Related Experiment Video
Updated: Mar 21, 2026

09:11
Controlled Rotation of Human Observers in a Virtual Reality Environment
Published on: April 21, 2022
3.1K
Steering chiral active Brownian motion via stochastic position-orientation resetting
1University of Vermont, Department of Physics, Burlington, Vermont 05405, USA.
Physical Review. E
|March 20, 2026
Summary
Stochastic resetting can control circular motion in chiral active particles. This method tunes particle dynamics, enhancing transport efficiency for applications like targeted delivery and search tasks.
Area of Science:
- Physics
- Statistical Mechanics
- Soft Matter
Background:
- Active systems often exhibit circular swimming, limiting transport efficiency.
- Chiral active Brownian particles display biased motion due to inherent asymmetry.
Purpose of the Study:
- Investigate the impact of stochastic position-orientation resetting on chiral active particle dynamics.
- Determine if resetting can overcome limitations imposed by circular motion and enhance transport.
Main Methods:
- Simulated two-dimensional chiral active Brownian particles.
- Implemented stochastic position-orientation resetting protocols.
- Analyzed steady-state mean-squared displacement, excess kurtosis, and orientation autocorrelation.
Main Results:
- Stochastic resetting effectively interrupts circular motion, enabling tunable dynamics.
- Mean-squared displacement shows non-monotonic dependence on rotational diffusion for infrequent resets.
- A spatiotemporal state diagram reveals three distinct states influenced by activity, chirality, and resetting.
Conclusions:
- Chirality enriches the dynamical landscape, allowing tunable transitions between transport modes.
- Resetting protocols can transform chiral active dynamics, optimizing search and transport.
- This strategy offers practical solutions for enhancing efficiency in micro- and nanomachines.
Related Concept Videos
Prochirality
5.3K
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...
5.3K
Properties of Enantiomers and Optical Activity
23.1K
It is essential to understand the difference between chiral and achiral interactions and the implications thereof in optical activity and their applications. Just as our feet, which are chiral, interact uniquely with chiral objects, such as a pair of shoes, but identically with achiral socks, enantiomers of a molecule exhibit different properties only when they interact with other chiral media. An example of a significant implication from this facet is the phenomenon known as optical activity,...
23.1K
Chirality in Nature
17.9K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
17.9K
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
3.7K
Replacing each alpha-hydrogen in chloroethane by bromine (or a different functional group) yields a pair of enantiomers. Such protons are called prochiral or enantiotopic and are related by a mirror plane. Enantiotopic protons are chemically equivalent in an achiral environment. Because most proton NMR spectra are recorded using achiral solvents, enantiotopic hydrogens yield a single signal.
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
3.7K
Molecules with Multiple Chiral Centers
16.3K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
16.3K
Chirality
31.9K
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...
31.9K

