Doping
rare-earth metals or introducing carbon into transition
metal phosphides (TMPs) can promote the property and stability of
water electrolysis. An original composite nanostructure, cerium-doped
and carbon-coated CoMoO4 (Ce-doped CoMoO4@C),
was obtained by a simple hydrothermal and annealing process successively.
Subsequently, chemical vapor deposition (CVD) was adopted to synthesize
carbon-coated and cerium-doped CoMoP/MoP (Ce-doped CoMoP/MoP@C) with
diammonium hydrogen phosphate as the phosphorus source. Ce-doped CoMoP/MoP@C
displayed superb bifunctional HER and OER catalytic performance under
alkaline conditions. The overpotential η10, Tafel
slope, and double-layer capacitance (C
dl) for the OER were 287.0 mV, 74.4 mV dec–1, and
10.44 mF cm–2, while for the HER, these values were
188.0 mV, 72.2 mV dec–1, and 33.00 mF cm–2, respectively. Meanwhile, only 1.59 V (@10 mA cm–2) was needed to drive the entire water splitting. In addition, there
was no apparent attenuation after electrolytic catalysis for 12 h
continuously. The superb performance and endurance gave credit to
the cooperative effect between carbon materials and metal phosphides
and the optimized electronic structure by the incorporation of the
Ce element.