Chemical Reactivity of Naphthalenecarboxylate-Protected Ruthenium Nanoparticles: Intraparticle Charge Delocalization Derived from Interfacial Decarboxylation

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• 作者：Limei Chen ; Peiguang Hu ; Christopher P. Deming ; Wei Li ; Ligui Li ; Shaowei Chen
• 刊名：Journal of Physical Chemistry C
• 出版年：2015
• 出版时间：July 9, 2015
• 年：2015
• 卷：119
• 期：27
• 页码：15449-15454
• 全文大小：365K
• ISSN：1932-7455

文摘

Ruthenium nanoparticles were prepared by thermolytic reduction of RuCl₃ in 1,2-propanediol containing sodium 2-naphthalenecarboxylate. Transmission electron microscopic measurements showed that the average diameter of the resulting 2-naphthalenecarboxylate-protected ruthenium nanoparticles (RuCOONA) was 1.30 卤 0.27 nm. Interestingly, hydrothermal treatment of the nanoparticles at controlled temperatures led to decarboxylation at the metal鈥搇igand interface, and the naphthalenyl moieties became directly bonded to the metal cores, which was confirmed by infrared and X-ray photoelectron spectroscopic measurements. In comparison with the as-produced RuCOONA nanoparticles, the decarboxylated nanoparticles (RuNA) exhibited markedly different optical and electronic properties, as manifested by an apparent red shift of the photoluminescence profiles, which was ascribed to electronic coupling between the particle-bound naphthalene groups. Electrochemical measurements exhibited consistent results where a negative shift was observed of the formal potential of the particle-bound naphthalene moieties. This was attributed to intraparticle charge delocalization that led to extended spilling of nanoparticle core electrons to the naphthalene moieties.