Project description:As supercapacitor electrode materials, their structures, including specific surface area, instability, and interconnection, determine the electrochemical performances (specific capacitance, cycle stability, and rate performance). In this study, 1T-MoS2 nanosheets were self-assembled into nanoflowers via a one-pot facile hydrothermal reaction. The nanoflowers retain the excellent electrical conductive performance and the feature of inherent high specific surface area of the nanosheets. For the sheets are interconnected to each other in flower structure, the structure is more stable and the charges are more easily transferred. Thus, compared to the nanosheet electrode, the nanoflower electrode shows the remarkable advantage when used as the electrode of the energy-storage device, whether it is 1T phase or 2H phase in KCl or in KOH. When measured at 0.5 A g-1 in KOH electrolyte, the MoS2 nanoflower electrode exhibits a high specific capacitance of 1120 F g-1. At the same time, when cycling 2000 times at a current density of 10 A g-1, the capacitance retention ratio can reach up to 96%.
Project description:Two-dimensional (2D) materials and their corresponding van der Waals heterostructures have drawn tremendous interest due to their extraordinary electrical and optoelectronic properties. Insulating 2D hexagonal boron nitride (h-BN) with an atomically smooth surface has been widely used as a passivation layer to improve carrier transport for other 2D materials, especially for Transition Metal Dichalcogenides (TMDCs). However, heat flow at the interface between TMDCs and h-BN, which will play an important role in thermal management of various electronic and optoelectronic devices, is not yet understood. In this paper, for the first time, the interface thermal conductance (G) at the MoS2/h-BN interface is measured by Raman spectroscopy, and the room-temperature value is (17.0 ± 0.4) MW · m-2K-1. For comparison, G between graphene and h-BN is also measured, with a value of (52.2 ± 2.1) MW · m-2K-1. Non-equilibrium Green's function (NEGF) calculations, from which the phonon transmission spectrum can be obtained, show that the lower G at the MoS2/h-BN interface is due to the weaker cross-plane transmission of phonon modes compared to graphene/h-BN. This study demonstrates that the MoS2/h-BN interface limits cross-plane heat dissipation, and thereby could impact the design and applications of 2D devices while considering critical thermal management.
Project description:Conductive polymers such as polypyrrole have been widely used as pseudo-capacitive electrodes for supercapacitors. This work demonstrates a simple method to improve the performance of conductive polymer electrodes by adding montmorillonite in order to perform capacitive behavior. Conductive composite polymers (CCPs) based on montmorillonite/polypyrrole (MMT/PPy(Cl)) have been synthesized by polymerization using FeCl3 as an oxidizing agent. During the preparation of CCP, the effect of MMT/pyrrole mass ratio and the influence of the amount of added H+ and temperature of the synthesis medium on the electrochemical performance of the composite have been investigated. The investigation associated with conductivity measurement allowed us to determine the best conditions to reach a high specific capacitance of 465 F gr-1 measured by cyclic voltammetry with respect to the CCP synthesized at ambient temperature (220 F gr-1) and a 35% increase in capacity compared to its homologue synthesized in neutral conditions at a low temperature. These performances have been advantageously correlated both to the edge acidity of the host material and to the evolution of its conductivity according to the preparation conditions. The galvanostatic charge/discharge tests also confirm the stability of the obtained composite, and a capacitance of 325 F g-1 for the best CCP is recorded with a regime of 1 A g-1. In addition, the durability of the device shows that the proposed material has a relatively good stability during cycling.
Project description:We report a gel polymer electrolyte (GPE) supercapacitor concept with improved pathways for ion transport, thanks to a facile creation of a coherent continuous distribution of the electrolyte throughout the electrode. Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) was chosen as the polymer framework for organic electrolytes. A permeating distribution of the GPE into the electrodes, acting both as integrated electrolyte and binder, as well as thin separator, promotes ion diffusion and increases the active electrode-electrolyte interface, which leads to improvements both in capacitance and rate capability. An activation process induced during the first charge-discharge cycles was detected, after which, the charge transfer resistance and Warburg impedance decrease. We found that a GPE thickness of 12 μm led to optimal capacitance and rate capability. A novel hybrid nanocomposite material, formed by the tetraethylammonium salt of the 1 nm-sized phosphomolybdate cluster and activated carbon (AC/TEAPMo12), was shown to improve its capacitive performance with this gel electrolyte arrangement. Due to the homogeneous dispersion of PMo12 clusters, its energy storage process is non-diffusion-controlled. In the symmetric capacitors, the hybrid nanocomposite material can perform redox reactions in both the positive and the negative electrodes in an ambipolar mode. The volumetric capacitance of a symmetric supercapacitor made with the hybrid electrodes increased by 40% compared to a cell with parent AC electrodes. Due to the synergy between permeating GPE and the hybrid electrodes, the GPE hybrid symmetric capacitor delivers three times more energy density at higher power densities and equivalent cycle stability compared with conventional AC symmetric capacitors.
Project description:Sodium ion capacitors are under extensive investigation as companionable pre-existing lithium ion batteries and sodium ion batteries. Finding a suitable host for sodium ion storage is still a major challenge. In this context, here we report a MoS2 nanoflowers@rGO composite produced via a hydrothermal method followed by an ultra sonication process as a sodium ion symmetric hybrid supercapacitor. The structural and electrochemical performances of the electrode material were investigated to establish its applicability in sodium ion capacitors. The electrochemical performance was evaluated using metallic sodium in a half cell configuration which delivered a maximum specific capacitance of 226 F g-1 at 0.03 A g-1. When examined as a symmetric hybrid electrode (full cell) it delivered a maximum capacitance of 55 F g-1 at 0.03 A g-1. This combination may be a new gateway for upcoming research work which deals with sodium ion storage applications. The results confirmed that the as-synthesized MoS2 nanoflowers@rGO heterostructure electrode exhibited notable electrochemical behaviour.
Project description:The design of bimetallic tellurides that exhibit excellent electrochemical properties remains a huge challenge for high-performance supercapacitors. In the present study, tellurium is consolidated on CoNi2@rGO for the first time, to synthesize NiTe2-Co2Te2@rGO nanocomposite by using a facile hydrothermal method. As-prepared NiTe2-Co2Te2@rGO nanocomposite was characterized by EDS, TEM, FESEM, Raman, BET, XRD, and XPS techniques to prove the structural transformation. Upon the electrochemical characterization, NiTe2-Co2Te2@rGO has notably presented numerous active sites and enhanced contact sites with the electrolyte solution during the faradic reaction. The as-prepared nanocomposite reveals a specific capacity of 223.6 mAh g-1 in 1.0 M KOH at 1.0 A g-1. Besides, it could retain 89.3% stability after 3000 consecutive galvanostatic charge-discharge cycles at 1.0 A g-1 current density. The hybrid supercapacitor, fabricated by activated carbon as an anode site, and NiTe2-Co2Te2@rGO as a cathode site, presents a potential window of 1.60 V with an energy density of 51 Wh kg-1 and a power density of 800 W kg-1; this electrode is capable of lighting up two red LED lamps and a yellow LED lamp for 20 min, which is connected in parallel. The present work opens new avenues to design and fabrication of nanocomposite electrode materials in the field of supercapacitors.
Project description:The bending process of 2D materials, subject to an external force, is investigated, and applied to graphene, molybdenum disulphide (MoS2), and imogolite. For graphene we obtained 3.43 eV Å2 per atom for the bending modulus, which is in good agreement with the literature. We found that MoS2 is ∼11 times harder to bend than graphene, and has a bandgap variation of ∼1 eV as a function of curvature. Finally, we also used this strategy to study aluminosilicate nanotubes (imogolite) which, in contrast to graphene and MoS2, present an energy minimum for a finite curvature radius. Roof tile shaped imogolite precursors turn out to be stable, and thus are expected to be created during imogolite synthesis, as predicted to occur by self-assembly theory.
Project description:The increasing global demand for energy storage solutions has spurred interest in advanced materials for electrochemical energy storage devices. Transition-metal carbides and nitrides, known as MXenes, are characterized by remarkable conductivity and tunable properties, They have gained significant attention for their potential in energy storage applications. The properties of two-dimensional (2-D) MXenes can be tuned by doping or composite formation. We report a novel Ti3C2Tx/NaF composite prepared via a straightforward hydrothermal process for supercapacitor electrode applications. Three composites with varying NaF concentrations (1%, 3%, and 5%) were synthesized under similar conditions. Structural characterization using X-ray diffraction (XRD) and scanning electron microscopy confirmed the successful formation of the composites, whereas distinct shifts in XRD peaks and new peaks revealed the presence of NaF. Electrochemical performance was evaluated by cyclic voltammetry, galvanostatic charging-discharging, and electrochemical impedance spectroscopy. The composites exhibited pseudo-capacitive behavior with reversible redox reactions during charge and discharge cycles. Specific capacitance of 191 F/g at scan rates of 2 mV/s was measured in 1 M KOH. Electrochemical impedance spectroscopy revealed an escalating impedance factor as NaF content increases within Ti3C2Tx. This study underscores the versatile energy storage potential of Ti3C2Tx/NaF composites, offering insights into their tailored properties and behavior.
Project description:One of the key challenges for pseudocapacitive electrode materials with highly effective capacitance output and future practical applications is how to rationally construct hierarchical and ordered hybrid nanoarchitecture through the simple process. Herein, we design and synthesize a novel NiMn-layered double hydroxide nanosheet@Ni3S2 nanorod hybrid array supported on porous nickel foam via a one-pot hydrothermal method. Benefited from the ultrathin and rough nature, the well-defined porous structure of the hybrid array, as well as the synergetic effect between NiMn-layered double hydroxide nanosheets and Ni3S2 nanorods, the as-fabricated hybrid array-based electrode exhibits an ultrahigh specific capacitance of 2703 F g-1 at 3 A g-1. Moreover, the asymmetric supercapacitor with this hybrid array as a positive electrode and wood-derived activated carbon as a negative electrode demonstrates high energy density (57 Wh Kg-1 at 738 W Kg-1) and very good electrochemical cycling stability.
Project description:Development of advanced materials for electrocatalytic and photocatalytic water splitting is the key in utilization of renewable energy. In the present work, we have synthesized MoS2 nanoparticles embedded over the graphene oxide (GO) and reduced graphene oxide (rGO) layer for superior catalytic activity in the hydrogen evolution process (HER). The nanocomposite materials are characterized using different spectroscopic and microscopic measurements. A Tafel slope of ∼40 mV/decade suggested the Volmer-Heyrovsky mechanism for the HER process with MoS2/GO composite as the catalyst, which indicated that electrochemical desorption of hydrogen is the rate-limiting step. The small Tafel slope indicates a promising electrocatalyst for HER in practical application. MoS2/GO composite material has shown superior catalytic behavior compared to that of MoS2/rGO composite material. The HER catalytic activity of the catalysts is explored using scanning electrochemical microscopy (SECM) using the feedback and redox competition mode in SECM. The activation energy for HER activity was calculated, and the values are in the range of 17-6 kJ/mol. The lower value of activation energy suggested faster HER kinetics.