Search for: All records

The intelligence of the human biological system is enabled by the highly distributed sensing receptors on soft skin that can distinguish various stimulations or environmental cues, thus establishing the fundamental logic of sensing and physiological regulation or response. To replicate biological perception, two approaches have emerged: artificial nervous systems that utilize soft electronics as biomimetic receptors to convert external stimuli into frequency-encoded signals, and biohybrid solutions that integrate living cells, plants, or even live animals with electronic components to decode environmental cues for life-like sensations. However, most current biohybrid approaches for artificial sensation are based on eukaryotic cells, which suffer from slow growth, stringent culture conditions, environmental susceptibility, and short lifespans, thus limiting their integration into practical wearables or robotic sensory skins. Here, we introduce fungi-based printable “Mycoelectronics”, which are created by additive bioprinting of living fungal mycelium networks onto stretchable electronics, as a practical living thermo-responsive sensory platform. This Mycoelectronics approach leverages fungi’s capacity for rapid biological responsiveness, cultivability with exponential growth, stability and self-healing in ambient conditions, bioprintability for scalable manufacturing, and mechanical flexibility for seamless integration with soft electronics. Critically, we discovered that the thermal responsiveness of the fungal network arises from intrinsic cellular processes—specifically, heat-induced vacuole remodeling and fusion, which modulate ionic transport and thus the electrical conductivity of the mycelial cells and networks, enabling a rapid temperature response. By bridging the gap between cell biology and soft electronics, the Mycoelectronics device with a living mycelium network functions as a thermal sensation system with rapid response and intrinsic self-healing properties, autonomously restoring sensing capabilities after damage or autonomously establishing sensor pathways in hard-to-reach locations. Furthermore, by integrating fungal thermal sensing with electronic circuits, we established a hybrid bioelectronic reflex arc that can actuate muscles and initiate diverse actions, suggesting promising applications in future neurorobotics and neuroprosthetics. 

Abstract Soft (flexible and stretchable) biosensors have great potential in real-time and continuous health monitoring of various physiological factors, mainly due to their better conformability to soft human tissues and organs, which maximizes data fidelity and minimizes biological interference. Most of the early soft sensors focused on sensing physical signals. Recently, it is becoming a trend that novel soft sensors are developed to sense and monitor biochemical signalsin situin real biological environments, thus providing much more meaningful data for studying fundamental biology and diagnosing diverse health conditions. This is essential to decentralize the healthcare resources towards predictive medicine and better disease management. To meet the requirements of mechanical softness and complex biosensing, unconventional materials, and manufacturing process are demanded in developing biosensors. In this review, we summarize the fundamental approaches and the latest and representative design and fabrication to engineer soft electronics (flexible and stretchable) for wearable and implantable biochemical sensing. We will review the rational design and ingenious integration of stretchable materials, structures, and signal transducers in different application scenarios to fabricate high-performance soft biosensors. Focus is also given to how these novel biosensors can be integrated into diverse important physiological environments and scenariosin situ, such as sweat analysis, wound monitoring, and neurochemical sensing. We also rethink and discuss the current limitations, challenges, and prospects of soft biosensors. This review holds significant importance for researchers and engineers, as it assists in comprehending the overarching trends and pivotal issues within the realm of designing and manufacturing soft electronics for biochemical sensing. 

Abstract The present study compares a single‐band chorus wave against a banded chorus wave observed by Van Allen Probes at adjacent times, and demonstrates that the single‐band chorus wave is associated with an anisotropic electron population over a broad energy range, while the banded chorus wave is accompanied by an electron phase space density plateau and an electron anisotropy reduction around Landau resonant energies. We further compare banded chorus waves with different spectral gap widths, and show that a wider spectral gap is associated with electron isotropization extending to higher energies with respect to the equatorial Landau resonant energy. We suggest that early generated chorus waves isotropize electrons via Landau resonant acceleration, and the waves that propagate to higher latitudes isotropize electrons at higher energies. The isotropization extending to higher energies leads to a larger spectral gap of new chorus waves after electrons bounce back to the equator. 

Abstract We recently reported the finding of elementary rising‐tone emissions embedded within each harmonic of magnetosonic waves, by investigating wave electric field waveforms measured by Van Allen Probes. The present study further uncovers a new set of fine structures of magnetosonic waves, namely, each elementary rising‐tone may consist of a series of mini harmonics spaced around the O⁺gyrofrequency. The measured ion distributions suggest that the proton ring distribution provides free energy to excite the waves, whilst the O⁺ions suppress the wave growth around multiples of O⁺gyrofrequency, resulting in the formation of mini harmonics. Further investigation suggests that the warm plasma dispersion relation, that is, the ion Bernstein mode instabilities, may contribute to the formation of mini harmonics. The mini harmonic structure implies a new mechanism of energy redistribution among ion species in space plasmas, potentially providing a new acceleration mechanism for O⁺ions in the magnetosphere. 

Microorganisms can efficiently navigate in anisotropic complex fluids, but the precise swimming mechanisms remain largely unexplored. Their dynamics are determined by the interplay between multiple effects, including the fluid's orientation order, swimmer's undulatory gait, and the finite length. Here we extend the numerical study of the two-dimensional undulatory motions of a flexible swimmer in lyotropic liquid-crystalline polymers (LCPs) by Lin et al. (2021) to the scenarios of arbitrary swimming directions with respect to the nematic director. The swimmer is modeled as a nearly inextensible yet flexible fiber with imposed traveling-wave like actuation. We investigate the orientation-dependent swimming behaviors in nematic LCPs for an infinite long sheet (i.e., Taylor's swimming sheet model) and finite-length swimmers. We demonstrate that the swimmer must be sufficiently stiff to produce undulatory deformations to gain net motions. Moreover, a motile finite-length swimmer can reorient itself to swim parallel with the nematic director, due to a net body torque arising from the asymmetric distribution of the polymer force along the body.