Fe-Co-Ni ternary single-atom electrocatalyst and stable quasi-solid-electrolyte enabling high-efficiency zinc-air batteries

38Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

The non-noble metal (Fe, Co, Ni, etc.) catalysts possess promising potential to replace noble metals (e.g., Pt, Ru, Ir, etc.) as catalysts for oxygen electrocatalysis. Up to now, various mono- and dual-single-atom catalysts have been fabricated, though it is still challenging to synthesise ternary single-atom catalysts due to the difference of interaction forces between different metal ions (Fe, Co, Ni, etc.) and ligands. Here, we report a Fe-Co-Ni ternary single-atom catalyst (FeCoNi-Nx) derived from a zeolitic imidazolate frameworks (ZIF) precursor as an efficient oxygen electrocatalyst, and an optimised flexible casting-drying polyvinyl alcohol (CD-PVA) film as a quasi-solid electrolyte host, for high-efficiency solid-state Zn-air batteries. The aberration-corrected HAADF-STEM and EELS spectrum confirm the co-existence of Fe, Co and Ni single atoms in the FeCoNi-Nx catalyst, and the electrochemical, mechanical, and durability tests prove the superiority of the CD-PVA film. As a result, the FeCoNi-Nx-based rechargeable Zn-air battery delivers superior specific capacity (846.8 mAh·gZn–1) and power density (135 mW·cm–2) in aqueous electrolyte, as well as an over 60 mW·cm–2 power density in quasi-solid electrolyte. As a result, the quasi-solid-state Zn-air battery with a small area of only 2 cm2 is able to charge a mobile phone, which outperforms all the reported devices to date.

Cite

CITATION STYLE

APA

Qin, S., Li, K., Cao, M., Liu, W., Huang, Z., He, G., … Li, H. (2024). Fe-Co-Ni ternary single-atom electrocatalyst and stable quasi-solid-electrolyte enabling high-efficiency zinc-air batteries. Nano Research Energy, 3(3). https://doi.org/10.26599/NRE.2024.9120122

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free