Effect of Thiophene Insertion on X-Shaped Anthracene-Based Hole-Transporting Materials in Perovskite Solar Cells.

In this work, two novel tetra-substituted X-shaped molecules X1 and X2 that were constructed with anthracene as the central core and arylamine as the donor groups have been synthesized. The HTMs X1 and X2 were synthesized in two steps from industrially accessible and moderately reasonable beginning reagents. These new HTMs are described in terms of utilization of light absorption, energy level, thermal properties, hole mobility (µh), and film-forming property. The photovoltaic performances of these HTMs were effectively assessed in perovskite solar cells (PSCs). The devices based on these HTMs accomplished an overall efficiency of 16.10% for X1 and 10.25% for X2 under standard conditions (AM 1.5 G and 100 mW cm-2). This precise investigation provides another perspective on the use of HTMs in PSCs with various device configurations.

Polycyclic Arenes Dihydrodinaphthopentacene-based Hole-Transporting Materials for Perovskite Solar Cells Application.

In this paper, two D-π-D type compounds, C1 and C2, containing dihydrodinaphthopentacene (DHDNP) as a π-bridge, p-methoxydiphenylamine and p-methoxytriphenylamine groups as the donor groups were synthesized. The four 4-hexylphenyl groups at the sp3 -carbon bridges of DHDNP were acquainted with control morphology and improving solubility. The light absorption, energy level, thermal properties, and application as hole-transporting materials in perovskite solar cells of these compounds were fully investigated. The HOMO/LUMO levels and energy gaps of these DHDNP-based molecules are suitable for use as hole-transporting materials in PSCs. The best power conversion efficiencies of the PVSCs based on the C1 and C2 are 15.96% and 12.86%, respectively. The performance of C1 is comparable to that of the reference compound spiro-OMeTAD (16.38%). Compared with spiro-OMeTAD, the C1-based PVSC device showed good stability, which was slightly decreased to 98.68% of its initial efficiency after 48 h and retained 81% of its original PCE after 334 h without encapsulation. These results reveal the potential usefulness of the DHDNP building block for further development of economical and highly efficient HTMs for PVSCs.