New light on the photocatalytic performance of NH4V4O10 and its composite with rGO.

Solar-driven photocatalysis has shown great potential as a sustainable wastewater treatment technology that utilizes clean solar energy for pollutant degradation. Consequently, much attention is being paid to the development of new, efficient and low-cost photocatalyst materials. In this study, we report the photocatalytic activity of NH4V4O10 (NVO) and its composite with rGO (NVO/rGO). Samples were synthesized via a facile one-pot hydrothermal method and successfully characterized using XRD, FTIR, Raman, XPS, XAS, TG-MS, SEM, TEM, N2 adsorption, PL and UV‒vis DRS. The results indicate that the obtained NVO and NVO/rGO photocatalysts exhibited efficient absorption in the visible wavelength region, a high content of V4+ surface species and a well-developed surface area. Such features resulted in excellent performance in methylene blue photodegradation under simulated solar light illumination. In addition, the composite of NH4V4O10 with rGO accelerates the photooxidation of the dye and is beneficial for photocatalyst reusability. Moreover, it was shown that the NVO/rGO composite can be successfully used not only for the photooxidation of organic pollution but also for the photoreduction of inorganic pollutants such as Cr(VI). Finally, an active species trapping experiment was conducted, and the photodegradation mechanism was discussed.

The valance state of vanadium-key factor in the flexibility of potassium vanadates structure as cathode materials in Li-ion batteries.

Potassium hexavanadate (K2V6O16·nH2O) nanobelts have been synthesized by the LPE-IonEx method, which is dedicated to synthesis of transition metal oxide bronzes with controlled morphology and structure. The electrochemical performance of K2V6O16·nH2O as a cathode material for lithium-ion batteries has been evaluated. The KVO nanobelts demonstrated a high discharge capacity of 260 mAh g-1, and long-term cyclic stability up to 100 cycles at 1 A g-1. The effect of the vanadium valence state and unusual construction of the nanobelts, composed of crystalline and amorphous domains arranged alternately were also discussed in this work. The ex-situ measurements of discharged electrode materials by XRD, MP-AES, XAS and XPS show that during the subsequent charge/discharge cycle the potassium in the K2V6O16·nH2O structure are replacing by lithium. The structural stability of the potassium hexavandate during cycling depends on the initial vanadium valence state on the sample surface and the presence of the "fringe free" domains in the K2V6O16·nH2O nanobelts.