Publications by authors named "Chengchao Li"

This paper proposes a co-design method of dynamic output feedback control law and periodic event-triggered control (PETC) strategy to tolerate a maximum allowable number of successive packet dropouts (MANSDs) in networked control systems (NCSs). For the purpose of striking a balance between saving limited communication resources and reducing complexity of the transmission implementation, we present the periodic event-triggering mechanism (PETM), in which the triggering conditions only needs to be monitored at each event-verifying instant. In NCSs, packets often suffer from some interference in network transmission, such as packet losses.

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Most in situ tool wear monitoring methods during micro end milling rely on signals captured from the machining process to evaluate tool wear behavior; accurate positioning in the tool wear region and direct measurement of the level of wear are difficult to achieve. In this paper, an in situ monitoring system based on machine vision is designed and established to monitor tool wear behavior in micro end milling of titanium alloy Ti6Al4V. Meanwhile, types of tool wear zones during micro end milling are discussed and analyzed to obtain indicators for evaluating wear behavior.

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The use of Li metal as the anode for Li-based batteries has attracted considerable attention due to its ultrahigh energy density. However, the formation of Li dendrites, uneven deposition, and huge volume changes hinder its reliable implementation. These issues become much more severe in commercial carbonate-based electrolytes than in ether-based electrolytes.

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We report the use of vinyl ethylene carbonate as a new solid electrolyte interface (SEI)-forming additive for Li-metal anodes in carbonate-based electrolyte, which has the advantages of both good storage performance and low price. Compared to the SEI formed in vinyl ethylene carbonate-free electrolyte, the SEI film formed in 10% vinyl ethylene carbonate electrolyte contains a higher relative content of polycarbonate species and a greater amount of decomposition products of LiPF salt. Both components are expected to have positive effects on the passivation of Li-metal surface and the accommodation of volume changes of anode during cycling.

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Novel composites made from monodispersed porous Al-glycolate spheres (NiMo/Al-SP) were synthesized through alcoholysis or hydrolysis treatments. The obtained samples were characterized by a complementary combination of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), N physisorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), hydrogen temperature-programmed reduction (H-TPR), and pyridine Fourier transform infrared spectroscopy (Py FT-IR). In addition, the catalytic performances of the resultant catalysts were evaluated in the simultaneous HDS of dibenzothiophene (DBT) and HYD of naphthalene (DBT and naphthalene represent the sulfur-containing compounds and polycyoalkanes, respectively).

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To further increase the energy and power densities of lithium-ion batteries (LIBs), monoclinic Li V (PO ) attracts much attention. However, the intrinsic low electrical conductivity (2.4 × 10 S cm ) and sluggish kinetics become major drawbacks that keep Li V (PO ) away from meeting its full potential in high rate performance.

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Novel two-dimensional (2D) FeO/SnSSe hexagonal nanoplates were prepared from hot-inject process in oil phase. The resulted hybrid manifests a typical 2D hexagonal nanoplate morphology covered with thin carbon layer. Serving as anode material of lithium-ion battery (LIB), the FeO/SnSSe hybrid delivers an outstanding capacity of 919 mAh g at 100 mA g and a discharge capacity of 293 mAh g after 300 cycles at the current density of 5 A g.

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Article Synopsis
  • A novel anode material, carbon-coated SnS/SnO heterostructures wrapped around carbon nanofibers (C@SnS/SnO@CNFs), shows impressive performance for lithium-ion batteries, achieving a reversible capacity of 826.8 mA h g after 500 cycles at a current density of 1.0 A g.
  • An unusual increase in capacity over cycling is attributed to a structural transformation from polycrystalline nanowalls to high-porosity amorphous nanosheets, enhancing effective surface area.
  • This lithiation-induced structural change improves charge transfer and reversibility in reactions involving SnS and SnO, offering insights into the optimization of electrode electrochemical performance.
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We demonstrate a facile hydrothermal method for growth of ultrathin NiCo2S4 nanosheets on reduced graphene oxide (RGO), which exhibit remarkable electrochemical performance with higher capacitance and longer cycle life than the bare NiCo2S4 hollow spheres (HSs).

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95 hair samples from traffic polices and 110 hair samples from ordinary people were collected from 6 areas of Guilin, China, and Hg, Pb contents in hairs were determined. The result shows that the heavier the traffic was, the higher hair Hg, Pb contents of traffic polices are. Hair Hg, Pb contents of traffic polices also increase with their working time.

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In this report, we present a hybrid structure involving a small quantity of Co element uniformly deposited on porous SnO(2) spheres as stable and high capacity anode materials for lithium-ion batteries. Specifically, Co element deposited on SnO(2) nanomaterials exhibited an exceptional reversible capacity of 810 mA h g(-1) after 50 cycles which is higher than the pure SnO(2) electrode. Based on the experiments results, a possible mechanism for the change of this structure during lithium ion insertion/extraction was proposed.

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Cobalt ion-based coordination polymer nanowires were synthesized by using nitrilotriacetic acid (NA) as a chelating agent by a one-step hydrothermal approach. In the synthesis, cobalt ions were bonded with amino or carboxyl groups of NA to form one-dimension polymer nanowires, which can be confirmed by FTIR and TGA results. Our experimental results show that the morphologies of polymer nanowires greatly depend on the precursor salts, ratios between deionized water and isopropyl alcohol.

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NiO hollow nanospheres were synthesized by controlled precipitation of metal ions with urea using carbon microspheres as templates, which were for the first time adopted to construct a novel amperometric glucose biosensor. Glucose oxidase was immobilized on the surface of hollow nanospheres through chitosan-assisted cross-linking technique. Due to the high specific active sites and high electrocatalytic activity of NiO hollow nanospheres, the constructed glucose biosensors exhibited a high sensitivity of 3.

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Colloidal carbon microspheres (CMS) are dispersed in chitosan (CHIT) solution to form an organic-inorganic hybrid with excellent micro-environment for the immobilization of biomolecules. A novel amperometric biosensor for the determination of hydrogen peroxide (H(2)O(2)) has been constructed by entrapping horseradish peroxidase (HRP) in as-synthesized CMS/CHIT hybrid. The modification of glassy carbon electrode is made by a simple solution-evaporation method.

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Rapid and ultrahigh sensing is realized from Au-coated ZnO rods with diameters down to 15 nm. Both the small diameters and the Au coating make the surface-depletion effect more pronounced for gas sensing. Such enhanced surface depletion increases the sensitivity, lowers the operation temperature and decreases the response time.

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