Homogeneous optical linewidths in hybrid Ruddlesden-Popper metal halides can only be measured using nonlinear spectroscopy
arXiv:2107.03199 · doi:10.1021/acs.jpcc.2c00658
Abstract
The homogeneous photoluminescence spectral linewidth in semiconductors carries a wealth of information on the coupling of primary photoexcitations with their dynamic environment as well as between multi-particles. In the limit in which inhomogeneous broadening dominates the total optical linewidths, the inhomogeneous and homogeneous contributions can be rigorously separated by temperature-dependent %linear spectral measurements such as steady-state photoluminescence spectroscopy. This is possible because the only temperature-dependent phenomenon is optical dephasing, which defines the homogeneous linewidth, since this process is mediated by scattering with phonons. However, if the homogeneous and inhomogeneous linewidths are comparable, as is the case in hybrid Ruddlesden-Popper metal halides, the temperature dependence of linear spectral measurement \emph{cannot} separate rigorously the homogeneous and inhomogeneous contributions to the total linewidth because the lineshape does \emph{not} contain purely Lorentzian components that can be isolated by varying the temperature. Furthermore, the inhomogeneous contribution to the steady-state photoluminescence lineshape is not necessarily temperature independent if driven by diffusion-limited processes, particularly if measured by photoluminescence. Nonlinear coherent optical spectroscopies, on the other hand, do permit separation of homogeneous and inhomogeneous line broadening contributions in all regimes of inhomogeneity. Consequently, these offer insights into the nature of many-body interactions that are entirely inaccessible to temperature-dependent linear spectroscopies. When applied to Ruddlesden-Popper metal halides, these techniques have indeed enabled us to quantitatively assess the exciton-phonon and exciton-exciton scattering mechanisms.
arXiv commentPerspective artile
References in corpus (15)
- Local polar fluctuations in lead halide perovskite crystals
- Intrinsic Exciton Linewidth in Monolayer Transition Metal Dichalcogenides
- Phonon coherences reveal the polaronic character of excitons in two-dimensional lead-halide perovskites
- Optical spectroscopy of two-dimensional layered perovskite
- Real-Time Observation of Exciton-Phonon Coupling Dynamics in Self-Assembled Hybrid Perovskite Quantum Wells
- Perspective: Exciton polarons in two-dimensional hybrid metal-halide perovskites
- Exciton-polaron spectral structures in two dimensional hybrid lead-halide perovskites
- Stable biexcitons in two-dimensional metal-halide perovskites with strong dynamic lattice disorder
- Electron-phonon couplings inherent in polarons drive exciton dynamics in two-dimensional metal-halide perovskites
- Vibrational Coupling Modifies Spectral Diffusion in Core-Shell Colloidal Quantum Dots
- Simultaneous Existence of Confined and Delocalized Vibrational Modes in Colloidal Quantum Dots
- Towards Engineering Intrinsic Linewidths and Line-Broadening in Perovskite Nanoplatelets
- Enhanced screening and spectral diversity in many-body elastic scattering of excitons in two-dimensional hybrid metal-halide perovskites
- Stochastic scattering theory for excitation induced dephasing: Time-dependent nonlinear coherent exciton lineshapes
- Stochastic scattering theory for excitation induced dephasing: Comparison to the Anderson-Kubo lineshape
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- QuDPy: A Python-Based Tool For Computing Ultrafast Non-linear Optical Responses
- Stochastic exciton-scattering theory of optical lineshapes: Renormalized many-body contributions