Related Experiment Video
Updated: Oct 13, 2025

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy
Published on: June 28, 2016
Tuning Spin-Polarized Lifetime in Two-Dimensional Metal-Halide Perovskite through Exciton Binding Energy
Xihan Chen1,2, Haipeng Lu1,3, Kang Wang1,4
1National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
Abstract:
Metal-halide perovskite semiconductors have attracted attention for opto-spintronic applications where the manipulation of charge and spin degrees of freedom have the potential to lower power consumption and achieve faster switching times for electronic devices. Lower-dimensional perovskites are of particular interest since the lower degree of symmetry of the metal-halide connected octahedra and the large spin-orbit coupling can potentially lift the spin degeneracy. To achieve their full application potential, long spin-polarized lifetimes and an understanding of spin-relaxation in these systems are needed. Here, we report an intriguing spin-selective excitation of excitons in a series of 2D lead iodide perovskite (n = 1) single crystals by using time- and polarization-resolved transient reflection spectroscopy. Exciton spin relaxation times as long as ∼26 ps at low excitation densities and at room temperature were achieved for a system with small binding energy, 2D EOA2PbI4 (EOA = ethanolamine). By tuning the excitation density and the exciton binding energy, we identify the dominant mechanism as the D'yakonov-Perel (DP) mechanism at low exciton densities and the Bir-Aronov-Pikus (BAP) mechanism at high excitation densities. Together, these results provide new design principles to achieve long spin lifetimes in metal-halide perovskite semiconductors.
More Related Videos
08:12Low Pressure Vapor-assisted Solution Process for Tunable Band Gap Pinhole-free Methylammonium Lead Halide Perovskite Films
Published on: September 8, 2017
09:00Experimental Methods for Spin- and Angle-Resolved Photoemission Spectroscopy Combined with Polarization-Variable Laser
Published on: June 28, 2018
Related Concept Videos
Spin–Spin Coupling Constant: Overview
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Valence Bond Theory
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Atomic Nuclei: Nuclear Spin State Overview