Boosting electrochemical stability of ultralow-Pt nanoparticle with Matryoshka-like structure in polymer electrolyte membrane fuel cells

[Display omitted] •Carbon-supported Pt-based materials with Matryoshka-like structure are proposed as ORR catalysts.•The catalyst has 3.4 times higher mass activity than commercial Pt/C in half-cell.•Pt@CuILPd/C-based polymer electrolyte membrane fuel cells show high and stable performance. Electroc...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2020-07, Vol.268, p.118450, Article 118450
Hauptverfasser: Lee, Hyunjoon, Park, Ji Eun, Kim, Ok-Hee, Hwang, Wonchan, Choi, Hee Ji, Yang, Jae Choon, Ahn, Chi-Yeong, Su Lim, Myung, Choi, Insoo, Cho, Yong-Hun, Sung, Yung-Eun
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Sprache:eng
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Zusammenfassung:[Display omitted] •Carbon-supported Pt-based materials with Matryoshka-like structure are proposed as ORR catalysts.•The catalyst has 3.4 times higher mass activity than commercial Pt/C in half-cell.•Pt@CuILPd/C-based polymer electrolyte membrane fuel cells show high and stable performance. Electrochemical catalysts with a core-shell structure have received much attention because of their enhanced efficiency and activity. Among them, those with a CuPd alloy core exhibit better activity than the ones with a single metal Pd core, which is known to be an excellent core-material. However, the superior performance of previously reported Pt catalysts with CuPd core has only been observed in half-cells, and was not reflected or even expanded to single-cells. We report catalysts having a Matryoshka-like structure with a Pt outer-layer, Cu interlayer, and Pd core for oxygen reduction reaction. This catalyst has 3.4 times higher Pt mass activity than the commercial Pt/C in half-cells, and also performs better in single-cells at only 0.056 mgPt cm−2. Particularly, the stability of this catalyst satisfies the 2020 DOE target, and electrochemical surface area loss during the stability test is only 40 % for this catalyst, while that of Pt/C is 80 %.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2019.118450