Carbon nanotubes decorated with Pt as a viable electrocatalyst system using electrochemical atomic layer deposition
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Drexler, Matthew
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Georgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USAGeorgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
Drexler, Matthew
[1
]
Abdelhafiz, Ali
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MIT, 77 Massachusetts Ave, Cambridge, MA 02139 USAGeorgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
Abdelhafiz, Ali
[2
]
Howe, Jane
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Univ Toronto, 27 Kings Coll Circle, Toronto, ON M5S 1A1, CanadaGeorgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
Howe, Jane
[3
]
Eres, Gyula
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Oak Ridge Natl Lab, POB 2008, Oak Ridge, TN 37831 USAGeorgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
Eres, Gyula
[4
]
Alamgir, Faisal
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Georgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USAGeorgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
Alamgir, Faisal
[1
]
机构:
[1] Georgia Inst Technol, Sch Mat Sci & Engn, North Ave 771 Ferst Dr, Atlanta, GA 30332 USA
[2] MIT, 77 Massachusetts Ave, Cambridge, MA 02139 USA
Surface limited redox replacement (SLRR) is an electrochemical deposition method designed to deposit metal thin films, typically onto other metals, that are mere monolayers in thickness, where such low dimensions allows catalyst-support interactions to affect catalyst efficiency. Here we explore the growth of Pt, using iterative Cumediated SLRR cycles, directly onto carbon nanotubes (CNTs) which are potentially good candidates as electrocatalyst supports due to their electrical conductivity and chemical resistance. Scanning electron microscope images showed that Pt grew as nanoparticles, and hydrogen underpotential deposition from cyclic voltammetry showed that the active surface area approached an asymptotic value around eight iterations. Catalytic activity, measured using the oxygen reduction reaction, reached a maximum at ten iterations. Both are shown to be influenced by the growth mode, but electrochemical modeling indicates that the trend in activity is also due to a change in activation energy, possibly due to changes in Pt electronic structure due to interactions with the CNTs. Durability cycling showed a greater than 85% retention of surface area for the first 10,000 cycles of accelerated stress testing but decayed steadily to about 50% after 30,000 cycles. This performance may be related to the phenomenon that limits surface area growth.