Development of a
low cost, high activity, and stable nonprecious
metal bifunctional catalyst for electrocatalytic water cracking is
a hot topic and big challenge. In this paper, we prepared a nitrogen-doped
carbon nanotube (NCNT)-enhanced three-dimensional self-supported electrocatalyst
with CoP and Co
2
P coexistence by a two-step strategy of
high-temperature carbonization and low-temperature phosphorylation.
Furthermore, the induced three-dimensional carbon network skeleton
facilitates rapid charge transfer. In addition, the active sites of
the carbon foam (CF) are greatly increased by the construction of
hollow structures. As a bifunctional electrocatalyst, CoP/Co
2
P/NCNT@CF exhibited excellent catalytic activity for both hydrogen
evolution reaction and oxygen evolution reaction in alkaline media,
requiring low overpotentials of 133 and 289 mV to obtain a current
density of 10 mA cm
–2
, respectively. Additionally,
the synthesized catalysts also exhibit good long-term stability, maintaining
high catalytic activity after 20 h of continuous operation. We also
confirmed the main driving force to improve the electron transfer
between the heterostructures of Co and P by XPS spectra. The excellent
electrocatalytic performance can be attributed to the close synergy
between the highly active CoP/Co
2
P/NCNT and CF. This study
provides a new strategy for the design of highly active bifunctional
self-supporting electrocatalysts.