The challenges of developing neuromorphic vision systems inspired by the human eye come not only from how to recreate the flexibility, sophistication, and adaptability of animal systems, but also how ...to do so with computational efficiency and elegance. Similar to biological systems, these neuromorphic circuits integrate functions of image sensing, memory and processing into the device, and process continuous analog brightness signal in real-time. High-integration, flexibility and ultra-sensitivity are essential for practical artificial vision systems that attempt to emulate biological processing. Here, we present a flexible optoelectronic sensor array of 1024 pixels using a combination of carbon nanotubes and perovskite quantum dots as active materials for an efficient neuromorphic vision system. The device has an extraordinary sensitivity to light with a responsivity of 5.1 × 10
A/W and a specific detectivity of 2 × 10
Jones, and demonstrates neuromorphic reinforcement learning by training the sensor array with a weak light pulse of 1 μW/cm
.
An extremely rare non‐Kramers holmium(III) single‐ion magnet (SIM) is reported to be stabilized in the pentagonal‐bipyramidal geometry by a phosphine oxide with a high energy barrier of 237(4) cm−1. ...The suppression of the quantum tunneling of magnetization (QTM) at zero field and the hyperfine structures originating from field‐induced QTMs can be observed even from the field‐dependent alternating‐current magnetic susceptibility in addition to single‐crystal hysteresis loops. These dramatic dynamics were attributed to the combination of the favorable crystal‐field environment and the hyperfine interactions arising from 165Ho (I=7/2) with a natural abundance of 100 %.
An extremely rare non‐Kramers holmium(III) single‐ion magnet is reported. The suppression of the quantum tunneling of magnetization at zero field and the hyperfine structures were observed in AC magnetic susceptibility measurements, and were attributed to the combination of a favorable crystal‐field environment and the hyperfine interactions arising from 165Ho (I=7/2) with a natural abundance of 100 %.
Quantum Fisher information matrix (QFIM) is a core concept in theoretical quantum metrology due to the significant importance of quantum Cramér-Rao bound in quantum parameter estimation. However, ...studies in recent years have revealed wide connections between QFIM and other aspects of quantum mechanics, including quantum thermodynamics, quantum phase transition, entanglement witness, quantum speed limit and non-Markovianity. These connections indicate that QFIM is more than a concept in quantum metrology, but rather a fundamental quantity in quantum mechanics. In this paper, we summarize the properties and existing calculation techniques of QFIM for various cases, and review the development of QFIM in some aspects of quantum mechanics apart from quantum metrology. On the other hand, as the main application of QFIM, the second part of this paper reviews the quantum multiparameter Cramér-Rao bound, its attainability condition and the associated optimal measurements. Moreover, recent developments in a few typical scenarios of quantum multiparameter estimation and the quantum advantages are also thoroughly discussed in this part.
High‐temperature dielectric polymers are in constant demand for the multitude of high‐power electronic devices employed in hybrid vehicles, grid‐connected photovoltaic and wind power generation, to ...name a few. There is still a lack, however, of dielectric polymers that can work at high temperature (> 150 °C). Herein, a series of all‐organic dielectric polymer composites have been fabricated by blending the n‐type molecular semiconductor 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTCDA) with polyetherimide (PEI). Electron traps are created by the introduction of trace amounts of n‐type small molecule semiconductor NTCDA into PEI, which effectively reduces the leakage current and improves the breakdown strength and energy storage properties of the composite at high temperature. Especially, excellent energy storage performance is achieved in 0.5 vol.% NTCDA/PEI at the high temperatures of 150 and 200 °C, e.g., ultrahigh discharge energy density of 5.1 J cm−3 at 150 °C and 3.2 J cm−3 at 200 °C with high discharge efficiency of 85–90%, which is superior to its state‐of‐the‐art counterparts. This study provides a facile and effective strategy for the design of high‐temperature dielectric polymers for advanced electronic and electrical systems.
This study reports the novel all‐organic dielectric composite films of 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTCDA)/polyetherimide (PEI) by using a facile solution casting method. By judiciously introducing semiconducting NTCDA into PEI, electron traps are successfully constructed, effectively reducing the leakage current and improving the breakdown strength. Finally, excellent high‐temperature energy storage performance is achieved in 0.5 vol.% NTCDA/PEI at 150 and 200 °C.
A large nonlinear optical (NLO) coefficient and a wide band gap are two crucial but contradictory parameters that are difficult to achieve simultaneously in a single infrared (IR) NLO compound. A ...salt‐inclusion chalcogenide (SIC), LiLiCs2ClGa3S6 (1), was prepared that presents a nanosized tunnel framework constructed from monotype chalcogenide tetrahedra. Highly oriented covalent GaS4 tetrahedra in the host lead to a moderate second harmonic generation response (0.7 AgGaS2), and ionic guests effectively broaden the band gap to the widest value (4.18 eV) among all IR NLO chalcogenides, thereby achieving a remarkable balance between NLO efficiency and band gap.
The salt‐inclusion chalcogenide LiLiCs2ClGa3S6 is presented, which features a 3D framework composed of Ga3S6 nanosized tunnels. Introduction of an ionic guest to the covalent chalcogenide host produces a material with a moderate nonlinear optical (NLO) coefficient and an ultrawide band gap (Eg). These characteristics are promising for the development of infrared (IR) NLO materials.
Necroptosis plays an essential role in acute kidney injury and is mediated by receptor-interacting protein kinase 1 (RIPK1), receptor-interacting protein kinase 3 (RIPK3), and mixed lineage kinase ...domain-like pseudokinase (MLKL). A novel RIPK3 inhibitor, compound 42 (Cpd-42) alleviates the systemic inflammatory response. The current study was designed to investigate whether Cpd-42 exhibits protective effects on acute kidney injury and reveal the underlying mechanisms.
The effects of Cpd-42 were determined in vivo through cisplatin- and ischaemia/reperfusion (I/R)-induced acute kidney injury and in vitro through cisplatin- and hypoxia/re-oxygenation (H/R)-induced cell damage. Transmission electron microscopy and periodic acid-Schiff staining were used to identify renal pathology. Cellular thermal shift assay and RIPK3-knockout mouse renal tubule epithelial cells were used to explore the relationship between Cpd-42 and RIPK3. Molecular docking and site-directed mutagenesis were used to determine the binding site of RIPK3 with Cpd-42.
Cpd-42 reduced human proximal tubule epithelial cell line (HK-2) cell damage, necroptosis and inflammatory responses in vitro. Furthermore, in vivo, cisplatin- and I/R-induced acute kidney injury was alleviated by Cpd-42 treatment. Cpd-42 inhibited necroptosis by interacting with two key hydrogen bonds of RIPK3 at Thr94 and Ser146, which further blocked the phosphorylation of RIPK3 and mitigated acute kidney injury.
Acting as a novel RIPK3 inhibitor, Cpd-42 reduced kidney damage, inflammatory response and necroptosis in acute kidney injury by binding to sites Thr94 and Ser146 on RIPK3. Cpd-42 could be a promising treatment for acute kidney injury.
This study aims to evaluate the effects of cold atmospheric plasma (CAP) treatment on the bonding of resin cement to high-translucency zirconia. Zirconia specimens were subjected to different ...treatments: no treatment (ZrT), 10-methacryloyloxydecyl dihydrogen phosphate (MDP)-containing primer (ZrT-M), alumina particle air-abrasion with/without MDP-containing primer (ZrT-AM/ZrT-A), CAP with/without MDP-containing primer (ZrT-PM/ZrT-P). The surface topography, wettability, and chemical composition were evaluated. The shear bond strength (SBS) was tested before and after thermocycling. CAP did not alter the morphology, increased the wettability, and decreased the carbon/oxygen ratio of zirconia surface. The SBSs of ZrT-PM and ZrT-P were significantly higher than the other groups. After thermocycling, ZrT-A, ZrT-M, ZrT-AM, and ZrT-P showed comparable SBSs, all of which were lower than ZrT-PM. It was concluded that CAP improved the bonding performance of high-translucency zirconia without damaging its surface. The combination of CAP with MDP further enhanced the bond strength and may enable durable bonding.
Resolving how Earth surface redox conditions evolved through the Proterozoic Eon is fundamental to understanding how biogeochemical cycles have changed through time. The redox sensitivity of cerium ...relative to other rare earth elements and its uptake in carbonate minerals make the Ce anomaly (Ce/Ce*) a particularly useful proxy for capturing redox conditions in the local marine environment. Here, we report Ce/Ce* data in marine carbonate rocks through 3.5 billion years of Earth’s history, focusing in particular on the mid-Proterozoic Eon (i.e., 1.8 – 0.8 Ga). To better understand the role of atmospheric oxygenation, we use Ce/ Ce* data to estimate the partial pressure of atmospheric oxygen (pO2) through this time. Our thermodynamics-based modeling supports a major rise in atmospheric oxygen level in the aftermath of the Great Oxidation Event (~ 2.4 Ga), followed by invariant pO2 of about 1% of present atmospheric level through most of the Proterozoic Eon (2.4 to 0.65 Ga).
•We report high-precision K isotopes of two weathering profiles developed on basalts.•Deposition of aeolian dust and formation of secondary minerals control K isotopic composition of bauxite ...profiles.•Weathering of igneous rocks leads to loss of isotopically heavy K from the continents.•Heavy K isotopic composition in modern seawater results from both continental weathering and silicate fixation.
Non-traditional stable isotopes (e.g., Li, Mg, and Si) are increasingly used as tracers for studying Earth's surface processes. The isotopes of potassium (K), a highly soluble and mobile element during weathering, could be a promising new tracer for continental weathering; however, the K isotopic variations in weathering profile has not been directly studied due to previous analytical difficulties. Recent high-precision measurements revealed that K isotopes in global river waters are fractionated from the Bulk Silicate Earth (BSE) value, indicating they are influenced by chemical weathering of the crust. Isotopic fractionation during chemical weathering is one of several processes that could ultimately lead to ∼0.6‰ difference of δ41K between the BSE and modern seawater. In order to determine the direction and controlling factors of K isotopic fractionation during basalt weathering, especially under intense weathering conditions, we measured K isotopic compositions in two sets of bauxite developed on the Columbia River Basalts, together with fresh parental basalt and aeolian deposit samples using a recently developed high-precision method. Results show that K isotopic variations among fresh basalts and aeolian dust are limited, close to the BSE value. Extreme K depletion (>99%) and K isotopic fractionation (δ41K up to 0.5 ‰) are observed in bauxite drill cores due to intense chemical weathering. The top of the weathering profiles shows less depletion in K abundances and the δ41K values are closer to those of the fresh basalts and aeolian dusts, likely due to addition of aeolian dust at the tops of both profiles. The weathered products are generally depleted in heavy K isotopes, which is consistent with heavier K isotopic compositions observed in river water and seawater. The δ41K in bauxites displays a positive correlation with K2O contents as well as δ7Li, indicating the behaviors of K and Li isotopes are comparable during chemical weathering. This study shows that K concentrations and its isotopic compositions are sensitive tracers of chemical weathering and could be good weathering proxies over Earth's history.
The feedback between CO2 sources and sinks through chemical weathering is one of the important reasons why Earth has maintained a habitable climate for over four billion years. The lithium (Li) ...isotopic system is a promising tracer of silicate weathering, but the mechanisms causing its isotope fractionation during weathering remain ambiguous. Here, we performed batch experiments of Li adsorption to one of the common clay minerals -kaolinite in three sets, including the time-series, pH-dependent, and concentration-control sets. Our results demonstrate that the liquid-solid Li isotope fractionation reaches up to 36‰, with up to 99% initial Li being adsorbed on kaolinite. The magnitudes of Li adsorption and isotope fractionation increase with reaction time, and reach the steady-state after ∼1000 min. The magnitude of Li isotope fractionation increases with the adsorption ratio of Li, in positive relationships with solute pH and ionic strength. At constant solute pH = 8.5 and ionic strength of 0.001 M, the adsorption ratio and isotope fractionation of Li on kaolinite reach the maximum with the lowest initial Li concentration of 2 μM. In experiments, Li is removed by kaolinite as the inner-sphere and/or outer-sphere complexes, likely followed by structural occupation as supported by incomplete desorption. We model the Li isotope fractionation in all three sets, which can be best described by Rayleigh distillation models. In summary, significant Li isotope fractionation occurs following a kinetic law in closed-systems during adsorption on kaolinite. Adsorption-driven isotope fractionation conforms to a kinetic solid-liquid isotope fractionation factor α ∼ 0.992, consistent with theoretical ion-desolvation between complexed and dissolved ions (α = 0.9925, Hofmann et al., 2012). This study reveals a vital kinetic role of clay uptake in Li isotope fractionation during chemical weathering, suggesting rapid forward adsorption reaction versus relatively slow backward reaction. The dominance of the kinetic mechanism over the equilibrium mechanism further explains field observations from rivers worldwide. Given above, the outcome of this study calls for additional attention on low-temperature kinetic Li isotope fractionation at Earth’s surface and further refinement of quantitative models using geological Li records to trace weathering and reconstruct climate.
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