Pt-based nanoframe catalysts have been explored extensively due to their superior activity toward the oxygen reduction reaction (ORR). Herein, we report the synthesis of Pt-Ni multiframes, which exhibit the unique structure of tightly fused multiple nanoframes and reinforced by an embedded dendrite. Rapid reduction and deposition of Ni atoms on Pt-Ni nanodendrites induce the alloying/dealloying of Pt and Ni in the overall nanostructures. After chemical etching of Ni, the newly formed dendrite-embedded Pt-Ni multiframes show an electrochemically active surface area (ECSA) of 73.4 m g and a mass ORR activity of 1.51 A mg at 0.93 V, which is 30-fold higher than that of the state-of-the-art Pt/C catalyst. We suggest that high ECSA and ORR performances of dendrite-embedded Pt-Ni multiframes/C can be attributed to the porous nanostructure and numerous active sites exposed on surface grain boundaries and high-indexed facets.

Pt-based alloy nanoframes have shown great potential as electrocatalysts toward the oxygen reduction reaction (ORR) in fuel cells. However, the intrinsically infirm nanoframes could be severely deformed during extended electro-cyclings, which eventually leads to the loss of the initial catalytic activity. Therefore, the structurally robust nanoframe is a worthy synthetic target. Furthermore, ternary alloy phase electrocatalysts offer more opportunities in optimizing the stability and activity than binary alloy ones. Herein, we report a robust PtCuNi ternary nanoframe, structurally fortified with an inner-lying PtCu dendrite, which shows a highly active and stable catalytic performance toward ORR. Remarkably, the PtCu@PtCuNi catalyst exhibited 11 and 16 times higher mass and specific activities than those of commercial Pt/C.

The synthesis of shape-, facet-, and composition-controlled Pd-based nanocrystals and the study of their catalytic reaction mechanisms are significant to and challenging for the development of advanced catalysts applicable to direct liquid-fuel cells (DLFCs). In the present study, we prepared (100)-faceted β-PdH cubes and ( 111)faceted β-PdH octahedra, which offered the opportunity to investigate the link between catalytic performance and the shape/facet/composition of nanocrystals. The β-PdH cubes and octahedra remarkably boosted catalytic activity and stability to the formic acid/methanol oxidation reaction (FAOR/MOR), due to the ligand effect originating from the interstitial alloying of β-PdH. Notably in this regard, β-PdH cubes exhibited the highest FAOR/MOR activity among Pdbased catalysts, owing to the relatively high CO tolerance on the Pd(100) facets. Our results confirm that simultaneous control of ligand and facet effects is an effective approach to the design of catalysts suitable for liquid fuel oxidation electrocatalysis.

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A layered β-NiOOH crystal with undercoordinated facets is an active and economically viable nonnoble catalyst for the oxygen evolution reaction (OER) in alkaline electrolytes. However, it is extremely difficult to enclose the β-NiOOH crystal with undercoordinated facets because of its inevitable crystal transformation to γ-NiOOH, resulting in the exfoliation of the catalytic surfaces. Herein, we demonstrate {111}-faceted Ni octahedra as the parent substrates whose surfaces are easily transformed to catalytically active β-NiOOH during the alkaline OER. Electron microscopic measurements demonstrate that the horizontally stacked β-NiOOH on the surfaces of Ni octahedra has resistance to further oxidation to γ-NiOOH. By contrast, significant crystal transformation and thus the exfoliation of the γ-NiOOH sheets can be observed on the surfaces of Ni cubes and rhombic dodecahedra (RDs). Electrocatalytic measurements show that the β-NiOOH formed on Ni octahedra exhibits highly enhanced OER durability compared to the Ni cubes, Ni RDs, and the state-of-the-art Ir/C catalysts.