Molecular engineering of oxadiazole-based small organic-functional molecules as hole transporting materials for dopant-free perovskite solar cells

Abstract

The present investigation concerns the synthesis and characterization of new hole-transporting materials (HTMs) for dopant free perovskite solar cells (PSCs). In this work, emphasis is placed on three new HTMs, specifically materials P-H, P-OMe, and P-CN, whose center-core is 2,2'-(4,8-bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene (OBDT) and combined with two donor units of substituted triphenylamine as at both ends along with oxadiazole acceptor units in between donor and OBDT. The fabrication of perovskite solar cell devices using new HTMs and compared the power conversion performance with the standard spiro-OMeTAD HTM. Several spectroscopic techniques were utilized to characterize the properties of the new HTMs, such as FESEM analysis of thin-film morphologies, time-dependent photoluminescence (PL) spectra, and mobility measurements. The HTMs P-OMe established a compressed and steady protective layer on the perovskite layer. This layer contributed to the development of open-circuit voltage (V_OC) and short-circuit current density (J_SC), both of which are crucial for accomplishing high power conversion efficiency (PCE) in PSCs. The PSC device integrating the P-OMe HTM displayed a superior PCE of 21.14 % over an active area of 0.22 cm². This activity was related to the standard device that utilized the standard Spiro-OMeTAD HTM, which accomplished a PCE of 17.46 %. The improved devices with the P-OMe HTM continued about 90 % of their initial PCE throughout maximum power point tracking (MPPT) for 90 days. Furthermore, these devices engaged in their activity over a further 2160 h under various temperature settings (25 °C and 35 °C), probably because of the hydrophobic property of the HTM.