Highly Efficient Spin-Filtering Transport in Chiral Hybrid Copper Halides
Ying Lu1, Qian Wang2, Ruilin He3
1Department of Materials Physics and Chemistry, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, China.
Angewandte Chemie (International Ed. in English)
|August 23, 2021
Summary
Researchers developed eco-friendly chiral copper halides for spintronics. These materials demonstrate high spin polarization efficiency, offering a stable, lead-free alternative for advanced spin filtering applications.
Area of Science:
- Materials Science
- Condensed Matter Physics
- Organic Chemistry
Background:
- Chiral hybrid organic-inorganic perovskites show promise for chiral-induced spin selectivity (CISS).
- There is a need for stable, non-toxic, lead-free materials for spintronic applications like spin filtering.
- Existing materials often contain toxic elements like lead, limiting their practical use.
Purpose of the Study:
- To synthesize and investigate novel chiral hybrid copper halides for CISS applications.
- To explore the potential of copper-based materials as stable and eco-friendly alternatives to lead-based perovskites.
- To evaluate the spin-polarized charge transport properties of these new materials.
Main Methods:
- Synthesis of chiral hybrid copper halides (R/S-MBA)₂CuX₄ (X=Cl, Br).
- Characterization of structural and electronic properties.
- Magnetic force microscopy measurements to assess spin-polarized charge transport.
Main Results:
- Successfully synthesized air-stable, low-toxicity chiral hybrid copper halides with 0D CuX₄ tetrahedral motifs.
- Observed efficient spin-polarized charge transport with up to 90% efficiency in both chloride and bromide compounds.
- Identified that (R/S-MBA)₂CuBr₄ exhibits lower chiroptical activity compared to its chloride counterpart despite similar structures.
Conclusions:
- Chiral hybrid copper halides expand the scope of the CISS effect into stable, eco-friendly metal-organic halide systems.
- These materials show significant potential for spintronic applications utilizing transition-metal hybrid systems.
- The findings pave the way for developing next-generation spintronic devices with enhanced safety and stability.
Related Concept Videos
Chirality
27.3K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
27.3K
Chirality at Nitrogen, Phosphorus, and Sulfur
6.2K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
6.2K
Prochirality
4.2K
The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
4.2K
Extraction: Advanced Methods
631
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
631
Stereoisomerism
12.7K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
12.7K
Colors and Magnetism
12.6K
Color in Coordination Complexes
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...
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...
12.6K


