Related Experiment Video
Updated: Jan 13, 2026

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Spin Qubits Candidate in Transition-Metal-Ion doped Halide Double Perovskites
Sakarn Khamkaeo1, Kunpot Mopoung1, Kingshuk Mukhuti2
1Department of Physics, Chemistry and Biology (IFM), Linköping University, Linköping, Sweden.
None:
Solid-state spin qubits offer a promising route toward scalable quantum technologies. Here we demonstrate that, despites of a nuclear-spin-rich host of halide double perovskites (HDPs), transition-metal centers (Cr3+ and Fe3+ ions) are a good candidate for spin qubits exhibiting long-lived electron spin coherence with = 29.5 µs and 21.2 µs at 4 K, respectively. Notably, spin localization facilitates a well-defined electron-nuclear (e-N) spin rotation between the electron spin and the neighboring nuclear spins of 35,37Cl and133Cs. The resulting e-N spin cluster is readily beneficial for a target nuclear-spin sensing. For the Cr3+ spin centers, the optical transitions associated with Cr3+ spin centers is spin-selective thereby paving a way for optical addressing of spins. Our findings from these spin ensemble studies establish HDPs as a new promising platform for creating solid-state spin qubits using simple and inexpensive solution-based single crystal growth methods, broadening material applications of halide perovskites.
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
04:14Facile Synthesis of Colloidal Lead Halide Perovskite Nanoplatelets via Ligand-Assisted Reprecipitation
Published on: October 1, 2019
Related Concept Videos
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...
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,...
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...