Overcoming Charge Confinement in Perovskite Nanocrystal Solar Cells

The small nanoparticle size and long-chain ligands in colloidal metal halide perovskite quantum dots (PeQDs) cause charge confinement, which impedes exciton dissociation and carrier extraction in PeQD solar cells, so they have low short-circuit current density J(sc), which impedes further increases in their power conversion efficiency (PCE). Here, a re-assembling process (RP) is developed for perovskite nanocrystalline (PeNC) films made of colloidal perovskite nanocrystals to increase J(sc) in PeNC solar cells. The RP of PeNC films increases their crystallite size and eliminates long-chain ligands, and thereby overcomes the charge confinement in PeNC films. These changes facilitate exciton dissociation and increase carrier extraction in PeNC solar cells. By use of this method, the gradient-bandgap PeNC solar cells achieve a J(sc) = 19.30 mA cm(-2) without compromising the photovoltage, and yield a high PCE of 16.46% with negligible hysteresis and good stability. This work provides a new strategy to process PeNC films and pave the way for high performance PeNC optoelectronic devices.

Automated summary

A re-assembling process is developed to increase J(sc) and PCE in perovskite nanocrystalline (PeNC) solar cells by eliminating long-chain ligands and increasing crystallite size in PeNC films. This work provides a new approach for the preparation of PeNC films and paves the way for high-performance PeNC optoelectronic devices.