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Carbon supported Pt-Y electrocatalysts for the oxygen reduction reaction

机译:碳负载的Pt-Y电催化剂用于氧还原反应

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Carbon supported Pt_3Y(Pt_3Y/C) and PtY(PtY/C) were investigated as oxygen reduction reaction (ORR)cat- alysts. After synthesis via reduction by NaBH_4, the alloy catalysts exhibited 10-20% higher mass activity (mA mgpt~(-1)) than comparably synthesized Pt/C catalyst. The specific activity (μAcm_(pt)~(-2)) was 23 and 65% higher for the Pt_3 Y/C and PtY/C catalysts, respectively, compared to Pt/C. After annealing at 900 ℃ under a reducing atmosphere, Pt_3Y/C-900 and PtY/C-900 catalysts showed improved ORR activity; the Pt/C and Pt/C-900 (Pt/C catalyst annealed at 900 ℃) catalysts exhibited specific activities of 334 and 393 μA cm_(pt)~(-2), respectively, while those of the Pt_3 Y/C-900 and PtY/C-900 catalysts were 492 and 1050μA cm_(pt)~(-2), respectively. X-ray diffraction results revealed that both the Pt_3Y/C and PtY/C catalysts have a fcc Pt structure with slight Y doping. After annealing, XRD showed that more Y was incorporated into the Pt structure in the Pt_3Y/C-900 catalyst, while the PtY/C-900 catalyst remained unchanged. Although these results suggested that the high ORR activity of the PtY/C-900 catalyst did not originate from Pt-Y alloy formation, it is clear that the Pt-Y system is a promising ORR catalyst which merits further investigation.
机译:研究了碳载Pt_3Y(Pt_3Y / C)和PtY(PtY / C)作为氧还原反应(ORR)催化剂。通过NaBH_4还原进行合成后,合金催化剂的质量活性(mA mgpt〜(-1))比比较合成的Pt / C催化剂高10-20%。与Pt / C相比,Pt_3 Y / C和PtY / C催化剂的比活度(μAcm_(pt)〜(-2))分别高23和65%。 Pt_3Y / C-900和PtY / C-900催化剂在还原气氛下于900℃退火后,ORR活性提高。 Pt / C和Pt / C-900(在900℃退火的Pt / C催化剂)的比活分别为334和393μAcm_(pt)〜(-2),而Pt_3 Y / C- 900和PtY / C-900催化剂分别为492和1050μAcm_(pt)〜(-2)。 X射线衍射结果表明,Pt_3Y / C和PtY / C催化剂均具有fcc Pt结构,并带有少量的Y掺杂。退火后,XRD显示在Pt_3Y / C-900催化剂中更多的Y掺入Pt结构,而PtY / C-900催化剂保持不变。尽管这些结果表明PtY / C-900催化剂的高ORR活性并非源于Pt-Y合金的形成,但显然Pt-Y体系是一种有前途的ORR催化剂,值得进一步研究。

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