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Updates every hour. Last Updated: 9-May-2026 17:15 ET (9-May-2026 21:15 GMT/UTC)
In a new Nature Physics study, researchers created particle-like so-called “vortex knots” inside chiral nematic liquid crystals, a twisted fluid similar to those used in LCD screens. For the first time, these knots are stable and could be reversibly switched between different knotted forms, using electric pulses to fuse and split them.
EurekAlert Summary
Order from Chaos: Technion and SJTU Researchers Reveal Hidden Photon Behavior
A collaborative team from the Technion–Israel Institute of Technology and Shanghai Jiao Tong University has identified a previously unknown physical phenomenon showing how order can emerge from complete disorder. Reported in Nature Materials, the study describes the discovery of photon “spin locking” generated by Brownian motion in nanometric systems.
The research was led by Prof. Erez Hasman of the Technion’s Faculty of Mechanical Engineering and the Helen Diller Quantum Center, together with Prof. Bo Wang, head of the Spin Nanophotonics Group at SJTU’s School of Physics and Astronomy and a former postdoctoral researcher in Prof. Hasman’s group.
The team uncovered a “spin-locking effect induced by Brownian motion,” demonstrating that photons scattered from randomly moving nanoparticles unexpectedly align into a specific spin state. This result overturns the long-standing assumption that Brownian motion produces fully chaotic, unpolarized scattering.
By illuminating nanoparticles suspended in a liquid, the researchers showed that sideways-scattered photons exhibit a locked spin state—an emergent form of order arising precisely from the particles’ random motion. The effect also enables characterization of particle size and material type, offering a new tool for nanoparticle identification.
“Our discovery beautifully illustrates the importance of experimental physics,” said Prof. Hasman. “It is often the most disordered systems that reveal the deepest order. We believe this phenomenon will open new avenues in nanoparticle characterization and future optical technologies.”
The study was supported by the National Science Foundations of Israel and China.
Osaka Metropolitan University researchers enhanced Saccharomyces cerevisiae to increase its tolerance for high 2,3-butanediol concentrations. This was achieved by introducing mutations into the genomic DNA and successfully obtaining a mutant strain that proliferates 122 times more than the parent strain.
Ocean data assimilation systems combine data assimilation with numerical ocean models to predict ocean conditions. Researchers recently created the Yin-He Global Ocean Data Assimilation and Forecast System (YHGO) to provide more accurate estimations of oceanic conditions than older platforms.
Researchers at Peking University and collaborators have revealed evidence of Mott insulator with thermally induced melting behavior in kagome compound Nb₃Cl₈. Using graphene-based chemical potential mapping, the team directly measured a strongly temperature-dependent Mott gap that remains robust up to 300 K, providing a new platform to study strong electron correlations and flat-band physics under ambient conditions.
Tokyo, Japan – Scientists from Tokyo Metropolitan University have re-engineered the popular Lattice-Boltzmann Method (LBM) for simulating the flow of fluids and heat, making it lighter and more stable than the state-of-the-art. By formulating the algorithm with a few extra inputs, they successfully got around the need to store certain data, some of which span the millions of points over which a simulation is run. Their findings might overcome a key bottleneck in LBM: memory usage.
Fluorine is critical for biomedicine. This element can help drug compounds be more potent and last longer in the body, and its radioactive isotope, fluorine-18, powers medical imaging techniques such as positron emission tomography (PET). But scientists have long struggled with adding fluorine to the most common chemical bonds—carbon–hydrogen (C–H) bonds—in a way that’s precise, efficient and compatible with the molecules used to create many modern medicines. There’s been particular interest in constructing carbon–fluorine bonds stereoselectively—that is, attaching fluorine from a specific direction in space to create the needed fluorinated stereoisomer (“mirror image” form) of the target molecule. Stereoselective C–H fluorination has remained one of the most challenging synthetic transformations, and the limited approaches developed to date have relied on expensive specialty chemicals or complicated, multi-step procedures. Now, chemists at Scripps Research have developed a long-sought method to stereoselectively attach fluorine atoms to complex, drug-like molecules in a single step using cheap, readily available fluoride salts.