Abstract

We thoroughly investigated the carrier-phonon relaxation process in 2D halide perovskites with the general formula of (BA)2(MA)n-1PbnI3n+1, where n = 2, 3, and 4, by femtosecond transient absorption spectroscopy. A significant enhancement of the hot phonon bottleneck effect is observed in the natural multiple quantum well with n = 2 and 3. Specifically, the sample with n = 3 shows a 1000 ps hot carrier relaxation time to reach room temperature, which is 10 times longer compared with its three-dimensional counterpart. We believe that both the organic cation and quantum confinement effect are responsible for this phenomenon. The acoustic phonon cannot propagate due to the decrease in group velocity caused by the confinement effect in such a quantum well structure. In addition, the confined acoustic phonons can up-convert to optical phonons due to the presence of a “hybrid phonon” induced by the organic cation. This result suggests a promising way to obtain long-live hot carrier materials.

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