2015
DOI: 10.1016/j.electacta.2015.10.058
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Effect of potential range on electrochemical performance of polyaniline as a component of lithium battery electrodes

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Cited by 16 publications
(8 citation statements)
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“…The most well‐known p‐type organic cathode materials are conducting polymers (e. g., polyaniline, [11,12] polytriphenylamine, [13] and polypyrrole [14] ) and nitroxyl radical polymers (e. g., PTMA [15] ). In recent years, researchers’ interest also shifts to polymers based on various electroactive heteroaromatics, including N ‐substituted phenazine, [16–19] conjugated pyridine dimer, [20] phenothiazine, [18,21–31] phenoxazine, [32] and thianthrene [33,34] .…”
Section: Introductionmentioning
confidence: 99%
“…The most well‐known p‐type organic cathode materials are conducting polymers (e. g., polyaniline, [11,12] polytriphenylamine, [13] and polypyrrole [14] ) and nitroxyl radical polymers (e. g., PTMA [15] ). In recent years, researchers’ interest also shifts to polymers based on various electroactive heteroaromatics, including N ‐substituted phenazine, [16–19] conjugated pyridine dimer, [20] phenothiazine, [18,21–31] phenoxazine, [32] and thianthrene [33,34] .…”
Section: Introductionmentioning
confidence: 99%
“…Such polymers have similar electronic, magnetic and optical properties to metals, whereas retaining the flexibility and processibility of conventional polymers. The outstanding properties afford PANI with potential practical applications such as in chemical sensor devices, light‐emitting diodes, electromagnetic interference shielding materials, anticorrosion coatings, separation membranes, lithium‐ion battery electrodes, supercapacitors, electromechanical actuators, and so forth.…”
Section: Introductionmentioning
confidence: 99%
“…[6] During the 1980s,P ANI was in fact one of the first organic materials tested as active material in electrochemical cells,a nd it showed an exceptional stability on cycling and excellent coulombic efficiency. [8] Even though some effort has been put into increasing the specific capacity of PA NI by improving the reversibility of the ES-PNS redox transition in non-aqueous electrolytes,t he most efficient strategy to date requires the use of high-molecular-weight anionic counterions,w hich limits the practical capacity of the PA NI electrodes. [2b] In practice,the capacity of PA NI in anonprotic environment is usually limited to half of that value due to the irreversible character of the redox transition between ES and PNS;either PNS is not chemically stable (PNS is too strong as an acid or electrophile) and reacts with the electrolyte,o rt he overpotential to incorporate the charge compensating anions is too high and the completely oxidized state cannot be reached within the stability window of the electrolyte.…”
mentioning
confidence: 99%
“…[2b] In practice,the capacity of PA NI in anonprotic environment is usually limited to half of that value due to the irreversible character of the redox transition between ES and PNS;either PNS is not chemically stable (PNS is too strong as an acid or electrophile) and reacts with the electrolyte,o rt he overpotential to incorporate the charge compensating anions is too high and the completely oxidized state cannot be reached within the stability window of the electrolyte. [8] Even though some effort has been put into increasing the specific capacity of PA NI by improving the reversibility of the ES-PNS redox transition in non-aqueous electrolytes,t he most efficient strategy to date requires the use of high-molecular-weight anionic counterions,w hich limits the practical capacity of the PA NI electrodes. [9] Compared to covalent functionalization reactions of PA NI, the deprotonation-induced n-doping of PA NI has been studied far too low,a si ti mplies the occurrence of formally negatively charged nitrogen atoms (nitrenes), the strong basicity of which requires strictly aprotic conditions.…”
mentioning
confidence: 99%