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Koushik Gayen

Publications and source records attributed to Koushik Gayen.

2 recordsLinked to original sources

Polaron-Driven Spin Funneling through Rashba-Split Bands in Mixed-Phase Quasi-Two-Dimensional Ruddlesden-Popper Perovskites

Metal halide perovskites (MHPs) exhibit pronounced spin-orbit coupling (SOC) as a result of their heavy metal constituents, leading to distinctive electronic properties such as Rashba type band splitting which make them promising candidates for next generation spintronic applications. Here, using circularly polarized luminescence (CPL) and polarization dependent pump-probe spectroscopy, we found that spin polarization is present across all phases of our two-dimensional (2D) Ruddlesden-Popper (RP) mixed-phase perovskites, (C6H7SNH3)2 (CH3NH3)n-1PbnI3n+1 (n=1-4), irrespective of the number of inorganic layers. The origin of these spin polarized bands is attributed to the Rashba effect. Interestingly, the highly disordered nature of this system facilitates remarkably efficient ultrafast funneling of photoexcited spin-polarized excitons from the pure 2D phase (n=1) to higher-n phases at room temperature. We demonstrate that significant polaron formation due to the inherent soft crystal lattice and higher exciton-phonon interaction is responsible for the observed spin funneling effect in mixed-phase 2D RP perovskites. Polaron act as a protective mechanism for spin-polarized excitons, preserving their spin information through the screening of omnipresent phonon-induced momentum scattering. These findings not only offer valuable guidance for the design of 2D RP perovskites with pronounced Rashba effects but also unveil a compelling class of solution-processed perovskites capable of efficient spin-preserving energy transport at room temperature.

cond-mat.mtrl-sci

Bidirectional Photoinduced Carrier Transfer in Fluorinated Quasi-2D Perovskites Governing Enhanced Photocurrent Generation

Quasi-two-dimensional (quasi-2D) metal halide perovskites exhibit rich phase heterogeneity that profoundly influences light-matter interactions and charge transport. However, the fundamental mechanisms governing carrier transfer across distinct phases remain poorly understood. Here, we demonstrate effective electron-hole separation in fluorinated multilayered quasi-2D perovskite films nominally prepared for three layers, using femtosecond transient absorption spectroscopy. The films are revealed to comprise a heterogeneous phase distribution (with 1, 2, 3 layers and bulk) naturally stacked along the growth direction. Our ultraviolet photoelectron spectroscopy (UPS) measurements, show the type-two band alignment between the small-n (layer number) phases and the bulk. This alignment drives charge separation via both direct and sequential carrier transfer mechanisms, whereby electrons preferentially migrate into the bulk domains while holes accumulate in the small-n layers, extending even to single layer phase-a process only rarely observed in previous studies. The nearly symmetric transfer times of electrons and holes yield an efficient and balanced spatial separation of carriers. Global target analysis employing a carrier transfer model quantitatively reproduces the spectral evolution, providing a rigorous validation of the mechanism. Nonetheless, we found photocurrent enhancement in the diode devices of this quasi-2D perovskite as a consequence of the efficient transfer of photocarriers in the opposite directions. This work delivers a comprehensive picture of interphase charge transfer in fluorinated quasi-2D perovskites and highlights strategies to engineer directional separation pathways for high-performance photovoltaic, optoelectronic, and quantum devices.

cond-mat.mtrl-sci