Publications by authors named "Jinglei Lei"

A cost-effective and highly efficient electrolyte with a wide electrochemical window, high reversibility of Mg plating/stripping, non-/low-corrosivity, good compatibility with cathode materials, and tolerance of trace water and impurity is crucial for the commercialization of rechargeable magnesium batteries. In this work, a novel boron-centered non-nucleophilic electrolyte that meets all the above requirements is prepared a facile and economic approach from the raw materials B(TFE)/MgCl/CrCl/Mg (BMCM). The as-prepared BMCM electrolyte is mainly composed of tetracoordinated anions [B(TFE)] and solvated cations [Mg(μ-Cl)(DME)].

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The application of magnesium alloys is seriously limited by their poor environmental adaptability. In this work, we report a robust superamphiphobic coating, which endows magnesium alloys with extraordinary environmental adaptability. The coating was fabricated on magnesium alloys by a facile, cost-effective, and scalable method, one-step particle-free spraying.

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The colorful and mechanically robust surfaces of metallic materials are important for their applications in electronics, automobile, aerospace, and so on, but it is challenging to prepare them at a reasonable cost. Herein, we propose a simple, environment-friendly, and cost-effective method, reagent-free hydrothermal treatment, to prepare colorful surfaces of magnesium alloys with mechanical robustness. The as-treated surface mainly composes of magnesium (hydr)oxides with a biomimetic microstructure, whose thickness and roughness increase linearly with the hydrothermal time.

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Amorphous molybdenum sulfide (MoS) is a highly active noble-metal-free electrocatalysts for the hydrogen evolution reaction (HER). The MoS was prepared by electrochemical deposition at room temperature. Low-cost precursors of Mo and S were adopted to synthesize thiomolybdates solution as the electrolyte.

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The effect of the oxygen evolution reaction (OER) is important in water splitting. In this work, we develop sphere-like morphology spinel oxide CoFeO/NF by hydrothermal reaction and calcination, and the diameter of the spheres is about 111.1 nm.

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High-tap-density silicon nanomaterials are highly desirable as anodes for lithium ion batteries, due to their small surface area and minimum first-cycle loss. However, this material poses formidable challenges to polymeric binder design. Binders adhere on to the small surface area to sustain the drastic volume changes during cycling; also the low porosities and small pore size resulting from this material are detrimental to lithium ion transport.

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The following facile approach has been developed to prepare a biomimetic-structural superhydrophobic surface with high stabilities and strong resistances on 2024 Al alloy that are robust to harsh environments. First, a simple hydrothermal treatment in a La(NO3)3 aqueous solution was used to fabricate ginkgo-leaf like nanostructures, resulting in a superhydrophilic surface on 2024 Al. Then a low-surface-energy compound, dodecafluoroheptyl-propyl-trimethoxylsilane (Actyflon-G502), was used to modify the superhydrophilic 2024 Al, changing the surface character from superhydrophilicity to superhydrophobicity.

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The present work demonstrates a generalized strategy using water-only hydrothermal oxidation to construct complex biomimetic micronanostructures on a series of metals and alloys, resulting in superhydrophilic surfaces. This general approach is environmentally-benign and cost-effective, which offers a unique clue for the rational fabrication of micronanoscale architectures and superhydrophilic surfaces.

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Kinetic characteristics of Li+ intercalation/deintercalation into/from individual LiNi0.8Co0.15Al0.

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