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This integrated approach provides a new method for designing high-energy and high-power cathodes for NICs and NIBs.The shuttle effect of lithium polysulfides (Li2Sn) in electrolyte and the low conductivity of sulfur are the two key hindrances of lithium sulfur (Li-S) batteries. In order to address the two issues, we propose a three-dimensional porous nitrogen-doped carbon nanosheet with embedded NixCo3-xS4 nanocrystals derived from metal-organic frameworks for the durable-cathode host material in Li-S batteries. Experiments and density functional theory simulations show that the large porosity, robust N-doped carbon framework, and evenly embedded NixCo3-xS4 nanocrystals with high polarity act as strong "traps" for the immobilization of Li2Sn, which leads to an effective suppressing of the shuttle effect and promotes efficient utilization of sulfur. The NixCo3-xS4/N-doped carbon hybrid material exhibits a high reversible capacity of 1122 mAh g-1 at a current density of 0.5 C after 100 cycles. Even at high areal sulfur loadings of 10 and 12 mg cm-2, the hybrid cathode materials can maintain good areal capacities of 7.2 and 7.6 mAh cm-2 after 100 cycles. The present study sheds light on the principles of the anchoring behaviors of Li2Sn species on bimetallic sulfide hybrid materials and reveals an attractive route to design the highly desirable cathode materials for Li-S batteries.Li has been regarded as the most attractive anode for next-generation high-energy-density batteries due to its high specific capacity and low electrochemical potential. However, its low electrochemical potential leads to the side reaction of Li with the solvent of the electrolyte (the solvation of Li ions exacerbates the reaction). selleck products This adverse side reaction results in uneven Li distribution and deposition, low Coulombic efficiency, and the formation of Li dendrites. Herein, we demonstrate an efficient method for achieving successive desolvation and homogeneous distribution of Li ions by using a double-layer membrane. The first layer is designed to enable the desolvation of Li ions. The second layer with controllable and ordered nanopores is expected to facilitate the homogeneous and exclusive transport of Li ions. The efficiency of the double-layer membrane on desolvation and exclusive transport of Li ions is confirmed by theoretical calculations, the significantly enhanced Li-ion transference number, improved Coulombic efficiency, and the inhibition of Li dendrites. These results will deepen our understanding of the modulation of ions and pave a way to the next-generation high-energy-density Li-metal batteries.Smart contact lenses have been put forward for years, but there is still no commercial product in the market; the high cost due to expensive fabrication techniques could be one of the reasons. In this paper, first, a cost-efficient and reliable route to fabricate graphene grating on contact lens was designed and demonstrated based on the direct laser interference patterning graphene film on commercial contact lenses using an NdYAG laser. The thickness of the film and the interference angle have been taken into consideration. Optical characterization and simulation have been applied to evaluate the quality of our final achieved grating patterns with a grating size from 0.92 to 3.04 μm. Two-dimensional (2D) patterns could also be obtained through double-time laser interference. Contact angles for samples with different interference angles were presented considering the service environment of smart contact lenses. Of course, the conductivity of the samples was evaluated using a four-probe method. The most conductive sample had the sheet resistance lower than 30 Ω/sq. This research study highlighted the possibility of patterning graphene with the laser ablation method and provided a candidate solution for the fabrication of smart contact lenses under controlled cost.The hard carbon (HC) has been emerging as one of the most promising anode materials for sodium-ion batteries (SIBs). Incorporation of cations into the HC lattice proved to be effective to regulate their d-interlayer spacing with a modified SIB performance. However, the complexity and high cost of current synthetic processes limited its large-scale application in SIBs. Through the natural hyperaccumulation process, a cost-effective and scale-up-driven procedure to produce Ca-ion self-incorporated HC materials was proposed by applying tamarind fruits as the precursor with the enrichment of Ca ions. In virtue of one-step pyrolysis, the self-incorporated and well-distributed Ca ions in tamarind fruits had successfully served as the buffer layer to expand the d-interlayer spacing of HC materials. Furthermore, the natural porosity hierarchy could be largely preserved by the optimization of calcination temperature. As a result, the Ca-rich HC material had exhibited the optimized cycling performance (326.7 mA h g-1 at 50 mA g-1 and capacity retention rate of 89.40% after 250 cycles) with a high initial Coulombic efficiency of 70.39%. This work provided insight into applying the hyperaccumulation effect of biomass precursors to produce doped HC materials with ion self-incorporation and the optimized d-interlayer spacing, navigating its large-scale application for high-performance SIBs.Laser-induced graphene (LIG) is a multifunctional graphene foam that is commonly direct-written with an infrared laser into a carbon-based precursor material. Here, a visible 405 nm laser is used to directly convert polyimide into LIG. This enabled the formation of LIG with a spatial resolution of ∼12 μm and a thickness of 60% reduction in LIG feature sizes reported in prior publications. This process occurs in situ in an SEM chamber, thus allowing direct observation of LIG formation. The reduced size of the LIG features enables the direct-write formation of flexible electronics that are not visible to the unaided eye. A humidity sensor is demonstrated which could detect human breath with a response time of 250 ms. With the growing interest in LIG for flexible electronics and sensors, finer features can greatly expand its utility.