Related Experiment Video
Updated: May 10, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Chiral symmetry breaking in superfluid 3He-A
H Ikegami1, Y Tsutsumi, K Kono
1Low Temperature Physics Laboratory, RIKEN, Wako, Saitama, Japan. hikegami@riken.jp
Researchers directly detected orbital chirality in superfluid helium-3 (3He-A) using electron transport measurements. This observation confirms chiral symmetry breaking and the selection of handedness at the superfluid transition.
Area of Science:
- Condensed Matter Physics
- Quantum Fluids
- Superfluidity
Background:
- Spontaneous symmetry breaking is crucial in physics.
- Superfluid helium-3 (3He-A) exhibits orbital chirality due to symmetry breaking.
- Direct detection of this chirality has been difficult.
Purpose of the Study:
- To directly detect the orbital chirality in superfluid helium-3 (3He-A).
- To demonstrate chiral symmetry breaking in this system.
- To investigate the selection of chirality handedness.
Main Methods:
- Transport measurements of electrons trapped below the free surface of superfluid 3He-A.
- Observation of the intrinsic Magnus force on moving electrons.
- Analysis of electron motion to infer chirality direction.
Main Results:
- Direct detection of electron chirality in superfluid 3He-A.
- Observed intrinsic Magnus force on moving electrons, reflecting chirality.
- Demonstrated selection of either right- or left-handed chirality at the superfluid transition.
Conclusions:
- Directly detected chirality in superfluid 3He-A.
- The intrinsic Magnus force serves as a direct probe of chirality.
- The observed selection of handedness confirms chiral symmetry breaking.
Related Concept Videos
Chirality
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...
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
Prochirality
Molecules with Multiple Chiral Centers
Symmetry Elements in a Crystal

