Scalable exothermic synthesis of sprout-like Ni-Co-Fe trimetallic oxide nanoparticles anchored on N-doped carbon nanotubes as bifunctional oxygen catalysts for zinc-air batteries

双功能 催化作用 材料科学 纳米颗粒 碳纤维 氧化物 过电位 碳纳米管 化学工程 析氧 纳米技术 化学 电化学 冶金 复合数 有机化学 电极 物理化学 复合材料 工程类
作者
Youngsun Cha,Taewon Kim,Kyungmin Kim,Jae Wook Seo,Ho Young Jang,Wonjoon Choi
出处
期刊:Carbon [Elsevier BV]
卷期号:: 118859-118859 被引量:11
标识
DOI:10.1016/j.carbon.2024.118859
摘要

Zn-air batteries (ZABs) offer a high specific energy density, cost-effectiveness, and eco-friendliness. Hence, they are attractive candidates for use as sustainable energy-storage devices. However, their practical applications are limited by their high bifunctional oxygen evolution reaction/oxygen reduction reaction (OER/ORR) overpotential and sluggish kinetics. To address these limitations, in this study, a highly active bifunctional oxygen catalyst, TNPs@N-CNT, is developed, in which Ni-Co-Fe trimetallic nanoparticles are anchored on N-doped carbon networks. TNPs@N-CNT is synthesized via the thermally driven combustion of collodion fuel. The carbonization of melamine foam containing pyridinic N in TNPs@N-CNT enhances the ORR and affords a high catalytic surface area and high electrical conductivity. Morphological studies and chemical characterization aid in finely tuning the thermal processing conditions, affording a TNPs@N-CNT suitable for charge transfer. TNPs@N-CNT shows enhanced ORR activity (half-wave potential = 0.62 V and onset potential = 1.49 V) in alkaline media. A ZAB with TNPs@N-CNT as the air cathode exhibits an output power density of 90 mW cm−2 and excellent cycling stability for over 200 h, outperforming previously reported carbon-supported precious-metal catalysts. This tunable and scalable fabrication strategy could promote the development of novel mesoporous structures combined with high-efficiency multi-metallic catalysts for applications in energy-storage systems.
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