RESUMO
We report here an expanded porphyrinoid, cyclo[2]pyridine[8]pyrrole, 1, that can exist at three closed-shell oxidation levels. Macrocycle 1 was synthesized via the oxidative coupling of two open chain precursors and fully characterized by means of NMR and UV-vis spectroscopies, MS, and X-ray crystallography. Reduction of the fully oxidized form (1, blue) with NaBH4 produced either the half-oxidized (2, teal) or fully reduced forms (3, pale yellow), depending on the amount of reducing agent used and the presence or absence of air. Reduced products 2 or 3 can be oxidized to 1 by various oxidants (quinones, FeCl3, and AgPF6). Macrocycle 1 also undergoes proton-coupled reductions with I-, Br-, Cl-, SO32-, or S2O32- in the presence of an acid. Certain thiol-containing compounds likewise reduce 1 to 2 or 3. This conversion is accompanied by a readily discernible color change, making cyclo[2]pyridine[8]pyrrole 1 able to differentiate biothiols, such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH).
RESUMO
The ability of carrier selective contact is mainly determined by the surface passivation and work function for dopant-free materials applied in crystalline silicon (c-Si) solar cells, which have received considerable attention in recent years. In this contribution, a novel electron-selective material, lanthanide terbium trifluoride (TbFx ), with an ultra-low work function of 2.4 eV characteristic, is presented, allowing a low contact resistivity (ρc ) of ≈3 mΩ cm2 . Additionally, the insertion of ultrathin passivated SiOx layer deposited by PECVD between TbFx and n-Si resulted in ρc only increase slightly. SiOx /TbFx stack eliminated fermi pinning between aluminum and n-type c-Si (n-Si), which further enhanced the electron selectivity of TbFx on full-area contacts to n-Si. Last, SiOx /TbFx /Al electron-selective contacts significantly improves the open circuit voltage (Voc ) for silicon solar cells, but rarely impacts the short circuit current (Jsc ) and fill factor (FF), thus champion efficiency cell achieved approaching 22% power conversion efficiency (PCE). This study indicates a great potential for using lanthanide fluorides as electron-selective material in photovoltaic devices.