Recently, the development of high-performance non-platinum electrocatalysts for fuel cell applications has been gaining attention. Palladium-based nanoalloys are considered as promising candidates to substitute platinum catalysts for cathodic and anodic reactions in fuel cells. Here, we develop a facile route to synthesize dendritic palladium–copper–cobalt trimetallic nanoalloys as robust multifunctional electrocatalysts for oxygen reduction and formic acid oxidation. To the best of our knowledge, the mass activities of the dendritic Pd₅₉Cu₃₀Co₁₁ nanoalloy toward oxygen reduction and formic acid oxidation are higher than those previously reported for non-platinum metal nanocatalysts. The Pd₅₉Cu₃₀Co₁₁ nanoalloys also exhibit superior durability for oxygen reduction and formic acid oxidation as well as good antimethanol/ethanol interference ability compared to a commercial platinum/carbon catalyst. The high performance of the dendritic Pd₅₉Cu₃₀Co₁₁ nanoalloys is attributed to a combination of effects, including defects, a synergistic effect, change of d-band center of palladium, and surface strain.

Edges are special sites in nanomaterials. The atoms residing on the edges have different environments compared to those in other parts of a nanomaterial and, therefore, they may have different properties. Here, recent progress in nanomaterial fields is summarized from the viewpoint of the edges. Typically, edge sites in MoS₂ or metals, other than surface atoms, can perform as active centers for catalytic reactions, so the method to enhance performance lies in the optimization of the edge structures. The edges of multicomponent interfaces present even more possibilities to enhance the activities of nanomaterials. Nanoframes and ultrathin nanowires have similarities to conventional edges of nanoparticles, the application of which as catalysts can help to reduce the use of costly materials. Looking beyond this, the edge structures of graphene are also essential for their properties. In short, the edge structure can influence many properties of materials.

External fields are introduced to catalytic processes to improve catalytic activities. The light field effect plays an important role in electrocatalytic processes, but is not fully understood. Here we report a series of photo-coupled electrocatalysts for CO₂ reduction by mimicking the structure of chlorophyll. The porphyrin-Au catalyst exhibits a high turnover frequency of 37,069 h⁻¹ at −1.1 V and CO Faradaic efficiency (FE) of 94.2% at −0.9 V. Under visible light, the electrocatalyst reaches similar turnover frequency and FE with potential reduced by ~ 130 mV. Interestingly, the light-induced positive shifts of 20, 100, and 130 mV for porphyrin-Co, porphyrin-Cu, and porphyrin-Au electrocatalysts are consistent with their energy gaps of 0, 1.5, and 1.7 eV, respectively, suggesting the porphyrin not only serves as a ligand but also as a photoswitch to regulate electron transfer pathway to the metal center.