A blue‐light emitting material based on a boron complex containing heteroaromatic phosphonate ligand is synthesized and characterized. The Phospho‐Fries rearrangement is used in the synthesis route of the ligand as a convenient method of introducing phosphonate groups into phenols. Structural, thermal and photophysical properties of the resulting oxazaborinin phosphonate compound have been characterized. DFT geometry optimizations were studied as well as the spatial position and symmetry of the HOMO and LUMO. Good thermal stability up to 250 °C enables vacuum deposition methods next to solution processing. Combining the work function with the optical band gap from UV‐Vis measurements shows that band alignment is possible with standard contact materials. Photoluminescence reveals an emission peak at 428 nm, which is suitable for a blue light‐emitter.

In this contribution, a nanoarchitectural approach was employed to produce a nanolayer of polyoxometalate (POM) on the surface of a glassy carbon electrode (GCE) to achieve a higher surface area with higher electrocatalytic activity toward the electrochemical hydrogen evolution reaction (HER). To accomplish this, the well-known layer-by-layer (LbL) technique was employed, which involved the alternate adsorption of the POM, Na 0, abbreviated as [(TBA)Mo 12 (AleThio) 4 ], and polyethyleneimine (PEI) polymer. This nanolayered electrode exhibited catalytic properties toward the HER in 0.5 M H 2 SO 4 with the resulting polarization curves indicating an increase in the HER activity with the increasing number of POM layers, and the overpotential required for this reaction was lowered by 0.83 V when compared with a bare GCE. The eighth PEI/[(TBA)Mo 12 (AleThio) 4 ] bilayer exhibited a significantly lower HER overpotential of −0.077 V at a current density of 10 mA cm −2 . Surface characterization of the LbL-assembled nanolayers was carried out using X-ray photoelectron spectroscopy, atomic force microscopy, and scanning electron microscopy. We believe that the synergetic effect of the positively charged PEI polymer and the catalytically active molybdate POM is the cause for the successful response to the electrochemical HER.

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