806
(Invited) Control of Film Morphology, Crystal Structure and Band Energy for Perovskite Solar Cells

Monday, 30 May 2016: 11:00
Aqua 314 (Hilton San Diego Bayfront)
E. W. G. Diau, C. M. Tsai, and H. P. Wu (National Chiao Tung University)
The development of all solid-state thin-film solar cells has reached a new milestone when the devices made of organometallic lead halide perovskite materials were reported with power conversion efficiency (PCE) exceeding 20 %. The key issue to make a device with a great photovoltaic performance for this kind of solar cells is to control the film morphology of perovskite under different experimental conditions. Varied mesoporous TiO2 nanostructures were applied to show the morphological effect of the scaffold on the device performance with a mesoscopic heterojuction. Anti-solvent method was applied to improve the morphology and crystallinity of the perovskite films to obtain device performance exceeding PCE 16 %. Varied additives were applied to control the formation morphology of the perovskite nanocrystals with a planar heterojunction. Moreover, we developed a simple drop-casting method via solvent-solvent extraction to grow dense and uniform perovskite nanocrystals at room temperature for carbon-based mesoscopic solar cells free of an organic hole-transport layer. The CH3NH3PbI3/ N-methyl-2-pyrrolidone (NMP) precursor solution (40 %) was first dripped onto a substrate with film configuration TiO2/Al2O3/C and infiltrated at 70 °C for 10 min. The perovskite substrate was next immersed in a bath of diethyl ether at 25 °C for 30 min. Third, the solvent-extracted substrate was stored in a dry box (humidity 50 %) at 25 °C for at least 100 h to complete the crystal growth. The device performance attained an efficiency 12.3 % of power conversion (PCE), which is significantly greater than that of DMF (6.3 %) and NMP (8.3 %) devices using traditional thermal annealing. For tin-rich perovskite, we designed and synthesized alloyed Sn-Pb mixed halide perovskites by dipping the precursor solutions on the mesoporous films with the TiO2/Al2O3/C configuration to form solar cells free of organic HTM. When 30 mol% of SnF2 additive was added in the tin-rich mix halide precursor solution, the device performance was improved from PCE 2.2 % (without SnF2) to PCE 4.3 % (with SnF2) with little effect of hysteresis; the short-circuit current density JSC has reached a remarkable level with 23.33±0.73 mA cm-2.