Pd-based alloys, especially for alloys containing early
transition
metals, have been extensively designed and applied to electro-oxidize
formic acid for direct formic acid fuel cells owing to their capability
to directly oxidize formic acid molecules via the dehydrogenation
pathway. Adjusting the strain and electronic effects of Pd-based alloys
is an effective method to regulate the adsorbing phenomena of intermediates
on catalysts during formic acid oxidation and improve the catalytic
activity and stability. The ordering degree of alloys plays an important
role in modulating the adsorbing ability. In this work, we report
a strategy varying the atomic ordering degree of PdCoNi/rGO trimetallic
alloys to manipulate the strain and electronic effects and electrocatalytic
performance toward formic acid oxidation. A series of PdCoNi/rGO-T trimetallic catalysts are synthesized, in which the atomic
order of the trimetallic catalysts is regulated by annealing the wet-chemistry-synthesized
PdCoNi/rGO alloy. As the annealing temperature increases, the atomic
arrangement among Pd, Co, and Ni is ordered. Eventually, ordered intermetallic
PdCoNi/rGO-T catalysts are generated. As the atomic
ordering degree increases, the lattice constant decreases, and more
charge transfers from Pd to Ni and Co, leading to enhanced strain
and electronic effects. Moreover, the ordered intermetallic structure
stabilizes Co and Ni atoms to prevent the dissolution of the transition
metals in acidic electrolyte, and the strain and electronic effects
in ordered PdCoNi/rGO catalysts are maintained. With an annealing
temperature of 700 °C, the intermetallic PdCoNi/rGO-700 exhibits
the highest specific activity of 8.33 mA/cm2, which is
1.95-fold improved compared to pristine PdCoNi/rGO alloy (3.23 mA/cm2) and 2.48 times compared to Pd/rGO-700 (2.54 mA/cm2). Moreover, PdCoNi/rGO-700 also shows outstanding catalytic durability
due to its excellent structural stability. We believe that this research
helps in developing Pd-based alloy catalysts with high activity and
stability for formic acid electro-oxidation.