Synthesis of Au/Pt bimetallic nanoparticles with a Pt-rich shell and their high catalytic activities for aerobic glucose oxidation

双金属片 化学 催化作用 纳米颗粒 酒精氧化 乙烯醇 化学工程 粒子(生态学) 粒径 聚合物 有机化学 物理化学 海洋学 工程类 地质学
作者
Haijun Zhang,Naoki Toshima
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:394: 166-176 被引量:77
标识
DOI:10.1016/j.jcis.2012.11.059
摘要

Integration of 'green chemistry' principles into nanotechnology is one of the key issues in nanoscience research today. In this work, three series of Au/Pt bimetallic nanoparticles (BNPs) with a structure of Au-rich core/Pt-rich shell were prepared using simultaneous reduction with rapid injection of NaBH(4), simultaneous reduction with dropwise addition of NaBH(4), and simultaneous alcohol reduction. The effects of particle size, electronic structure and composition upon the catalytic activities for aerobic glucose oxidation of the BNPs were also investigated. Catalytically highly active PVP-protected Au/Pt BNPs of about 1.5 nm in diameter were synthesized using simultaneous reduction with rapid injection of NaBH(4). The prepared colloidal Au/Pt BNPs catalysts possessed a high and durable catalytic activity for aerobic glucose oxidation, which were stably kept for more than 2 months under ambient conditions. The maximum activities normalized with Au content of the BNPs with Au/Pt atomic ratio of 4/6 were nearly 10 times higher than that of Au nanoparticles (NPs) with nearly the same particle size. The higher catalytic activity of the prepared Au/Pt BNPs than the Au NPs can be ascribed to the following two factors; (1) the small average diameter, usually about 1.5 nm, and (2) the presence of negatively charged Au and Pt atoms due to electron donation from protecting polymer (PVP: poly(N-vinyl-2-pyrrolidone)) by electronic charge transfer effects upon catalytically active sites. In contrast, the Au/Pt BNPs, synthesized by alcohol reduction and dropwise addition of NaBH(4) into the starting solution and having the large mean particle sizes, showed a low catalytic activity.

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