Issue 33, 2024

Facile synthesis of MnO/NC nanohybrids toward high-efficiency ORR for zinc–air battery

Abstract

The development of inexpensive non-precious metal materials as high-efficiency stable oxygen reduction reaction (ORR) catalysts holds significant promise for application in metal–air batteries. Here, we synthesized a series of nanohybrids formed from MnO nanoparticles anchored on N-doped Ketjenblack carbon (MnO/NC) via a facile hydrothermal reaction and pyrolysis strategy. We systematically investigated the influence of pyrolysis temperature (600 to 900 °C) on the ORR activities of the MnO/NC samples. At the optimized pyrolysis temperature of 900 °C, the resulting MnO/NC (referred to as MnO/NC-900) exhibited superior ORR activity (onset potential = 0.85 V; half-wave potential = 0.74 V), surpassing other MnO/NC samples and nitrogen-doped Ketjenblack carbon (NC). Additionally, MnO/NC-900 demonstrated better stability than the Pt/C catalyst. The enhanced ORR activity of MnO/NC-900 was attributed to the synergy effect between MnO and NC, abundant surface carbon defects and surface-active components (N species and oxygen vacancies). Notably, the Zinc–air battery (ZAB) equipped MnO/NC-900 as the cathode catalyst delivered promising performance metrics, including a high peak power density of 146.5 mW cm−2, a large specific capacity of 795 mA h gZn−1, and an excellent cyclability up to 360 cycles. These results underscore the potential of this nanohybrid for applications in energy storage devices.

Graphical abstract: Facile synthesis of MnO/NC nanohybrids toward high-efficiency ORR for zinc–air battery

Supplementary files

Article information

Article type
Paper
Submitted
10 Jun 2024
Accepted
19 Jul 2024
First published
31 Jul 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 24031-24038

Facile synthesis of MnO/NC nanohybrids toward high-efficiency ORR for zinc–air battery

Q. Zhuang, C. Hu, W. Zhu, G. Cheng, M. Chen, Z. Wang, S. Cai, L. Li, Z. Jin and Q. Wang, RSC Adv., 2024, 14, 24031 DOI: 10.1039/D4RA04237A

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