Developing highly active and cost-effective electrocatalysts
is
critical for enhancing the intrinsic performance of electrocatalytic
water splitting. Oxoanion-based compounds, such as phosphates and
molybdates, have emerged as promising electrocatalysts owing to their
advantageous properties of nontoxicity, low price, and strong water
adsorption ability. However, their relatively inferior activity has
impeded extensive investigation into electrochemical applications.
Herein, an amorphous phosphate-adsorbed and RuNi-doped molybdate (RuNiMo-P)
composite is synthesized on nickel foam (NF) support by using a simple
two-step method. Significantly, an acidic solution of phosphomolybdic
acid (PMo12), containing a low concentration of Ru, can
etch the NF, contributing to the in situ growth of the RuNi-doped
molybdate precursor. Subsequent phosphating ensures the surface formation
of the amorphous phosphate layer due to abundant oxygen in the precursor.
The strong structural interaction between RuNi-doped molybdate and
amorphous phosphate in RuNiMo-P prompts an enhanced hydrogen evolution
reaction (HER) performance, delivering an overpotential of 38 mV at
a current density of −10 mA cm–2, a Tafel
slope of 53 mV dec–1, and good stability in an alkaline
medium. Characterizations after HER reveal that RuNi doping, partial
dissolution of phosphate and molybdate species, and newly formed NiOOH
nanosheets can expose active sites, facilitate charge transfer, and
modify electronic structures, thereby improving the HER performance
effectively.