Long Exciton Dephasing Time and Coherent Phonon Coupling in CsPbBr2Cl Perovskite Nanocrystals.
Michael A BeckerLorenzo ScarpelliGeorgian NedelcuGabriele RainòFrancesco MasiaPaola BorriThilo StöferleMaksym V KovalenkoWolfgang LangbeinRainer F MahrtPublished in: Nano letters (2018)
Fully inorganic cesium lead halide perovskite nanocrystals (NCs) have shown to exhibit outstanding optical properties such as wide spectral tunability, high quantum yield, high oscillator strength as well as blinking-free single photon emission, and low spectral diffusion. Here, we report measurements of the coherent and incoherent exciton dynamics on the 100 fs to 10 ns time scale, determining dephasing and density decay rates in these NCs. The experiments are performed on CsPbBr2Cl NCs using transient resonant three-pulse four-wave mixing (FWM) in heterodyne detection at temperatures ranging from 5 to 50 K. We found a low-temperature exciton dephasing time of 24.5 ± 1.0 ps, inferred from the decay of the photon-echo amplitude at 5 K, corresponding to a homogeneous line width (fwhm) of 54 ± 5 μeV. Furthermore, oscillations in the photon-echo signal on a picosecond time scale are observed and attributed to coherent coupling of the exciton to a quantized phonon mode with 3.45 meV energy.
Keyphrases
- energy transfer
- room temperature
- diffusion weighted imaging
- diffusion weighted
- quantum dots
- optical coherence tomography
- contrast enhanced
- magnetic resonance
- solar cells
- living cells
- ionic liquid
- blood pressure
- high efficiency
- working memory
- dual energy
- label free
- perovskite solar cells
- monte carlo
- cerebral ischemia
- fluorescent probe
- brain injury
- blood brain barrier