A facile synthesis of heteroatom-doped carbon framework anchored with TiO<Subscript>2</Subscript> nanoparticles for high performance lithium ion battery anodes

Titanium dioxide (TiO₂)-based materials have been well studied because of the high safety and excellent cycling performance when employed as anode materials for lithium ion batteries (LIBs), whereas, the relatively low theoretical capacity (only 335 mAh g^?1) and serious kinetic problems such as poor electrical conductivity (~?10^?13S cm^?1) and low lithium diffusion coefficient (~?10^?9 to 10^?13 cm² s^?1) hinder the development of the TiO₂-based anode materials. To overcome these drawbacks, we present a facile strategy to synthesize N/S dual-doping carbon framework anchored with TiO₂ nanoparticles (NSC@TiO₂) as LIBs anode. Typically, TiO₂ nanoparticles are anchored into the porous graphene-based sheets with N, S dual doping feature, which is produced by carbonization and KOH activation process. The as-obtained NSC@TiO₂ electrode exhibits a high specific capacity of 250 mAh g^?1 with a coulombic efficiency of 99% after 500 cycles at 200 mA g^?1 and excellent rate performance, indicating its promising as anode material for LIBs.     

Effect of passivating Al<Subscript>2</Subscript>O<Subscript>3</Subscript> thin films on MnO<Subscript>2</Subscript>/carbon nanotube composite lithium-ion battery anodes

MnO₂/carbon nanotube composite electrodes for Li-ion battery application were directly coated with ultrathin thicknesses of aluminum oxide film by atomic layer deposition (ALD). The non-reactive Al₂O₃ layer not only provides a stable film to protect the manganese oxide and carbon nanotubes from undesirable reaction with the electrolyte but also restrains the volume change strain of manganese oxide during cycling. The first cycle Coulombic efficiency of coated samples was increased to different extents depending on the coating thickness. In the following cycles, the coated electrodes denote high specific capacity, good capacity retention ability, and perfect rate charge/discharge performance.     

Fabrication and electrochemical investigation of Li<Subscript>0.5</Subscript>TiO<Subscript>2</Subscript> as anode materials for lithium ion batteries

Hexagonal and cubic Li_0.5TiO₂ particles have been fabricated through magnesiothermic reduction of Li₂TiO₃ particles in a temperature range of 600 to 640 °C. The prolonged reduction time results in lattice transition from hexagonal to cubic structure of Li_0.5TiO₂. Their microstructures, valance state, chemical composition, as well as electrochemical performance as anode candidates for lithium ion batteries have been characterized and evaluated. The hexagonal Li_0.5TiO₂ exhibits better electrochemical activity compared with the cubic one. Further, the carbon-coated hexagonal Li_0.5TiO₂ displays improved electrochemical performance with initial reversible capacity of 176.6 mAh g^?1 and excellent cyclic behavior except capacity fading in the initial 10 cycles, which demonstrate a novel anode candidate for long lifetime lithium ion batteries.     

Conductive TiN thin layer-coated nitrogen-doped anatase TiO<Subscript>2</Subscript> as high-performance anode materials for sodium-ion batteries

Nitrogen-doped anatase titanium oxide (N-TiO₂) with enhanced electronic conductivity induced by titanium nitride (TiN) thin layer coating was employed as high-performance anode material for sodium-ion batteries. The TiN thin layer can not only dramatically increase the electronic conductivity among crystal grains but also alleviate the volume expansion to consolidate the structure during long-term sodiation and desodiation process. The composite exhibits an excellent electrochemical performance, delivering a high specific capacity of 226.9 mA h g^?1 at 0.1 C and owning excellent rate capability of 158.3 mA h g^?1 at 10 C high rate. Moreover, the composite has no obvious capacity decay after 500 cycles at 1 C, showing its superior cycling performance. The enhancement of electrochemical performance may be attributed to the faster kinetics of sodium ion sodiation/desodiation, which could be a result of enhanced electronic conductivity due to the formation of TiN thin layer coating.     

Photocatalytic properties of nanocrystalline TiO<Subscript>2</Subscript> thin films doped with Tb

In this work photocatalytic properties of TiO₂ thin films doped with different amount of Tb have been described. Thin films were prepared by high energy reactive magnetron sputtering process. Comparable photocatalytic activity has been found for all doped TiO₂ thin films, while different amounts of Tb dopant (0.4 and 2.6 at. %) results in either an anatase or rutile structure. It was found that the terbium dopant incorporated into TiO₂ was also responsible for the amount of hydroxyl groups and water particles adsorbed on the thin film surfaces and thus photocatalytic activity was few times higher in comparison with results collected for undoped TiO₂ thin films.     

Binder-free combination of amorphous TiO<Subscript>2</Subscript> nanotube arrays with highly conductive Cu bridges for lithium ion battery anode

Binder-free combination of highly conductive Cu bridges with amorphous TiO₂ nanotube arrays for lithium ion battery anode were designed and achieved via one-step facile electrodeposition. The obtained composite Cu/TiO₂ nanotubes electrode was studied in terms of XRD, SEM, EDX, galvanostatic charge/discharge, cycle stability, rate performance, and AC impedance. As expected, the composite electrode delivered higher discharge capacity, rate performance, and cycle stability than the bare one, possibly due to improved electrical conductivity and the synergy effect between conductive Cu bridges and amorphous TiO₂ nanotube arrays.     

Physical properties of Ba<Subscript>0.8</Subscript>Sr<Subscript>0.2</Subscript>TiO<Subscript>3</Subscript> thin films

The behavior of material constants in ferroelectric Ba_0.8Sr_0.2TiO₃ thin films is studied depending on the misfit strain at room temperature in the context of nonlinear thermodynamic potential of the phenomenological theory. Some constants are found to undergo drastic changes with the alternating strain at the interfaces. The gathered results allow one to evaluate the material constants for a specific film and to outline the direction in searching the ways to synthesize films with the needed properties.     

Electrospinning preparation of one-dimensional Co<Superscript>2+</Superscript>-doped Li<Subscript>4</Subscript>Ti<Subscript>5</Subscript>O<Subscript>12</Subscript> nanofibers for high-performance lithium ion battery

One-dimensional Co²⁺-doped Li₄Ti₅O₁₂ nanofibers with a diameter of approximately 500 nm have been synthesized via a one-step controllable electrospinning method. The Co²⁺-doped Li₄Ti₅O₁₂ nanofibers were systematically characterized by XRD, ICP, TEM, SEM, BET, EDS mapping, and XPS. Based on the cubic spinel structure and one-dimensional effect of Li₄Ti₅O₁₂, Co²⁺-doped Li₄Ti₅O₁₂ nanofibers exhibit the enlarged lattice volume, reduced particle size and enhanced electrical conductivity. More importantly, Co²⁺-doped Li₄Ti₅O₁₂ nanofibers as a lithium ion battery anode electrode performs superior electrochemical performance than undoped Li₄Ti₅O₁₂ electrode in terms of electrochemical measurements. Particularly, the reversible capacity of Co²⁺-doped Li₄Ti₅O₁₂ electrode reaches up to 140.1 mAh g^?1 and still maintains 136.5 mAh g^?1 after 200 cycles at a current rate of 5 C. Therefore, one-dimensional Co²⁺-doped Li₄Ti₅O₁₂ nanofiber electrodes, showing high reversible capacity and remarkable recycling property, could be a potential candidate as an anode material.     

Nonlinear dielectric response of epitaxial Ba<Subscript>0.6</Subscript>Sr<Subscript>0.4</Subscript> TiO<Subscript> 3</Subscript> thin films

Based on Landau-Devonshire (LD)-type phenomenological thermodynamic theory, the electric field dependence of the dielectric properties of tetragonal single-domain barium strontium titanate(Ba_1-xSr_xTiO₃) films on cubic substrates is theoretically investigated by taking into account the high order terms of the polarization. At room temperature, the nonlinear dielectric responses of epitaxial Ba_0.6Sr_0.4TiO₃ films are provided by adjusting the film thickness and growth temperature. The strong nonlinearity of relative dielectric constant and pyroelectric coefficient are attained around critical film thickness on MgO (69 nm) and LaAlO₃ (132 nm) substrates or critical growth temperature on MgO (337 °C) substrate with respect to epitaxy-induced lattice misfit and thermal stresses during deposition. This can be explained that small compressive stresses are effective to support high nonlinearity of dielectric constant and pyroelectric coefficient for Ba_0.6Sr_0.4TiO₃ films irrespective of whether they are on compressive substrate or tensile substrate. It is also predicted that a large tunability may be achieved by altering processing conditions, such as the film thickness and growth temperature for different substrates. Our theoretical results are in good agreement with the experimental data reported in literature.     

Evaluation of LiMn<Subscript>2</Subscript>O<Subscript>4</Subscript>-LiNi<Subscript>0.80</Subscript>Co<Subscript>0.15</Subscript>Al<Subscript>0.05</Subscript>O<Subscript>2</Subscript> hybrid material as cathode in soft-packed lithium ion battery

The major electrochemical performances of LiMn₂O₄ (LMO)-LiNi_0.80Co_0.15Al_0.05O₂ (NCA) blending cathodes with full-range ratios are evaluated in industrial perspective. The results indicate that the reversible lithium ions can be fully utilized when NCA percentage reaches up to 50 %. The median voltages of blends are higher than the value calculated from a linear relationship of the two pristine cathodes, which is beneficial to energy density. But a synergy effect on room-temperature cycle performance is not observed for the hybrid cathode. However, the high-temperature (45 °C) capacity retention with 70 % NCA is 97.9 % after 100 cycles, higher than both pristine cathodes. It is not until NCA content increases to more than 50 % that the high-rate performance is much deteriorated. Additionally, the swelling of fully charged pouch-type battery after 4 h storage at 85 °C disappears when NCA percentage is less than 50 %. Hence, it is practically manifested that critical flaws of NCA and LMO can be compromised by blending with each other in a critical ratio. In this way, NCA can be practically used in soft-packed battery.     

Optoelectronics properties of TiO<Subscript>2</Subscript>:Cu thin films obtained by sol gel method

In this research, Cu-doped TiO₂ thin films have been successfully deposited onto a glass substrate by Sol–gel technique using dip coating method. The films were annealed at different annealing temperatures (400–500 °C) for 1 h. The structural, optical and electrical properties of the films were investigated and compared using X-ray Diffraction, UV–visible spectrophotometer and 4-point probe method. Optical analysis by mean transmittance T(λ) and absorption A(λ) measurements in the wavelength range between 300 to 800 nm allow us to determine the indirect band gap energy. DRX analysis of our thin films of TiO₂:Cu shows that the intensities of the line characteristic of anatase phase increasing in function of the temperature.     

Enhanced electrochemical performance of lithium ion battery cathode Li<Subscript>3</Subscript>V<Subscript>2</Subscript>(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>/C

Li-ion battery cathode material lithium-vanadium-phosphate Li₃V₂(PO₄)₃ was synthesized by a carbon-thermal reduction method, using stearic acid, LiH₂PO₄, and V₂O₅ as raw materials. And stearic acid acted as reductant, carbon source, and surface active agent. The effect of its content on the crystal structure and electrochemical performance of Li₃V₂(PO₄)₃/C were characterized by XRD and electrochemical performance testing, respectively. The results showed that the content of carbon source has no significant effect on the crystal structure of lithium vanadium phosphate. Lihtium vanadium phosphate obtained with 12.3% stearic acid demonstrated the best electrochemical properties with a typical discharge capacity of 119.4 mAh/g at 0.1 C and capacity retention behavior of 98.5% after 50 cycles. And it has high reversible discharge capacity of 83 mAh/g at 5 C with the voltage window of 3 to 4.3 V.     

Sulfonated poly(phenylene oxide)/Ti<Superscript>3+</Superscript>/TiO<Subscript>2</Subscript> nanotube arrays membrane/electrode with high performances for lithium ion battery

Sulfonated poly(phenylene oxide) (SPPO) film was electrodeposited on Ti³⁺-doped TiO₂ nanotube arrays (Ti³⁺/TiO₂NT) electrode via the electropolymerization of sulfonated phenol. The as-synthesized SPPO/Ti³⁺/TiO₂NT membrane/electrode was investigated in terms of SEM, FESEM, EDX, FTIR, XPS, galvanostatic charge/discharge, and cycle voltammetry (CV). As expected, the porous SPPO film did form on the surface of Ti³⁺/TiO₂NT electrode; furthermore, the resultant SPPO/Ti³⁺/TiO₂NT membrane/electrode delivered higher electrochemical performances than PPO/Ti³⁺/TiO₂NT, mainly attributed to the contributions of the ionic conductivity induced by –SO₃H groups within SPPO.     

Photoaccumulating film systems based on TiO<Subscript>2</Subscript>/MoO<Subscript>3</Subscript> and TiO<Subscript>2</Subscript>/MoO<Subscript>3</Subscript>:V<Subscript>2</Subscript>O<Subscript>5</Subscript> nanoheterostructures

The thin-film photocatalysts TiO₂/MoO₃ and TiO₂/MoO₃:V₂O₅ obtained by a combination of sol–gel and sintering techniques were studied using the photooxidation of probing dyes, EPR spectroscopy, X-ray diffraction analysis, and electron microscopy. It was shown that due to charge accumulation caused by UV irradiation, these photocatalysts retain their oxidative activity and ability for self-sterilization in the dark for a long time after irradiation was terminated (up to 5 h for TiO₂/MoO₃:V₂O₅).     

NiCo<Subscript>2</Subscript>O<Subscript>4</Subscript> polyhedra with controllable particle size as high-performance anode for lithium-ion battery

Different particle sizes of dodecahedron precursors are synthesized by controlling the polarity of the solution. Through the results of scanning electron microscope (SEM) images, it can be found that different particle sizes of precursors present obvious edge angles and their morphology can be well retained after annealing. X-ray diffraction (XRD) measurements suggest that the annealed polyhedral products are pure single-phase NiCo₂O₄. When tested as lithium-ion battery anode, 0.5 μm NiCo₂O₄ polyhedra exhibits a specific capacity of 1050 mAh g^?1 at 0.1 C at the 60th cycle, which was higher than theoretical capacity of single metal oxide (NiO 718 mAh g^?1 and Co₃O₄ 890 mAh g^?1). It also exhibits the highest rate capability with an average discharge capacity of 890, 700, 490, 330, and 300 mAh g^?1 at 0.5, 2, 4, 8, and 10 C, respectively. Those advantages are attributed to that small-sized particle with great surface areas decrease the actual current density at the surface and inner of the prepared electrode.     

Influence of nanocrystalline structure and composition on hardness of thin films based on TiO<Subscript>2</Subscript>

In this work, the influence of Tb-doping on structure, and especially hardness of nanocrystalline TiO₂ thin films, has been described. Thin films were formed by a high-energy reactive magnetron sputtering process in a pure oxygen atmosphere. Undoped TiO₂-matrix and TiO₂:Tb (2 at. % and 2.6 at. %) thin films, had rutile structure with crystallite sizes below 10 nm. The high-energy process produces nanocrystalline, homogenous films with a dense and close packed structure, that were confirmed by X-ray diffraction patterns and micrographs from a scanning electron microscope. Investigation of thin film hardness was performed with the aid of a nanoindentation technique. Results of measurements have shown that the hardness of all manufactured nanocrystalline films is above 10 GPa. In the case of undoped TiO₂ matrix, the highest hardness value was obtained (14.3 GPa), while doping with terbium results in hardness decreasing down to 12.7 GPa and 10.8 GPa for TiO₂:(2 at. % Tb) and TiO₂:(2.6 at. % Tb) thin films, respectively. Incorporation of terbium into TiO₂-matrix also allows modification of the elastic properties of the films.     

Absorption spectrum of thin K<Subscript>2</Subscript>CdI<Subscript>4</Subscript> films

The absorption spectrum of thin films of a new compound, K₂CdI₄, was studied. It was established that this compound belongs to direct-bandgap dielectrics and that its low-frequency electronic and excitonic excitations are localized in CdI ₄ ^2? structural blocks of the crystal lattice. It was found that, in M₂CdI₄ compounds (M = K, Rb, Cs), the bandgap width E _g grows and the spin-orbit splitting of the valence band top decreases with increasing ionic radius of the alkali metal.     

Antibacterial effect of silver modified TiO<Subscript>2</Subscript>/PECVD films

This paper deals with photocatalytic activity of silver treated TiO₂ films. The TiO₂ films were deposited on glass substrates by plasma enhanced chemical vapor deposition (PECVD) in a vacuum reactor with radio frequency (RF) low temperature plasma discharge in the mixture of oxygen and titanium isopropoxide vapors (TTIP). The depositions were performed under different deposition conditions. Subsequently, the surface of TiO₂ films was modified by deposition of silver nanoparticles. Photocatalytic activity of both silver modified and unmodified TiO₂ films was determined by decomposition of the model organic matter (acid orange 7). Selected TiO₂ samples were used for tests of antibacterial activity. These tests were performed on Gram-negative bacteria Escherichia coli. The results clearly proved that presence of silver clusters resulted in enhancement of the photocatalytic activity, which was up to four times higher than that for pure TiO₂ films.     

Magnetotransport in thin epitaxial Bi<Subscript>2</Subscript>Se<Subscript>3</Subscript> films

The magnetoconductivity of thin Bi₂Se₃ films covered by a protective Se layer and grown at (111) BaF₂ substrates is studied. It is shown that the negative magnetoconductivity observed at low magnetic fields and caused by the effect of weak antilocalization, as well as the Shubnikov?de Haas oscillations at higher fields, is determined only by the magnetic field component perpendicular to the film plane. The obtained experimental results can be reasonably interpreted under the assumption that the studied films exhibit two-dimensional topologically protected electron states. Moreover, the contribution of these states to the total conductivity turns out to be the dominant one.