Publications by authors named "Y J Dappe"

Capturing sunlight to fuel the water splitting reaction (WSR) into O and H is the leitmotif of the research around artificial photosynthesis. Organic semiconductors have now joined the quorum of materials currently dominated by inorganic oxides, where for both families of compounds the bandgaps and energies can be adjusted synthetically to perform the Water Splitting Reaction. However, elaborated and tedious synthetic pathways are necessary to optimize the photophysical properties of organic semiconductors.

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There has been considerable interest in building switching functions into self-assembled monolayers with switching actuated by external stimuli such as light, electrical current, heat, pressure or chemical changes. In this study, dual switching functionality has been built into azobenzene based molecular monolayers. Switching behaviour has been compared for unsubstituted azobenzene monolayer adsorbates and two other monolayers whose position on the terminal phenyl group is substituted by ethyl and isopropyl chains, respectively.

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Phosphorene, a semiconducting two-dimensional material, has recently attracted huge interest due to its potential applications in opto-electronics. The first attempts to synthesize phosphorene were based mainly on mechanical and chemical exfoliations. A few years later, different groups reported the synthesis of phosphorene using the molecular beam epitaxy process, which opened the way for research on physical properties.

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Due to its diverse allotropes and intriguing properties, 2D phosphorus, also known as phosphorene, is a material of great interest. Here, the successful growth of flat hexagonal 2D phosphorus on Au(111) is reported. Starting from phosphorus linear chains at low coverage, a porous network and finally an extended 2D flat hexagonal (HexP) layer while increasing phosphorus deposition is formed.

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We synthesized a sublimable molecular spin crossover Fe(II) complex based on the Schiff base tridentate ligand qsal-NEt (5-diethylamino-2-((quinolin-8-ylimino)methyl)phenol). The compound undergoes a transition in temperature with thermally induced excited spin state-trapping (TIESST) for high-temperature sweep rates, which can be suppressed by reducing the sweep rate. The X-ray absorption spectroscopy (XAS) studies on the microcrystalline powder confirm the TIESST effect.

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