posted on 2017-02-22, 00:00authored byJoseph L. Garrett, Elizabeth M. Tennyson, Miao Hu, Jinsong Huang, Jeremy N. Munday, Marina S. Leite
Hybrid organic–inorganic
perovskites based on methylammonium lead (MAPbI3) are an
emerging material with great potential for high-performance and low-cost
photovoltaics. However, for perovskites to become a competitive and
reliable solar cell technology their instability and spatial variation
must be understood and controlled. While the macroscopic characterization
of the devices as a function of time is very informative, a nanoscale
identification of their real-time local optoelectronic response is
still missing. Here, we implement a four-dimensional imaging method
through illuminated heterodyne Kelvin probe force microscopy to spatially
(<50 nm) and temporally (16 s/scan) resolve the voltage of perovskite
solar cells in a low relative humidity environment. Local open-circuit
voltage (Voc) images show nanoscale sites
with voltage variation >300 mV under 1-sun illumination. Surprisingly,
regions of voltage that relax in seconds and after several minutes
consistently coexist. Time-dependent changes of the local Voc are likely due to intragrain ion migration
and are reversible at low injection level. These results show for
the first time the real-time transient behavior of the Voc in perovskite solar cells at the nanoscale. Understanding
and controlling the light-induced electrical changes that affect device
performance are critical to the further development of stable perovskite-based
solar technologies.