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Meysoun Jabrane

Publications and source records attributed to Meysoun Jabrane.

2 recordsLinked to original sources

Scalable Conformal MoSx Catalyst for Efficient Hydrogen Evolution at Industrial-Level Current Density in Alkaline Electrolyzers

The development of simple and scalable fabrication strategies for cost-effective electrodes is crucial to advance water splitting in alkaline water electrolyzers (AWEs). Here, we present a coating-annealing method to conformally coat a MoSx catalyst layer onto a porous Ni foam (NF) substrate. By controlling the annealing process, the composition of the MoSx layer could be tuned from MoS2 to MoS3 and its catalytic performance for hydrogen evolution reaction (HER) in alkaline media was optimized. The MoS3@NF synthesized by this method achieved industrially relevant HER current densities of 200 mA/cm2 at a low overpotential of 246 mV, maintaining stable operation for over 240 h. The MoS3@NF cathode, combined with a stainless steel anode, enabled an alkaline water electrolyzer (AWE) cell to operate steadily at 1.96 V and 1 A/cm2 for 1000 h. This performance surpasses that of most of the previously reported water electrolyzers employing MoSx-based cathodes. Our work demonstrates the potential of MoS3 (with its abundant edge-sulfur atoms serving as active sites) as a high-performance cathode material for industrial AWEs.

cond-mat.mtrl-sci

A Nanocrystal Synthesis Derived Approach to Silver Bismuth Iodide Layered Double Perovskites with Aliphatic Amines: (CnH(2n+1)NH3)4AgBiI8

Lead-free iodide double perovskites are an interesting class of materials since they combine a relatively low toxicity (compared to the lead counterpart) with the small bandgap typical of iodide-based perovskite structures. Their reported number is small due to their lower structural stability compared to the chloride and bromide analogues, hence their difficult synthesis. The structural constraints that limit stability, on the other hand, can be much relieved in layered, organic-inorganic perovskites. Following this line of thought, we report here a successful fast precipitation route to iodide layered (CnH(2n+1)NH3)4AgBiI8 (n = 10, 12, and 14) double perovskites that borrow concepts from the synthesis of colloidal nanocrystals. X-ray diffraction studies revealed for these compounds a monoclinic crystal structure containing edge-sharing alternated [AgI6] and [BiI6] octahedra. These materials have experimental band gaps of 2.1 eV, as also corroborated by theoretical calculations. We have also investigated their phase transitions by thermal analysis and temperature-dependent diffraction and found them to be similar to their lead-based layered perovskite counterparts.

cond-mat.mtrl-sci