cathode and a liquid drop placed on a graphite disk anod
55 large interfacial resistance between a solid cathode and a solid electrolyte that increases with each
56 ped using a single LiVPO4 F material as both cathode and anode in a "water-in-salt" gel polymer elect
57 cal conductivity and structural stability of cathode and anode materials based on NASICON structure.
58 e to coat conformal protective thin films on cathode and anode particles of lithium ion batteries to
59 e electrical conductivity to the paper-based cathode and anode, commercially available eyeliner conta
60 When utilized as electrocatalysts for both cathode and anode, Ni3S2/NF demonstrated outstanding dur
62 elithiation of lithium iron phosphate at the cathode and electrons utilized in the formation of a sol
64 issolved intermediate products from the SeS2 cathode and lithium metal and eliminates lithium dendrit
65 cyclability of a 4-volt lithium cobalt oxide cathode and operation as low as -60 degrees C, with exce
66 ructured materials are suitable for both the cathode and the anode, where the operation potential can
68 ort ions between the sulfur/carbon composite cathode and the lithium anode in lithium-sulfur batterie
70 earch in the development of electrolytes and cathodes and discuss some of the significant challenges
71 s that coupled with industrially established cathodes and electrolytes exhibit long cycle life (up to
72 on batteries with aluminium anodes, graphite cathodes and ionic liquid electrolytes has increased; ho
74 t uses a microporous carbon-sulfur composite cathode, and a liquid carbonate electrolyte containing t
75 the ternary electrode as both the anode and cathode, and the performance surpasses that of the Ir/C-
76 82% and 91% capacity retention for anode and cathode are achieved after 500 stretch-release cycles.
77 al properties of CaP solids collected on the cathode are still related to bulk solution pH, as confir
78 cells consisting of gSi@C anodes and LiCoO2 cathodes are assembled and achieve good initial cycling
82 V, were the same as those obtained with a Pt cathode at a loading of 0.1 milligram of Pt per centimet
87 roduction, successfully delayed the onset of cathode biofouling and improved reactor performance.
88 anode, garnet electrolyte and a high-voltage cathode by applying the newly developed interface chemis
89 el structure, alpha-MnO2 can be applied to a cathode by insertion reaction and to an anode by convers
90 r cracks in a commercial LiNi1/3Mn1/3Co1/3O2 cathode by using advanced scanning transmission electron
91 ver, much remains to be done to increase the cathode capacity and to understand details of the anion-
93 ygen through an ionomer contained within the cathode catalyst layer in an anion exchange membrane fue
94 nylimidazole)10Cl](+) as mediator, while the cathode catalysts were bilirubin oxidase and [Os(2,2'-bi
98 yzed urine was fed to the caustic-generating cathode compartment for ammonia stripping with redirecti
100 versus 2) plastic-crystal electrolyte in the cathode composites shows that the former suffers from a
101 arlier batteries in which both the anode and cathode consisted of organic material required significa
103 lucose oxidizing anode and a O2 reducing MCO cathode, could become the in vivo source of electricity
106 by an inexpensive precipitation method, the cathode delivers a specific capacity of 142 mAh g(-1).
107 e acidic single-cell with such a catalyst as cathode delivers high performance, with power density up
108 composite electrolyte, and Sm0.5 Sr0.5 CoO3 cathode demonstrates excellent performance with maximum
109 olar polysulfides can be anchored within the cathode due to the internal electric field originated fr
110 ir dissolution into the electrolyte from the cathode during each redox cycle leads to a shortened cyc
113 AORFB) technology utilizing a newly designed cathode electrolyte containing a highly water-soluble fe
114 de side of a lithium ion battery, termed the cathode electrolyte interface (CEI), whose composition a
116 secondary-ion mass spectrometry shows that a cathode-electrolyte interphase, initially formed on carb
118 mpetitive transport, the textile-based Li-O2 cathode exhibits a high discharge capacity of 8.6 mAh cm
121 tional system operated with a flowing liquid cathode (FLC-APGD) were studied in detail and discussed.
125 In an effort to develop high-energy-density cathodes for sodium-ion batteries (SIBs), low-cost, high
126 lts demonstrated that HA could contribute to cathode fouling, but the extent of power reduction was r
127 f multiple electron collectors with multiple cathodes had much higher total voltage/current output th
128 grafted skin paired with LiNi0.5Co0.2Mn0.3O2 cathode has a 90.0% capacity retention after 400 charge/
129 current by thermionic electron emission, the cathode has to be at sufficiently high temperature, whic
130 Ni-rich LiNi0.8Co0.1Mn0.1O2 layered oxide cathodes have been highlighted for large-scale energy ap
132 e KxMnFe(CN)6 (0 </= x </= 2) as a potassium cathode: high-spin Mn(III)/Mn(II) and low-spin Fe(III)/F
133 raphene stack is showcased as suitable model cathode host for unveiling the challenging surface chemi
135 osition of aerosol particles on the tip of a cathode in a coaxial microelectrode system, followed by
137 s in the presence of a dye as a hybrid photo-cathode in a two-electrode system, with lithium metal as
141 hermodynamics and reaction pathway of sulfur cathode in MgTFSI2 -DME electrolyte, as well as the asso
142 power densities of the ssDNA probe modified cathode in the absence and presence of complementary seq
144 , hollow-fiber porous membranes were used as cathodes in anaerobic electrochemical membrane bioreacto
146 (1-x >/= 0.5), are appealing candidates for cathodes in next-generation lithium-ion batteries (LIBs)
148 polymorph mixed with bismuth oxide (Bi2O3)) cathodes intercalated with Cu(2+) that deliver near-full
150 etal oxide, reveals the dynamic behaviour of cathode interphases driven by conductive carbon additive
151 e insights on the formation and evolution of cathode interphases, facilitating development of in situ
155 nvestigation, a novel graphene/cotton-carbon cathode is presented here that enables sulfur loading an
156 n rate reaches ~1200 mumol/h when the liquid cathode is purified water or an aqueous solution of NaCl
157 ode, the electron current emanating from the cathode is regulated by the electric potential on a grid
158 of previous reports on related Li-excess LIB cathodes, it is proposed that part of the charge compens
159 The battery consists of printed anode and cathode layers based on graphite and lithium cobalt oxid
160 he cell voltage by the use of high potential cathodes like bilirubin oxidase (BOx) or iron-aminoantip
161 on and low electronic conductivity of sulfur cathodes limit the practical application of Li-S batteri
162 -ion batteries (LIBs) based on layered LiMO2 cathodes (M = Ni, Mn, Co: NMC; M = Ni, Co, Al: NCA) need
163 e achieved with the boron-rich anode and the cathode made from a refractory metal which has a melting
164 latinum consumption are desirable for use as cathode material during the oxygen reduction reaction in
167 rganotrisulfide is a promising high-capacity cathode material for high-energy rechargeable lithium ba
168 this study proposes K0.5 MnO2 as a potential cathode material for K-ion batteries as an alternative t
169 te a novel crosslinked disulfide system as a cathode material for Li-S cells that is designed with th
171 hium-sulfur (Li-S) batteries and a candidate cathode material for lithium-metal-free Li-S cells.
172 ersulfurated coronene renders it a promising cathode material for lithium-sulfur batteries, displayin
173 has demonstrated promising performance as a cathode material in lithium ion batteries (LIBs), by ove
174 treatment on spinel LiNi0.5 Mn1.5 O4 (LNMO) cathode material is developed to optimize the performanc
175 d insertion and extraction of Li ions from a cathode material is imperative for the functioning of a
176 he synthesis was achieved independent of the cathode material suggesting that under such conditions t
179 pectroscopy revealed that independent of the cathode material, the tubes are primarily single and dou
180 ounds (Li2Fe)ChO (Ch = S, Se) were tested as cathode materials against graphite anodes (single cells)
181 h, focusing on a wide range of intercalation cathode materials and the mechanisms of multivalent ion
182 ategies for the practical viability of these cathode materials are discussed along with the optimizat
183 environment around O in paramagnetic Li-ion cathode materials are essential in order to understand t
184 ributed to the slower particle growth of the cathode materials at the lower operating temperature.
189 al to serve as low-cost and highly efficient cathode materials in direct methanol fuel cells (DMFCs).
190 lex frameworks also demonstrate potential as cathode materials in Li-ion batteries because of the fav
192 prevent the use of many high-energy-density cathode materials in practical lithium-ion batteries.
193 were recently identified as high-performance cathode materials in the context of electro-organic synt
196 interaction between Li polysulfides and Li-S cathode materials originates from the electron-rich dono
198 deep comprehension, which is helpful to the cathode materials rational design and practical applicat
199 f lithium-excess cation-disordered oxides as cathode materials relies on the extent to which the oxyg
200 spatially resolved element analysis of such cathode materials will help in understanding the observe
201 ed as an example of a new class of promising cathode materials, Na(Li1/3 M2/3 )O2 (M: transition meta
202 oupling a sulfur anode with different Li-ion cathode materials, the aqueous Li-ion/sulfur full cell d
210 he design of high-capacity cation-disordered cathode materials.The performance of lithium-excess cati
211 quest for safe, low-cost positive electrode (cathode) materials with desirable energy and power capab
212 hase between a solid electrolyte and a solid cathode may be extended to other all-solid-state battery
214 tic trunk bilaterally with anode cephalad to cathode (n = 8, 'cardiac' configuration) or with electro
215 olyte, neither the reaction mechanism at the cathode nor the nature of the reaction product is known.
216 ysulphides generated during discharge in the cathode of a lithium-sulphur redox cell are important, b
217 phology evolution on a carbon nanotube (CNT) cathode of a working solid-state Li-O2 nanobattery and c
218 brane-electrode assembly was deployed as the cathode of an electrochemical cell, and showed good resi
219 densities recorded in the kinetic region of cathode operation, at fuel cell voltages greater than 0
221 nomaterials that coat (V2 O5 @graphene@V2 O5 cathode) or are coated by (graphene@Si@graphene anode) g
222 l together with a multicopper oxidase at the cathode, or in a proton exchange membrane fuel cell (PEM
224 rphase between a solid electrolyte and solid cathode particles reduces the interfacial resistance, in
225 hemical bias applied, readily passivates the cathode particles through mutual exchange of surface spe
232 ells (EFCs), EFCs with laccase air-breathing cathodes prepared from TBA(+) modified Aquivion ionomers
234 ctive Nafion/carbon powder layer is a stable cathode producing CO in pH neutral water with 90% farada
236 nes, desktop and laptop computers, monitors, cathode ray tube and flat panel display televisions, DVD
238 ug L(-1) and-upon coupling lead to a mineral cathode-release due to galvanic corrosion by 990 mug L(-
240 glucose oxidase and laccase at the anode and cathode respectively; no external mediators are used; an
241 nd hydrogen evolution reactions at anode and cathode, respectively, achieving a very high electrolysi
242 DH) and bilirubin oxidase (BOD) at anode and cathode, respectively, in the biofuel cell arrangement.
243 s and phase changes in the sulfur conversion cathode result in highly complex phenomena that signific
244 of and capturing free radicals formed at the cathode, resulting in enhanced membrane durability.The p
245 )Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveals a combination of degradation species: n
248 ere is a lesser-known analogous layer on the cathode side of a lithium ion battery, termed the cathod
249 s for high energy density and alleviation of cathode side reactions/corrosions, but introduces drawba
252 of the carbon cloth current distributor, the cathode significantly lowered the total cell resistance
255 e provide suggestions for future multivalent cathode studies, including a strong emphasis on the unam
257 e Li-O2 battery can form a Li2O2 film on the cathode surface, leading to low capacities, low rates an
258 suppressing direct reduction to Li2O2 on the cathode surface, which would otherwise lead to Li2O2 fil
261 ilitate CO2 reduction at perovskite titanate cathode surfaces, promoting adsorption/activation by mak
265 fur battery research is the design of sulfur cathodes that exhibit high electrochemical efficiency an
266 structure and high catalytic activity of the cathode, the as-prepared Li-CO2 batteries exhibit high r
267 erplay between the reaction mechanism at the cathode, the chemical structure and the morphology of th
268 rroelectrics (BaTiO3 nanoparticles) into the cathode, the heteropolar polysulfides can be anchored wi
270 However, in conventional porous carbon-air cathodes, the oxygen gas and electrolyte often compete f
271 nisms were transported from the anode to the cathode through an external circuit, which could be dete
272 rging and discharging of lithium-ion-battery cathodes through the de- and reintercalation of lithium
273 cycling of hydrogen gas (H2) produced at the cathode to the anode in an electrochemical system allows
276 ful for developing the next generation of MV-cathodes to targeted in-depth studies rationalizing comp
277 eveloping a low cost, highly active, durable cathode towards an oxygen reduction reaction (ORR) is on
279 ndence of the H2 and CO current densities on cathode voltage that are in strikingly good agreement wi
280 here was no such significant effect when the cathode was placed on the supraorbital ridge (bipolar-un
282 Selenium, which dissolves from the SeS2 cathode, was found to become a component of the anode so
283 the thermodynamically optimal coatings for a cathode, we further present optimal hydrofluoric-acid sc
284 nase-based anode and bilirubin oxidase-based cathode were assembled to a quasi-2D capillary-driven mi
287 ole in fouling from organic matter in water, cathodes were exposed to high concentrations of humic ac
288 nificantly limited by the performance of the cathode which is based on oxygen reduction for in vivo a
289 stretchable Li4 Ti5 O12 anode and a LiFePO4 cathode with 80% stretchability are prepared using a 3D
292 y, we combined the light-protected TiO2 |MnP cathode with a CdS-sensitized photoanode to enable solar
293 node paired with a selenium disulfide (SeS2) cathode with high capacity and long-term stability.
294 LiNO3-KNO3 eutectic) and a porous carbon O2 cathode with high energy efficiency ( approximately 95%)
297 cycles with excellent rate capability using cathodes with areal sulfur loadings up to 8.1 mg cm(-2).
300 A electrodes are employed as both anodes and cathodes with polarity switching at a set frequency.
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