Matthew Flynn-Hepford1,Arya Ahmadi1,Holland Hysmith1,Yongtao Liu2,Mahshid Ahmadi1,Anton Ievlev2,Bobby Sumpter2,Olga Ovchinnikova2
University of Tennessee- Knoxville1,Oak Ridge National Laboratory2
Matthew Flynn-Hepford1,Arya Ahmadi1,Holland Hysmith1,Yongtao Liu2,Mahshid Ahmadi1,Anton Ievlev2,Bobby Sumpter2,Olga Ovchinnikova2
University of Tennessee- Knoxville1,Oak Ridge National Laboratory2
Hybrid perovskite materials have drawn a lot of attention recently for solar energy applications, but the instability of these materials makes long term efficiency a major issue that needs to be addressed. The weak bonding in methylammonium lead iodide (MAPbI<sub>3</sub>) that enables ion migration can be leveraged for memristivie applications where ion migration needs to be controlled rather than eliminated. We show that in modeled structures, cesium (Cs) doping the MA site (A-site) can enable stronger local bonding with the iodine (I) ions allowing for weak bonding ion conductivity channels that can help control ion migration under applied bias. Cs doped MAPbI<sub>3</sub> films were spin coated on glass/ITO substrates to act as an active layer for memristive devices. Local IV measurements were conducted using an AFM tip and a DC bias was applied to the tip in contact mode in order to induce ion migration. Kelvin probe force microscopy (KPFM) was used to probe the resulting variation in surface potential. The chemical origins of the surface potential variations were investigated using specially resolved time-of-flight scanning ion mass spectroscopy.