3 research outputs found

    In-Situ Growth of Few-Layered MoS<sub>2</sub> Nanosheets on Highly Porous Carbon Aerogel as Advanced Electrocatalysts for Hydrogen Evolution Reaction

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    Molybdenum disulfide-based hybrids, acting as cost-effective and acid-stable electrocatalysts for hydrogen evolution reaction (HER), have been developed fast for providing sustainable hydrogen energy in recent years. Herein, few-layered molybdenum disulfide (MoS<sub>2</sub>) nanosheets/carbon aerogel (CA) hybrids were successfully obtained through the combination of sol–gel process, aging, freeze-drying, high temperature carbonization, and solvothermal reaction. CA with highly continuous porosity and high specific surface area is used as a matrix material for construction of hierarchical MoS<sub>2</sub>/CA hybrids where few-layered MoS<sub>2</sub> nanosheets are uniformly covered on a CA surface. In this heterostructured system, CAs not only provide three-dimensional (3D) conductive pathway for fast transportation of electrons and ions, but also offer highly active regions for the growth of MoS<sub>2</sub>, greatly preventing the aggregation of MoS<sub>2</sub> nanosheets. Due to the rationally designed hybrids with 3D porous nanostructures, the as-prepared MoS<sub>2</sub>/CA hybrids with optimized MoS<sub>2</sub> content exhibit enhanced catalytic performance for electrocatalytic HER with a low onset potential of −0.14 V, large current density, and excellent stability

    Cotton Wool Derived Carbon Fiber Aerogel Supported Few-Layered MoSe<sub>2</sub> Nanosheets As Efficient Electrocatalysts for Hydrogen Evolution

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    Recent studies have proven that newly emerging two-dimensional molybdenum diselenide (MoSe<sub>2</sub>) is a promising noble-metal-free electrocatalyst for hydrogen evolution reaction (HER). Increasing the exposures of the active edges of MoSe<sub>2</sub> nanostructures is a key issue to fully realize the excellent electrochemical properties of MoSe<sub>2</sub>. In this work, a few-layered MoSe<sub>2</sub>/carbon fiber aerogel (CFA) hybrids have been facilely obtained through the combination of high-temperature carbonization and one-pot solvothermal reaction. CFA derived from cotton wool is used as a three-dimensional conductive network for construction of hierarchical MoSe<sub>2</sub>/CFA hybrids, where few-layered MoSe<sub>2</sub> nanosheets are uniformly and perpendicularly decorated on the surfaces of CFA. In the designed and prepared hybrids, CFA effectively increases the exposures of the active edges of MoSe<sub>2</sub> nanosheets as well as provides reduced lengths for both electron transportation and ion diffusion. Therefore, the obtained optimal MoSe<sub>2</sub>/CFA hybrid exhibits excellent electrochemical activity as HER electrocatalyst with a small onset potential of −0.104 V vs reversible hydrogen electrode and a small Tafel slope of 62 mV per decade, showing its great potential as a next-generation Pt-free electrocatalyst for HER

    Molybdenum Carbide Anchored on Graphene Nanoribbons as Highly Efficient All-pH Hydrogen Evolution Reaction Electrocatalyst

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    The demand for exploiting hydrogen as a new energy source has driven the development of feasible, efficient, and low-cost electrocatalysts for hydrogen evolution reaction (HER) in different reaction media. Herein, we report the synthesis of molybdenum carbide (Mo<sub>2</sub>C) nanoparticles anchored on graphene nanoribbons (GNRs) as HER electrocatalyst that can function well under acidic, basic, and neutral conditions. GNRs obtained by unzipping carbon nanotubes (CNTs) display strip-like structure, offering abundant active sites for growing Mo<sub>2</sub>C nanoparticles. Furthermore, GNRs could provide a fast electron transport pathway as well as large exposed surface area to allow full impregnation of electrolytes. Coupling with the anticorrosion feature of Mo<sub>2</sub>C nanoparticles, the Mo<sub>2</sub>C–GNR hybrid exhibits outstanding electrocatalytic performance in all of the acidic, basic, and neutral media, making it promising as a highly efficient electrocatalyst under conditions at all pH values
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