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Ultrafast oscillatory transient absorption (TA) dynamics are observed in single crystals of hybrid organic-inorganic perovskite (CHNH)PbX with X = I, Br, Cl. High-density photoinduced charges, low binding energy of the excitons, efficient generation and high mobility of charges, and long diffusion length of both excitons and charges led to transient interconversion between excitons and charges with high efficiency, which is responsible for the oscillatory TA dynamics at re-excitation by the probe pulses. The pump pulses initiated a quasi-equilibrium scheme of coexisting excitons and charges with high densities, the probe pulse triggered a perturbation through interconversion between these two kinds of excited "particles," which was overlapped on the intrinsic exciton relaxation dynamics, producing an oscillatory modulation with time delay.

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All-inorganic perovskite films have emerged as promising candidates for laser gain materials owing to their outstanding optoelectronic properties and straightforward solution processing. However, the performance of blue perovskite lasing still lags far behind due to the inevitable high density of defects. Herein, we demonstrate that defects can be utilized instead of passivated/removed to form bound excitons to achieve excellent blue stimulated emission in perovskite films.

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