4.7 Article

Ultrasonic Plasma Engineering Toward Facile Synthesis of Single-Atom M-N4/N-Doped Carbon (M = Fe, Co) as Superior Oxygen Electrocatalyst in Rechargeable Zinc-Air Batteries

期刊

NANO-MICRO LETTERS
卷 13, 期 1, 页码 -

出版社

SHANGHAI JIAO TONG UNIV PRESS
DOI: 10.1007/s40820-020-00581-4

关键词

Single-atom-doped M-N-4/NC catalyst; Plasma engineering; ORR/OER bifunctional activity; DFT calculation; Rechargeable Zn-air battery

资金

  1. Global Frontier Program through the Global Frontier Hybrid Interface materials (GFHIM) of the National Research Foundation of Korea (NRF) - ministry of science, ICT and Future Planning [2013M3A6B1078874]
  2. Busan Innovation Institute of Industry, Science & Technology Planning (BISTEP)
  3. Federal Ministry of Education and Research (BMBF) under the Make Our Planet Great Again -German Research Initiative (MOPGAGRI) [57429784]

向作者/读者索取更多资源

In this study, ultrasonic plasma engineering was utilized to fabricate uniform single-atom M-N-4 carbon catalysts with high production rate and superior performance, outperforming conventional noble-metal catalysts in practical applications.
As bifunctional oxygen evolution/reduction electrocatalysts, transition-metal-based single-atom-doped nitrogen-carbon (NC) matrices are promising successors of the corresponding noble-metal-based catalysts, offering the advantages of ultrahigh atom utilization efficiency and surface active energy. However, the fabrication of such matrices (e.g., well-dispersed single-atom-doped M-N-4/NCs) often requires numerous steps and tedious processes. Herein, ultrasonic plasma engineering allows direct carbonization in a precursor solution containing metal phthalocyanine and aniline. When combining with the dispersion effect of ultrasonic waves, we successfully fabricated uniform single-atom M-N-4 (M = Fe, Co) carbon catalysts with a production rate as high as 10 mg min(-1). The Co-N-4/NC presented a bifunctional potential drop of Delta E = 0.79 V, outperforming the benchmark Pt/C-Ru/C catalyst (Delta E = 0.88 V) at the same catalyst loading. Theoretical calculations revealed that Co-N-4 was the major active site with superior O-2 adsorption-desorption mechanisms. In a practical Zn-air battery test, the air electrode coated with Co-N-4/NC exhibited a specific capacity (762.8 mAh g(-1)) and power density (101.62 mW cm(-2)), exceeding those of Pt/C-Ru/C (700.8 mAh g(-1) and 89.16 mW cm(-2), respectively) at the same catalyst loading. Moreover, for Co-N-4/NC, the potential difference increased from 1.16 to 1.47 V after 100 charge-discharge cycles. The proposed innovative and scalable strategy was concluded to be well suited for the fabrication of single-atom-doped carbons as promising bifunctional oxygen evolution/reduction electrocatalysts for metal-air batteries.

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