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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 991 records · Page 55
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Pseudocapacitive Storage in Nanolayered Ti 2 NT x MXene Using Mg-Ion Electrolyte

Electrochemical supercapacitors are hybrids of a capacitor and battery that rely on materials capable of storing charges via pseudocapacitive reactions in addition to conventional electrostatic double-layer charge storage. MXenes, a relatively new class of two-dimensional (2D) transition metal carbides and nitrides, are ideal candidates for supercapacitors due to their high electronic conductivity, high surface area, and ability to store charges via pseudocapacitive mechanisms. Nitride MXenes such as Ti 2 NT x are predicted to have higher pseudocapacitance than carbide MXenes but have not been explored experimentally. Here, we report on the synthesis, characterization, and pseudocapacitive charge storage mechanism in the Ti 2 NT x nitride MXene. Successful formation of nanolayered Ti 2 NT x MXene is characterized by XRD, SEM, and N 2 physisorption analyses. The identity of the surface terminating groups T x are assigned to primarily O and/or OH based on Raman, FTIR, and STEM-EELS. When tested in various electrolytes, the nanolayered Ti 2 NT x MXene exhibits pronounced reversible redox peaks and high areal capacitances (~1350 uF cm -2 in 1 M MgSO 4 aqueous electrolyte) well exceeding that expected from a double-layer charge storage (~50 uF cm -2 ) showing that charge is stored in the Ti 2 NT x MXene via a pseudocapacitive mechanism. We report a trend in the capacitance as a function of cation as follows: Mg 2+ > Al 3+ > H + > Li + > Na + > K + , that matches theoretical predictions. Remarkably, nanolayered Ti 2 NT x MXene exhibits >200 F g -1 capacitance over a 1.0 V range in the Mg-ion electrolyte, and the capacitance increases to 160% of its initial value after 1000 cycles owing to the 2 e - process and the distinctive multilayer adsorption characteristic of the Mg 2+ cation on the Ti 2 NT x MXene. Furthermore, these findings identify Ti 2 NT x MXene as a new pseudocapacitive material that possesses high capacitance and wide working voltage in a safe and environmentally friendly Mg-ion electrolyte.

2D MXene↗
DOE OSTI2017

Unrivaled combination of surface area and pore volume in micelle-templated carbon for supercapacitor energy storage

Here, we created Immense Surface Area Carbons (ISACs) by a novel heat treatment that stabilized the micelle structure in a biological based precursor prior to high temperature combined activation – pyrolysis. While displaying a morphology akin to that of commercial activated carbon, ISACs contain an unparalleled combination of electrochemically active surface area and pore volume (up to 4051 m 2 g –1 , total pore volume 2.60 cm 3 g –1 , 76% small mesopores). The carbons also possess the benefit of being quite pure (combined O and N: 2.6–4.1 at%), thus allowing for a capacitive response that is primarily EDLC. Tested at commercial mass loadings (~10 mg cm –2 ) ISACs demonstrate exceptional specific capacitance values throughout the entire relevant current density regime, with superior rate capability primarily due to the large fraction of mesopores. In the optimized ISAC, the specific capacitance ( C g ) is 540 F g –1 at 0.2 A g –1 , 409 F g –1 at 1 A g –1 and 226 F g –1 at a very high current density of 300 A g –1 (~0.15 second charge time). At intermediate and high currents, such capacitance values have not been previously reported for any carbon. Tested with a stable 1.8 V window in a 1 M Li 2 SO 4 electrolyte, a symmetric supercapacitor cell yields a flat energy–power profile that is fully competitive with those of organic electrolyte systems: 29 W h kg –1 at 442 W kg –1 and 17 W h kg –1 at 3940 W kg –1 . The cyclability of symmetric ISAC cells is also exceptional due to the minimization of faradaic reactions on the carbon surface, with 80% capacitance retention over 100 000 cycles in 1 M Li 2 SO 4 and 75 000 cycles in 6 M KOH.

25 ENERGY STORAGE↗
DOE OSTI2016

Si:SrTiO 3 -Al 2 O 3 -Si:SrTiO 3 multi-dielectric architecture for metal-insulator-metal capacitor applications

We present that metal-insulator-metal (MIM) capacitors comprised of amorphous Si:SrTiO 3 -Al 2 O 3 -Si:SrTiO 3 multi-dielectric architecture have been fabricated employing a combination of pulsed laser and atomic layer deposition techniques. The voltage linearity, temperature coefficients of capacitance, dielectric and electrical properties upon thickness were studied under a wide range of temperature (200–400 K) and electric field stress (61.5 MV/cm). A high capacitance density of 31 fF/μm 2 , a low voltage coefficient of capacitance of 363 ppm/V 2 , a low temperature coefficient of capacitance of <644 ppm/K, and an effective dielectric constant of 133 are demonstrated in a MIM capacitor with 1.4 nm capacitance equivalent thickness in a 40 nm thick ultra high-k multi-dielectric stack. Finally, all of these properties make this dielectric architecture of interest for next generation, highly scaled MIM capacitor applications.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Increased Multilayer Fabrication and RF Characterization of a High-Density Stacked MIM Capacitor Based on Selective Etching

This paper presents the fabrication and characterization of a high-density multilayer stacked metal-insulator-metal (MIM) capacitor based on a novel process of depositing the MIM multilayer on pillars followed by polishing and selective etching steps to form a stacked capacitor with merely three photolithography steps. In this paper, the pillars were made of glass to prevent substrate loss, whereas an oxide-nitride-oxide dielectric was employed for lower leakage, better voltage/frequency linearity, and better stress compensation. MIM capacitors with six dielectric layers were successfully fabricated, yielding capacitance density of 3.8 fF/mu m(2), maximum capacitance of 2.47 nF, and linear and quadratic voltage coefficients of capacitance below 21.2 ppm/V and 2.31 ppm/V-2. The impedance was measured from 40 Hz to 3 GHz, and characterized by an analytically derived equivalent circuit model to verify the radio frequency applicability. The multilayer stacking-induced plate resistance mismatch and its effect on the equivalent series resistance (ESR) and effective capacitance was also investigated, which can be counteracted by a corrected metal thickness design. A low ESR of 800 m Omega was achieved, whereas the self-resonance frequency was >760 MHz, successfully demonstrating the feasibility of this method to scale up capacitance densities for high-quality-factor, high-frequency, and large-value MIM capacitors.

Tseng, VFG↗
DOE OSTI2021

Do Deep Eutectic Solvents Behave Like Ionic Liquid Electrolytes? A Perspective from the Electrode-Electrolyte Interface

The differential capacitance as a function of potential and composition for choline chloride (ChCl) and ethylene glycol (EG) at 1:2,1:4, 1:6, and 1:20 molar ratios were studied using electrochemical impedance spectroscopy (EIS) on glassy carbon. In addition, ChCl:EG at the known ethaline DES composition (1:2) and 1:20 molar ratio were studied on Au and Pt electrodes, and compared to glyceline (ChCl:glycerol, 1:2). The capacitance-potential curves on glassy carbon were best interpreted by the modified Gouy-Chapman model. A dampened U-shape was observed similar to dilute electrolytes, however, the non-negligible ionic and H-bonding interactions in these electrolytes resulted in ambiguity about the point of zero charge where capacitance was weakly dependent on potential. Additionally, the differential capacitance was independent of composition on glassy carbon due to limited availability of mobile free ions and constraints by solvated ion sizes within the interface. Increases in capacitance are observed with Au as a result of desolvation and specific adsorption of Cl, and with Pt upon decreased Cl concentrations. These results indicate DESs and H-bonded electrolytes with high salt concentrations are distinct from ionic liquids and present no pronounced over screening or crowding with applied potential.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Multidimensional Cyclic Voltammetry Simulations of Pseudocapacitive Electrodes with a Conducting Nanorod Scaffold

This paper aims to understand the effect of nanoarchitecture on the performance of pseudocapacitive electrodes consisting of conducting scaffold coated with pseudocapacitive material. To do so, two-dimensional numerical simulations of ordered conducting nanorods coated with a thin film of pseudocapacitive material were performed. The simulations reproduced three-electrode cyclic voltammetry measurements based on a continuum model derived from first principles. Two empirical approaches commonly used experimentally to characterize the contributions of surface-controlled and diffusion-controlled charge storage mechanisms to the total current density with respect to scan rate were theoretically validated for the first time. Moreover, the areal capacitive capacitance, attributed to EDL formation, remained constant and independent of electrode dimensions, at low scan rates. However, at high scan rates, it decreased with decreasing conducting nanorod radius and increasing pseudocapacitive layer thickness due to resistive losses. By contrast, the gravimetric faradaic capacitance, due to reversible faradaic reactions, decreased continuously with increasing scan rate and pseudocapacitive layer thickness but was independent of conducting nanorod radius. Note that the total gravimetric capacitance predicted numerically featured values comparable to experimental measurements. Finally, an optimum pseudocapacitive layer thickness that maximizes total areal capacitance was identified as a function of scan rate and confirmed by scaling analysis.

42 ENGINEERING↗
DOE OSTI2024

Assessment of Readout Techniques for Passive Monitors

This fiscal year (FY) 2023 report on passive temperature sensors covers two main objectives: to demonstrate that the optical dilatometer can successfully process disc shaped silicon carbide (SiC) temperature monitors (TMs), and to demonstrate proof of concept for using the capacitance readout method to read printed melt wires. The SiC objective was successfully met by annealing and analyzing, via optical dilatometry, all eight 3-mm SiC discs provided by the Nuclear Science User Facilities (NSUF) Idaho State University (ISU) Nanostructured Steels for Enhanced Radiation Tolerance (N SERT) experiment, which was irradiated at Idaho National Laboratory (INL)’s Advanced Test Reactor (ATR). Per the ISU N SERT experiment, capsule 1 (KGT 3828 1 and KGT 3828-2) had a design temperature of 300°C +/- 50°C and an exposure of 2 dpa +/- 10%; capsule 2 (KGT 4600 and KGT 4609) had a design temperature of 300°C +/- 50°C and an exposure of 6 dpa +/- 10%; capsule 3 (KGT 4639 C and KGT 4639-D) had a design temperature of 500°C +/- 50°C and an exposure of 6 dpa +/- 10%; and capsule 4 (KGT 3841 3 and KGT 3841 4) had a design temperature of 500°C +/- 50°C and an exposure of 2 dpa +/- 10%. The target exposure rates, in dpa, are the neutron damage for various types of nanostructured steels. All but three SiC TMs (KGT 4600, KGT 4639 D, and KGT 3841 4) revealed averaged peak irradiation temperatures that fell within the design temperature ranges. The three SiC TMs that did not fall within the design temperatures ranges were at least 100°C below that target temperature. Furthermore, SiC TM KGT 3841 C revealed two irradiation regimes: one closer to the 300°C design temperature, and the other closer to the 500°C design temperature. Also, all the SiC TMs’ averaged peak irradiation temperatures came in anywhere between 20°C and 240°C below the irradiation temperatures predicted by the thermal models. This showed the optical dilatometry method to be a reliable and less time intensive process for determining averaged peak irradiation temperatures from passive SiC TMs such as rods and discs. Under the Advanced Sensors and Instrumentation (ASI) program in FY-23, Boise State University (BSU) proposed to demonstrate proof of concept for using a capacitance readout technique applicable to printed melt wires; however, they were stymied by the complexity of the capacitance readout method. In support of the BSU work, INL developed an additively manufactured (AM) ceramic package for encapsulating the new melt wires. Inks were synthesized at BSU that used new protocols rather than following previously established protocols implemented at INL, and testing of various temperatures was conducted at BSU to evaluate the melting behaviors of the printed melt wires. The result was that the capacitance readout technique showed promise but also created more challenges than originally anticipated. For example, the tin ink synthesized at BSU showed unusual melting behaviors that did nothing to enhance the performance of the final printed melt wire prototype in terms of the capacitance readout method. To make the proof of concept work when applied to the printed melt wires, the ASI program would need to invest further resources and time. Consequently, the program is not planning to continue this proof of concept work in FY-24, based on the progress and findings achieved in FY-23.

36 MATERIALS SCIENCE↗
NASA NTRS1990

Fabrication and optimization of a whiskerless Schottky barrier diode for submillimeter wave applications

The following accomplishments were made towards the goal of an optimized whiskerless diode chip for submillimeter wavelength applications. (1) Surface channel whiskerless diode structure was developed which offers excellent DC and RF characteristics, reduced shunt capacitance and simplified fabrication compared to mesa and proton isolated structures. (2) Reliable fabrication technology was developed for the surface channel structure. The new anode plating technology is a major improvement. (3) DC and RF characterization of the surface channel diode was compared with whisker contacted diodes. This data indicates electrical performance as good as the best reported for similar whisker contacted devices. (4) Additional batches of surface channel diodes were fabricated with excellent I-V and reduced shunt capacitance. (5) Large scale capacitance modelinng was done for the planar diode structure. This work revealed the importance of removing the substrate gallium arsenide for absolute minimum pad capacitance. (6) A surface channel diode was developed on quartz substrate and this substrate was completely removed after diode mounting for minimum parasitic capacitance. This work continues with the goal of producing excellent quality submillimeter wavelength planar diodes which satisfy the requirements of easy handling and robustness. These devices will allow the routine implementation of Schottky receivers into space-based applications at frequencies as high as 1 THz, and, in the future, beyond.

Bishop, W.↗
NASA NTRS2001

Silicon micromachined accelerometer/seismometer and method of making the same

A silicon-based microaccelerometer for seismic application is provided using a low-resonant frequency (10 Hz), large proof mass (1 gram), and high Q suspension to achieve high sensitivity of less than 1 ng with a bandwidth a 0.05 to 50 Hz. The proof mass is cut away from a planar substrate in the form of a disk using abrasive cutting, which disk closely fits but does not touch a surrounding angular frame. The spring of the microaccelerometer between the angular frame and the proof mass is provided from two continuous, 3 microns thick membranes. The fixed capacitive electrodes are provided on separate, subsequently bonded substrates, and movable capacitive plates are provided on the membranes. By fabricating capacitive plates on the separate substrates, the gap between the fixed and movable capacitive plates in the differential capacitive sensor is closely controlled. The use of continuous membranes for the spring produces a shock resistant, robust sensor.

Martin, Richard D.↗
NASA NTRS2003

Capacitor-Chain Successive-Approximation ADC

A proposed successive-approximation analog-to-digital converter (ADC) would contain a capacitively terminated chain of identical capacitor cells. Like a conventional successive-approximation ADC containing a bank of binary-scaled capacitors, the proposed ADC would store an input voltage on a sample-and-hold capacitor and would digitize the stored input voltage by finding the closest match between this voltage and a capacitively generated sum of binary fractions of a reference voltage (Vref). However, the proposed capacitor-chain ADC would offer two major advantages over a conventional binary-scaled-capacitor ADC: (1) In a conventional ADC that digitizes to n bits, the largest capacitor (representing the most significant bit) must have 2(exp n-1) times as much capacitance, and hence, approximately 2(exp n-1) times as much area as does the smallest capacitor (representing the least significant bit), so that the total capacitor area must be 2(exp n) times that of the smallest capacitor. In the proposed capacitor-chain ADC, there would be three capacitors per cell, each approximately equal to the smallest capacitor in the conventional ADC, and there would be one cell per bit. Therefore, the total capacitor area would be only about 3(exp n) times that of the smallest capacitor. The net result would be that the proposed ADC could be considerably smaller than the conventional ADC. (2) Because of edge effects, parasitic capacitances, and manufacturing tolerances, it is difficult to make capacitor banks in which the values of capacitance are scaled by powers of 2 to the required precision. In contrast, because all the capacitors in the proposed ADC would be identical, the problem of precise binary scaling would not arise.

Cunningham, Thomas↗
DOE OSTI2013

Giant Molecular Magnetocapacitance

Capacitance of a nanoscale system is usually thought of having two contributions, a classical electrostatic contribution and a quantum contribution dependent on the density of states and/or molecular orbitals close to the Fermi energy. In this letter we demonstrate that in molecular nano-magnets and other magnetic nanoscale systems, the quantum part of the capacitance becomes spin-dependent, and is tunable by an external magnetic field. This molecular magnetocapacitance can be realized using single molecule nano-magnets and/or other nano-structures that have antiferromagnetic ground states. As a proof of principle, first-principles calculation of the nano-magnet [Mn3O(sao)3(O2CMe)(H2O)(py)3] shows that the charging energy of the high-spin state is 260 meV lower than that of the low-spin state, yielding a 6% difference in capacitance. A magnetic field of ~40T can switch the spin state, thus changing the molecular capacitance. A smaller switching field may be achieved using nanostructures with a larger moment. Molecular magnetocapacitance may lead to revolutionary device designs, e.g., by exploiting the Coulomb blockade magnetoresistance whereby a small change in capacitance can lead to a huge change in resistance.

Wu, Yuning↗
DOE OSTI2016

MnO{sub 2}-wrapped hollow graphitized carbon nanosphere electrode for supercapacitor

Highlights: • MnO{sub 2}/HGC nanospheres are prepared by a cooperative template wrapping method. • MnO{sub 2}/HGC nanospheres possess large specific surface area. • MnO{sub 2}/HGC nanospheres are benefit for transmission of ions and electrons. • MnO{sub 2}/HGC electrodes exhibit a high specific capacitance. - Abstract: MnO{sub 2}-wrapped hollow graphitized carbon nanospheres (MnO{sub 2}/HGC) electrodes are prepared by a cooperative template wrapping method. hollow Graphitized carbon nanospheres (HGC) are firstly obtained by carbonizing phenolic resin followed by etching the SiO{sub 2} template, then the MnO{sub 2} ultrathin nanoplates are coated on the surfaces of the HGC nanospheres through a redox reaction between KMnO{sub 4} and HGC nanospheres. The as-prepared MnO{sub 2}/HGC hollow nanospheres possess porous structure and large specific surface area (∼230 m{sup 2} g{sup −1}). The specific capacitances of MnO{sub 2}/HGC nanosphere electrodes with different mass ratios of MnO{sub 2} to HGC are about 340–380 F g{sup −1} at a scan rate of 5 mV s{sup −1} in Na{sub 2}SO{sub 4} solution, and shows relative good cycling performance of the initial capacitance after 1000 cycles. The good specific capacitance is ascribed to the novel hollow nanosphere structure, which possesses high surface-to-volume ratio, and makes it easy for the mass diffusion of electrolyte and transmission of ions and electrons and also maintains the mechanical integrality.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Ceria nanoparticles uniformly decorated on graphene nanosheets with coral-like morphology for high-performance supercapacitors

Graphical abstract: The study reported the synthesis of coral-like CeO{sub 2}/GNs for supercapacitors. The unique architecture with overall connected framework and good conducting network of the graphene greatly boosts the Faradaic redox reaction. Therefore, the CeO{sub 2}/GNs delivers an excellent electrochemical performance. - Highlights: • The study reported the synthesis of CeO{sub 2}/GNs. • The graphene was woven into CeO{sub 2}, acting as a good conducting network. • The CeO{sub 2}/GNs shows a coral-like structure. • The architecture creates an overall connected framework. • The CeO{sub 2}/GNs delivers good capacitive performances. - Abstract: CeO{sub 2}/graphene was synthesized by a simple microwave method along with subsequent calcination. CeO{sub 2} nanoparticles with an average size of 68.8 nm are uniformly decorated on graphene nanosheets (CeO{sub 2}/GNs). The CeO{sub 2}/GNs displays a like-coral morphology. The architecture including overall connected framework, abundant intercrossed and interconnected nanochannels and perfect conducting network of the graphene, endows the CeO{sub 2}/GNs material with a superior electron and mass transport. As a result, the CeO{sub 2}/GNs gives a high specific capacitance of 503.4 F/g at 2 A/g and good cycle performance with 91.8% capacitance retention after 3000 cycles. Further, an asymmetric supercapacitors was assembled by using CeO{sub 2}/GNs as the positive electrode and activated carbon as the negative electrode, the asymmetric device demonstrate a favorable energy density of 30.2 Wh/kg at the power density of 750.0 W/kg and superior cycle life with 86.4% the capacitance retenion at 5 A/g after 3000 cycles.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Synthesis of MnO{sub 2}/C composite nanotubes as advanced cathode of supercapacitors

Graphical abstract: Self-supported porous MnO{sub 2}/C nanotube arrays are prepared by combined hydrothermal plus carbonization methods and demonstrated with high capacitance and good cycling life as cathode of supercapacitors. - Highlights: • MnO{sub 2}/C nanotube arrays are synthesized by a hydrothermal method. • MnO{sub 2}/C nanotube arrays show good high-rate performance. • MnO{sub 2}/C nanotube arrays show an excellent cycling performance. - Abstract: Controllable synthesis of high-capacity cathode is the research hotspot in the field of supercapacitors. In this work, with the help of sacrificial ZnO template, MnO{sub 2}/C nanotube arrays are formed by hydrothermal synthesis plus glucose carbonization. MnO{sub 2}/C composite nanotubes of 120–130 nm are formed and grow vertically to the substrate forming the final nanotube arrays. Fast ion/electron transfer is realized in this unique porous nanotube architecture. As cathode of supercapacitors, the MnO{sub 2}/C nanotube arrays exhibit high specific capacitance (790 F g{sup −1} at 5 A g{sup −1}), excellent rate performance (570 F g{sup −1} at 30 A g{sup −1}) and long-term cycling stability (90.7% capacitance retention after 20,000 cycles). The proposed electrode construction strategy is favorable for fabrication of other capacitive cathodes for energy storage.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Single-step hydrothermal synthesis of wrinkled graphene wrapped TiO2 nanotubes for photocatalytic hydrogen production and supercapacitor applications

Highlights: • Wrinkle rGO wrapped TiO{sub 2} nanotubes were prepared by alkanine hydrothermal method. • Improved visible absorption and reduced recombination was witnessed in rGO-TiO{sub 2}. • H{sub 2} production of 24,880 μmole/g/h was achieved by rGO-TiO{sub 2}, 12.9 folds to P25 TiO{sub 2}. • Double layer and pseudo capacitance of rGO-TiO{sub 2} showed specific capacitance 160 F/g. - Abstract: Herein, we discuss the synthesis of reduced graphene oxide and TiO{sub 2} (rGO-TiO{sub 2}) nanocomposites with varying ratios of rGO to TiO{sub 2} by hydrothermal method. Photocatalytic ability of the nanocomposites was assessed for H{sub 2} production under natural sunlight. At 5 wt% GO loading, the rGO-TiO{sub 2} exhibited 24,880 μmol/g/h H{sub 2}, 12.9 times to commercial P25-TiO{sub 2} (1920 μmol/g/h). The symmetric supercapacitor device fabricated using rGO-TiO{sub 2} demonstrated 160 F/g specific capacitance with 99% retention. The efficient charge carrier separation and transportation between TiO{sub 2} nanotubes and rGO resulted high photocatalytic activity. The synergistic double layer pseudo capacitor behavior of rGO-TiO{sub 2} is the reason for improved specific capacitance.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Facile preparation of porous nickel oxide membrane for flexible supercapacitors electrode via phase-separation method of polymer

Highlights: • Polymer/metal oxide hybrid membrane is fabricated for supercapacitors electrode. • Effects of membrane components on structure and performance are investigated. • The prepared electrode membrane shows high flexible property. • A capacitance of 794 F/g is obtained at a current density of 1.0 A/g. • Symmetric supercapacitor device exhibits an energy density of 39.6 Wh/kg. - Abstract: In this article, a porous flexible membrane electrode of nickel oxide is developed by a facile method based on liquid-liquid phase-separation. The effects of the membrane components on structures and electrochemical behaviors of membrane electrode are investigated. The results reveal that nano NiO and conducting graphite are imbedded into the polymer membrane of polyethersulfone to form a flexible hybrid membrane (M-NiO-G), which shows the highest specific capacitance of 794.0 F/g at a current density of 1.0 A/g. The asymmetrical supercapacitor device based on the as-synthesized of M-NiO-G (positive electrode) and activated carbon membrane (negative electrode) exhibits a high specific capacitance of 154.0 F/g at a current density of 0.2 A/g. The coulombic efficiency remains about 95.0%, and the capacitance retention is 84.8% after 5000 charging-discharging cycles at 1.0 A/g. The energy density of the asymmetrical supercapacitor device reaches 39.6 Wh/kg at a power density of 516.9 W/kg, still remains 20.0 Wh/kg at a high power density of 2567.4 W/kg in the potential window from 0 to 1.36 V in 6 M KOH aqueous solution.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Fabrication of CeO2/PANI composites for high energy density supercapacitors

Highlights: • Fabrication of CeO{sub 2}/PANI composite was successfully prepared using easy solution mixing method. • Combinational approaches of rare earth oxides with conducting polymer composites posses’ excellent pseudocapacitive nature. • Superior specific capacitance, rate capacitance and cyclic stability. • Outstanding performance of asymmetric and symmetric devices. - Abstract: Combinational approaches of rare earth oxides with conducting polymer composites have gained vast attention in supercapacitor field due to the outstanding pseudocapacitive property. Here we detail the redox reaction based on CeO{sub 2}/polyaniline nanostructure to grasp the superior electrochemical nature of the composite. The CeO{sub 2}/polymer nanostructure showed the improved specific capacitance of 1452 F g{sup −1} at 2 A g{sup −1} when compared to pristine CeO{sub 2} (927 F g{sup −1} at 2 A g{sup −1}). The composite also maintains excellent rate capacitance (875 F g{sup −1} at 10 A g{sup −1}) and good cyclic stability upto 1500 cycles at high current density of 20 A g{sup −1}. Symmetric and asymmetric supercapacitor devices were fabricated using CeO{sub 2}/ PANI as an electrode. Moreover, the asymmetric supercapacitor possesses excellent specific capacity (256 F g{sup −1} at 2 mV s{sup −1}) with high energy density (75 Whkg{sup −1}) and high power density (566 Wkg{sup −1}). These results suggest a potential usefulness of CeO{sub 2}/ PANI composite exploit as an efficient electrode for supercapacitor applications.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Morphological behaviour, electronic bond formation and electrochemical performance study of V2O5-polyaniline composite and its application in asymmetric supercapacitor

Highlights: • Interlinked V{sub 2}O{sub 5}-PANI composites are synthesized by chemical polymerization. • V{sub 2}O{sub 5}-PANI exhibits the highest capacitance of 529.56 F g{sup −1} with wide window of 1.6 V. • Correlation between electrochemical performances with IR peak shifts is studied. • Inorganic-organic synergistic effect plays crucial role for wide working window. • Asymmetric supercapacitor exhibits high energy and power in wide potential windows. - Abstract: To meet the demand of high-energy density supercapacitors, development of suitable electrode material with a wide potential window and high specific capacitance is most important. In this report, we have synthesized V{sub 2}O{sub 5}-PANI nanocomposite through in-situ intercalation and polymerization reaction of aniline with V{sub 2}O{sub 5}, which shows a wide potential window as well as high specific capacitance. XRD, SEM and FTIR have been used to characterize the electrode materials. Their electrochemical activity and pseudocapacitive performances were investigated. The correlation between morphology and electrochemical performances were investigated which is a vital way for the selection of electrode materials. Due to the organic-inorganic compatibility, V{sub 2}O{sub 5}-PANI exhibits good electrochemical charge storage in a wide potential window of 1.6 V (ranging between −0.4 V to 1.2 V) with excellent stability of 84.2% capacitance retention after 5000 GCD cycles. Moreover, asymmetric supercapacitor was assembled V{sub 2}O{sub 5}-PANI composite and NiMn{sub 2}O{sub 4} electrodes which yield remarkable energy and power density.

77 NANOSCIENCE AND NANOTECHNOLOGY↗