Abstract
Constructing a potentially stable and highly active nanostructured catalyst for hydrazine electro-oxidation is of substantial importance in direct-hydrazine fuel cells (DHFCs) application. In this work, we grow layered prickly-like Fe/Co di-hydroxide porous nanostructures as bifunctional catalysts on the surface of nickel mesh (Fe/Co/NiMn D-HPNs) via controllable electroplating method for an efficient electrooxidation reaction of hydrazine. The layered prickly-like Fe/Co/NiMn D-HPNs samples are explored as potential catalysts for electrooxidation of hydrazine with the enhanced catalytic current response (32.4 mA cm−2), which is higher than the mono-hydroxide nanostructured electrodes (Fe@ D-HPNs and Co@ D-HPNs). The obtained higher catalytic activity is mainly attributed to layered prickly-like nanostructures with a large electroactive surface area (116.5 cm−2), Fe and Co elements that promoted synergetic effect, and the presence of grain-boundaries on the surface of prickly-like porous layers. The layered prickly-like Fe/Co/NiM30 D-HPNs catalyst displayed a low Tafel slope (67.4 mV dec−1) and longer stability of its original morphology of layered prickly-like porous nanostructures toward the electrooxidation of hydrazine even after >10000 sec. Thus, the layered prickly-like Fe/Co/NiM30 D-HPNs are considered as a potential and robust catalyst, and provide new insights in the construction of highly-active and low-cost alternative non-noble nanostructured materials for DHFCs applications.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.