4.6 Article

Nitrogen-coordinated single-atom catalysts with manganese and cobalt sites for acidic oxygen reduction

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 11, 页码 5930-5936

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta08029f

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资金

  1. Fundamental Research Funds for the Central Universities [2232019A3-03, JUSRP121035]
  2. National Natural Science Foundation of China [21875033, 52103260]
  3. China Postdoctoral Science Foundation [2021M690067]
  4. Natural Science Foundation of Jiangsu Province for Youths [BK20210482]
  5. Jiangsu Province Postdoctoral Science Foundation [2021K053A]

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This study developed an efficient catalyst based on Mn, Co, and N-co-doped carbon for acidic oxygen reduction reaction. Through analysis using electron microscopy, X-ray absorption spectroscopy, and Raman spectroscopy, it was found that the MnCo-N-C catalyst had a higher degree of graphitization, improving corrosion resistance and catalytic durability. After 50 hours of testing, the current retention of the MnCo-N-C catalyst was significantly higher (81%) compared to the Co-N-C catalyst.
Developing a low-cost, highly active and durable catalyst for acidic oxygen reduction reaction (ORR) is of significant importance for proton-exchange electrolyte membrane fuel cell. In this work, we report an efficient catalyst based on Mn, Co and N co-doped carbon (MnCo-N-C) for acidic ORR. Electron microscopy and X-ray absorption spectroscopy indicate that atomic CoNx and MnNx sites are dispersed in the carbon matrices of MnCo-N-C. Raman spectroscopy verifies that the doping of Mn into carbon matrices can enable a higher graphitization degree, which can improve the corrosion resistance and catalytic durability of the MnCo-N-C catalyst towards ORR in challenging acidic media. As a result, the MnCo-N-C catalyst exhibits significantly improved ORR durability with a higher current retention of 81% after 50 h of test compared with that (52%) of the Co-N-C catalyst. Moreover, the half-wave potential of the MnCo-N-C catalyst increases by 100 mV compared with that of the Co-N-C catalyst.

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