Pt-Co truncated octahedral nanocrystals: A class of highly active and durable catalysts toward oxygen reduction

Min Shen, Minghao Xie, John Slack, Krysta Waldrop, Zitao Chen, Zhiheng Lyu, Shaohong Cao, Ming Zhao, Miaofang Chi, Peter N. Pintauro, Rong Cao, Younan Xia

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

We report a facile and scalable synthesis of Pt-Co truncated octahedral nanocrystals (TONs) by employing Pt(acac)2 and Co(acac)2 as precursors, together with CO molecules and Mn atoms derived from the decomposition of Mn2(CO)10 as a reductant and a {111} facet-directing agent, respectively. Both the composition and yield of the Pt-Co TONs could be varied through the introduction of CHCl3. When tested at 80 °C using membrane electrode assembly (MEA), the 4 nm Pt2.6Co TONs gave a mass activity of 294 A gPt-1 at beginning-of-life (BOL) and it increased to 384 A gPt-1 during recovery cycles. The mass activity at BOL only dropped by 24% after 30 000 voltage cycles at end-of-life (EOL) in a metal dissolution accelerated stress test. The Pt2.6Co/C catalyst outperformed the commercial TKK Pt3Co/C (230 A gPt-1 at BOL and 40% loss after 30 000 cycles at EOL) in terms of both activity and durability. Our systematic analysis suggested that the enhancement in activity can be attributed to the combination of small, uniform size and well-defined {111} facets. This new class of catalysts holds promise for applications in proton-exchange membrane fuel cells.

Original languageEnglish
Pages (from-to)11718-11727
Number of pages10
JournalNanoscale
Volume12
Issue number21
DOIs
StatePublished - Jun 7 2020

Funding

This work was supported in part by U.S. Department of Energy (DOE) Fuel Cell Technologies Office (DOE contract No. DE-EE-000765) and start-up funds from the Georgia Institute of Technology. TEM imaging, high-resolution TEM imaging, XRD, and XPS analyses were performed at the Georgia Tech Institute for Electronics and Nanotechnology, a member of the National Nanotechnology Coordinated Infrastructure, which is supported by the NSF (Grant ECCS-1542174). The STEM and EDX characterizations were performed at the Oak Ridge National Laboratory’s Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. This work was supported in part by U.S. Department of Energy (DOE) Fuel Cell Technologies Office (DOE contract No. DE-EE-000765) and start-up funds from the Georgia Institute of Technology. TEM imaging, high-resolution TEM imaging, XRD, and XPS analyses were performed at the Georgia Tech Institute for Electronics and Nanotechnology, a member of the National Nanotechnology Coordinated Infrastructure, which is supported by the NSF (Grant ECCS-1542174). The STEM and EDX characterizations were performed at the Oak Ridge National Laboratory's Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility.

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