Zinc phthalocyanine absorbance in the near-infrared with application for transparent and colorless dye-sensitized solar cells

Transparent and colorless solar cells are attractive new photovoltaic devices as they could bring new opportunities to harness sunlight energy and particularly for their integration in windows. In this work, a new zinc phthalocyanine was synthesized and investigated as sensitizer in dye-sensitized solar cell (DSSC) for this purpose. The zinc phthalocyanine features a benzoic acid anchoring group and six thio(4-tertbutylphenyl) substituents in ${\alpha }$ position of the phtalocyanine. The dye was characterized by absorption and emission spectroscopy and by electrochemistry. The physico-chemical properties show that the dye fulfills the criteria for such an application. A detailed computational study indicates that the electronic communication with $\mathrm{TiO}_{2}$ conduction is weak owing to the absence of overlapping of the wavefunctions of the dye with those of the $\mathrm{TiO}_{2}$ semiconductor. The photovoltaic performances of the zinc phthalocyanine were measured in $\mathrm{TiO}_{2}$-based DSSC that revealed inefficient electron injection, which certainly can be explained by the weak electronic coupling of the dye with $\mathrm{TiO}_{2}$ that limits electron injection efficiency. A strategy is proposed to make better-performing sensitizers

Voltage-induced modulation of the magnetic exchange in binuclear Fe(iii) complex deposited on Au(111) surface

We present a complete computational study devoted to the deposition of a magnetic binuclear complex on a metallic surface, aimed to obtain insight into the interaction of magnetically coupled complexes with their supporting substrates, as well as their response to external electrical stimuli applied through a surface-molecule-STM molecular junction-like architecture. Our results not only show that the deposition is favorable in two of the four studied orientations, but also, that the magnetic coupling is only slightly perturbed once the complex is adsorbed. We observe that the effects of the applied bias voltage on the magnetic coupling strongly depend on the molecule orientation with respect to the surface and the voltage polarity. Further analysis shows that this behavior is attributable to the stabilization/destabilization of the d-type singly occupied orbitals of the iron centers, reinforced by the strong local electric fields and induced charge densities only present in certain orientations of the deposited molecule and applied voltage polarity.Ministerio de Ciencia e InnovacionFondos Fede