4.8 Article

Silver based single atom catalyst with heteroatom coordination environment as high performance oxygen reduction reaction catalyst

期刊

NANO RESEARCH
卷 15, 期 9, 页码 7968-7975

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-4499-8

关键词

Ag; single-atom; heteroatom coordination; oxygen reduction; zinc-air battery

资金

  1. National Key Research and Development Program of China [2019YFA0210300]
  2. National Natural Science Foundation of China [21971008]
  3. Fundamental Research Funds for the Central Universities [buctrc201916, buctrc201823]

向作者/读者索取更多资源

In this study, an Ag-based single atom catalyst, Ag-1-h-NPCISC, with heteroatom coordination was synthesized and shown to greatly improve the performance of oxygen reduction reaction (ORR). A zinc-air battery with Ag-1-h-NPCISC as the air electrode achieved a high peak power density, attributed to the advantages of the hollow structure, single atom metal center, and heteroatom coordination environment. Density functional theory (DFT) calculations revealed that Ag-1-h-NPCISC lowered the energy barrier for the formation of OOH*, improving the ORR activity. This work demonstrates the promising potential of well manipulated Ag-based single atom catalysts in electrocatalysis.
Ag is a potential low-cost oxygen reduction reaction (ORR) catalyst in alkaline condition, which is important for the zinc-air batteries. Here, we report that an Ag based single atom catalyst with heteroatom coordination. Ag-1-h-NPCISC, has been synthesized and shown much improved performance towards ORR by manipulating the coordination environment of the Ag center. It shows a high half wave potential (0.896 V) and a high turnover frequency (TOF) (5.9 s(-1)) at 0.85 V, which are higher than the previously reported Ag based catalysts and commercial Pt/C. A zinc-air battery with high peak power density of 270 mW.cm(-2) is fabricated by using the Ag-1-h-NPCISC as air electrode. The high performance is attributed to (1) the hollow structure providing good mass transfer; (2) the single atom metal center structure providing high utility of the Ag; (3) heteroatom coordination environment providing the adjusted binding to the ORR intermediates. Density functional theory (DFT) calculations show that the energy barrier for the formation of OOH*, which is considered as the rate determine step for ORR on Ag nanoparticles, is lowered on Ag-1-h-NPCISC, thus improving the ORR activity. This work demonstrates that the well manipulated Ag based single atom catalysts are promising in electrocatalysis.

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