Unveiling Charge Transfer and Recombination Dynamics in 3D/2D Heterostructure via Ultrafast Spectroscopy for Efficient Perovskite Solar Cells

Abstract Charge transfer properties between 3D and 2D perovskite layers play a key role in determining the performance of 3D/2D heterostructure perovskite solar cells (PSCs). However, the exact photophysical behaviors at 3D/2D perovskite heterostructure remain ambiguous, which makes it challenging to form the desired 3D/2D heterostructure. Herein, via combining the state‐of‐the‐art ultrafast spectroscopies of femtosecond transient absorption spectroscopy, transient absorption microscopy and time‐resolved photoluminescence spectroscopy, charge transfer and recombination dynamics are unveiled at 3D/2D perovskite heterostructure, for comparison, where the 2D layers are fabricated through the two distinct approaches of organic ligand surface reaction (2D L ) and 2D crystal seed direct deposition (2D S ), respectively. 3D/2D S heterostructure exhibits superior hole transfer from 3D to 2D S , featuring a large spatial diffusion constant and high charge mobility compared to 3D/2D L , attributed to the higher phase purity and the lower defects in 2D S . Moreover, 3D/2D S heterostructure yields suppressed nonradiative recombination, reduced Langevin recombination, and increased quasi‐Fermi level splitting, significantly aiding fast photoinduced charge transfer at such heterostructure. These advantages are further confirmed by a remarkably improved PSC efficiency using 3D/2D S , especially in terms of enhanced open‐circuit voltage and diminished energy loss. This work sheds light on the dynamics at 3D/2D heterostructures, providing a promising guideline for designing 3D/2D high‐performance PSCs.