4.6 Article

A gel-limiting strategy for large-scale fabrication of Fe-N-C single-atom ORR catalysts

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 11, Pages 7137-7142

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta09228b

Keywords

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Funding

  1. National Natural Science Foundation of China [21972111, 21773188]
  2. Fundamental Research Funds for the Central Universities [XDJK2019AA002, XDJK2019B052]
  3. Natural Science Foundation of Chongqing [cstc2018jcyjAX0714]
  4. Venture AMP
  5. Innovation Support Program for Chongqing Overseas Returnees [cx2019073]
  6. Chongqing Engineering Research Center for Micro-Nano Biomedical Materials and Devices
  7. Chongqing Key Laboratory for Advanced Materials and Technologies

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This study presents a gel-limiting strategy for fabricating Fe-N-C single-atom catalysts and evaluates its feasibility for large-scale applications. The Fe-SASCs exhibited superior electrocatalytic performance compared to commercial Pt/C and were successfully used in a homemade Zn-air battery, demonstrating practical application value. The reported strategy has the potential to be further developed for the preparation of more transition metal SASCs in the future.
Although transition metal single atom site catalysts (SASCs) show great potential for electrocatalysis, their large-scale controllable and flexible preparation remains a great challenge. In this article, we report a simple gel-limiting strategy for fabricating Fe-N-C single-atom catalysts and evaluate its feasibility in large-scale applications. The results show that the production of Fe-SASCs can be controlled by the limiting immobilization of a hydroxyl-rich temperature-controlled gel combined with simple centrifugal treatment, even if the amount of Fe-feeding fluctuates within a certain range. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and X-ray photoelectron spectroscopy (XPS) confirmed the formation of Fe-N single-atom sites and the uniform distribution of Fe on commercial activated carbon. As an ORR electrocatalyst, the Fe-SASC delivered a higher limiting diffusion current, and more positive onset potential and half-wave potential (E-onset = 1.00 V, E-1/2 = 0.87 V), and excellent methanol resistance compared to commercial Pt/C (E-onset = 0.97 V, E-1/2 = 0.85 V). Using the prepared Fe-SASCs, a homemade Zn-air battery was assembled which demonstrated a higher open circuit voltage, power density, and stability, further proving the practical application value of our proposed method and as-prepared catalyst. More importantly, our reported strategy can be further developed and extended to the future preparation of more transition metal SASCs.

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