In the present work, a combination of imaging, spectroscopic and computational methods shows that 1-dodecanethiol undergoes S-deprotonation to form 1-dodecanethiolate on the surface of palladium nanoparticles, which then self-assembles into a structure that shows a high degree of order. The alkyl chain is largely in the all-trans conformation, which occurs despite the small size of the nanoparticle, (mean diameter = 3.9 nm). Inelastic neutron scattering spectroscopy is readily able to characterise organic surface layers on nanoparticles; the nature of the material is irrelevant: whether the nanoparticle core is an oxide, a metal or a semiconductor makes no difference. Comparison to DFT calculations allows insights into the nature and conformation of the adsorbed layer.

The adsorbed state of a thiol on palladium nanoparticles / Rogers, Scott M.; Dimitratos, Nikolaos; Jones, Wilm; Bowker, Michael; Kanaras, Antonios G.; Wells, Peter P.; Catlow, C. Richard A.; Parker, Stewart F.. - In: PHYSICAL CHEMISTRY CHEMICAL PHYSICS. - ISSN 1463-9076. - STAMPA. - 18:26(2016), pp. 17265-17271. [10.1039/c6cp00957c]

The adsorbed state of a thiol on palladium nanoparticles

Dimitratos, Nikolaos;
2016

Abstract

In the present work, a combination of imaging, spectroscopic and computational methods shows that 1-dodecanethiol undergoes S-deprotonation to form 1-dodecanethiolate on the surface of palladium nanoparticles, which then self-assembles into a structure that shows a high degree of order. The alkyl chain is largely in the all-trans conformation, which occurs despite the small size of the nanoparticle, (mean diameter = 3.9 nm). Inelastic neutron scattering spectroscopy is readily able to characterise organic surface layers on nanoparticles; the nature of the material is irrelevant: whether the nanoparticle core is an oxide, a metal or a semiconductor makes no difference. Comparison to DFT calculations allows insights into the nature and conformation of the adsorbed layer.
2016
The adsorbed state of a thiol on palladium nanoparticles / Rogers, Scott M.; Dimitratos, Nikolaos; Jones, Wilm; Bowker, Michael; Kanaras, Antonios G.; Wells, Peter P.; Catlow, C. Richard A.; Parker, Stewart F.. - In: PHYSICAL CHEMISTRY CHEMICAL PHYSICS. - ISSN 1463-9076. - STAMPA. - 18:26(2016), pp. 17265-17271. [10.1039/c6cp00957c]
Rogers, Scott M.; Dimitratos, Nikolaos; Jones, Wilm; Bowker, Michael; Kanaras, Antonios G.; Wells, Peter P.; Catlow, C. Richard A.; Parker, Stewart F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/659463
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