4.8 Article

Hierarchical N-doped carbon spheres anchored with cobalt nanocrystals and single atoms for oxygen reduction reaction

期刊

NANO ENERGY
卷 87, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.nanoen.2021.106153

关键词

Oxygen reduction reaction; Zn-air battery; Electrocatalysis; Co-N-C; Zeolitic imidazole frameworks

资金

  1. National Key Research and Development Program of China, China [2020YFA0715000]
  2. National Natural Science Foundation of China, China [51832004]
  3. Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory, China [XHT2020-003]

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This study presents an efficient carbon-based catalyst derived from bimetallic zeolitic imidazole frameworks for the oxygen reduction reaction. The ultrasonic strategy enables uniform anchoring of the catalyst on resin microspheres, improving synthesis efficiency and distribution uniformity. By rational design of the catalyst structure, the performance of oxygen reduction reaction is enhanced.
Carbon-supported transition metal catalysts have attracted intense interest for oxygen reduction reaction (ORR) due to their high activity and low cost. Herein, we report bimetallic zeolitic imidazole frameworks (BMZIF)derived hierarchical N-doped carbon spheres anchored with graphene-encapsulated Co nanocrystals (Co@C) and spatially isolated single Co atoms (Co SAs) (denoted as Co-NCS) for highly efficient ORR. An ultrasonic strategy has been developed to uniformly anchor BMZIF on resin microspheres. The ultrasonic method significantly shortens the synthesis time and contributes to the homogeneous distribution of BMZIF. The inner resin spheres act as ideal support to anchor Zn/Co ions and prevent the aggregation of BMZIF nanocrystals, and the derived products provide adequate structural support and high conductivity after carbonization. Meanwhile, the outer BMZIF-derived porous carbon framework provides large specific surface area, promoted electron transport, and abundant exposed active sites. The co-existence of Co SAs and Co@C plays a vital role in the ORR process. The resultant catalyst demonstrates superior ORR performance with a half-wave potential (J1/2) of 0.90 V, outperforming the commercial Pt/C. This work opens a new path to construct efficient Co-N-C based catalysts.

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