2006
DOI: 10.1021/cm0518978
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Pt Nanoparticle Binding on Functionalized Multiwalled Carbon Nanotubes

Abstract: To create new catalyst materials for fuel cell applications, multiwalled carbon nanotubes (CNTs) were functionalized with sCdO, sCsOsCs, sCOOs, and sCsOH groups using a sonochemical treatment method under acidic aqueous solution (HNO 3 /H 2 SO 4 ) conditions to make them amenable to deposition of highly dispersed, ∼4 nm diameter Pt nanoparticles. The Pt-CNT interface was probed with X-ray photoelectron spectroscopy (XPS), extended X-ray absorption fine structure spectroscopy (EXAFS), and Raman and attenuated t… Show more

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Cited by 267 publications
(194 citation statements)
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References 51 publications
(78 reference statements)
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“…We note that the interaction we observe differs from that of Hull et al who deposited pre-prepared Pt nanoclusters onto functionalised carbon nanotubes [31]. In this case, while the majority of the Pt was present in metallic form, they observed a weak XPS signal indicating PtO x formation on the nanocluster surfaces.…”
Section: Resultscontrasting
confidence: 71%
“…We note that the interaction we observe differs from that of Hull et al who deposited pre-prepared Pt nanoclusters onto functionalised carbon nanotubes [31]. In this case, while the majority of the Pt was present in metallic form, they observed a weak XPS signal indicating PtO x formation on the nanocluster surfaces.…”
Section: Resultscontrasting
confidence: 71%
“…Figure 3 shows the Pt 4f and Co 2p XPS spectra obtained from CZTS−Pt and CZTS−PtCo nanoheterostructures. As for monometallic CZTS−Pt (Figure 3a), 19 the Pt 4f spectrum of CZTS−PtCo (Figure 3b) presented relatively broad bands, which pointed to the presence of at least two pairs of doublets and thus two Pt chemical states, Pt 0 and Pt 2+ . From the fitting of the spectra it became clear that in both samples the metallic Pt 0 state is the main component.…”
Section: ■ Results and Discussionmentioning
confidence: 89%
“…The loss of intensity of the peak at 3450 cm -1 confirms the involvement and reduction of oxygen-containing groups in the formation of the Ag nanoparticles. Besides, it also suggests that strong interactions may exist between the Ag nanoparticles and the remaining surface hydroxyl O atoms [67]. Interestingly, the interactions between the nanoparticles and CCG were strong enough to ensure the nanoparticles remained attached even after chemical cleaning and ultrasonication.…”
Section: Resultsmentioning
confidence: 99%