Liguo Ma

Fabrication of highly ordered nanoporous alumina films by stable high-field anodization

Stable high-field anodization (1500–4000 A m −2 ) for the fabrication of highly ordered porous anodic alumina films has been realized in a H3PO4–H2O–C2H5OH system. By maintaining the self-ordering voltage and adjusting the anodizing current density, high-quality self-ordered alumina films with a controllable inter-pore distance over a large range are achieved. The high anodizing current densities lead to high-speed film growth (4–10 µ mm in −1 ). The inter-pore distance is not solely dependent on the anodizing voltage, but is also influenced by the anodizing current density. This approach is simple and cost-effective, and is of great value for applications in diverse areas of nanotechnology.

Synthesis of chiral TiO 2 nanofibre with electron transition-based optical activity

The optical chirality induced at the absorption bands due to electronic exciton coupling of the transition dipole moments between chromophores in close proximity is ubiquitous in helical organic materials. However, inorganic materials with optical activity resulting from electronic transitions have not been explored. Here we report the synthesis of chiral TiO2 fibres via transcription of the helical structure of amino acid-derived amphiphile fibres through coordination bonding interactions between the organics and the TiO2 source. Upon calcination, the as-prepared amorphous TiO2 double-helical fibres with a pitch length of ~100 nm were converted to double-helical crystalline fibres with stacks of anatase nanocrystals in an epitaxial helical relationship. Both the amorphous and anatase crystalline helical TiO2 fibres exhibited optical response to circularly polarized light at the absorption edge around ~350 nm. This was attributed to the semiconductor TiO2-based electronic transitions from the valence band to the conduction band under an asymmetric electric field.

High-speed growth and photoluminescence of porous anodic alumina films with controllable interpore distances over a large range

Highly ordered porous anodic alumina (PAA) films are fabricated with high efficiency by stable high-field anodization in oxalic acid/ethanol/water electrolytes at 100–180V and sulfuric acid/oxalic acid/ethanol/water electrolytes at 30–80V, giving interpore distances in the range of 225–450nm and 70–140nm, respectively. The photoluminescence of PAA films prepared by high-field anodization shows remarkable redshift of the peak position and decrease of the intensity compared to that of PAA films formed by conventional low-field anodization.

Facile synthesis of superhydrophobic surface of ZnO nanoflakes: chemical coating and UV-induced wettability conversion

This work reports an oriented growth process of two-dimensional (2D) ZnO nanoflakes on aluminum substrate through a low temperature hydrothermal technique and proposes the preliminary growth mechanism. A bionic superhydrophobic surface with excellent corrosion protection over a wide pH range in both acidic and alkaline solutions was constructed by a chemical coating treatment with stearic acid (SA) molecules on ZnO nanoflakes. It is found that the superhydrophobic surface of ZnO nanoflake arrays shows a maximum water contact angle (CA) of 157° and a low sliding angle of 8°, and it can be reversibly switched to its initial superhydrophilic state under ultraviolet (UV) irradiation, which is due to the UV-induced decomposition of the coated SA molecules. This study is significant for simple and inexpensive building of large-scale 2D ZnO nanoflake arrays with special wettability which can extend the applications of ZnO films to many other important fields.

High-speed growth of TiO2 nanotube arrays with gradient pore diameter and ultrathin tube wall under high-field anodization

Highly ordered TiO(2) nanotubular arrays have been prepared by two-step anodization under high field. The high anodizing current densities lead to a high-speed film growth (0.40-1.00 microm min(-1)), which is nearly 16 times faster than traditional fabrication of TiO(2) at low field. It was found that an annealing process of Ti foil is an effective approach to get a monodisperse and double-pass TiO(2) nanotubular layer with a gradient pore diameter and ultrathin tube wall (nearly 10 nm). A higher anodic voltage and longer anodization time are beneficial to the formation of ultrathin tube walls. This approach is simple and cost-effective in fabricating high-quality ordered TiO(2) nanotubular arrays for practical applications.

Optically Active Nanostructured ZnO Films

Inorganic nanomaterials endowed with hierarchical chirality could open new horizons in physical theory and applications because of their fascinating properties. Here, we report chiral ZnO films coated on quartz substrates with a hierarchical nanostructure ranging from atomic to micrometer scale. Three levels of hierarchical chirality exist in the ZnO films: helical ZnO crystalline structures that form primary helically coiled nanoplates, secondary helical stacking of these nanoplates, and tertiary nanoscale circinate aggregates formed by several stacked nanoplates. These films exhibited optical activity (OA) at 380 nm and in the range of 200-800 nm and created circularly polarized luminescence centered at 510 nm and Raman OA at 50-1400 cm(-1) , which was attributed to electronic transitions, scattering, photoluminescent emission, and Raman scattering in a dissymmetric electric field. The unprecedented strong OA could be attributed to multiple light scattering and absorption-enhanced light harvesting in the hierarchical structures.

Ammonia intercalated flower-like MoS2 nanosheet film as electrocatalyst for high efficient and stable hydrogen evolution

Ammonia intercalated flower-like MoS2 electrocatalyst film assembled by vertical orientated ultrathin nanosheet on graphite sheethas been successfully synthesized using one-step hydrothermal method. In this strategy, ammonia can effectively insert into the parallel plane of the MoS2 nanosheets, leading to the expansion of lattice and phase transfer from 2H to 1T, generating more active unsaturated sulfur atoms. The flower-like ammoniated MoS2 electrocatalysts with more active sites and large surface area exhibited excellent HER activity with a small Tafel slope and low onset overpotential, resulting a great enhancement in hydrogen evolution. The high efficient activity and recyclable utilization, as well as large-scale, indicate that it is a very promising electrocatalyst to replace Pt in industry application.

One-step synthesis of highly efficient three-dimensional Cd1-xZnxS photocatalysts for visible light photocatalytic water splitting

Visible light accounts for about 43% of the solar spectrum, and developing highly efficient visible-light-driven photocatalyst is of special significance. In this work, highly efficient three-dimensional (3D) Cd1−xZnxS photocatalysts for hydrogen generation under the irradiation of visible light were synthesized via one-step solvothermal pathway. Scanning electron microscope, X-ray diffractometer, Raman spectrometer, and X-ray photoelectron spectrometer were utilized to characterize the morphology, crystal structure, vibrational states, and surface composition of the obtained 3D Cd1−xZnxS. UV-Vis spectra indicated that the as-synthesized Cd1−xZnxS had appropriate bandgap and position of the conduction band that is beneficial for visible light absorption and photo-generated electron-hole pair separation. Moreover, the 3D structure offers a larger surface area thus supplying more surface reaction sites and better charge transport environment, and therefore, the efficiency of water splitting was improved further.

Self-assembly of versatile tubular-like In2O3 nanostructures

Versatile indium oxide tubular nanostructures (well-aligned nanotube arrays, flower-like tubular structures, and square nanotubes) were fabricated by a facile and reliable chemical vapor deposition (CVD) technique, taking advantage of the self-assembly property and substrate-induced epitaxial growth mechanism. The technique has a few advantages, such as low growth temperature, nonexistence of catalyst, template-free synthesis, direct bonding to the semiconductor substrates, etc. This strategy might extend the approach of synthesizing desirable nanostructures of other important low-melting metal oxides for potential applications.

Electrochemically induced Ti3+ self-doping of TiO2 nanotube arrays for improved photoelectrochemical water splitting

AbstractWe report a facile electrochemical reduction method to synthesize Ti3+-self-doped TiO2 nanotube arrays (TNTs), where the effects of reduction duration and potential on the photoelectrochemical performance were systematically investigated. The X-ray photoelectron spectroscopy and electron paramagnetic resonance spectra confirmed the presence of Ti3+ in the TNTs. Under the optimum reduction condition, the Ti3+-self-doped TNTs exhibited remarkably enhanced photocurrent density and photoconversion efficiency, which were nearly 3.1 and 1.75 times that of pristine TNTs, respectively. The enhancement of PEC performance is due to the improved electrical conductivity, accelerated charge transfer rate at the TNTs/electrolyte interface, as well as the improved visible light response, which is elucidated by electrochemical impedance spectra, Mott–Schottky, and UV–Vis diffuse reflection spectra.