Designing nonprecious but efficient electrocatalysts for the hydrogen evolution reaction (HER) in alkaline solution still remains a significant challenge. Herein, we report the NiMoP nanosheets on hollow Cu3P nanotube arrays...
The fabrication of low-cost and high-performance electrocatalysts is essential for water splitting to achieve sustainable oxygen evolution reaction. In this work, spinel oxides (CuCo2O4 and Co3O4) are mounted on nickel...
The development of multifunctional electrocatalysts with
rich resources,
excellent performance, and stability is necessary for water splitting
to achieve sustainable hydrogen and oxygen production. Herein, we
report the preparation of a bifunctional coral-like nanostructured
electrocatalyst (p-MoS2/NiS2) by in situ vulcanization
of polymeric sulfur with a MoO3/Ni as the precursor. It
is exciting that the whole preparation process of the electrocatalyst
can be completed in a few hours. The as-fabricated multimetallic sulfide
not only exhibits well-defined heterointerfaces and the defect-rich
two-dimensional (2D) nanoconfiguration with high conductivity to overcome
the poor hydrogen evolution reaction (HER) activity, but also promotes
the formation of the 1T phase. The obtained p-MoS2/NiS2 nanostructures exhibit low overpotentials of −115
mV at −10 mA cm–2 and 337 mV at 100 mA cm–2 toward the HER and oxygen evolution reaction (OER),
respectively, which surpass most of the previously reported bimetallic
sulfide-based electrocatalysts. Benefiting from the stability of the
hierarchical heterostructure and the coupling effect between the inner
layer of NiS2 and outer layers of MoS2, the
p-MoS2/NiS2 catalyst is endowed with high activity
for water splitting. It can be used as a bifunctional electrocatalyst
for water splitting with a cell voltage of 1.51 V at a current density
of 10 mA cm–2. Overall, this work proposes a simple
in situ vulcanization method to synthesize MoS2, which
expands the interlayer spacing and realizes the coexistence of a metastable
structure and metal doping.
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