Preparation and capacitive properties of cobalt-nickel oxides/carbon nanotube composites

In this paper, nickel-cobalt oxides/carbon nanotube (CNT) composites were prepared by adding and thermally decomposing nickel and cobalt nitrates directly onto the surface of carbon nanotube/graphite electrode to form nickel and cobalt oxides. Carbon nanotubes used in this paper were grown directly on graphite substrate by chemical vapor deposition technique. The capacitive behavior of nickel-cobalt oxides/CNT electrode was investigated by cyclic voltammetry and galvanostatic charge-discharge method in 1 M KOH aqueous solutions. The results show that nickel-cobalt oxides/CNT composite electrode has excellent charge-discharge cycle stability (0.2% and 3.6% losses of the specific capacitance are found at the 1000th and 2000th charge-discharge cycles, respectively) and good charge-discharge properties at high currrent density. Additionally, the effect of Ni/Co molar ratio on specific capacitance of the composite electrode was investigated and the highest specific capacitance (569 F g⁻¹ at 10 mA cm⁻²) is obtained at Ni/Co molar ratio = 1:1.     

TiO2 nanotubes manufactured by anodization of Ti thin films for on-chip Li-ion 2D microbatteries

The use of self-organized TiO₂ nanotube arrays electrochemically grown onto Si is investigated for the fabrication of an alternative electrode dedicated to on-chip Li-ion 2D microbatteries. Discharge/charge curves and cycling performance are studied in lithium-anode electrochemical test cells for both amorphous and crystalline titania nanotubes. At 5 μA cm⁻² amorphous TiO₂ nanotube layers onto Si deliver a maximum areal capacity of 89 μAh cm⁻² in the first reversible discharge and 56 μAh cm⁻² over 50 cycles. We demonstrate that these nanostructured thin film electrodes showing such electrochemical performances are compatible with IC technology.     

Preparation of high surface area nickel electrodeposit using a liquid crystal template technique

We show in this work that template electrodeposition of nickel at room temperature from a nickel sulphamate bath prepared in a new hexagonal liquid crystalline phase of water-Triton X-100-poly (acrylic acid) results in a highly porous surface. The roughness factor value of about 3620 obtained for this coating is the highest value reported in the literature for any electrodeposited nickel. The scanning electron microscopy (SEM) and scanning tunneling microscopy (STM) pictures show the formation of porous deposit with granular features in between the pores. The single electrode double layer capacitance value measured for the deposit is 338 mF cm⁻², which translates into a specific capacitance of 50 F g⁻¹ without any post-thermal treatment of the electrode, suggesting its utility in super capacitors. Electrochemical studies using cyclic voltammetry (CV), Tafel plots and electrochemical impedance spectroscopy (EIS) and comparison of these results with some existing high surface area Ni catalysts show that the material has potential application as an excellent hydrogen evolving cathode.     

The preparation of titania nanotubes and its application in flexible dye-sensitized solar cells

Anatase titania nanotube (TNT) is prepared by two-steps hydrothermal growth method. Using the TNTs and titania particles (P25), a highly stable and uniform titania colloid without any sedimentation in 180 days is prepared by hydrothermal treatment. Based on the titania colloid, a flexible dye-sensitized solar cell (DSSC) is fabricated at low temperature. The influence of preparation conditions on the properties of TNTs and titania colloid is discussed by transmitting electron microscopy, scanning electron microscopy, selected area electron diffraction, X-ray diffraction, UV-vis absorption spectra, and Brunauer-Emmet-Teller surface area measurements. Under an optimized condition, a flexible DSSC with light-to-electric energy conversion efficiency of 4.0% is achieved under a simulated solar light irradiation of 100 mW cm⁻² (AM 1.5).     

Electrochemically multi-anodized TiO2 nanotube arrays for enhancing hydrogen generation by photoelectrocatalytic water splitting

An enhanced hydrogen production by photoelectrocatalytic water splitting was obtained using extremely highly ordered nanotubular TiO₂ arrays in this work. Highly ordered TiO₂ nanotube arrays with a regular top porous morphology were grown by a facile and green three-step electrochemical anodization. The well ordered hexagonal concaves were uniformly distributed on titanium substrate by the first anodization, served as a template for further growth of TiO₂ nanotubes. As a result, the TiO₂ nanotube arrays constructed through the third anodization showed appreciably more regular architecture than that of the sample by conventional single anodization under the same conditions. The enhanced photoelectrochemical activity was demonstrated through the hydrogen generation by photoelectrocatalytic water splitting, with an exact H₂ evolution rate up to 420 μmol h⁻¹ cm⁻² (10 mL h⁻¹ cm⁻²) in 2 M Na₂CO₃ + 0.5 M ethylene glycol. The photocurrent density of the third-step anodic TiO₂ nanotubes is about 24 mA cm⁻² in 0.5 M KOH, which is 2.2 times higher than that of the normal TiO₂ nanotubes (∼11 mA cm⁻²) by a single electrochemical anodization.     

Electrostatic heterocoagulation of carbon nanotubes and LiCoO2 particles for a high-performance Li-ion cell

Nanotubes were coated on the surface of active LiCoO₂ particles using electrostatic heterocoagulation to enhance the electrochemical properties of a Li-ion battery. Only 0.5 wt% of multiwalled carbon nanotubes (MWCNTs) was added as a conducting agent into the LiCoO₂ cathode, which had a density of 4.0 g cm⁻³. We found that our electrode that was prepared using heterocoagulation with 0.5 wt% of thin MWCNTs maintained a volumetric capacitance of 403 mAh cm⁻¹ after 40 cycles from the initial 624 mAh cm⁻¹, compared with previous result of 310 mAh cm⁻¹ obtained from simple mixing with 3 wt% MWCNTs. The high volumetric capacity with smaller swelling using less amount of MWCNTs was attributed to the self-assembled nanotube network formed between active particles during coagulation, which was maintained with volume expansion during cycle testing.     

Electrochemical study of NiO nanoparticles electrode for application in rechargeable lithium-ion batteries

Nickel oxide nanoparticles were synthesized via a simple and inexpensive microwave-assisted synthesis method within a fast reaction time of less than 20 min. The calcination of as-prepared precursor at 600 °C produces single phase nickel oxide. The lattice structure and morphology of the sample were investigated by X-ray diffraction, field-emission scanning electron microscopy and field-emission transmission electron microscopy. The particle size range of the nickel oxide nanoparticles varied from 50 to 60 nm. Nickel oxide nanoparticles exhibited good electrochemical performances as an anode material for lithium-ion batteries. The prepared nickel oxide anode revealed a large initial discharge capacity of 1111.08 mAh g⁻¹ at 0.03 C rate and retained 80% of initial capacity (884.30 mAh g⁻¹) after 20 cycles. Furthermore, at elevated rate of 3.7 C, the charge capacity of the nickel oxide electrode was as high as 253.1 mAh g⁻¹, which was 35% greater than that of commercial bulk nickel oxide (188 mAh g⁻¹). The enhancement of the electrochemical performance was attributed to the high specific surface area, good electric contact among the particles and easier lithium ion diffusion.     

Large-area TiO2 nanotube dye-sensitized solar cells using thermal-sprayed Ti layers on stainless steel

This work presents large-scale dye-sensitized solar cells and methods for their manufacture. A dye-sensitized solar cell device contains a photosensitive dye adsorbed on a large surface of the anode, and a transparent conductive cathode disposed opposite the anode, wherein platinum nano-catalytic particles adhere to its surface, and an electrolytic solution is sealed between the anode and the transparent conductive cathode. A titania nanotube film was fabricated by thermo-spraying titanium film on 304 stainless-steel substrate. The photo-current conversion efficiency was tested under an AM 1.5 solar simulator. The dye-sensitized solar cell device has a short current density of 8.22 mA cm^–2, open voltage of 0.71 V, fill factor of 0.59, and conversion efficiency of 3.4%. The internal impedance of the dye-sensitized solar cell was detected and simulated using an electrical impedance spectra technique with inductance, resistance, and capacitance characteristics. The stainless-steel/titania, titania/electrolyte, electrolyte, and electrolyte/(platinum/indium tin oxide) interfaces were simulated using an resistor–capacitor parallel circuit, and bulk materials such as stainless steel, tin doped indium oxide, and conducting wire were simulated by using a series of resistors and inductance.     

Thermal oxidative cutting of multi-walled carbon nanotubes

Commercially available, multi-walled carbon nanotubes grown by CVD are usually inherently entangled, but can be separated by cutting. However, most cutting methods both cause damage to the nanotubes and involve a lengthy work-up procedure. The use of abrupt, repeated exposure to oxidising conditions in air proved to be an efficient (68% yield) means of producing material with open ends, moderate functionalisation, and enhanced solvent dispersibility; the average lengths were reduced from over 5 μm to approximately 650 nm. Additionally, the character of the surface oxides can be tuned to have either an acidic or basic character by using a simple thermal treatment. These approaches could be deliberately integrated into conventional CVD processes, but also have implications for the products of standard nanotube syntheses. Raman spectroscopy and electron microscopy were used to study the impact of cutting on the intrinsic graphitic structure and the length distribution. X-ray photoelectron spectroscopy was used to determine the extent of functionalisation. The cut carbon nanotubes were dispersed in dimethylformamide (DMF), a Lewis basic solvent, and chloroform, a Lewis acidic solvent, using mild sonication. Through the use of an experimentally determined extinction coefficient (ε = 35.10 ml mg⁻¹ cm⁻¹), the relative dispersibility of the cut and functionalised carbon nanotubes in DMF and chloroform was determined.     

Capacitance behavior of activated carbon fibers with oxygen-plasma treatment

Modified activated carbon fibers (ACFs) were used as the electrodes of an electric double-layer capacitor and showed an enhanced capacitance effect after a RF-plasma treatment. The capacitance and the surface functional groups of the ACFs were studied. For the plasma-treated ACFs having a specific surface area of 1500 m² g⁻¹, the capacitance increased by 28% compared to the untreated sample and the highest electric capacitance value of 142 F g⁻¹ was achieved with an oxygen feed concentration of 10 vol.%. The Brunauer-Emmett-Teller (BET) surface area was 2103 m² g⁻¹, which was 34% higher than that of the untreated sample. The pore volume was similarly increased to 483.1 cm³ g⁻¹ STP, and from the pore distribution plot, quantities of mesopores of 10 nm or less and micropores also increased. However, in order to enhance the capacitance, the quinone functional group had a significant influence in addition to the BET surface area. The correlation between the capacitance and the number of quinone functional groups was confirmed because quinone is an electron acceptor.     

Near-infrared photorefractive polymer composites based on carbon nanotubes

A photorefractive effect at the wavelength of 1064 nm is demonstrated for a composite consisting of an aromatic polyimide and carbon single wall nanotubes. The two-beam gain coupling coefficient and the net gain coefficient are equal to 90 and 65 cm⁻¹, respectively, at 80 V/μm for a nanocomposite containing 0.25 wt% crude nanotube material. The refractive index modulation measured at E₀ = 50 V/μm is close to Δn = 0.004.     

Optimal synthesis of mesostructured hollow titania nanotubes templated on CaCO3 nanoparticles

Approximate 10 µm length of mesostructured hollow titania nanotubes with intact configuration was successfully prepared by using needle-like calcium carbonate and octadecylamine as double templates at room temperature in nonaqueous system. During the whole preparation, two parameters i.e. tetrabutoxytitanium/calcium carbonate molar ratio and annealing temperature, were optimized to obtain titania nanotubes with well-defined tubular morphology and mesoporous structure in tube walls. The as-prepared samples were characterized by scanning electron microscopy, transmission electron microscopy, broad-angle X-ray diffraction, pore size distribution and Brunauer-Emmett-Teller. The results showed that under optimal experimental conditions i.e. tetrabutoxytitanium/calcium carbonate molar ratio (50 wt.%) and annealing temperature (773 K), the tube materials exhibited uniform tubular structure with a length of 8-15 µm and an inner diameter of ∼ 400 nm, a wall thickness of ∼ 40 nm, a surface area of 112.2 m²/g and a pore volume of 0.18 cm³/g. The optimized titania nanotubes were utilized as a carrier for the immobilized of ibuprofen via a simple adsorption method. It was found that the loaded drug presented good sustained release property in three release media, i.e. simulated body fluid, normal saline and pure water.     

Lithium-ion battery anode properties of TiO2 nanotubes prepared by the hydrothermal synthesis of mixed (anatase and rutile) particles

From mixed (anatase and rutile) bulk particles, anatase TiO₂ nanotubes are synthesized in this study by an alkaline hydrothermal reaction and a consequent annealing at 300-400 °C. The physical and electrochemical properties of the TiO₂ nanotube are investigated for use as an anode active material for lithium-ion batteries. Upon the first discharge-charge sweep and simultaneous impedance measurements at local potentials, this study shows that interfacial resistance decreases significantly when passing lithium ions through a solid electrolyte interface layer at the lithium insertion/deinsertion plateaus of 1.75/2.0 V, corresponding to the redox potentials of anatase TiO₂ nanotubes. For an anatase TiO₂ nanotube containing minor TiO₂(B) phase obtained after annealing at 300 °C, the high-rate capability can be strongly enhanced by an isotropic dispersion of TiO₂ nanotubes to yield a discharge capacity higher than 150 mAh g⁻¹, even upon 100 cycles of 10 C-rate discharge-charge operations. This is suitable for use as a high-power anode material for lithium-ion batteries.     

Nickel oxide/hydroxide nanoplatelets synthesized by chemical precipitation for electrochemical capacitors

Nickel hydroxide powder prepared by directly chemical precipitation method at room temperature has a nanoplatelet-like morphology and could be converted into nickel oxide at annealing temperature higher than 300 °C, confirmed by the thermal gravimetric analysis and X-ray diffraction. Annealing temperature influences significantly both the electrical conductivity and the specific surface area of nickel oxide/hydroxide powder, and consequently determines the capacitor behavior. Electrochemical capacitive behavior of the synthesized nickel hydroxide/oxide film is investigated by cyclic voltammetry and electrochemical impedance spectroscope methods. After 300 °C annealing, the highest specific capacitance of 108 F g⁻¹ is obtained at scan rate of 10 mV s⁻¹. When annealing temperature is lower than 300 °C, the electrical conductivity of nickel hydroxide dominates primarily the capacitive behavior. When annealing temperature is higher than 300 °C, both electrical conductivity and specific surface area of the nickel oxide dominate the capacitive behavior.     

Single-source precursor route to carbon nanotubes at mild temperature

Carbon nanotubes were synthesized via a single-source precursor route at 500 °C, using iron carbonyl both as carbon source and catalyst. The X-ray power diffraction pattern indicates that the products are hexagonal graphite. Transmission electron microscope (TEM) images of the sample reveal carbon nanotubes with an average inner (outer) diameter of 30 nm (60 nm). High-resolution TEM indicates that fabrication of the carbon nanotube walls was composed of ca. 40 graphene layers. The Raman spectrum shows two strong peaks at 1587 and 1346 cm⁻¹, corresponding to the typical Raman peaks of graphitized carbon nanotubes. This method avoids the separation of raw material from solvent and simplifies the operation process. At the same time, the research provides a new route to large-scale synthesis of carbon nanotubes.     

Coating manganese oxide onto graphite electrodes by immersion for electrochemical capacitors

In this study, manganese oxide was coated on a graphite electrode by immersion. Durations for immersion were varied to control the amount of manganese oxide coated onto the electrode surface. Maximum capacitance of 556 mF cm⁻² was obtained in 0.5 M LiCl and with better/superior conditions (immersion time = 80 min and potential scan rate = 10 mV s⁻¹). In addition, cyclic voltammograms of the prepared electrode at different potential scan rates exhibited the approximately rectangular and symmetric current-potential characteristics of a capacitor. Furthermore, the chronopotentiometry (CP) charge-discharge curves of the electrode prepared at 80 min of immersion time with a constant current of 1 mA were symmetric and similar isosceles triangles, which demonstrate its high electrochemical reversibility and good stability. Finally, under scanning electron microscope (SEM), the surface of the electrode prepared at 80 min of immersion time and after 1500 cycles of potential cycling revealed that numerously three-dimensional network of macropores appeared on large spherical grains.     

Influence of water content on nanotubular anodic titania formed in fluoride/glycerol electrolytes

A study has been carried out of nanotubular anodic films formed on titanium at 20 V in fluoride/glycerol electrolyte, containing up to 50 vol.% water. Anodizing was terminated at a charge of 1 C cm⁻². Addition of water resulted in an increased current and significantly reduced tube length associated with increased oxygen gas evolution. Films formed in the absence of added water were amorphous by electron diffraction, whereas water addition also led to the formation of anatase and rutile. The barrier layer was relatively thin for electrolyte of low water content, due to either a voltage drop in the electrolyte close to the anode or to a change in the film composition affecting the electric field across the layer. Ribbing of the external walls of the nanotubes was more evident in the presence of water. It is suggested that dissolution of a fluoride-rich layer, which separates the nanotubes, accompanies the nanotube growth, with the dissolution allowing transient film formation at the external walls of the nanotubes when the residual layer is sufficiently thin.     

Electropolymerization of polyaniline on titanium oxide nanotubes for supercapacitor application

Vertically aligned polyaniline (PANI) nanotubes have great potential application in supercapacitor electrode material. In this paper we have investigated facile growth of PANI nanotubes on a titanium nanotube template (TNT) using electrochemical polymerization. The morphology of PANI nanostructures grown over TNT is strongly influenced by the scan rate in the electrochemical polymerization. The growth morphology of PANI nanotubes has been carefully analyzed by field emission scanning electron microscopy. The detailed growth mechanism of PANI nanotubes has been put forward. Specific capacitance value of 740 F g⁻¹ was obtained for PANI nanotube structures (measured at charge–discharge rate of 3 A g⁻¹).     

Raman spectroscopy and nitrogen vapour adsorption for the study of structural changes during purification of single-wall carbon nanotubes

Raman spectroscopy and nitrogen adsorption measurements were combined to study the surface features of semi-conducting and metallic single-wall nanotubes (SWNTs). The nanotubes were treated chemically and with heat under moderate conditions that more than doubled the mesopore volume of the tested samples, which consistently led to a significant rise in the total surface area of up to 1550 m²/g. The large increase in the number of micropores of less than 1 nm in diameter was associated with the loosening of nanotube bundles as well as the creation of structural flaws on the surface of individual SWNTs due to chemical treatment. Micropores in the 1.0-1.8 nm range were associated with the holes created on the surface of individual tubes. Heating at 1000 °C was shown to restore nanotube diameter to their initial pre-chemical treatment levels with the change in the chirality of SWNTs and diminish the porosity by closing small holes. It was assumed that the intermediate frequency range (500-1100 cm⁻¹) was associated with the degree of imperfection of HiPco SWNTs crystalline structures, and therefore provided information about the degree of tube surface damage due to the presence of functional groups. A hypothesis explaining the transformation of SWNT porous structure during heat treatment is proposed.     

Spark plasma sintering of double-walled carbon nanotubes

Bulk samples of double-walled carbon nanotubes are prepared for the first time. The best spark plasma sintering conditions are (1100 °C, 100 MPa). Raman spectroscopy and scanning electron microscopy show that the nanotubes are undamaged. The density is equal to 1.29 g cm⁻³ and the pores are all below 6 nm in diameter. The electrical conductivity is equal to 1650 S cm⁻¹. The transverse fracture strength is equal to 47 MPa.