Enhancement of hydrogen storage performance in cost effective novel g–C3N4–MoS2–Ni(OH)2 ternary nanocomposite fabricated via hydrothermal method

Energy from hydrogen has been looked upon with great favours to encounter the shortage of fossil fuels in energy generation. Safety issues and storage concerns of hydrogen has been a major drawback in this regard. Here, a novel material g–C3N4–MoS2–Ni(OH)2 is crafted to achieve promisingly sufficient storage capacity for hydrogen. Hydrothermal route is optimized in a best possible way to achieve flower like structure of MoS2. It is then blended with fine sheets of Ni(OH)2 and as synthesized g-C3N4 to develop the promising nanocomposite g–C3N4–MoS2–Ni(OH)2. Morphological investigation using TEM and SEM analyses revealed flower-like structure near fine sheets of Ni(OH)2 and g-C3N4. Fruitfully, the modified surface of the nanocomposite resulted in an enhanced hydrogen storage capability. The hydrogen sorption experiments were carried out at 150 °C for 15 and 30 min intervals under 10 bar hydrogen pressure, and the hydrogen desorption process was carried out from room temperature (RT) to 200 °C with a ramping rate of 15 °C min−1 in an argon medium with a flow rate of 100 mL min−1. During non-isothermal H2 desorption, S150 composite exhibits better hydrogen storage capacity of 2.79 and 3.21 wt% under hydrogenation intervals of 15 and 30 min respectively. Furthermore, S150 desorbed 3.7 wt% H2 in 20 min at isothermal desorption of 200 °C

Construction novel highly active photocatalytic H2 evolution over noble-metal-free trifunctional Cu3P/CdS nanosphere decorated g-C3N4 nanosheet

Hydrogen energy possesses immense potential in developing a green renewable energy system. However, a significant problem still exists in improving the photocatalytic H2 production activity of metal-free graphitic carbon nitride (g-C3N4) based photocatalysts. Here is a novel Cu3P/CdS/g-C3N4 ternary nanocomposite for increasing photocatalytic H2 evolution activity. In this study, systematic characterizations have been carried out using techniques like X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HR-TEM), Raman spectra, UV–Vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), surface area analysis (BET), electrochemical impedance (EIS), and transient photocurrent response measurements. Surprisingly, the improved 3CP/Cd-6.25CN photocatalyst displays a high H2 evolution rate of 125721 μmol h−1 g−1. The value obtained exceeds pristine g-C3N4 and Cu3P/CdS by 339.8 and 7.6 times, respectively. This could be the maximum rate of hydrogen generation for a g–C3N4–based ternary nanocomposite ever seen when exposed to whole solar spectrum and visible light (λ > 420 nm). This research provides fresh perspectives on the rational manufacture of metal-free g-C3N4 based photocatalysts that will increase the conversion of solar energy. By reusing the used 3CP/Cd/g-C3N4 photocatalyst in five consecutive runs, the stability of the catalyst was investigated, and their individual activity in the H2 production activity was assessed. To comprehend the reaction mechanisms and emphasise the value of synergy between the three components, several comparison systems are built