Carbon fiber (CF) reinforced composites are widely used due to their excellent properties. However, the smooth surface and few functional groups of CFs can lead to fiber fractures and pullout, which reduce the service life of the composites. The overall performance of composites can be improved by growing carbon nanotubes (CNTs) on the CF surface. Before this, CF surface should be modified to enhance the loading amount of catalyst particles and thus make the CNTs more uniform. In this paper, CNTs were grown on a CF surface by one-step chemical vapor deposition to prepare multi-scale CNTs/CF reinforcements, and the effects of different methods on the CF surface modification were explored. After setting four intensities of electrochemical anodic oxidation, i.e., 50 C/g, 100 C/g, 150 C/g and 200 C/g, it was found that the distribution and quantity of CNTs were improved under both the 100 C/g and 150 C/g conditions. Considering the influence of electrical intensity on the (002) interplanar spacing of CFs, which affects the mechanical properties of the samples, 100 C/g was finally selected as the optimal electrochemical treatment intensity. This finding provides a reference for continuous and large-scale modification of CF surfaces to prepare CNTs/CF multi-scale reinforcements.Keywords:carbon nanotube;carbon fiber;surface modification;electrochemical anodic oxidation
Photoactive WO 3 is attractive as a photocatalyst for green energy evolution through water splitting. In the present work, an electrochemical anodic oxidation method was used to fabricate a photo-responsive nanotube array-like WO 3 /W (NA-WO 3 /W) photoanode from W foil as a precursor. Compared with a reference commercial WO 3 /W electrode, the NA-WO 3 /W photoanode exhibited enhanced and stable photoelectrocatalytic (PEC) activity for visible-light-driven water splitting with a typical H 2 /O 2 stoichiometric ratio of 2:1 and quantum efficiency of approximately 5.23% under visible-light irradiation from a light-emitting diode ( λ = 420 nm, 15 mW/cm 2 ). The greatly enhanced PEC performance of the NA-WO 3 /Wphotoanode was attributed to its fast electron–hole separation rate, which resulted from the one-dimensional nanotube array-like structure, high crystallinity of monoclinic WO 3 , and strong interaction between WO 3 and W foil. This work paves the way to a facile route to prepare highly active photoelectrodes for solar light transfer to chemical energy .
In this work, we reported the utilization of mesoporous α-Fe2O3 films as optical sensors for detecting organic vapors. The mesoporous α-Fe2O3 thin films, which exhibited obvious Fabry–Perot interference fringes in the reflectance spectrum, were successfully fabricated through electrochemical anodization of Fe foils. Through monitoring the optical thickness of the interference fringes, three typical organic species with different vapor pressures and polarities (hexane, acetone and isopropanol) were applied as probes to evaluate the sensitivity of the α-Fe2O3 based interferometric sensor. The experiment results showed that the as-synthesized mesoporous α-Fe2O3 interferometer displayed high reversibility and stability for the three organic vapors, and were especially sensitive to isopropanol, with a detection limit of about 65 ppmv. Moreover, the photocatalytic properties of α-Fe2O3 under visible light are beneficial for degradation of dodecane vapor residues in the nano-pores and refreshment of the sensor, demonstrating good self-cleaning properties of the α-Fe2O3-based interferometric sensor.
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