Calcination of metal–organic frameworks (MOFs)
to prepare
porous-carbon-based nanocomposites has emerged as a facile and viable
method for various applications. Here, the Cu-based HKUST-1 MOF is
chosen as the synthesis precursor and growth template owing to its
large surface area, high pore volume, as well as facile and large-scale
preparation. Through the direct phosphorization at elevated temperatures,
a hierarchical porous matrix consisting of HKUST-1 MOF-derived zero-dimensional
(0D) Cu3P nanoparticles embedded on the surface of conductive
carbon matrices is produced in a single step, in which its hydrogen
evolving electrocatalytic performances are assessed as a representative
application. The Cu3P/C-300 composite, at a loading mass
as small as 0.1 mg cm–2, demonstrates an overpotential
of 233 mV at 10 mA cm–2 and a Tafel slope of 91
mV dec–1 for hydrogen evolution with robust durability
in a 1 M KOH solution, which are both lower than other metal phosphides
directly dropcasted onto the conductive substrates (overpotentials
mainly >250 mV at 10 mA cm–2 and Tafel slopes
mainly
>100 mV dec–1). Such an improved hydrogen evolution
reaction performance is attributed to high specific surface area,
improved interfacial contact with the conductive substrate, and the
synergistic effects of the intrinsically active Cu3P nanoparticles
of ultrasmall sizes with carbon matrices. The synthesis strategy may
shed light on the development of cost-effective and stable electrocatalysts
with excellent electrochemical performances in energy-conversion fields.