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Inspired by the human visual system, photonic synapses with photonic sensing and data memorization offer a promising alternative to traditional von Neumann architectures for neuromorphic computing. This study introduces a multifunctional artificial photonic synapse based on solution-processed PEASnI 2D Ruddlesden-Popper perovskite. By modulation of the applied bias voltage, the PEASnI device can switch between two distinct optoelectronic modes. In the absence of bias, the device operates in the photodetector mode, demonstrating a responsivity of 42.4 mA W. The low dark current of the device allows for a high detectivity of 3.6 × 10 Jones and a broad linear dynamic range of 140 dB. Under reverse bias, the device transitions into a synaptic mode, enabling the observation of several synaptic behaviors, including paired-pulse facilitation, long-term potentiation, spike-frequency-dependent plasticity, and spike-number-dependent plasticity. The synaptic behavior is attributed to band alignment and carrier accumulation in the interfacial layer. Moreover, the synaptic performance of the PEASnI device is further illustrated through simulations of image contrast enhancement and edge detection. This work reveals the potential of PEASnI-based photonic synapses for next-generation neuromorphic vision systems, offering an energy-efficient and highly adaptable approach to optoelectronic computing applications.
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http://dx.doi.org/10.1021/acsami.5c10557 | DOI Listing |
eNeuro
September 2025
Department of Neurology, Long School of Medicine, University of Texas Health Science Center San Antonio, San Antonio, Texas, USA, 78229.
The corticospinal tract (CST) is essential for forelimb-specific fine motor skills. In rodents, it undergoes extensive structural remodeling across development, injury, and disease states, with major implications for motor function. A vast body of literature, spanning numerous injury models, frequently assesses these projections.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Institute of Neuroscience, Technical University of Munich, Munich 80802, Germany.
Amyloid β (Aβ)-dependent circuit dysfunction in Alzheimer's disease (AD) is determined by a puzzling mix of hyperactive and inactive ("silent") brain neurons. Recent studies identified excessive glutamate accumulation as a key Aβ-dependent determinant of hyperactivity. The cellular mechanisms underlying neuronal silence depend on both Aβ and tau protein pathologies, with an unknown role of Aβ.
View Article and Find Full Text PDFNat Commun
August 2025
Department of Neuroscience, Del Monte Institute for Neuroscience, University of Rochester Medical Center, Rochester, NY, USA.
Adolescence is a sensitive period for frontal cortical development and cognitive maturation, marked by heightened structural plasticity in the dopaminergic (DA) mesofrontal circuit. However, the cellular and molecular mechanisms underlying this plasticity remain unclear. Here, we show that microglia, the brain's innate immune cells, are highly responsive to mesofrontal DA signaling during adolescence.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
Inspired by the human visual system, photonic synapses with photonic sensing and data memorization offer a promising alternative to traditional von Neumann architectures for neuromorphic computing. This study introduces a multifunctional artificial photonic synapse based on solution-processed PEASnI 2D Ruddlesden-Popper perovskite. By modulation of the applied bias voltage, the PEASnI device can switch between two distinct optoelectronic modes.
View Article and Find Full Text PDFJ Neurosci
August 2025
Sanders-Brown Center on Aging, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
While cerebrovascular dysfunction and reactive astrocytosis are extensively characterized hallmarks of Alzheimer's disease (AD) and related dementias, the dynamic relationship between reactive astrocytes and cerebral vessels remains poorly understood. Here, we used jGCaMP8f and two photon microscopy to investigate calcium signaling in multiple astrocyte subcompartments, concurrent with changes in cerebral arteriole activity, in fully awake seven-to-eight-month-old male and female 5xFAD mice, a model for AD-like pathology, and wild-type (WT) littermates. In the absence of movement, spontaneous calcium transients in barrel cortex occurred more frequently in astrocyte somata, processes, and perivascular regions of 5xFAD mice.
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