High-performance flexible supercapacitors based on C/Na<Subscript>2</Subscript>Ti<Subscript>5</Subscript>O<Subscript>11</Subscript> nanocomposite electrode materials

A new solution method to synthesize Na₂Ti₅O₁₁ with titanium powder is presented, and the C/Na₂Ti₅O₁₁ nanocomposite with high specific surface area and tunnel structure as the electrode material has excellent electrochemical performance. The single electrode composed of the C/Na₂Ti₅O₁₁ nanocomposite based on carbon fiber fabric (CFF) has the highest area capacitance of 1066 mF cm^?2 at a current density of 2 mA cm^?2, which is superior to other titanates and Na-ion materials for supercapacitors (SCs). By scan-rate dependence cyclic voltammetry analysis, the capacity value shows both capacitive and faradaic intercalation processes, and the intercalation process contributed 81.7% of the total charge storage at the scan rate of 5 mV s^?1. The flexible symmetric solid-state SCs (C/Na₂Ti₅O₁₁/CFF//C/Na₂Ti₅O₁₁/CFF) based on different C/Na₂Ti₅O₁₁ mass were fabricated, and 7 mg SCs show the best supercapacitive characteristics with an area capacitance of 309 mF cm^?2 and a specific capacitance of 441 F g^?1, it has a maximum energy density of 22 Wh kg^?1 and power density of 1286 W kg^?1. As for practical application, three SCs in series can power 100 green light-emitting diodes (LEDs) to light up for 18 min, which is much longer than our previous work by Wang et al. lighting 100 LEDs for 8 min. Thus, the C/Na₂Ti₅O₁₁ nanocomposite has promising potential application in energy storage devices.     

Ionic liquid-derived Co<Subscript>3</Subscript>O<Subscript>4</Subscript>/carbon nano-onions composite and its enhanced performance as anode for lithium-ion batteries

In this work, a novel composite of Co₃O₄ nanoparticle and carbon nano-onions (CNOs) is synthesized by using ionic liquid as carbon and nitrogen source through a facile carbothermic reduction followed by low-temperature oxidation method. The SEM and HRTEM images reveal that the Co₃O₄ particles are homogenously embedded in the CNOs. Due to the unique nano-structure, the electrolyte contacts well with the active materials, leading to a better transfer of lithium ions. Moreover, the unique nano-structure not only buffers the volume changes but also facilitates the shuttling of electrons during the cycling process. As a result, the electrode made up of Co₃O₄/CNOs composite delivers favorable cycling performance (676 mAh g^?1 after 200 cycles) and rate capability (557 mAh g^?1 at the current of 1 C), showing a promising prospect for lithium-ion batteries as anode materials.     

Enhanced electrochemical performance of Na<Subscript>3</Subscript>V<Subscript>2</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>F<Subscript>3</Subscript> for Na-ion batteries with nanostructure and carbon coating

Carbon-coating Na₃V₂(PO₄)₂F₃ nanoparticles (NVPF@C NP) were prepared by a hydrothermal assisted sol–gel method and applied as cathode materials for Na-ion batteries. The as-prepared nanocomposites were composed of Na₃V₂(PO₄)₂F₃ nanoparticles with a typical size of ~?100 nm and an amorphous carbon layer with the thickness of ~?5 nm. Cyclic voltammetry, rate and cycling, and electrochemical impedance spectroscopy tests were used to discuss the effect of carbon coating and nanostructure. Results display that the as-prepared NVPF@C NP demonstrates a higher rate capability and better long cycling performance compared with bare Na₃V₂(PO₄)₂F₃ bulk (72 mA h g^?1 at 10 C vs 39 mA h g^?1 at 10 and 1 C capacity retention of 95% vs 88% after 50 cycles). The remarking electrode performance was attributed to the combination of nanostructure and carbon coating, which can provide short Na-ion diffusion distance and rapid electron migration.     

Samarium-doped Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles with improved magnetic and supercapacitive performance: a novel preparation strategy and characterization

Sm³⁺-doped magnetite (Fe₃O₄) nanoparticles were synthesized through a one-pot facile electrochemical method. In this method, products were electrodeposited on a stainless steel (316L) cathode from an additive-free 0.005 M Fe(NO₃)₃/FeCl₂/SmCl₃ aqueous electrolyte. The structural characterizations through X-ray diffraction, field-emission electron microscopy, and energy-dispersive X-ray indicated that the deposited material has Sm³⁺-doped magnetite particles with average size of 20 nm. Magnetic analysis by VSM revealed the superparamagnetic nature of the prepared nanoparticles (Ms = 41.89 emu g^?1, Mr = 0.12 emu g^?1, and H _Ci = 2.24 G). The supercapacitive capability evaluation of the prepared magnetite nanoparticles through cyclic voltammetry and galvanostat charge–discharge showed that these materials are capable to deliver specific capacitances as high as 207 F g^?1 (at 0.5 A g^?1) and 145 F g^?1 (at 2 A g^?1), and capacity retentions of 94.5 and 84.6% after 2000 cycling at 0.5 and 1 A g^?1, respectively. The results proved the suitability of the electrosynthesized nanoparticles for use in supercapacitors. Furthermore, this work provides a facile electrochemical route for the synthesis of lanthanide-doped magnetite nanoparticles.     

Cathodic electrosynthesis of CuFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/CuO composite nanostructures for high performance supercapacitor applications

In this work, CuFe₂O₄/CuO nanocomposites have been synthesized by galvanostatic cathodic electrodeposition. The obtained nanocomposites were characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray powder diffraction, Fourier Transform Infrared, and Brunauer–Emmett–Teller surface area analysis. The electrochemical properties of CuFe₂O₄/CuO nanocomposites were evaluated by cyclic voltammetry, galvanostatic charge–discharge cycling, and electrochemical impedance spectroscopy in 1.0 M KOH. The CuFe₂O₄/CuO nanocomposites have shown the high specific capacitance of 322.49 F g^?1 at the scan rate of 1 mV s^?1. After 5000 cycles, 92% of this specific capacitance was retained. Although the prepared nanocomposite has shown a mediocre specific capacitance compared to other metal oxide-based materials, the low cost of the starting materials and the ease of preparation make this nanocomposite a good candidate for supercapacitor applications.     

Ordered mesoporous carbon-supported CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> composite with enhanced lithium storage properties

A high and stable reversible specific capacity (1277.7 mAh g^?1) was successfully achieved by the CoFe₂O₄/ordered mesoporous carbon nanohybrids (CFO/CMK-3) composite anode at the current density of 0.1 A g^?1 after 100 cycles. CFO/CMK-3 electrode also exhibited a stable capacity up to 733.2 and 482.6 mAh g^?1 at the current densities of 0.5 and 1 A g^?1 after 500 cycles, respectively. The CFO particles were found to be uniformly distributed inside the pore channels of CMK-3. Structure characterization before and after 100 tests revealed that the specific CMK-3 mesoporous structure and CFO crystallites remained unchanged. The stability of the anode composite stability and the rapid redox capability of CFO gave rise to superior lithium storage capacity and excellent cycling stability. CFO/CMK-3 showed a great promise to serve as anode for high-performance lithium-ion battery.     

Preparation and electrochemical properties of nanorods and nanosheets structural Li<Subscript>4</Subscript>Ti<Subscript>5</Subscript>O<Subscript>12</Subscript> as anode for lithium ion batteries

In this study, nanorods and nanosheets structure of Li₄Ti₅O₁₂ (LTO) with higher capacity and cycle performance are prepared by hydrothermal synthesis. We can obtain different nanostructural LTO by changing heating time in autoclave and molar ratio between lithium (Li) and titanium (Ti). Precursor was calcined at 600 °C for 6 h in air after heating to 180 °C with the holding time of 12 and 24 h in Teflon-lined PTFE autoclave vessel, nanorods and nanosheets structure of LTO were prepared successfully, respectively. Specially, when the molar ratio between Li and Ti was 4.2:5, the discharge capacities were 177.7 and 230.7 mAh g^?1 at 20 mA g^?1, respectively. When the holding time was 24 h as well as molar ratio between Li and Ti was 4.2:5, the band gap was least, and this pure LTO reversible capacities reached 90.36 and 73.12% after 200 and 3000 cycles at 100 mA g^?1 and 1 A g^?1, respectively.     

Co<Subscript>9</Subscript>S<Subscript>8</Subscript> nanotubes: facile synthesis and application in the catalytic reduction of 4-nitrophenol

Co₉S₈ nanotubes have been successfully synthesized via a facile two-step solvothermal method without the assistance of any template or surfactant, using cobalt sulphate (CoSO₄?7H₂O), urea and sodium sulphide (Na₂S?9H₂O) as starting reactants, and deionized water and glycol as the reactive medium. The phase and the morphology of the as-obtained product were characterized by means of powder X-ray diffraction, energy dispersive spectrometry and scanning electron microscopy. The result displays that the Co₉S₈ nanotubes have hexagonal cross-sections, the diameter of the nanotubes is about 200 nm and the wall thickness is of 50 nm. The experiments showed that the Co₉S₈ nanotubes could be used as new-type catalysts for the reduction of 4-nitrophenol. It was found that the as-obtained Co₉S₈ nanotubes contributed to the best catalytic activity.     

EPR and optical investigation of ultraviolet-emitting Gd<Subscript>3</Subscript>Ga<Subscript>5</Subscript>O<Subscript>12</Subscript> garnet

Gd₃Ga₅O₁₂ garnet was prepared by a solution combustion method and characterized using powder X-ray diffraction, electron paramagnetic resonance (EPR) and optical spectroscopic techniques. EPR spectrum of the samples at ambient and low temperatures exhibited resonance signal at g?≈?2 attributed to Gd³⁺ ions disposed in an octahedral symmetry. The optical absorption spectrum showed a band centered at 274 nm attributed to ⁸S_7/2→⁶I_J transition of the Gd³⁺ ions. The excitation spectrum showed a maximum at 273 nm along with two relatively weaker peaks at 276 and 279 nm. These three excitation bands were assigned to the transitions ⁸S_7/2→⁶I_J. The emission spectrum showed two peaks centered at 311 and 306 nm that were assigned to the transitions ⁶P_7/2→⁸S_7/2 and ⁶P_5/2→⁸S_7/2 of Gd³⁺, respectively. To evaluate the phosphor performance, several magnetic and thermodynamic parameters for the system were calculated adopting standard procedure.     

Low temperature sintering and dielectric properties of Ba<Subscript>3</Subscript>(VO<Subscript>4</Subscript>)<Subscript>2</Subscript> microwave ceramics using Co<Subscript>2</Subscript>O<Subscript>3</Subscript> additives

The Ba₃(VO₄)₂–x wt% Co₂O₃ (x?=?0.5–5) ceramics were prepared by the solid state reaction method in order to reduce the sintering temperature. The effects of the Co₂O₃ additions on the phase composition, microstructures, sintering characteristics and microwave dielectric properties of Ba₃(VO₄)₂ ceramics are investigated by an X-ray diffractometer, a scanning electron microscope and a network analyzer. As a result, the Q?×?f value of 54,000 GH, the ε _r of 14.6 and the τ_f value of +58.5 ppm/°C were obtained in the sample of the Ba₃(VO₄)₂–3 wt% Co₂O₃ ceramic sintered at the temperature of 925 °C, which is capable to co-fire with electrode metal of high conductivity such as Ag (961 °C). Moreover, the Q?×?f values of the sample with Co₂O₃ higher than that of 3 wt% additions decreased because of the formation of Ba₂V₂O₇ phase.     

Facile synthesis and characterization of MnO<Subscript>2</Subscript> nanomaterials as supercapacitor electrode materials

MnO₂ nanomaterials are synthesized via calcinations in air at various temperatures. Amorphous MnO₂ masses appear between 100 and 300 °C and nanorods form above 400 °C. Transmission and scanning electron microscopy are used to observe the geometries of each material, with further structural analyses conducted using X-ray photoelectron spectroscopy, X-ray diffraction, and BET method. The electrochemical properties are investigated through galvanostatic charge/discharge cycling, electrochemical impedance spectra, and cyclic voltammetry within a three-electrode test cell filled with 1 mol L^?1 Na₂SO₄ solution. The slightly asymmetric galvanostatic cycling curves suggest that the reversibility of the Faradaic reactions are imperfect, requiring a larger time to charge than discharge. The specific capacitances of each sample are calculated and trends are identified, proving that the samples synthesized at higher temperatures exhibit poorer electrochemical behaviors. The highest calculated specific capacitance is 175 F g^?1 by the sample calcinated at 400 °C. However, the lower temperature samples exhibit more favorable geometric properties and higher overall average specific capacitances. For future research, it is suggested that surface modifications such as a carbon coating could be used in conjunction with the MnO₂ nanorods to reach the electrochemical properties required by contemporary industrial applications.     

Synthesis of polypyrrole/Fe-kanemite nanocomposite through in situ polymerization: effect of iron exchange,acid treatment,and CO<Subscript>2</Subscript> adsorption properties

This paper focuses on the synthesis of polypyrrole/Fe-kanemite nanocomposites by in situ polymerization of pyrrole. Different percentages of PPy/Fe-kan have been prepared and tested for the CO₂ adsorption. Fe-exchanged kanemite was prepared using various iron contents and used as an oxidant for the preparation of PPy/Fe-kan nanocomposite. The obtained materials were characterized using various techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy, ultraviolet–visible (UV–vis), thermogravimetric analysis TGA, energy dispersive X-ray analysis, scanning and transmission electronic microscopy (SEM, TEM). Based on the XRD and UV–vis analysis, the exchange process leads to the formation of various iron species on the external and internal surface. The thermal stability of PPy/Fe-kan was improved and increased in the following order PPy/Fe-kan (1%) > PPy/Fe-kan (3%) > PPy/Fe-kan (5%) > PPy/Fe-kan (10%) > PPy. SEM and TEM analysis show that the nanocomposite particles have spherical morphology with a high dispersion of the Fe-kanemite in the polymer matrix. CO₂ adsorption at 0 and 15 °C was carried using a volumetric method, and the recorded isotherm indicated that the CO₂ adsorption capacity of PPy/Fe-kan can be enhanced through modification by polypyrrole. The unmodified Na-kanemite has low CO₂ adsorption capacity around 0.05 mmol g^?1 at 15 °C, while the PPy/Fe-kan (5%) nanocomposite presented the best CO₂ adsorption capacity around 1.7 mmol g^?1 at 0 °C under low pressure that is mainly attributable to physical adsorption.     

Synthesis and characterization of LiNi<Subscript>0.9</Subscript>Co<Subscript>0.1</Subscript>O<Subscript>2</Subscript> for lithium batteries

LiNi_0.9Co_0.1O₂ cathode material is prepared from LiOH·H₂O and Ni_0.9Co_0.1(OH)₂ by co-precipitation and subsequent two-stage heat treatment in flowing oxygen based on the results of thermogravimetric. The structural and electrochemical properties of the samples are characterized by means of inductively coupled plasma-atomic emission spectrometer (ICP-AES), X-ray diffraction (XRD), scanning electron microscope (SEM), cyclic voltammogram (CV) and charge–discharge studies. All the samples sintered at different temperatures have a typical layered structure with space group R3-m and good electrochemical performances. The sintering temperature has a remarkable effect on the electrochemical performance of the samples. The sample sintered at 730 °C shows the largest initial discharge capacity 191.1 mAh g⁻¹ (50 mA g⁻¹, 3.0–4.3 V) and the best cycling performance. The initial discharge capacity rises to above 200 mAh g⁻¹ with the voltage range 3.0–4.5 V.     

Preparation and characterization of Co<Subscript>9</Subscript>S<Subscript>8</Subscript> nanocrystalline and nanorods

Hexagonal Co₉S₈ nanocrystal and nanorods were synthesized using cobalt chloride (CoCl₂·6H₂O), dimethyl sulfoxide (DMSO) and non-aqueous alcohol as the starting materials, and taking dimethyl sulfoxide as both sulfur source and strong infiltrator in nanorods preparation. The Co₉S₈ samples were characterized by X-ray diffraction (XRD), scanning tunneling microscope (SEM), transmission electron microscope (TEM), vibrating sample magnetometer (VSM) and laser Raman spectrometer. The results show that the as-prepared Co₉S₈ nanocrystal with a size of 6 nm take on weak paramagnetism at room temperature. The lengths and diameters of the nanorods were about 4 μm and 200 nm, respectively. The reason for the relative lower synthesis temperature of nanorods was discussed and a ‘micro-autoclave reactor’ model was suggested as well.     

Removal of lead (II) and nickel (II) ions from aqueous solution using activated carbon prepared from rapeseed oil cake by Na<Subscript>2</Subscript>CO<Subscript>3</Subscript> activation

In this study, rapeseed oil cake as a precursor was used to prepare activated carbons by chemical activation with sodium carbonate (Na₂CO₃) at 600 and 800 °C. The activated carbon with the highest surface area of 850 m² g^?1 was produced at 800 °C. The prepared activated carbons were mainly microporous. The activated carbon having the highest surface area was used as an adsorbent for the removal of lead (II) and nickel (II) ions from aqueous solutions. The effects of pH, contact time, and initial ion concentration on the adsorption capacity of the activated carbon were investigated. The kinetic data of adsorption process were studied using pseudo-first-order, pseudo-second-order kinetic models and intraparticle diffusion model. The experimental data were well adapted to the pseudo-second-order model for both tested ions. The adsorption data for both ions were well correlated with Langmuir isotherm. The maximum monolayer adsorption capacities of the activated carbon for the removal of lead (II) and nickel (II) ions were determined as 129.87 and 133.33 mg g^?1, respectively.     

Cr<Subscript>2</Subscript>O<Subscript>3</Subscript> nanocrystal anode materials with improved cyclic stability for lithium ion batteries

The cyclic stability of Cr₂O₃ is very poor due to the large volume change during lithiation/delithiation. In this study, we have found that Cr₂O₃ nanocrystals synthesized by using a simple hydrothermal method can improve its cyclic stability. Sample calcined at 430 °C has uniform size, compact structure and high crystallization degree. These Cr₂O₃ nanocrystals exhibit a stable cyclic performance of 185 mAh g^?1 after 100 cycles at 100 mA g^?1. It is useful in real life, such as providing power consumption for minitype device, etc.     

Investigation for the synthesis of hierarchical Co<Subscript>3</Subscript>O<Subscript>4</Subscript>@MnO<Subscript>2</Subscript> nanoarrays materials and their application for supercapacitor

We designed and fabricated hierarchical Co₃O₄@MnO₂ nanoarrays directly grown on nickel foam by hydrothermal and calcination methods. After the investigation of growth mechanism, we found that the deposition of MnO₂ was based on the self-decomposition of KMnO₄ and the reducibility of Co₃O₄ during the hydrothermal process. Thanks to the hierarchical structure, the obtained electrode exhibited excellent capacitive performance in supercapacitor. It delivered 21.72 F cm^?2 at a current density of 5 mA cm^?2 and retained ~94 % capacitance of initial value after 5000 cycles.     

Enhanced electrochemical reduction of hydrogen peroxide by Co<Subscript>3</Subscript>O<Subscript>4</Subscript> nanowire electrode

Crystalline Co₃O₄ nanowire arrays with different morphologies grown on Ni foam were investigated by varying the reaction temperature, the concentration of precursors, and reaction time. The Co₃O₄ nanowires synthesized under typical reaction condition had a diameter range of approximately 500–900 nm with a length of 17 µm. Electrochemical reduction of hydrogen peroxide (H₂O₂) of the optimized Co₃O₄ nanowire electrode was studied by cyclic voltammetry. A high current density of 101.8 mA cm^?2 was obtained at ?0.4 V in a solution of 0.4 M H₂O₂ and 3.0 M NaOH at room temperature compared to 85.8 mA cm^?2 at ?0.35 V of the Co₃O₄ nanoparticle electrode. Results clearly indicated that the Ni foam supported Co₃O₄ nanowire electrode exhibited superior catalytic activity and mass transport kinetics for H₂O₂ electrochemical reduction.     

Scalable synthesis of TiO<Subscript>2</Subscript> crystallites embedded in bread-derived carbon matrix with enhanced lithium storage performance

TiO₂/carbon (C/TiO₂) composites have been synthesized via an in-situ pyrolysis method using bread as carbon source and investigated as anodes for lithium-ion batteries. As a cheap and common staple food with a sponge-like structure, bread contains a certain amount of moisture, enabling the hydrolysis of tetrabutyl orthotitanate. It is characterized that TiO₂ nanocrystallites are embedded in bread-derived carbon matrix, and their synergetic effect on improving electrochemical properties is demonstrated as well. Partially surface lithium storage of ultrasmall TiO₂ particles is credited to the unique embedment structure. Meanwhile, the carbon species are of importance in enhancing reversible capacities and accelerating interfacial charge transfer. It delivers a reversible capacity of 231 mAh g^?1 at a specific current of 100 mA g^?1 after 200 cycles for the resultant C/TiO₂ composite with 38.8 wt.% carbon. This work presents a facile strategy toward scalable and eco-friendly preparation of metal oxides compositing with carbonaceous materials.     

Facial synthesis of MnO<Subscript>2</Subscript>/three dimensional graphene composite and its application in supercapacitors

MnO₂ nanoparticle/three dimensional graphene composite (MnO₂/3DG) was synthesized by a hydrothermal template-free method and subsequent ultrasonic treatment in KMnO₄ solution. The MnCO₃/3DG particles can be detected after the hydrothermal process, which may be produced through the reaction between Mn²⁺ and \({\text{C}}{{\text{O}}_{\text{3}}}^{{\text{2}} - }\) due to the decarboxylation of GO under the hydrothermal condition. The final product MnO₂/3DG displayed high specific capacitance (324 F g^??1 at 0.4 A g^?1) and good cycle stability (91.1% capacitance retention after 5000 cycles). Furthermore, the asymmetric supercapacitor assembled with MnO₂/3DG and activated carbon (AC) exhibits an energy density of 33.78 Wh kg^?1 at the powder density of 380 W kg^?1. The excellent supercapacitance of the MnO₂/3DG composite may be due to the high pseudocapacitance of the dispersed MnO₂ nanoparticles and the conductive graphene with three dimensional porous microstructure.