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
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
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
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