supercapacitors based on tungsten trioxide nanorods
DESCRIPTION
Outline Introduction Synthesis of tungsten trioxide nanorods Characterization of tungsten trioxide nanorods Electrochemical studies for supercapacitive behaviour ConclusionsTRANSCRIPT
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J. Rajeswari, B. Viswanathan and T. K. VaradarajanJ. Rajeswari, B. Viswanathan and T. K. VaradarajanNational Centre for Catalysis ResearchNational Centre for Catalysis Research
Department of ChemistryDepartment of ChemistryIndian Institute of Technology MadrasIndian Institute of Technology Madras
Chennai – 600 036Chennai – 600 036IndiaIndia
Supercapacitors based on tungsten trioxide nanorodsSupercapacitors based on tungsten trioxide nanorods
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Introduction Introduction
Synthesis of tungsten trioxide nanorodsSynthesis of tungsten trioxide nanorods
Characterization of tungsten trioxide nanorodsCharacterization of tungsten trioxide nanorods
Electrochemical studies for supercapacitive behaviourElectrochemical studies for supercapacitive behaviour
ConclusionsConclusions
OutlineOutline
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Two types of capacitors - Electric double layer capacitors (EDLCs) and pseudocapacitors (redox capacitors)
EDLCs - An electrochemical double layer capacitor uses the physical separation of electronic charge in the electrode and ions of the electrolyte adsorbed at the surface
A Faradaic supercapacitor is charged by chemisorption of a working cation of the electrolyte at a reduced complex at the surface of the electrode (or)
Faradaic supercapacitor – electrochemical redox process involving charge transfer by the electrode material – called as pseudo or redox capacitors
Electrochemical supercapacitance –redox process accompanied by the non Faradaic charging-discharging at the interface
EDLCs have a lower specific capacitance than an optimal faradaic supercapacitor
Electrochemical SupercapacitorsElectrochemical Supercapacitors
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Amorphous hydrated ruthenium oxide, RuO2.nH2O, in strong acid is capable of chemisorbing one proton per Ru atom to give a capacity of 720 F/g and excellent cyclability
RuO2.nH2O is too expensive to be commercially attractive - search for alternate materials
Small size of proton offers the best chance to achieve optimal chemisorption, the search has been restricted mostly to materials stable in strong acids
Transition metal oxides such as RuO2, Co3O4, MnO2, IrOx etc., have been shown to be excellent materials for supercapacitors
Charge storage property of WO3 has been used extensively as electrochromic materials
Very few reports are available on WO3 as capacitors – as a second component in RuO2 systems to reduce the loading of Ru
Electrochemical SupercapacitorsElectrochemical Supercapacitors
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Tungsten trioxides form tungsten bronzes (MxWO3) – M is a metal other than tungsten, most commonly an alkali metal or hydrogen
Tungsten bronzes – electron and proton conductors – desired property for a Faradaic supercapacitor
The redox processes that take place in tungsten trioxides are as follows:
First process (I) occurs at potential more positive than -0.3 V Second process (II) occur at potential more negative than -0.3 V
Hence, in WO3, charge separation at the electrode-electrolyte interface and redox processes due to the formation of HxWO3 and WO3-y contribute capacitance to the system
WO3 + xH+ + e- HxWO3
(0 < x <1) (I)
WO3 + 2yH+ + 2ye- WO3-y + yH2O (0 < y < 1) (II)
Electrochemical behaviour of tungsten trioxidesElectrochemical behaviour of tungsten trioxides
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Under experimental conditions, in W-RuO2 film, W is in the form of WO3 – revealed from XRD
Presence of W – increased charging and discharging time – evident from chronopotentiometry
Specific capacitance per volume after one cycle is 54.2 mF/cm2m for W-RuO2
30.4 mF/cm2 m for RuO2
Increased specific capacitance and stability over cyle numer in the presence of W J. Vac. Sci. Technol. B 21, (2003), 949
Solid state thin film containing W cosputtered RuOSolid state thin film containing W cosputtered RuO22 supercapacitor electrodes supercapacitor electrodes
Tungsten based supercapacitors reported in literatureTungsten based supercapacitors reported in literature
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Amorphous tungsten oxide – ruthenium oxide composites for Amorphous tungsten oxide – ruthenium oxide composites for Electrochemical capacitorsElectrochemical capacitors
J. Electrochem.Soc., 148, (2001), A189
To reduce the cost of RuO2, WO3 has been added by precipitation method
Results have shown that WO3 can constitute an alternate electrode material for the high cost RuO2 for supercapacitor applications
100 % RuO2
~50%WO3 + ~50% RuO2
Tungsten based supercapacitors reported in literatureTungsten based supercapacitors reported in literature
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Tungsten trioxide systems for supercapacitors studied in the present workTungsten trioxide systems for supercapacitors studied in the present work
Aim of the present study: Supercapacitive behaviour of nanorods of WO3
Tungsten trioxide nanorods - Method employed: Thermal decomposition using tungsten containing precursor
Supercapacitive behaviour of nanorods have been compared with bulk WO3
Bulk WO3: Commercially obtained from Alfa Aesar ( A Johnson Matthey Company)
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Different synthetic approaches Solvothermal methodSolvothermal method Template directed synthesisTemplate directed synthesis Sonochemiccal synthesisSonochemiccal synthesis Thermal MethodsThermal Methods
DecompositionDecomposition Chemical vapor depositionChemical vapor deposition
Thermal decomposition – simple, easy, inexpensive and contaminants free methodsimple, easy, inexpensive and contaminants free methodOne report for synthesis of WOOne report for synthesis of WO33 nanorods by thermal decomposition method nanorods by thermal decomposition method
Disadvantages of the existing report:
Tedious synthetic method for the precursor compound [WO(OMe)4] Highly unstable precursor compound A relatively higher pyrolysis temperature Multisteps from precursor to product
Pol et.al, Inorg. Chem. 44 (2005) 9938
Reported methods for the synthesis of WOReported methods for the synthesis of WO33 nanorods nanorods
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Preparation of tetrabutylammonium decatungstate ((CPreparation of tetrabutylammonium decatungstate ((C44HH99))44N)N)44WW1010OO3232
Chemseddine et.al, Inorg. Chem. 23 (1984) 2609
Na2WO4.2H2O + 3M HCl
Clear yellow solution
White precipitate
Filtered, washed with boiling water and ethanol
Tetrabutyl ammonium bromide (TBABr)
Recrystallized in hot DMF
Yellow crystals of ((C4H9)4N)4W10O32
Sodium tungstate and tetrabutylammonium bromide – starting materials – to synthesizethe precursor
Synthesis of the precursorSynthesis of the precursor
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Recrystallized ((CRecrystallized ((C44HH99))44N)N)44WW1010OO3232
pyrolyzed at 450 pyrolyzed at 450 C, 3h, NC, 3h, N22
(tubular furnace)(tubular furnace)
WOWO3 3 nanorodsnanorods blue powderblue powder
Synthesis of Tungsten trioxide nanorodsSynthesis of Tungsten trioxide nanorods
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WO3 nanorods prepared by our group
WO3 nanorods from literature
Preparation of precursor
Nature of the precursor
Precursor Tunability
No of steps
Simple, easy and economicalSimple, easy and economical
StableStable
Easy storageEasy storageMetal and the cation can be Metal and the cation can be tuned to give a tuned to give a variety of metal oxide variety of metal oxide nanorodsnanorods
Single stepSingle step
Relatively not economical Relatively not economical and also tedious methodand also tedious method
Highly volatile, evaporates to Highly volatile, evaporates to give W(OMe)give W(OMe)66 and and WOWO22(OMe)(OMe)22
Limitation in storageLimitation in storage
No such possibilityNo such possibility
Multiple stepsMultiple steps
Comparison of the features of the synthesis of WOComparison of the features of the synthesis of WO3 3 nanorodsnanorods by our group vs. existing report by our group vs. existing report
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The WO42- octahedra are surrounded by the ((C4H9)4)N+ groups
This allows the growth of WO3 in one dimension
When pyrolysed at 450 C, ((C4H9)4)N+ group decomposes off leaving WO3 nanorods
Scheme for the formation of tungsten trioxide (WOScheme for the formation of tungsten trioxide (WO33) nanorods) nanorods
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Single crystalline monoclinic WOSingle crystalline monoclinic WO33 (JCPDS: 75-2072) (JCPDS: 75-2072)
To study the structure and composition, powder XRD pattern was obtained
X-ray diffraction pattern of tungsten trioxide nanorodsX-ray diffraction pattern of tungsten trioxide nanorods
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260 and 334 cm-1 : O-W-O bending modes of WO3
703 and 813 cm-1 : O-W-O stretching modes of WO3
Confirms the formation of WOConfirms the formation of WO33
Raman Spectrum of tungsten trioxide nanorods Raman Spectrum of tungsten trioxide nanorods
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The synthesized WOThe synthesized WO33 has rod morphology – evident from SEM images has rod morphology – evident from SEM images
Scanning electron microscopic images of tungsten trioxide nanorodsScanning electron microscopic images of tungsten trioxide nanorods
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Bulk WO3 : No specific morphology – aggregates of particles
Scanning electron microscopic images of bulk tungsten trioxide Scanning electron microscopic images of bulk tungsten trioxide
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Transmission electron microscopic images of tungsten trioxide nanorods Transmission electron microscopic images of tungsten trioxide nanorods
Dimensions of WODimensions of WO33 nanorods calculated from TEM images : nanorods calculated from TEM images : Length: 130 – 480 nmLength: 130 – 480 nm
Width: 18-56 nmWidth: 18-56 nm
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Interplanar spacing, d: 0.375 nm – corresponds to (020) plane of monoclinic WO3 This observation agrees with the d value obtained from the XRD
High resolution transmission electron microscopic image ofHigh resolution transmission electron microscopic image of tungsten trioxide nanorodstungsten trioxide nanorods
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Presence of constituent elements, W and O is confirmed from the corresponding EDAX peaks Cu peak – from the grid
Energy dispersive X-ray analysis of tungsten trioxide nanorods Energy dispersive X-ray analysis of tungsten trioxide nanorods
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Electrochemical measurements were carried out using CHI660 electrochemical workstation
Three-electrode set up
Pt wire - counter electrode : Ag/AgCl/ (sat KCl) - reference electrode
Glassy carbon coated with electrode material as working electrode
The electrolyte used was 1 M H2SO4 at room temperature and geometrical area of electrode = 0.07cm2
Cyclic voltammetry (CV)
Galvanostatic charge–discharge studies (Chronopotentiometry)
The electrochemical properties were studied using
Electrode fabrication
5 mg of WO3 nanorods or bulk WO3 - dispersed in 100L H2O by ultrasonication
10 L of dispersion has been coated on GC and dried in an oven at 70 C
5 L of Nafion (binder) coated and dried at room temperature
Electrochemical Studies Electrochemical Studies
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Electrolyte: 1M H2SO4 ; Scan rate : 50 mV/s
Anodic peak (~0.1 V) due to the formation of tungsten bronzes (HxWO3) can be observed
WO3 nanorods Bulk WO3
Cyclic voltammograms of tungsten trioxide nanorods and bulk tungsten trioxideCyclic voltammograms of tungsten trioxide nanorods and bulk tungsten trioxide
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Anodic peak current density: WOWO33 Nanorods: 24.7 mAcm Nanorods: 24.7 mAcm-2-2
Bulk WOBulk WO3 3 : 3.5 mAcm: 3.5 mAcm-2-2
Peak current density of WO3 nanorods is ~ 7 times higher than the bulk WO3
Higher redox current for nanorod system shows its higher charge storage by pseudocapacitance
An overlay of cyclic voltammograms of tungsten trioxide An overlay of cyclic voltammograms of tungsten trioxide nanorods and bulk tungsten trioxidenanorods and bulk tungsten trioxide
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Electrolyte: 1M H2SO4 ; Constant current density: 3 mAcm-2
Symmetric inverted ‘V’ type chronopotentiograms will be exhibited by ideal supercapacitors
For WO3 nanorods, a symmetric curve can be observed
For the bulk WO3, an unsymmetry can be seen
This shows that WO3 nanorods constitute desired ideal supercapacitive behaviour
Charge- discharge time has increased for nanorods several folds than the bulk sytem
WO3 nanorods Bulk WO3
Chronopotentiograms of tungsten trioxide nanorods and bulk tungsten trioxideChronopotentiograms of tungsten trioxide nanorods and bulk tungsten trioxide
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Specific Capacitance, C(F/g) = it/mV
where i is the current density used for charge/discharge = 3 mA/cm2
t is the time elapsed for the discharge cycle,
m is the mass of the active electrode = 7 mg/cm2
V is the voltage interval of the discharge = 0.7 V
Capacitance values are calculated from the chronopotentiograms
Increased t value (evident from chronopotentiogram) for WO3 nanorods – higher capacitance
Specific Capacitance for WOSpecific Capacitance for WO33 nanorods : 436 F/g nanorods : 436 F/g Bulk WOBulk WO3 3 : 57 F/g: 57 F/g
Specific CapacitanceSpecific Capacitance
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Higher capacitance for WO3 nanorods can be attributed to the following factors:
Faradaic supercapacitance arise from (1) charge accumulation due to chemisorption of smaller cations such as H+ or Li+ on the redox active material and (2) redox process by the active material
Facile formation of HxWO3 acts as driving force for the redox process – pseudocapacitance
The chemisorption of H+ ion on WO3 is more facile than on RuO2 as H+ is an inherent part of the HxWO3 system (formed by WO3 in acid medium)
Reduction of particle size to nanoregion – increased surface to volume ratio- lead to signal amplification
In electrochemical studies the above factor contributed to enhanced redox process (Faradaic process)
Increased electrode electrolyte interface (EDLC) due to increased number of particles
Contribution of all these facts has lead to enhancement of supercapacitance of WO3 nanorods
Factors for the capacitance in WOFactors for the capacitance in WO33 nanorods nanorods
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Potential vs time at a constant current density of 3 mAcm-2 for 40 cyclesDesired property for devices – stability over long timeWO3 nanorods - Stable over a long period of time – better cycling performance
Cycling performance of tungsten trioxide nanorods electrode Cycling performance of tungsten trioxide nanorods electrode
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Inorder to observe the stability, specific capacitance vs no of cycles has been plotted
Specific capacitance values are taken from the previous chronopotentiogram at every 10 cycles and has been plotted
After 40 cycles, % loss in specific capacitance for WO3 nanorods: 10%
Cycling performance of tungsten trioxide nanorods electrode Cycling performance of tungsten trioxide nanorods electrode
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Potential vs time at a constant current density of 3 mAcm-2 for 40 cyclesDesired property for devices – stability over long time
Cycling performance of bulk tungsten trioxide electrodeCycling performance of bulk tungsten trioxide electrode
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0 5 10 15 20 25 30 35 400
10
20
30
40
50
Spec
ific
capa
cita
nce
(Fg-1
)
Cycle number
Inorder to observe the stability, specific capacitance vs no of cycles has been plotted
Specific capacitance values are taken from the previous chronopotentiogram at every 10 cycles and has been plotted
After 40 cycles, % loss in specific capacitance for bulk WO3 : 30%
Cycling performance of bulk tungsten trioxide electrodeCycling performance of bulk tungsten trioxide electrode
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Tungsten trioxide nanorods have better performance and stability over its counterpartAfter 40 cycles, % loss in specific capacitance for WO3 nanorods: 10%After 40 cycles, % loss in specific capacitance for bulk WO3 : 30%
Overlay of cycling performances of WOOverlay of cycling performances of WO33 nanorods and bulk WO nanorods and bulk WO33
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MaterialMaterial Specific Specific CapacitanceCapacitance
(F/g)(F/g)
WOWO33 nanorods nanorods 436436
Bulk WOBulk WO33 5757
Tabulation of specific capacitance Tabulation of specific capacitance
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Tungsten trioxide nanorods by a single step pyrolysis technique has been prepared
The synthesized nanorods have been employed for supercapacitor electrode applications
Tungsten trioxide nanorods showed higher performance and stability than its bulk counterpart
In terms of the Faradaic capacitance due to the chemisorption of H+ ion on the WO3, it appears better than RuO2
ConclusionsConclusions