Enhanced stability of sub-nanometric iridium decorated graphitic carbon nitride for H2 production upon hydrous hydrazine decomposition.

Stabilizing metal nanoparticles is vital for large scale implementations of supported metal catalysts, particularly for a sustainable transition to clean energy, e.g., H2 production. In this work, iridium sub-nanometric particles were deposited on commercial graphite and on graphitic carbon nitride by a wet impregnation method to investigate the metal-support interaction during the hydrous hydrazine decomposition reaction. To establish a structure-activity relationship, samples were characterized by transmission electron microscopy and X-ray photoelectron spectroscopy. The catalytic performance of the synthesized materials was evaluated under mild reaction conditions, i.e. 323 K and ambient pressure. The results showed that graphitic carbon nitride (GCN) enhances the stability of Ir nanoparticles compared to graphite, while maintaining remarkable activity and selectivity. Simulation techniques including Genetic Algorithm geometry screening and electronic structure analyses were employed to provide a valuable atomic level understanding of the metal-support interactions. N anchoring sites of GCN were found to minimise the thermodynamic driving force of coalescence, thus improving the catalyst stability, as well as to lead charge redistributions in the cluster improving the resistance to poisoning by decomposition intermediates.

Selective decomposition of hydrazine over metal free carbonaceous materials.

Herein we report a combined experimental and computational investigation unravelling the hydrazine hydrate decomposition reaction on metal-free catalysts. The study focuses on commercial graphite and two different carbon nanofibers, pyrolytically stripped (CNF-PS) and high heat-treated (CNF-HHT), respectively, treated at 700 and 3000 °C to increase their intrinsic defects. Raman spectroscopy demonstrated a correlation between the initial catalytic activity and the intrinsic defectiveness of carbonaceous materials. CNF-PS with higher defectivity (ID/IG = 1.54) was found to be the best performing metal-free catalyst, showing a hydrazine conversion of 94% after 6 hours of reaction and a selectivity to H2 of 89%. In addition, to unveil the role of NaOH, CNF-PS was also tested in the absence of alkaline solution, showing a decrease in the reaction rate and selectivity to H2. Density functional theory (DFT) demonstrated that the single vacancies (SV) present on the graphitic layer are the only active sites promoting hydrazine decomposition, whereas other defects such as double vacancy (DV) and Stone-Wales (SW) defects are unable to adsorb hydrazine fragments. Two symmetrical and one asymmetrical dehydrogenation pathways were found, in addition to an incomplete decomposition pathway forming N2 and NH3. On the most stable hydrogen production pathway, the effect of the alkaline medium was elucidated through calculations concerning the diffusion and recombination of atomic hydrogen. Indeed, the presence of NaOH helps the extraction of H species without additional energetic barriers, as opposed to the calculations performed in a polarizable continuum medium. Considering the initial hydrazine dissociative adsorption, the first step of the dehydrogenation pathway is more favourable than the scission of the N-N bond, which leads to NH3 as the product. This first reaction step is crucial to define the reaction mechanisms and the computational results are in agreement with the experimental ones. Moreover, comparing two different hydrogen production pathways (with and without diffusion and recombination), we confirmed that the presence of sodium hydroxide in the experimental reaction environment can modify the energy gap between the two pathways, leading to an increased reaction rate and selectivity to H2.

Effects of oxygen functionalities on hydrous hydrazine decomposition over carbonaceous materials.

Metal-free heterogeneous catalysis is promising in the context of H2 generation. Therefore, establishing structure-activity relationships is a crucial issue to improve the development of more efficient catalysts. Herein, to evaluate the reactivity of the oxygen functionalities in carbonaceous materials, commercial functionalized pyrolytically stripped carbon nanofibers (CNFs) were used as catalysts in the liquid-phase hydrous hydrazine decomposition process and its activity was compared to that of a pristine CNF material. Different oxygenated groups were inserted by treating CNFs with hydrogen peroxide for 1 h (O1-H2O2) and HNO3 for 1 h (O1-HNO3) and 6 h (O6-HNO3). An increase in activity was observed as a function of the oxidizing agent strength (HNO3 > H2O2) and the functionalization time (6 h > 1 h). A thorough characterization of the catalysts demonstrated that the activity could be directly correlated with the oxygen content (O6-HNO3 > O1-HNO3 > O1-H2O2 > CNFs) and pointed out the active sites for the reaction at carbon-oxygen double bond groups (CO and COOH). Systematic DFT calculations supported rationalization of the experimental kinetic trends with respect to each oxygen group (CO, C-O-C, C-OH and COOH).

Hydrous Hydrazine Decomposition for Hydrogen Production Using of Ir/CeO2: Effect of Reaction Parameters on the Activity.

In the present work, an Ir/CeO2 catalyst was prepared by the deposition-precipitation method and tested in the decomposition of hydrazine hydrate to hydrogen, which is very important in the development of hydrogen storage materials for fuel cells. The catalyst was characterised using different techniques, i.e., X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) equipped with X-ray detector (EDX) and inductively coupled plasma-mass spectroscopy (ICP-MS). The effect of reaction conditions on the activity and selectivity of the material was evaluated in this study, modifying parameters such as temperature, the mass of the catalyst, stirring speed and concentration of base in order to find the optimal conditions of reaction, which allow performing the test in a kinetically limited regime.