Bowei Zhang

Hybrid vertical graphene/lithium titanate–CNTs arrays for lithium ion storage with extraordinary performance

In the present study, we report a synthetic strategy for the direct fabrication of hybrid vertical graphene/lithium titanate–CNTs arrays via atomic layer deposition in combination with chemical vapor deposition. A novel array architecture was formed where active lithium titanate (Li4Ti5O12, LTO) was uniformly sandwiched by a vertical graphene backbone and an interconnected CNTs shell. The hybrid omnibearing conductive network was identified to be an extremely stable porous structure and demonstrated superior ultra-high rate capability (146 mA h g−1 at 50C and 131 mA h g−1 at 100C) with a capacity of 136 mA h g−1 at 20C after 10u2006000 cycles when used as an electrode in lithium ion batteries. This special electrode construction strategy is expected to provide a new route for the manufacture of electrochemical energy storage with ultra-high rate capability and ultra-stability.

A novel synthesis of carbon nanotubes directly from an indecomposable solid carbon source for electrochemical applications

Carbon nanotubes (CNTs) are synthesized through a novel low cost self-vaporized chemical vapor deposition (SCVD) technique from an indecomposable solid carbon source for the first time. This method was manipulated to avoid the injection of flammable gasses, by producing gaseous carbon (e.g. CO) through an in situ catalyzed gasification of the intermediate product induced by KOH. Simultaneously, the as-produced gaseous carbons will deposit onto the pre-imbedded Ni nanocatalyst surface and form CNTs. The growth mechanism is discussed in detail by adjusting the KOH amount. The as-prepared CNTs are rich in oxygen and deficiencies, which endow them with abundant active sites for electrochemical applications. Superior supercapacitor performance is achieved with a specific capacitance 6 times higher than that of commercial CNTs. This technique represents a novel, convenient approach toward large scale production of CNTs directly from a solid carbon precursor, and would show promising applications in various industrial fields.

Phase transition of hollow-porous α-Fe2O3 microsphere based anodes for lithium ion batteries during high rate cycling

In the present paper, hollow-porous α-Fe2O3 microspheres are prepared via cation etching of zinc citrate microspheres and subsequent thermal treatment. The superior performance of the as-obtained α-Fe2O3 microspheres as an anode material for lithium ion batteries is evaluated. After 1000 cycles, the capacity still remains more than 1100 mA h g−1 at a current rate of 1 A g−1. Meanwhile, the crystal size induced phase transition of Fe2O3 microspheres (α → γ → β) is observed during cycling by the measurements of ex situ XRD and TEM, which is responsible for their abnormal performance fluctuation.

Nanoscale ion intermixing induced activation of Fe2O3/MnO2 composites for application in lithium ion batteries

Herein, we demonstrate a facile method to prepare hollow-structured oxygen-vacancy-rich Fe2O3/MnO2 nanorods. Our results show that oxygen vacancies are induced by nanoscale ion intermixing between Fe and Mn ions during the annealing process. Owing to their unique core–shell hollow nanostructure and the presence of oxygen vacancies, the Fe2O3/MnO2 nanorods show excellent electrochemical performances as an anode material for lithium ion batteries and a reversible capacity higher than 700 mA h g−1 after 2000 cycles.

Evidence of a nanosized copper anodic reaction in an anaerobic sulfide aqueous solution

The present paper reports the use of TEM to investigate the electrochemical behavior of a copper subject to the both free corrosion and polarization in a 0.1 M NaCl + 5 × 10−4 M Na2S aqueous solution at the nano scale. The pure copper is found to be transformed into nano-crystalline Cu2S in the thin region of the copper needle in the solution at open circuit conditions. However, a rough Cu2S layer is formed in the active region of electrochemical polarization, which is then converted to the passive CuS layer with a uniform thickness at higher potentials. Upon the continuous increase of an applied potential, cubic CuS particles with sizes of ∼100 nm are precipitated on the needle surface due to the breakdown of the passive layer. Meanwhile, the growth of a large amount of nanosized CuCl particles is also found, indicating that Cl− ions participate in the electrochemical reaction in the transpassive region. It is worth noting that the present work also provides a simple and cost-effective way for the synthesis of copper sulfides (Cu2S and CuS) through electrochemical processes.

The Electrochemical Response of Single Crystalline Copper Nanowires to Atmospheric Air and Aqueous Solution

In this paper, single crystalline copper nanowires (CuNWs) have been electrochemically grown through anodic aluminum oxide template. The environmental stability of the as-obtained CuNWs in both 40% relative humidity (RH) atmosphere and 0.1 m NaOH aqueous solution has been subsequently studied. In 40% RH atmosphere, a uniform compact Cu2 O layer is formed as a function of exposure time following the logarithmic law and epitaxially covers the CuNW surfaces. It is also found that the oxide layers on CuNWs are sequentially grown when subjected to the cyclic voltammetry measurement in 0.1 m NaOH solution. An epitaxially homogeneous Cu2 O layer is initially formed over the surface of the CuNW substrates by solid-state reaction (SSR). Subsequently, the conversion of Cu2 O into epitaxial CuO based on the SSR takes place with the increase of applied potential. This CuO layer is partially dissolved in the solution forming Cu(OH)2 , which then redeposited on the CuNW surfaces (i.e., dissolution-redeposition (DR) process) giving rise to a mixed polycrystalline CuO/Cu(OH)2 layer. The further increase of applied potential allows the complete oxidation of Cu2 O into CuO to form a dual-layer structure (i.e., CuO inner layer and Cu(OH)2 outer layer) with random orientations through an enhanced DR process.

In Situ Formation of Decavanadate-Intercalated Layered Double Hydroxide Films on AA2024 and their Anti-Corrosive Properties when Combined with Hybrid Sol Gel Films

A layered double hydroxide (LDH) film was formed in situ on aluminum alloy 2024 through a urea hydrolysis method, and a decavanadate-intercalated LDH (LDH-V) film fabricated through the dip coating method. The microstructural and morphological characteristics were investigated by scanning electron microscopy (SEM). The corrosion-resistant performance was analyzed by electrochemical impedance spectroscopy (EIS), scanning electrochemical microscopy (SECM), and a salt-spray test (SST).The SEM results showed that a complete and defect-free surface was formed on the LDH-VS film. The anticorrosion results revealed that the LDH-VS film had better corrosion-resistant properties than the LDH-S film, especially long-term corrosion resistance. The mechanism of corrosion protection was proposed to consist of the self-healing effect of the decavanadate intercalation and the shielding effect of the sol-gel film.

Electrochemical behaviors of hierarchical copper nano-dendrites in alkaline media

In this study, hierarchical copper nano-dendrites (CuNDs) are fabricated via the electrodeposition method. The electrochemical behaviors of the as-obtained hierarchical CuNDs in 0.1 M NaOH aqueous solution are subsequently studied. The CuNDs experience a non-equilibrium oxidation process when subjected to cyclic voltammetry (CV) measurements. The first oxidation peak O1 in CV is attributed to the formation of an epitaxial Cu2O layer over the surface of the hierarchical CuNDs. However, the second oxidation peak O2 in CV appears unusually broad across a wide potential range. In this region, the reaction process starts with the nucleation and growth of Cu(OH)2 nanoneedles, followed by the oxidation of Cu2O. Upon the increase of potential, Cu2O is gradually transformed to CuO and Cu(OH)2, forming a dual-layer structure with high productivity of Cu(OH)2 nanoneedles.

Morphology controlled lithium storage in Li3VO4 anodes

Li3VO4 (LVO) anode materials with controllable morphologies ranging from spherical-assemblies, single-crystal nanorods, and flower shapes to bulk-shapes were fabricated via a solvothermal approach using different alcohols (i.e., ethanol, methanol, propanol, and butanol). XRD, SEM, BET, Raman and FTIR and galvanostatic charge/discharge measurements were carried out to correlate their structure/morphology with their electrochemical characteristics. The experimental results reveal that both structure and morphology play important roles in the Li+ ion storage of LVO, which degrades in the sequential order from nanorods, to spheres, to flowers and finally to bulk. The LVO nanorods are hierarchical and have a small particle size, high specific surface area, and high crystallinity; thus, they exhibit the largest Li+ ion diffusion coefficient and best electrochemical performance among the four electrodes. Moreover, coating carbon on the single-crystal LVO nanorods further enhances their Li+ ion storage ability. Consequently, the carbon-coated LVO nanorods deliver a high reversible capacity of 440 mA h g−1 at 0.1 A g−1 with good cycling stability and demonstrate great practical application. In addition, the results promote a better fundamental understanding of the Li+ ion storage behavior in LVO and provide insight into the optimal design of LVO and other vanadium-based electrode materials.

Extraordinary catalysis induced by titanium foil cathode plasma for degradation of water pollutant

The present paper reports a rapid and cost-effective bifunctional approach to the degradation of organic pollutants in the aqueous solution. This in situ hybrid induced photocatalytic method involves the advanced oxidation process, and photocatalytic process induced by ultraviolet radiated from the plasma discharge to improve the degradation efficiency. This powerful plasma allows the organic molecules to be cleaved either in the plasma zone or on the plasma/solution interface through hydrogen abstraction and electron transfer. Four parallel metal foil electrodes (i.e. Ta, Cu, Ti and Au coated Ti), used as cathodes in the two-electrode system, were evaluated in terms of their degradable performance to organic pollutants. It was found that the degradation rates are dependent on the electrical conduction of metal cathodes. During the discharge process, the Ti-based foil produces TiO2 particles, which then act as catalyst in the electrolyte and perform the photocatalytic process along with the plasma discharge process to degrade organic pollutants. It is of particular interest that gold nanoparticles, generated from Au coated Ti foil film during electrode discharging, are less than 5u202fnm in size and further enhance the TiO2 photocatalytic activity. In fact, this bifunctional plasma discharge process to the degradation of water pollutant provides an insight into more applications such as chemical conversion, water purification and dust pollution.