New 'optical neural engine’ solves partial differential equations
Peer-Reviewed Publication
Updates every hour. Last Updated: 4-Jul-2025 19:11 ET (4-Jul-2025 23:11 GMT/UTC)
University of Utah engineers encode partial differential equations in light and feed them into newly designed optical neural engine, or ONE, to accelerate machine learning.
A study in Science Advances that describes a new soft robotic system was co-led by Harvard Professor L. Mahadevan in collaboration with Professor Ho-Young Kim at Seoul National University. Their work paves new directions for future, low-power swarm robotics.
The new robots, called link-bots, are comprised of centimeter-scale, 3D-printed particles strung into V-shaped chains via notched links and are capable of coordinated, life-like movements without any embedded power or control systems.
Washington, D.C., June 2025: In a defining moment for global public health and the fight against chronic disease, more than 350 leading scientists, policy makers, ethicists, journalists and civil society representatives from over 50 countries and 150 major organizations gathered at the inaugural Human Exposome Moonshot Forum. What is expected by participants to be seen, in-time, as a historic event, this Washington, D.C. gathering marks the formal launch of a bold and globally coordinated, bottom-up initiative to map the physical, chemical, biological and psychosocial exposures that people experience during their lifetime. Known as the "exposome" experts agree that these influences account for over 80% of chronic disease today. As Professor Thomas Hartung of Johns Hopkins University, Member of the Organizing Committee and the Forum’s Host stated: “We are not promising a rocket launch to a ready destination. We are building the launchpad. The exposome is not the rocket, it is the moon. Each new data point, each discovery, is a step towards that distant but vital world where prevention replaces reaction and science empowers health.”
Physicists at the University of Oxford have set a new global benchmark for the accuracy of controlling a single quantum bit, achieving the lowest-ever error rate for a quantum logic operation—just 0.000015%, or one error in 6.7 million operations. This record-breaking result represents nearly an order of magnitude improvement over the previous benchmark, set by the same research group a decade ago.
Biological cells exhibit nearly transparent characteristics with weak absorption properties in the visible light spectrum, resulting in extremely low optical contrast between cells and the surrounding medium under traditional bright-field microscopy. To enhance imaging contrast, conventional methods rely on chemical staining or fluorescent labeling, introducing exogenous absorption/fluorescence probes to visualize cellular structures. However, these approaches suffer from drawbacks such as phototoxicity, photobleaching, and poor biocompatibility, severely limiting long-term dynamic observation of living cells. Quantitative phase imaging (QPI) utilizes the inherent physical property of cellular phase (thickness) as an endogenous “probe”, resolving cellular thickness, refractive index, and 3D topography with nanoscale accuracy. It provides a new avenue for dynamic observation of living cells and nanoscale biological studies.
As a significant branch of QPI technology, differential phase contrast (DPC) has attracted considerable attention due to its advantages of being non-interferometric and low-cost. However, its theoretical framework relies on the “weak object approximation”, linking intensity images to sample phase through a linear model. This simplified model introduces two fundamental limitations. First, the phase reconstruction result is highly dependent on the precise modeling of the phase transfer function (PTF) under an ideal pupil. In practical optical systems, however, wavefront aberrations couple with the sample phase, leading to significant reconstruction errors. Second, the conventional half-circle illumination suffers from the problem of PTF response cancellation, resulting in the loss of low-frequency phase information and making it difficult to accurately reconstruct the fine structure of weak phase objects. These limitations significantly compromise the robustness of DPC in non-ideal optical environments and restrict its practical applicability in frontier biological research, such as cellular morphology characterization and tracking of subcellular dynamic processes.