ABSTRACT
Fully ambient-processed and highly efficient methylammonium lead iodide (MAPbI3) perovskite films are very desirable for industrial manufacturing of perovskite solar cells (PSCs). To date, most reported highly efficient MAPbI3 PSCs rely on the fabrication of lead iodide (PbI2) films inside the glovebox. Here we report a simple fabrication method using extra dry isopropanol (IPA100) for obtaining uniform and loosely packed PbI2 film, which leads to a uniform and highly crystalline MAPbI3 film under ambient conditions. Compared with recently reported results (10%-15%) using IPA treatment in the glovebox, we achieved over 16% efficiency of PSCs while fabricating perovskite films in fully ambient conditions. We have found the removal of even trace amounts of water from IPA to be a key factor for the successful ambient fabrication of PbI2 films, as the high polarity of water negatively influences the crystallinity and morphology of the PbI2 film.
ABSTRACT
The charge separation and charge recombination dynamics in P3HT-ZnO and P3HT-dye-ZnO bulk heterojunction organic-inorganic hybrid solar cells (OIHSCs) prepared by a one-pot method were studied using a transient absorption (TA) method, both for optical absorption of P3HT in the visible region and for optical absorption of SQ36 in the NIR region. In the case of P3HT-ZnO, the charge separation was very fast, occurring within 1 ps. On the other hand, high charge recombination between electrons in the surface states and/or the conduction band of ZnO and holes in P3HT was observed. In the case of P3HT-dye-ZnO, we found that the charge recombination could be greatly suppressed by locating the dye at the P3HT/ZnO interfaces while maintaining a fast charge separation rate (a few ps to 10 ps). Our findings provide one methodology for the design of OIHSCs for improving their conversion efficiency, which is to position the dye at the appropriate BHJ interfaces.
