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Meenakshi Pegu

Publications and source records attributed to Meenakshi Pegu.

2 recordsLinked to original sources

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

Improving the Stability of Colloidal CsPbBr3 Nanocrystals with an Alkylphosphonium Bromide as Surface Ligand Pair

In this study, we synthesised a phosphonium-based ligand, trimethyl(tetradecyl)phosphonium bromide (TTP-Br), and employed it in the post-synthesis surface treatment of Cs-oleate-capped CsPbBr3 NCs. The photoluminescence quantum yield (PLQY) of the NCs increased from 60% to more than 90%, as a consequence of replacing Cs-oleate with TTP-Br ligand pairs. Density functional theory calculations revealed that TTP+ ions bind to the NC surface by occupying Cs+ surface sites and orienting one of their P-CH3 bonds perpendicular to the surface, akin to quaternary ammonium passivation. Importantly, TTP-Br-capped NCs exhibited higher stability in air compared to didodecyldimethylammonium bromide-capped CsPbBr3 NCs (which is considered a benchmark system), retaining 90% of their PLQY after six weeks of air exposure. Light-emitting diodes fabricated with TTP-Br-capped NCs achieved a maximum external quantum efficiency of 17.2 %, demonstrating the potential of phosphonium-based molecules as surface ligands for CsPbBr3 NCs in optoelectronic applications.

cond-mat.mtrl-sci