134 research outputs found
Highly efficient single atom based materials in energy conversion
Since the size of metal components plays a pivotal role in determining the reactivity and selectivity of the heterogeneous catalysts; enormous efforts are invested in downsizing the metal particles to atomic level for ultimate catalysis over last decade. Single atoms (SAs) become an interesting research field towards material synthesis and performance optimization for diverse catalytic reactions. Significantly, various single atoms show remarkable catalytic activity and selectivity toward a variety of electrocatalytic reactions, including hydrogen evolution reaction (HER), oxygen evolution reaction (OER), oxygen reduction reaction (ORR), CO oxidation reaction, CO2 reduction reaction, water gas shift reaction, and hydrogenation with a high efficiency. It is noteworthy that the same foreign isolated substitutions can be tuned to show distinguishing catalytic activities via anchoring on different supports
Box Spline Wavelet Frames for Image Edge Analysis
We present a new box spline wavelet frame and apply it for image edge analysis. The wavelet frame is constructed using a box spline of eight directions. It is tight and has seldom been used for applications. Due to the eight different directions, it can find edges of various types in detail quite well. In addition to step edges (local discontinuities in intensity), it is able to locate Dirac edges (momentary changes of intensity) and hidden edges (local discontinuity in intensity derivatives). The method is simple and robust to noise. Many numerical examples are presented to demonstrate the effectiveness of this method. Quantitative and qualitative comparisons with other edge detection techniques are provided to show the advantages of this wavelet frame. Our test images include synthetic images with known ground truth and natural, medical images with rich geometric information
Room-Temperature Sodium-Sulfur Batteries: A Comprehensive Review on Research Progress and Cell Chemistry
Room temperature sodium-sulfur (RT-Na/S) batteries have recently regained a great deal of attention due to their high theoretical energy density and low cost, which make them promising candidates for application in large-scale energy storage, especially in stationary energy storage, such as with electrical grids. Research on this system is currently in its infancy, and it is encountering severe challenges in terms of low electroactivity, limited cycle life, and serious self-charging. Moreover, the reaction mechanism of S with Na ions varies with the electrolyte that is applied, and is very complicated and hard to detect due to the multi-step reactions and the formation of various polysulfides. Therefore, understanding the chemistry and optimizing the nanostructure of electrodes for RT-Na/S batteries are critical for their advancement and practical application in the future. In the present review, the electrochemical reactions between Na and S are reviewed, as well as recent progress on the crucial cathode materials. Furthermore, attention also is paid to electrolytes, separators, and cell configuration. Additionally, current challenges and future perspectives for the RT-Na/S batteries are discussed, and potential research directions toward improving RT-Na/S cells are proposed at the end
Promoted Photocharge Separation in 2D Lateral Epitaxial Heterostructure for VisibleâLightâDriven CO2 Photoreduction
Photocarrier recombination remains a big barrier for the improvement of solar energy conversion efficiency. For 2D materials, construction of heterostructures represents an efficient strategy to promote photoexcited carrier separation via an internal electric field at the heterointerface. However, due to the difficulty in seeking two components with suitable crystal lattice mismatch, most of the current 2D heterostructures are vertical heterostructures and the exploration of 2D lateral heterostructures is scarce and limited. Here, lateral epitaxial heterostructures of BiOClâ@âBi2O3 at the atomic level are fabricated via sonicatingâassisted etching of Cl in BiOCl. This unique lateral heterostructure expedites photoexcited charge separation and transportation through the internal electric field induced by chemical bonding at the lateral interface. As a result, the lateral BiOClâ@âBi2O3 heterostructure demonstrates superior CO2 photoreduction properties with a CO yield rate of about 30 ”mol gâ1 hâ1 under visible light illumination. The strategy to fabricate lateral epitaxial heterostructures in this work is expected to provide inspiration for preparing other 2D lateral heterostructures used in optoelectronic devices, energy conversion, and storage fields
Nickel sulfide nanocrystals on nitrogen-doped porous carbon nanotubes with high-efficiency electrocatalysis for room-temperature sodium-sulfur batteries
Polysulfide dissolution and slow electrochemical kinetics of conversion reactions lead to low utilization of sulfur cathodes that inhibits further development of room-temperature sodium-sulfur batteries. Here we report a multifunctional sulfur host, NiS2 nanocrystals implanted in nitrogen-doped porous carbon nanotubes, which is rationally designed to achieve high polysulfide immobilization and conversion. Attributable to the synergetic effect of physical confinement and chemical bonding, the high electronic conductivity of the matrix, closed porous structure, and polarized additives of the multifunctional sulfur host effectively immobilize polysulfides. Significantly, the electrocatalytic behaviors of the Lewis base matrix and the NiS2 component are clearly evidenced by operando synchrotron X-ray diffraction and density functional theory with strong adsorption of polysulfides and high conversion of soluble polysulfides into insoluble Na2S2/Na2S. Thus, the as-obtained sulfur cathodes exhibit excellent performance in room-temperature Na/S batteries
A High-Kinetics Sulfur Cathode with a Highly Efficient Mechanism for Superior Room-Temperature Na-S Batteries
2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Applications of room-temperature-sodium sulfur (RT-Na/S) batteries are currently impeded by the insulating nature of sulfur, the slow redox kinetics of sulfur with sodium, and the dissolution and migration of sodium polysulfides. Herein, a novel micrometer-sized hierarchical S cathode supported by FeS2 electrocatalyst, which is grown in situ in well-confined carbon nanocage assemblies, is presented. The hierarchical carbon matrix can provide multiple physical entrapment to polysulfides, and the FeS2 nanograins exhibit a low Na-ion diffusion barrier, strong binding energy, and high affinity for sodium polysulfides. Their combination makes it an ideal sulfur host to immobilize the polysulfides and achieve reversible conversion of polysulfides toward Na2S. Importantly, the hierarchical S cathode is suitable for large-scale production via the inexpensive and green spray-drying method. The porous hierarchical S cathode offers a high sulfur content of 65.5 wt%, and can deliver high reversible capacity (524 mAh gâ1 over 300 cycles at 0.1 A gâ1) and outstanding rate capability (395 mAh gâ1 at 1 A gâ1 for 850 cycles), holding great promise for both scientific research and real application
Betulinic Acid Derivatives as Human Immunodeficiency Virus Type 2 (HIV-2) Inhibitors â„
We previously reported that [[N-[3ÎČ-hydroxyl-lup-20(29)-en-28-oyl]-7-aminoheptyl]-carbamoyl]methane (A43D, 4) was a potent HIV-1 entry inhibitor. However, 4 was inactive against HIV-2 virus, suggesting the structural requirements for targeting these two retroviruses are different. In this study, a series of new betulinic acid derivatives were synthesized, and some of them displayed selective anti-HIV-2 activity at nanomolar concentrations. In comparison to compounds with anti-HIV-1 activity, a shorter C-28 side chain is required for optimal anti-HIV-2 activity
Early Microglial Activation Following Closed-Head Concussive Injury Is Dominated by Pro-Inflammatory M-1 Type
Microglial activation is a pathological hallmark of traumatic brain injury (TBI). Following brain injury, activated microglia/macrophages adopt different phenotypes, generally categorized as M-1, or classically activated, and M-2, or alternatively activated. While the M-1, or pro-inflammatory phenotype is detrimental to recovery, M-2, or the anti-inflammatory phenotype, aids in brain repair. Recent findings also suggest the existence of mixed phenotype following brain injury, where activated microglia simultaneously express both M-1 and M-2 markers. The present study sought to determine microglial activation states at early time points (6â72 h) following single or repeated concussive injury in rats. Closed-head concussive injury was modeled in rats using projectile concussive impact injury, with either single or repeated impacts (4 impacts, 1 h apart). Brain samples were examined using immunohistochemical staining, inflammatory gene profiling and real-time polymerase chain reaction analyses to detect concussive injury induced changes in microglial activation and phenotype in cortex and hippocampal regions. Our findings demonstrate robust microglial activation following concussive brain injury. Moreover, we show that multiple concussions induced a unique rod-shaped microglial morphology that was also observed in other diffuse brain injury models. Histological studies revealed a predominance of MHC-II positive M-1 phenotype in the post-concussive microglial milieu following multiple impacts. Although there was simultaneous expression of M-1 and M-2 markers, gene expression results indicate a clear dominance in M-1 pro-inflammatory markers following both single and repeated concussions. While the increase in M-1 markers quickly resolved after a single concussion, they persisted following repeated concussions, indicating a pro-inflammatory environment induced by multiple concussions that may delay recovery and contribute to long-lasting consequences of concussion
Discovery of diarylpyridine derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors
Two series (4 and 5) of diarylpyridine derivatives were designed, synthesized, and evaluated for anti-HIV-1 activity. The most promising compound, 5e, inhibited HIV-1 IIIB, NL4-3, and RTMDR1 with low nanomolar EC50 values and selectivity indexes of >10,000. The results of this study indicate that diarylpyridine can be used as a novel scaffold to derive a new class of potent NNRTIs, active against both wild-type and drug resistant HIV-1 strains
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