Effect of nano-dispersed silica on the ion-conducting behavior of PMMA-based polymer gel electrolytes containing LiPF<Subscript>6</Subscript>

Nano-sized silica poly(methylmethacrylate)-based gel electrolyte containing lithium hexafluorophosphate (LiPF₆) was synthesized by using different binary solvent mixture (propylene carbonate(PC) and dimethylformamide (DMF) in different volume ratio). Role of DMF in PC: Higher DMF content in PC-based electrolyte shows higher ionic conductivity at all polymer content and at wide temperature regions (10-70 °C). A small increment in ionic conductivity at lower content of polymer in liquid/gel electrolyte was observed and having maximum conductivity of 13.12 mS/cm at 25 °C. Stability (mechanically and electrically), viscosity and ionic conductivity of gel electrolytes were improved with the addition of nano-sized silica at ambient temperature. Ionic conductivity of nano-sized silica-based gel electrolyte does not change much over 5^o–70 °C temperature range and is factor-wise only which make indispensable in different electrochemical devices. Also polymer gel electrolyte membranes as such and with dispersed silica nano-particles were characterized through scanning electron microscope to study the morphology of gel matrix.     

Preparation and ionic conductivity of composite polymer electrolytes based on hyperbranched star polymer

Hyperbranched star polymer HBPS-(PPEGMA) _x was synthesized by atom transfer radical polymerization (ATRP) using hyperbranched polystyrene (HBPS) as macroinitiator and poly(ethylene glycol) methyl ether methacrylate (PEGMA) as monomer. The structure of the prepared hyperbranched star polymer was characterized by ¹H NMR, ATR-FTIR, and GPC. Polymer electrolytes based on HBPS-(PPEGMA) _x , lithium salt, and/or nano-TiO₂ were prepared. The influences of lithium salt concentration and type, nano-TiO₂ content, and size on ionic conductivity of the obtained polymer electrolytes were investigated. The results showed that the low crystallinity of the prepared polymer electrolyte was caused by the interaction between lithium salt and polymer. The addition of TiO₂ into HBPS-(PPEGMA) _x /LiTFSI improved the ionic conductivity at low temperature. The prepared composite polymer electrolyte showed the highest ionic conductivity of 9?×?10^?5 S cm^?1 at 30 °C when the content of TiO₂ was 15 wt% and the size of TiO₂ was 20 nm.     

Poly(ethyleneglycol methacrylate phosphate) and heterocycle based proton conducting composite materials

Novel anhydrous proton conducting polymer electrolytes based on poly(ethyleneglycol methacrylate phosphate) (PEGMAP) and heterocycle have been investigated. The materials were synthesized via conventional radical bulk polymerization of ethylene glycol methacrylate phosphate in the presence of proton solvents such as imidazole (Im) or benzimidazole (BnIm). The poly(EGMAP–Im_x) or poly(EGMAP–BnIm_x) composites were produced where x is the molar ratio of heterocycle to monomer in the feed. The polymer–heterocycle electrolytes were characterized by elemental analysis (EA), FT-IR spectroscopy, thermogravimetry analysis (TG), differential scanning calorimetry (DSC) and impedance spectroscopy. Maximum proton conductivity of 2 × 10^− 4 S/cm has been obtained for the anhydrous composite electrolytes at 160 °C.     

Local configurations and atomic intermixing in as-quenched and annealed Fe1−xCrx and Fe1−xMox ribbons

Local atomic configuration, phase composition and atomic intermixing in Fe-rich Fe_1?xCr_x and Fe_1?xMo_x ribbons (x = 0.05, 0.10, 0.15), of potential interest for high-temperature applications and nuclear devices, are investigated in this study in relation to specific processing and annealing routes. The Fe-based thin ribbons have been prepared by induction melting, followed by melt spinning and further annealed in He at temperatures up to 1250 °C. The complex structural, compositional and atomic configuration characterisation has been performed by means of X-ray diffraction (XRD), transmission Mössbauer spectroscopy and differential scanning calorimetry (TG-DSC). The XRD analysis indicates the formation of the desired solid solutions with body-centred cubic (bcc) structure in the as-quenched state. The Mössbauer spectroscopy results have been analysed in terms of the two-shell model. The distribution of Cr/Mo atoms in the first two coordination spheres is not homogeneous, especially after annealing, as supported by the short-range order parameters. In addition, high-temperature annealing treatments give rise to oxidation of Fe (to haematite, maghemite and magnetite) at the surface of the ribbons. Fe_1?xCr_x alloys are structurally more stable than the Mo counterpart under annealing at 700 °C. Annealing at 1250 °C in He enhances drastically the Cr clustering around Fe nuclei.     

Poly(ethylene glycol)/poly(2-acrylamido-2-methyl-1-propane sulfonic acid) gel electrolytes: a detailed investigation of their conductivity and characterization

Poly(ethylene glycol)/poly(2-acrylamido-2-methyl-1-propane sulfonic acid) (PEG/PAMPS) with a transparent appearance were prepared in the presence of ammonium persulfate (APS) as an initiator at 70 °C for 24 h. PEG/PAMPS-based polymer gel electrolytes in a motionless and uniform state were obtained by adding the required amount of liquid electrolytes to a dry PEG/PAMPS polymer. Liquid electrolytes include organic solvents with high boiling points (-1-methyl-2-pyrrolidone (NMP) and γ-butyrolactone (GBL)) and a redox couple (alkali metal iodide salt/iodine). The optimized conditions for PEG/PAMPS-based gel electrolytes based on the salt type, the concentration of alkali metal iodide salt/iodine, and solvent volume ratio were determined to be NaI, 0.4 M NaI/0.04 M I₂, and NMP:GBL (7:3, v/v), respectively. The highest ionic conductivity and the liquid electrolyte absorbency were 2.58 mS cm^?1 and 3.6 g g^?1 at 25 °C, respectively. The ion transport mechanism in both the polymer gel electrolytes and liquid electrolytes is investigated extensively, and their best fits with respect to the temperature dependence of the ionic conductivity are determined with the Arrhenius equation.     

Genesis,structural, and transport properties of La<Subscript>2</Subscript>Mo<Subscript>2-x</Subscript>W<Subscript>x</Subscript>O<Subscript>9</Subscript> prepared via mechanochemical activation

Fast oxide-ion conductors La₂Mo_2-xW_xO₉ (x = 0–1) have been prepared using mechanochemical activation (MA) of starting oxides in a high-power planetary ball mill. Studies of La₂Mo_2-xW_xO₉ genesis and structural properties using thermal analysis, XRD, SEM, IR, and Raman spectroscopy have revealed that MA results in the formation of an amorphous precursor, while the cubic β-phase is formed after calcination at 700–900 °C. Due to a high dispersion of powders, high-density pellets of W-LAMOX ceramics have been obtained already after sintering at 950 °C. Their electrical conductivity measured by the impedance spectroscopy depends on the W concentration being sufficiently high (up to 5.6?10^?3 S/cm at 630 °C) at temperatures below 650 °C.     

Electrochemical and structural properties of a polymer electrolyte system based on the effect of CeO<Subscript>2</Subscript> nanofiller with PVDF-co-HFP for energy storage devices

In the present work, a series of five different nanocomposite polymer electrolytes (NCPEs) have been reported with varying contents of ceria, CeO₂ nanofiller suitably incorporated within an optimized composition having 75:25 wt% ratio of poly(vinylidenefluoride-co-hexafluoropropylene) [(PVDF-co-HFP)] and zinc trifluoromethanesulfonate (ZnTf) in the form of films obtained by mean of solution casting technique with a general formula [75 wt% PVDF-co-HFP:25 wt% ZnTf]-x wt% CeO₂ where x = 1, 3, 5, 7, and 10, respectively. The chosen NCPE system is found to exhibit the maximum electrical conductivity of 3 × 10^?4 S cm^?1 for 5 wt% loading of CeO₂ nanofiller at ambient temperature. The observed conductivity enhancement has been attributed to the occurrence of an increase in the amorphous content as confirmed by X-ray diffraction (XRD) analysis. Detailed Fourier transform infrared (FTIR) spectral analysis has indicated the feasibility of complexation of the host polymer matrix with ZnTf salt and CeO₂ nanofiller. The incorporation of CeO₂ nanofiller has further increased the decomposition voltage of the polymer electrolyte from 2.4 to 2.7 V as revealed from the voltammetric studies performed on such NCPEs, thereby suggesting the suitability of these NCPE films with an enhanced electrical conductivity as new electrolytes in order to design and fabricate eco-friendly zinc rechargeable batteries and other electrochemical devices.     

Electrochemical characterization of ionic liquid based gel polymer electrolyte for lithium battery application

High molecular weight polymer poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP), ionic liquid 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMIMFSI), and salt lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)-based free-standing and conducting ionic liquid-based gel polymer electrolytes (ILGPE) have been prepared by solution cast method. Thermal, electrical, and electrochemical properties of 80 wt% IL containing gel polymer electrolyte (GPE) are investigated by thermogravimetric (TGA), impedance spectroscopy, linear sweep voltammetry (LSV), and cyclic voltammetry (CV). The 80 wt% IL containing GPE shows good thermal stability (~?200 °C), ionic conductivity (6.42?×?10^?4 S cm^?1), lithium ion conductivity (1.40?×?10^?4 S cm^?1 at 30 °C), and wide electrochemical stability window (~?4.10 V versus Li/Li⁺ at 30 °C). Furthermore, the surface of LiFePO₄ cathode material was modified by graphene oxide, with smooth and uniform coating layer, as confirmed by scanning electron microscopy (SEM), and with element content, as confirmed by energy dispersive X-ray (EDX) spectrum. The graphene oxide-coated LiFePO₄ cathode shows improved electrochemical performance with a good charge-discharge capacity and cyclic stability up to 50 cycles at 1C rate, as compared with the without coated LiFePO₄. At 30 °C, the discharge capacity reaches a maximum value of 104.50 and 95.0 mAh g^?1 for graphene oxide-coated LiFePO₄ and without coated LiFePO₄ at 1C rate respectively. These results indicated improved electrochemical performance of pristine LiFePO₄ cathode after coating with graphene oxide.     

Effect of H<Subscript>3</Subscript>PO<Subscript>2</Subscript> on the mechanical,thermal, and electrical properties of polymers based on poly (vinyl alcohol) (PVA) and chitosan (CS)

A polymer based on poly (vinyl alcohol) (PVA) and chitosan (CS) with a weight ratio of 80:20 was prepared by solvent casting processes, and the effect of H₃PO₂ was investigated. Thermal analysis shows miscibility of the two polymer amorphous phases since a single T_g was located between those of the individual components and the melting point of the crystalline phase was depressed to 189 °C. It was found that the acid acts as a plasticizer for the PVA-CS blends and its T_g is depressed significantly to 23 °C as the acid concentration increases to 50%. Strain-stress tests also corroborate this effect. The DC conductivity of the blends follows an Arrhenius-type thermal activation behavior with activation energy of 0.1 eV in the 30–90 °C temperature range. Moreover, the conductivity increases with increasing acid content up to a maximum value of approximately 1.4 × 10^?2 S/cm for the blend with an acid concentration of 50%.     

Effect of tetrabutylammonium iodide content on PVDF-PMMA polymer blend electrolytes for dye-sensitized solar cells

The influence of tetrabutylammonium iodide on the polyvinylidene fluoride-poly(methyl methacrylate)-ethylene carbonate (PVDF-PMMA-EC)-I₂ polymer blend electrolytes was investigated and optimized for use in a dye-sensitized solar cell. The different weight ratios (50, 60, 70, and 80 %) of tetrabutylammonium iodide (TBAI)-added PVDF-PMMA-EC-I₂ polymer electrolytes were prepared. The prepared solid polymer blend electrolytes were characterized by using various techniques such as Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and electrochemical impedance spectroscopy (EIS). The FT-IR spectra revealed the interaction among all composition of polymer electrolytes. The influence of TBAI salt on the ionic conductivity of polymer electrolytes was studied using electrochemical impedance spectroscopy. The polymer electrolyte containing 60 % of TBAI in PVDF-PMMA-EC-I₂ showed the highest room temperature conductivity of 5.10?×?10^?3 S cm^?1. The fabricated DSSC using PVDF-PMMA-EC-I₂ polymer electrolytes with 60 % of TBAI showed the best performance with a short-circuit current density of 8.0 mA cm^?2, open-circuit voltage of 0.66 V, fill factor of 0.65, and the overall power conversion efficiency of 3.45 % under an illumination of 100 mW cm^?2. Hence, the weight content of organic iodide salt in polymer electrolytes influences the overall performance of dye-sensitized solar cells.     

Preparation of LiNi<Subscript>0.5</Subscript>Mn<Subscript>1.5</Subscript>O<Subscript>4</Subscript> cathode materials by electrospinning

LiNi_0.5Mn_1.5O₄ cathode material was prepared by electrospinning using lithium hydroxide, manganese acetate, nickel acetate, acetic acid, ethanol, and poly(vinyl pyrrolidone) as raw materials. The effect of calcination temperature on the structure, morphology, and electrochemical properties was investigated. XRD results indicate that the LiNi_0.5Mn_1.5O₄ composite is well crystallized as a spinel structure at calcination temperature of 650 °C for 3 h. SEM results reveal that this composite has a nanofiber shape with average size of about 300–500 nm. Electrochemical performance tests reveal that this composite shows the initial discharge capacity of 127.8 and 105 mAhg^?1 at 0.1 and 3 C rates, respectively, and exhibits good cycling performance.     

Thermal stability of amorphous SiOC/crystalline Fe composite

We examined the thermal stability of amorphous silicon oxycarbide (SiOC) and crystalline Fe composite by in situ and ex situ annealing. The Fe/SiOC multilayer thin films were grown via magnetron sputtering with controlled length scales on a surface-oxidized Si (100) substrate. These Fe/SiOC multilayers were in situ or ex situ annealed at temperature of 600 °C or lower. The thin multilayer sample (~10 nm) was observed to have a layer breakdown after 600 °C annealing. Diffusion starts from low groove angle triple junctions in Fe layers. In contrast, the thick multilayer structure (~70 nm) was found to be stable and an intermixed layer (Fe_xSi_yO_z) was observed after 600 °C annealing. The thickness of the intermixed layer does not vary as annealing time goes up. The results suggest that the Fe_xSi_yO_z layer can impede further Fe, Si and O diffusion, and assists in maintaining morphological stability.     

The Effect of Supercritical CO2 on the Macromolecules Parallel Conformation and Its Relation to the Electrical Conductivity and Dielectric Behavior of Epichlorohydrin Terpolymer

The effect of supercritical CO₂ on the electrical conductivity of poly(epichlorohydrin–Ethylene oxide–Allyl glycidal ether) terpolymer is investigated using dielectric spectroscopy. Impedance measurements were carried out in the frequency range from 100–10 MHz and the temperature range of ?35–70°C with intervals of 5°C. The experimental results of the dielectric constant and the dielectric loss were fitted with the Cole–Cole equation to obtain the maximum relaxation frequencies of the different relaxation processes. As a result of the CO₂ treatment process, enhancement in the polymer chain mobility without noteworthy change in the glass transition temperature was determined. In addition, the level of the DC conductivity and the dielectric strength were increased. These effects were attributed to improvement in the chain dynamics, which arises from enhancement in the parallel conformation of macromolecules.     

Excellent organic/inorganic transparent thin film moisture barrier entirely made by hot wire CVD at 100 °C

We present a silicon nitride/polymer hybrid multilayer moisture barrier for flexible electronics made entirely by hot wire chemical vapor deposition (HWCVD) at substrate temperatures below 100 °C. Using the initiated CVD (iCVD) variant of HWCVD for the polymer layers, these can be extremely thin, while efficiently decoupling the defects in consecutive inorganic layers. Although a single layer of low temperature SiN_x is more prone to have pinholes than its state‐of‐the‐art high temperature equivalent, we have achieved a simple three‐layer structure consisting of two low‐temperature SiN_x layers with a polymer layer in between, which is pinhole free and shows a water vapor transmission rate (WVTR) as low as 5 × 10^–6 g/m²/day at a temperature of 60 °C and a relative humidity of 90%. This WVTR is low enough for organic devices. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Photovoltaic structures using AgSb(S x Se1−x )2 thin films as absorber

Photovoltaic structures were prepared using AgSb(S _x Se_1?x )₂ as absorber and CdS as window layer at various conditions via a hybrid technique of chemical bath deposition and thermal evaporation followed by heat treatments. Silver antimony sulfo selenide thin films [AgSb(S _x Se_1?x )₂] were prepared by heating multilayers of sequentially deposited Sb₂S₃/Ag dipped in Na₂SeSO₃ solution, glass/Sb₂S₃/Ag/Se. For this, Sb₂S₃ thin films were deposited from a chemical bath containing SbCl₃ and Na₂S₂O₃. Then, Ag thin films were thermally evaporated on glass/Sb₂S₃, followed by selenization by dipping in an acidic solution of Na₂SeSO₃. The duration of dipping was varied as 3, 4 and 5 h. Two different heat treatments, one at 350 °C for 20 min in vacuum followed by a post-heat treatment at 325 °C for 2 h in Ar, and the other at 350 °C for 1 h in Ar, were applied to the multilayers of different configurations. X-ray diffraction results showed the formation of AgSb(S _x Se_1?x )₂ thin films as the primary phase and AgSb(S,Se)₂ and Sb₂S₃ as secondary phases. Morphology and elemental detection were done by scanning electron microscopy and energy dispersive X-ray analysis. X-ray photoelectron spectroscopic studies showed the depthwise composition of the films. Optical properties were determined by UV–vis–IR transmittance and reflection spectral analysis. AgSb(S _x Se_1?x )₂ formed at different conditions was incorporated in PV structures glass/FTO/CdS/AgSb(S _x Se_1?x )₂/C/Ag. Chemically deposited post-annealed CdS thin films of various thicknesses were used as window layer. J–V characteristics of the cells were measured under dark and AM1.5 illumination. Analysis of the J–V characteristics resulted in the best solar cell parameters of V _oc = 520 mV, J _sc = 9.70 mA cm^?2, FF = 0.50 and η = 2.7 %.     

Improving the performance of pure sulfide Cu(InGa)S2 solar cells via injection annealing system

In this study, we present an effective method of improving the performance of pure sulfide Cu(InGa)S₂ (CIGS) solar cells via injection annealing system. The injection annealing system can perform annealing at desired temperatures, and therefore, the CIGS thin film passed over the temperature range in which secondary phases occurs. Via the injection annealing system, secondary phase InS_x was effectively removed from the surface of the CIGS thin films at the temperatures over 550°C. This resulted in the formation of good-quality P–N junction CIGS devices, thereby improving significantly the performance of the CIGS solar cell. In addition, the open-circuit-voltage (V_OC) and fill factor (FF) of the CIGS devices increased gradually with increasing annealing temperature in the range of 550–640°C. It is speculated that the bulk defects were decreased as the annealing temperature increased. Finally, via injection annealing system, a pure sulfide CIGS solar cell with an efficiency of 12.16% was achieved.     

Adhesion,morphology, and heat resistance properties of polyurethane coated poly(methyl methacrylate)/fullerene-C60 composite films

Novel polyurethane (PU) adhesive was prepared and coated on poly(methyl methacrylate) (PMMA) and poly(methyl methacrylate)/fullerene (PMMA/Full-C₆₀) composite. Dip-coating technique was employed as facile and cost-effective procedure to coat polyurethane on film substrate. The properties of PU/PMMA and PU/PMMA/Full-C₆₀ composite were studied using Fourier transform infrared spectroscopy, Field Emission Scanning Electron Microscopy, tensile, adhesion, thermal and flammability measurement. Testing polyurethane-coated PMMA exhibited crumpled surface while fullerene addition formed unique pattern of dispersed spherical structures. Fullerene nanofiller loading improved the adhesion and mechanical properties of composite films due to polymer–carbon interaction. In PU/PMMA/Full-C₆₀ 0.5 composite with 0.5 wt.% nanofiller, tensile strength (71.4 MPa) was increased by 18.6% while tensile modulus was increased by 143.85% compared with PU/PMMA. In PU/PMMA/Full-C₆₀ 0.5, T₀ of 473 °C and T_max of 655 °C were observed. Increasing the fullerene content up to 0.5 wt.% decreased the peak heat release rate to 131 kW/m². Novel polyurethane-coated PMMA/Full-C₆₀ composite have potential applications as adhesive coatings in electronic and automotive appliances.     

Characterization of high ionic conducting PVAc–PMMA blend-based polymer electrolyte for electrochemical applications

A solid polymer blend electrolyte is prepared using poly(vinyl acetate) (PVAc) and poly(methyl methacrylate) (PMMA) polymers with different molecular weight percentage (wt%) of ammonium thiocyanate (NH₄SCN) by solution casting technique with tetrahydrofuran (THF) as a solvent. The structural, morphological, vibrational, thermal and electrical properties of the prepared polymer blend electrolytes have been studied. The incorporation of NH₄SCN into the polymeric matrix causes decrease in the degree of crystallinity of the samples. The complex formation between the polymer and salt has been confirmed by FTIR technique. The increase in T _g with increase in salt concentration has been investigated. The maximum conductivity of 3.684?×?10^?3 S cm^?1 has been observed for the composition of 70PVAc/30PMMA/30 wt% of NH₄SCN at 303 K. This value of ionic conductivity is five orders of magnitude greater than that of 70PVAc/30PMMA polymer membrane. Dielectric and transport studies have been done. The highest conducting polymer electrolyte is used to fabricate proton battery with the configuration Zn/ZnSO₄·7H₂O (anode) ||polymer electrolyte||PbO₂/V₂O₅ (cathode). The open circuit voltage of the fabricated battery is 1.83 V, and its performance has been studied.     

PPV/PVA/ZnO nanocomposite prepared by complex precursor method and its photovoltaic application

In this article, we describe a new method to prepare a ZnO and conjugated polymer nanocomposite and its application in bulk-heterojunction solar cells. The composite was composed of zinc oxide (ZnO) and poly(phenylene vinylene)/poly(vinyl alcohol) (PPV/PVA). For the preparation, the composite was prepared first through the complex reaction between Zn²⁺ ion and –OH of the PVA–PPV precursor by simply mixing zinc salts and a PVA–PPV precursor aqueous solution at 70 °C. By addition of a concentrated aqueous ammonia into the system, highly regular Zn(OH)₂ nanodots were formed and dispersed in the PVA/PPV precusor mixed solution. The PVA/PPV precursor can well bind Zn²⁺ ion through complex interaction, so act as a template to direct the distribution of ZnO in the process. The nanocomposite films were finally obtained by solution casting and subsequently treated by heating samples at 160 °C for 6 h. TEM observations showed that ZnO nanodots uniformly dispersed in PVA–PPV mixtures. The resulting nanocomposite films possess a large interfacial area between the electron donor and acceptor of the bulk-heterojunction. Improved charge seperation and collection are evidenced by the large photoluminescence intensity difference between pure PPV and composites films, which result in the increase in both open circuit voltage and short circuit current of the hybrid solar cells.     

Co-substitution effect on the structural,electrical, and electrochemical properties of nanostructured Co<Subscript>x</Subscript>Ni<Subscript>1-x</Subscript>MnP<Subscript>2</Subscript>O<Subscript>7</Subscript> (x = 0, 0.25, 0.5, and 0.75)

Cobalt-nickel-manganese pyrophosphate nanostructures with formula Co_xNi_1-xMnP₂O₇ were prepared via the hydrothermal method at 150 °C, with further calcinations at 500 °C. A structural analysis of Co_xNi_1-xMnP₂O₇ samples was carried out using X-ray diffraction (XRD). The effect of Co substitution on the structural, electrical, and electrochemical properties of Co_xNi_1-xMnP₂O₇ is reported. The electrochemical results show that the specific capacity increases from 59 to 205 mAh/g with increasing Co content. This study demonstrates the Co substitution effect on the mixed electrical conductivity. The temperature dependence of the dc electrical conductivity, for both pure and Co²⁺-doped samples, obeys the Arrhenius law. The frequency dependence of ac conductivity for the materials exhibited a Jonscher’s universal power law. The plots of pre-exponent (n) versus temperature suggested that the conduction mechanism can be described using correlated barrier hopping model. The improved electrical conductivity and electrochemical proprieties of Co_xNi_1-xMnP₂O₇ nanomaterials could be ascribed to the synergistic effect of nickel and cobalt ions. The best results have been obtained for the composition x(Co) = 0.75, where the electrical conductivity is maximum, and the Co_0.75Ni_0.25MnP₂O₇ demonstrates the highest specific capacity, implying their promising potential applications in the energy storage.