01717nas a2200217 4500008004100000022001400041245009500055210006900150260006900219300001200288490000700300520095400307653001301261653001401274653001901288653001601307653000801323100001801331700002201349856012801371 2006 eng d a0300-944000aConducting polymer based hybrid nano-composites for enhanced corrosion protective coatings0 aConducting polymer based hybrid nanocomposites for enhanced corr aPO BOX 564, 1001 LAUSANNE, SWITZERLANDbELSEVIER SCIENCE SAcDEC a332-3360 v573 a

Hybrid composite coatings containing zinc oxide (ZnO) and polyaniline (PANI) as nano-additives dispersions were prepared with poly(vinyl acetate) (PVAc) as the major matrix. The steel plates dip-coated with these formulations were tested for corrosion protection by immersion in saline water over long periods. The Tafel plots for the determination of open circuit potential (OCP) and corrosion current (I-corr) were recorded. The coatings containing both ZnO and PANI showed improved corrosion resistance as compared to the single component coating. The I-corr values of PVAc-ZnO-PANI are found to be two-order magnitude lower than that of PVAc and PVAc-ZnO coatings. The results are explained on the basis of enhancement in barrier properties due to nano-particulate additives in PVAc-ZnO-PANI film together with the redox behaviour of PANI and protective oxide layer formation near the substrate. (C) 2006 Elsevier B.V All rights reserved.

10aCoatings10acorrosion10anano-additives10apolyaniline10aZnO1 aPatil, R., C.1 aRadhakrishnan, S. uhttps://library.ncl.res.in/content/conducting-polymer-based-hybrid-nano-composites-enhanced-corrosion-protective-coatings-001522nas a2200229 4500008004100000022001400041245013300055210006900188260010600257300001400363490000700377520063200384653001701016653001601033653001501049653002601064100001901090700002001109700001701129700002001146856012601166 2007 eng d a0013-468600aCorrelation between mobility enhancement and conformational change in polyaniline and its derivatives: polaron lattice formation0 aCorrelation between mobility enhancement and conformational chan aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcMAR a3615-36200 v523 a

Conformational changes in polyaniline, poly(methyl aniline), and poly(methoxyaniline) are studied in perchloric acid and acetonitrile by means of an in situ reflection technique with oxidation level as a parameter. Stretching of polymer chains leading to enhancement of specular reflection at the polymer-coated electrodes is found to be well correlated with the increase in carrier mobility. The concomitant change in mobility and chain conformation observed with the polyaniline family is explained in terms of the formation of polaron lattice at increased oxidation levels. (c) 2006 Elsevier Ltd. All rights reserved.

10aConformation10apolyaniline10areflection10ascattering : mobility1 aHarima, Yutaka1 aOgawa, Fumiyuki1 aPatil, Rahul1 aJiang, Xiaoqing uhttps://library.ncl.res.in/content/correlation-between-mobility-enhancement-and-conformational-change-polyaniline-and-its00847nas a2200241 4500008004100000022001400041245007900055210006900134260010700203300001200310490000700322653001700329653001300346653001000359653001600369653001500385100001900400700002200419700002000441700002000461700001700481856010700498 2007 eng d a0032-389600aNew technique to study kinetics of chain conformation in polyaniline films0 aNew technique to study kinetics of chain conformation in polyani aTSUKIJI DAISAN NAGAOKA BLDG, 2-4-2 TSUKIJI, CHUO-KU, TOKYO, 104, JAPANbSOC POLYMER SCIENCE JAPANcFEB a296-2970 v3910aConformation10akinetics10alaser10apolyaniline10areflection1 aHarima, Yutaka1 aKishimoto, Kazuya1 aOgawa, Fumiyuki1 aJiang, Xiaoqing1 aPatil, Rahul uhttps://library.ncl.res.in/content/new-technique-study-kinetics-chain-conformation-polyaniline-films-001743nas a2200217 4500008004100000022001400041245010700055210006900162260009800231300001400329490000700343520089500350653002101245653002301266653003201289653001601321100001701337700001901354700002201373856013001395 2007 eng d a0959-810300aSynthesis, characterization and actuation behavior of polyaniline-coated electroactive paper actuators0 aSynthesis characterization and actuation behavior of polyaniline aTHE ATRIUM, SOUTHERN GATE, CHICHESTER PO19 8SQ, W SUSSEX, ENGLANDbJOHN WILEY & SONS LTDcDEC a1530-15360 v563 a

This investigation deals with the synthesis, characterization and actuation behavior of conductive polyaniline-coated electroactive paper actuators. The actuator is made by electrochemical deposition of conductive polyaniline on a cellulose paper. The aim of the investigation was to improve the bending displacement of electroactive paper actuators. The displacement outputs of the actuators show that a trilayer is better than a bilayer configuration. The nature of the dopant ion used in the electro-generation affects the performance. A change in humidity plays a vital role in actuation performance of the actuators. Comparing the performance of electroactive paper actuators with and without a conductive polyaniline coating, the coating improves the displacement output threefold. Finally, the actuation principle mechanism is addressed. (C) 2007 Society of Chemical Industry.

10abending actuator10aconducting polymer10aelectroactive polymer (EAP)10apolyaniline1 aKim, Jaehwan1 aYun, Sung-Ryul1 aDeshpande, S., D. uhttps://library.ncl.res.in/content/synthesis-characterization-and-actuation-behavior-polyaniline-coated-electroactive-paper-001929nas a2200217 4500008004100000022001400041245008300055210006900138260006900207300001200276490000700288520116800295653002501463653001001488653001601498653001901514100002201533700002301555700001701578856011601595 2009 eng d a0300-944000aEpoxy powder coatings containing polyaniline for enhanced corrosion protection0 aEpoxy powder coatings containing polyaniline for enhanced corros aPO BOX 564, 1001 LAUSANNE, SWITZERLANDbELSEVIER SCIENCE SAcMAR a383-3860 v643 a

Incorporation of polyaniline (PANI) in epoxy type powder coating formulations has not been attempted earlier. Using specific grade of PANI with low doping, it can be incorporated in epoxy powder coating formulations by twin screw extrusion process. The powder formulations were deposited on steel substrates by electrostatic spray coating at -60 W and baked at 140 degrees C for 20 min. These were extensively tested for corrosion resistance by exposure to hot saline conditions followed by electrochemical impedance spectroscopy and also salt spray testing. PANI incorporated coatings showed no deterioration even after 1400 h of hot (65 degrees C) saline treatment. The coatings intentionally scratched also exhibited self healing property and there was no rust formation even after prolonged exposure to hot saline conditions. These results could be explained on the basis of additional crosslinking due to PANI, as confirmed by DSC results, which gave rise to improved barrier property and self healing was associated with the scavenging of ions by PANI which prevented corrosion of the underlying substrate. (C) 2008 Elsevier B.V. All rights reserved.

10aCorrosion resistance10aEpoxy10apolyaniline10aPowder coating1 aRadhakrishnan, S.1 aSonawane, Narendra1 aSiju, C., R. uhttps://library.ncl.res.in/content/epoxy-powder-coatings-containing-polyaniline-enhanced-corrosion-protection-002729nas a2200241 4500008004100000022001400041245011500055210006900170260007300239300001400312490000800326520182600334653002502160653002702185653001602212100002002228700002102248700002102269700002402290700001802314700002302332856013202355 2010 eng d a0304-885300aCobalt nanoparticles doped emaraldine salt of polyaniline: a promising room temperature magnetic semiconductor0 aCobalt nanoparticles doped emaraldine salt of polyaniline a prom aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcDEC a3926-39310 v3223 a

Incorporation of magnetic nanoparticles in polymers with organic functional groups working as semiconducting substrate is of immense interest in the field of dilute magnetic semiconductors (DMS) and spintronics. In this article we report on synthesis and evaluation of dilutely doped (0-10 wt%) cobalt nanoparticles in emaraldine salt (ES) of polyaniline in the presence of dodecyl benzene sulfonic acid (DBSA) and p-toluene sulfonic acid (p-TSA) using a sonochemical-assisted-reduction approach as a possible DMS candidate. The X-ray diffraction pattern and high resolution transmission electron microscopy (HRTEM) image show the ES to be polycrystalline, in which 10 nm sized Co nanoparticles get embedded in its FCC structural form. From Fourier transform infrared (FT-IR) and UV-visible (UV-vis) spectroscopy studies, it is predicted that cobalt particles get electrostatically bound to the specific SO(3)(-) ion sites of ES, thereby modifying torsional degrees of freedom of the system. The applied field dependent magnetization study shows that the sample exhibits hysteresis loop with a minimal doping of 3 wt% of Co nanoparticles and increases with the amount of Co nanoparticles in ES due to dipolar interaction. The electron transport data show that with increase in Co wt% there is a gradual shift from ohmic to non-ohmic response to the sample bias, accompanied by opening of electrical hysteresis and an increased resistance. The non-linear response of higher doped systems has been attributed to the combination of direct and Fowler-Nordheim tunneling phenomena in these systems. Persistence of optical and transport properties of the polymer, with an introduction of magnetic moment in the system, envisages the system to be a fine magnetic semiconductor. (C) 2010 Elsevier B.V. All rights reserved.

10aCobalt nanoparticles10aMagnetic semiconductor10apolyaniline1 aHatamie, Shadie1 aKulkarni, M., V.1 aKulkarni, S., D.1 aNingthoujam, R., S.1 aVatsa, R., K.1 aKale, Sangeeta, N. uhttps://library.ncl.res.in/content/cobalt-nanoparticles-doped-emaraldine-salt-polyaniline-promising-room-temperature-magnetic-001966nas a2200241 4500008004100000022001400041245005800055210005800113260006900171300001200240490000800252520118600260653002701446653002001473653002001493653001601513100002301529700002301552700002201575700002101597700001801618856008801636 2011 eng d a0379-677900aPolyaniline modified electrodes for detection of dyes0 aPolyaniline modified electrodes for detection of dyes aPO BOX 564, 1001 LAUSANNE, SWITZERLANDbELSEVIER SCIENCE SAcMAY a659-6640 v1613 a

Polyaniline (PANI) is one of the most extensively used conjugated polymers in the design of electrochemical sensors. In this study, we report electrochemical dye detection based on PANI for the adsorption of both anionic and cationic dyes from solution. The inherent property of PANI to adsorb dyes has been explored for the development of electrochemical detection of dye in solution. The PANI film was grown on electrode via electrochemical polymerization. The as grown PANI film could easily adsorb the dye in the electrolyte solution and form an insulating layer on the PANI coated electrode. As a result, the current intensity of the PANI film was significantly altered. Furthermore, PANI coated stainless steel (SS) electrodes show a change in the current intensity of Fe(2+)/Fe(3+) redox peaks due to the addition of dye in electrolyte solution. PANI films coated on both Pt electrodes and non-expensive SS electrodes showed the concentration of dye adsorbed is directly proportional to the current intensity or potential shift and thus can be used for the quantitative detection of textile dyes at very low concentrations. (C) 2011 Elsevier B.V. All rights reserved.

10aElectrochemical sensor10aEmeraldine base10aEmeraldine salt10apolyaniline1 aMahanta, Debajyoti1 aMunichandraiah, N.1 aRadhakrishnan, S.1 aMadras, Giridhar1 aPatil, Satish uhttps://library.ncl.res.in/content/polyaniline-modified-electrodes-detection-dyes-002301nas a2200277 4500008004100000022001400041245013200055210006900187260007100256300001600327490000600343520126900349653002001618653002201638653002301660653001601683653002201699653001901721100002501740700002401765700002801789700002501817700002501842700002401867856013201891 2013 eng d a1944-824400aDesign of a high performance thin all-solid-state supercapacitor mimicking the active interface of its liquid-state counterpart0 aDesign of a high performance thin allsolidstate supercapacitor m a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcDEC a13397-134040 v53 a

Here we report an all-solid-state supercapacitor (ASSP) which closely mimics the electrode-electrolyte interface of its liquid-state counterpart by impregnating polyaniline (PANO-coated carbon paper with polyvinyl alcohol-H2SO4 (PVA-H2SO4) gel/plasticized polymer electrolyte. The well penetrated PVA-H2SO4 network along the porous carbon matrix essentially enhanced the electrode-electrolyte interface of the resulting device with a very low equivalent series resistance (ESR) of 1 Omega/cm(2) and established an interfacial structure very similar to a liquid electrolyte. The designed interface of the device was confirmed by cross-sectional elemental mapping and scanning electron microscopy (SEM) images. The PANI in the device displayed a specific capacitance of 647 F/g with an areal capacitance of 1 F/cm(2) at 0.5 A/g and a capacitance retention of 62% at 20 A/g. The above values are the highest among those reported for any solid-state-supercapacitor. The whole device, including the electrolyte, shows a capacitance of 12 F/g with a significantly low leakage current of 16 mu A(2). Apart from this, the device showed excellent stability for 10000 cycles with a coulombic efficiency of 100%. Energy density of the PANI in the device is 14.3 Wh/kg.

10aall-solid-state10acyclic voltametry10aimpedance analysis10apolyaniline10apolyvinyl alcohol10asupercapacitor1 aAnothumakkool, Bihag1 aTorris, Arun, A. T.1 aBhange, Siddheshwar, N.1 aUnni, SreeKuttan, M.1 aBadiger, Manohar, V.1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/design-high-performance-thin-all-solid-state-supercapacitor-mimicking-active-interface-its-002446nas a2200325 4500008004100000022001400041245015900055210006900214260005700283300001400340490000800354520126400362653003101626653002801657653001301685653001501698653001601713653001801729653002701747653001501774100002801789700002101817700002701838700002401865700002401889700002601913700002601939700002501965856013001990 2014 eng d a0303-402X00aStudies on morphology of polyaniline films formed at liquid-liquid and solid-liquid interfaces at 25 and 5 A degrees C, respectively, and effect of doping0 aStudies on morphology of polyaniline films formed at liquidliqui a233 SPRING ST, NEW YORK, NY 10013 USAbSPRINGERcMAY a1079-10890 v2923 a

It is well accepted that the morphology of the nanomaterials has great effect on the properties and hence their applications. Therefore, morphology of materials has become a focus of research in the scientific world. The present study shows that interfacial polymerization and subsequent self-assembly provides a control over the morphology, nanorod/nanosheet, of polyaniline (PANI) films synthesized by liquid-liquid interface reaction technique and solid-liquid interface reaction technique. The synthesized PANI films and its particulate structure are characterized by using various spectroscopic techniques such as UV-visible, ATR-IR, Raman and XPS. The study confirmed the formation, the structure, the size and shape of particles and morphology of PANI by using analytical techniques namely, SAED, SEM and TEM. An important observation is that doping with HCl significantly improves the nanorod formation at the interface. The doped PANI electrode exhibits a higher area with rectangular shape in CV cycle and better cycle stability when compared with the performance of undoped PANI films. We believe that the results of these studies can give valuable leads to manoeuvre formation of PANI films with desired morphology for various applications.

10ainterfacial polymerization10aLiquid-liquid interface10aNanorods10ananosheets10apolyaniline10aSelf-assembly10aSolid-liquid interface10aThin films1 aWaghmode, Babasaheb, J.1 aPatil, Sagar, H.1 aJahagirdar, Mandar, M.1 aPatil, Virendra, S.1 aWaichal, Rupali, P.1 aMalkhede, Dipalee, D.1 aSathaye, Shivaram, D.1 aPatil, Kashinath, R. uhttps://library.ncl.res.in/content/studies-morphology-polyaniline-films-formed-liquid-liquid-and-solid-liquid-interfaces-25-002995nas a2200241 4500008004100000022001400041245015500055210006900210260007100279300001400350490000600364520208400370653001502454653002402469653001602493653001402509653001602523653001502539100002102554700002502575700002402600856012902624 2015 eng d a1944-824400a3D polyaniline porous layer anchored pillared graphene sheets: enhanced interface joined with high conductivity for better charge storage applications0 a3D polyaniline porous layer anchored pillared graphene sheets en a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcAPR a7661-76690 v73 a

Here, we report synthesis of a 3-dimensional (3D) porous polyaniline (PANI) anchored on pillared graphene (G-PANI-PA) as an efficient charge storage material for supercapacitor applications. Benzoic acid (BA) anchored graphene, having spatially separated graphene layers (G-Bz-COOH), was used as a structure controlling support whereas 3D PANI growth has been achieved by a simple chemical oxidation of aniline in the presence of phytic acid (PA). The BA groups on G-Bz-COOH play a critical role in preventing the restacking of graphene to achieve a high surface area of 472 m(2)/g compared to reduced graphene oxide (RGO, 290 m(2)/g). The carboxylic acid (-COOH) group controls the rate of polymerization to achieve a compact polymer structure with micropores whereas the chelating nature of PA plays a crucial role to achieve the 3D growth pattern of PANI. This type of controlled interplay helps G-PANI-PA to achieve a high conductivity of 3.74 S/cm all the while maintaining a high surface area of 330 m(2)/g compared to PANI-PA (0.4 S/cm and 60 m(2)/g). G-PANI-PA thus conceives the characteristics required for facile charge mobility during fast charge-discharge cycles, which results in a high specific capacitance of 652 F/g for the composite. Owing to the high surface area along with high conductivity, G-PANI-PA displays a stable specific capacitance of 547 F/g even with a high mass loading of 3 mg/cm(2), an enhanced areal capacitance of 1.52 F/cm(2), and a volumetric capacitance of 122 F/cm(3). The reduced charge-transfer resistance (RCT) of 0.67 O displayed by G-PANI-PA compared to pure PANI (0.79 O) stands out as valid evidence of the improved charge mobility achieved by the system by growing the 3D PANI layer along the spatially separated layers of the graphene sheets. The low RCT helps the system to display capacitance retention as high as 65% even under a high current dragging condition of 10 A/g. High charge/discharge rates and good cycling stability are the other highlights of the supercapacitor system derived from this composite material.

10adurability10aionic accessibility10aphytic acid10apillaring10apolyaniline10arestacking1 aSekar, Pandiaraj1 aAnothumakkool, Bihag1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/3d-polyaniline-porous-layer-anchored-pillared-graphene-sheets-enhanced-interface-joined-001631nas a2200241 4500008004100000245015900041210006900200260000800269300001100277490000700288520079100295653000901086653001601095653001901111653002201130100001701152700002101169700002201190700001601212700001701228700001701245856012701262 2017 eng d00aFacile synthesis and electrochemical evaluation of PANI/CNT/MoS2 ternary composite as an electrode material for high performance supercapacitor0 aFacile synthesis and electrochemical evaluation of PANICNTMoSinf cSEP a 24-340 v233 aSynthesis of a novel ternary composite consisting of polyaniline (PANI), functionalized multi-walled carbon nanotubes (CNTs) and molybdenum disulfide (MoS2), via an in-situ polymerization method is reported. Detailed structural and electrochemical characterization shows that incorporation of a small amount of MoS2 in PANI/CNT composite tends to eliminate agglomeration problem of CNT. The PANI/CNT/MoS2 ternary composite reaches a specific capacitance of 350 F/g at the current density 1 A/g corresponding to a 5% MoS2 content. This ternary composite shows good cycling stability even at a higher energy density of 10 A/g. Further, PANI/CNT/MoS2 composite electrode shows higher energy density (7.77 Wh/kg) and power density (2140 W/kg) as compared to PANI/CNT composite without MoS2.10aMoS210apolyaniline10asupercapacitor10aTernary Composite1 aThakur, A.K.1 aDeshmukh, A., B.1 aChoudhary, R., B.1 aKarbhal, I.1 aMajumder, M.1 aShelke, M.V. uhttps://library.ncl.res.in/content/facile-synthesis-and-electrochemical-evaluation-panicntmos2-ternary-composite-electrode02522nas a2200253 4500008004100000022001400041245015300055210006900208260000800277300001200285490000700297520158900304653004001893653003801933653002601971653001601997653001902013653002102032100001502053700002402068700002002092700002402112856013202136 2018 eng d a1944-824400aRealizing high capacitance and rate capability in polyaniline by enhancing the electrochemical surface area through induction of superhydrophilicity0 aRealizing high capacitance and rate capability in polyaniline by cJAN a676-6860 v103 a

Polyaniline (PANI) as a pseudocapacitive material has very high theoretical capacitance of 2000 F g(-1). However, its practical capacitance has been limited by low electrochemical surface area (ESA) and unfavorable wettability toward aqueous electrolytes. This work deals with a strategy wherein the high ESA of PANI has been achieved by the induction of superhydrophilicity together with the alignment of PANI exclusively on the surface of carbon fibers as a thin layer to form a hybrid assembly. Superhydrophilicity is induced by electrochemical functionalization of the Toray carbon paper, which further induces superhydrophilicity to the electrodeposited PANI layer on the paper, thereby ensuring a high electrode-electrolyte interface. The Toray paper is electrochemically functionalized by the anodization method, which generates a highly active electrochemical surface as well as greater wettability (superhydrophilic) of the carbon fibers. Because of the strong interaction of anilinium chloride with the hydrophilic carbon surface, PANI is polymerized exclusively over the surface of the fibers without any appreciable aggregation or agglomeration of the polymer. The PANI-Toray paper assembly in the solid-state prototype supercapacitor can provide a high gravimetric capacitance of 1335 F g(-1) as well as a high areal capacitance of 1.3 F cm(-2) at a current density of 10 A g(-1). The device also exhibits high rate capability, delivering 1217 F g(-1) at a current density of 50 A g(-1) and a high energy density of 30 W h kg(-1) at a power density of 2 kW kg(-1).

10aelectrochemical active sulfate area10aelectrochemical functionalization10aelectropolymerization10apolyaniline10asupercapacitor10asuperhydrophilic1 aSoni, Roby1 aKashyap, Varchaswal1 aNagaraju, Divya1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/realizing-high-capacitance-and-rate-capability-polyaniline-enhancing-electrochemical-surface03124nas a2200241 4500008004100000022001400041245017300055210006900228260000900297300001200306490000800318520223900326653000802565653003002573653002002603653001602623653002002639100002102659700002302680700002602703700002502729856012802754 2018 eng d a0013-468600aTo form layer by layer composite film in view of its application as supercapacitor electrode by exploiting the techniques of thin films formation just around the corner0 aTo form layer by layer composite film in view of its application cMAR  a556-5680 v2653 aA method is described to form robust composite supercapacitor electrodes consisting of polyaniline (PANI)-graphene (GNS) and PANI-MoS2 nanosheets wherein composites are formed by Layer by Layer (LbL) deposition. PANI layer consisting of 10-15 nm particle size was formed by LLIRT, while GNS and MoS2 layers were formed by modified LLIRT. A special feature of the development is the architecture which is rarely found in the literature wherein singular components are stacked over each other to form a composite. The architecture is found to show strong synergistic effects suitable for high performance supercapacitor applications. The composites were characterized by using X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM) etc. The characterization indicates the formation of composites having uniform distribution of PANI nanoparticles over the 2D nanosheets of GNS and MoS2 respectively. The electrochemical performance of the composites was evaluated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and Galvanostatic Charge Discharge (GCD). The composite layer consisting of PANI-GNS alternate layers, showed an excellent specific capacitance (C-sp) of 549 Fg(-1) while PANI-MoS2 alternate layers and PANI layers showed C-sp to be (413 F g(-1)) and (185 F g(-1)) respectively. It is proposed that C-sp stability of the composites is greatly enhanced by the architecture of composite formation through LbL deposition approach. PANI-GNS showed high stability (95% retention of C-sp), PANI-MoS2 (94% retention of C-sp) as against single component capacitance of PANI (67% retention of C-sp). The results reveal the importance of the architecture of composite formation. The architecture of depositing alternate layers of components to form a composite would have special properties leading to synergistic effect in the applications. The present communication is a proof of this concept. It shows the boost in the charge storage resulting in stable robust supercapacitors formation. We predict similar advantages in other applications such as solar energy conversion, sensors, catalysis, etc. (C) 2018 Elsevier Ltd. All rights reserved.10aGNS10aLayer-by-Layer deposition10aMoS2 nanosheets10apolyaniline10aSupercapacitors1 aPatil, Sagar, H.1 aGaikwad, Aarti, P.1 aSathaye, Shivaram, D.1 aPatil, Kashinath, R. uhttps://library.ncl.res.in/content/form-layer-layer-composite-film-view-its-application-supercapacitor-electrode-exploiting01036nas a2200313 4500008004100000022001400041245011400055210006900169260000900238300001100247490000700258653001400265653001600279653003100295100001700326700001900343700001900362700002600381700002200407700001900429700002200448700002100470700002000491700002800511700001900539700002400558700002200582856011800604 2024 eng d a2352-152X00aPANI-grafted boron, nitrogen co-doped carbon fiber: An outstanding, high-performance supercapacitor electrode0 aPANIgrafted boron nitrogen codoped carbon fiber An outstanding h cAUG  a1126680 v9610aComposite10apolyaniline10aSolid-state supercapacitor1 aNayan, Rajiv1 aSinha, Shubhra1 aDixit, Vaibhav1 aSatnami, Manmohan, L.1 aGhosh, Kallol, K.1 aPervez, Shamsh1 aDeb, Manas, Kanti1 aShrivas, Kamlesh1 aRai, Manish, K.1 aYenchalwar, Sandeep, G.1 aWasnik, Kundan1 aJadkar, Sandesh, R.1 aKarbhal, Indrapal uhttps://library.ncl.res.in/content/pani-grafted-boron-nitrogen-co-doped-carbon-fiber-outstanding-high-performance