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Adsorption of molecules at the electrode/solution interface is of great significance in understanding heterogeneous electron transfer processes. Herein, we study the interfacial properties of coppe...

Platinum (Pt) is one of the most well-known catalytic/electrocatalytic materials for many important (electro)chemical conversion reactions. Their low availability and high cost limit their commercial applications. In the quest for alternative catalytic materials, core–shell nanostructures are evolving as a major alternative. Herein, we report a novel strategy for preparing copper–platinum core–shell nanostructures on a pencil graphite substrate (Cu@Pt/PGE), wherein copper nanostructures are prepared by template electrodeposition. This was followed by a galvanic replacement reaction for Pt modification. We show that the entire preparation could be completed in less than an hour at room temperature. The catalytic efficiency of the resulting dendritic Cu@Pt core–shell nanostructures is explored toward the ammonia oxidation reaction (AOR), since it is of great importance for environmental monitoring, ammonia removal and recently in ammonia fuel cells. Using the Cu@Pt/PGE nanozyme, the ammonia oxidation reaction could be carried out at −0.28 V vs. Ag/AgCl with promising catalytic performance, which is much higher than commercially available Pt disc electrodes. The catalyst could also be used for selective ammonia detection towards aquatic monitoring with a maximum sensitivity of 62 μA μM−1 cm−2 and a lower limit of detection of 613 nM. The results presented here may be highly useful for the development of next-generation alternative ammonia fuel cells and aquatic monitoring/purification as well as for the development of novel, high performance and affordable nanocatalytic systems.

Herein we report preparation of copper-silver bimetallic nanostructures with excellent electrocatalytic properties. Copper nanostructures were formed by template electrodeposition method while bimetallic nanostructures were prepared by galvanic replacement of copper with silver. Electrocatalytic activity of these nanocatalysts were demonstrated using electroanalysis of dopamine as model analyte. A maximum sensitivity of 1.56 μA/μM/cm2 and a lower limit of detection of 26 nM together with good recovery in real sample analysis provided the practical feasibility of the sensor. In summary, this work demonstrates a facile route for the fabrication of cost-effective bimetallic nanoelectrocatalysts under ambient conditions within a short duration of time.