Key Laboratory of Fuel Cell Technology of Guangdong Province, Department of Chemistry, College of Chemistry and Chemical Engineering , South China University of Technology , Guangzhou 510640 , China.
Langmuir. 2018 May 22;34(20):5719-5727. doi: 10.1021/acs.langmuir.8b00328. Epub 2018 May 8.
Pt-based catalysts with novel structure have attracted great attention due to their outstanding performance. In this work, HPtCl was used as both precursor and etching agent to realize the shape-controlled synthesis of Pt-modified Au@Ag nanorods (NRs). During the synthesis, the as-prepared Ag shell played a crucial role in both protecting the Au NRs from being etched away by PtCl and leading to an unusual growth mode of Pt component. The site-specified etching and/or growth depended on the concentration of HPtCl, where high-yield core-shell structure or dumbbell-like structure could be obtained. The shape-controlled synthesis also led to a tunable longitudinal surface plasmon resonance from ca. 649 to 900 nm. Meanwhile, the core-shell Pt-modified Au@Ag NRs showed approximately 4-fold enhancement in catalytic reduction reaction of p-nitrophenol than that of the Au NRs, suggesting the great potential for photocatalytic reaction.
基于铂的催化剂具有新颖的结构,由于其出色的性能而引起了极大的关注。在这项工作中,使用 HPtCl 作为前体和蚀刻剂来实现 Pt 修饰的 Au@Ag 纳米棒(NRs)的形状控制合成。在合成过程中,所制备的 Ag 壳在保护 Au NRs 免受 PtCl 刻蚀和导致 Pt 组分异常生长模式方面起着至关重要的作用。特定位置的刻蚀和/或生长取决于 HPtCl 的浓度,可以获得高产率的核壳结构或哑铃状结构。形状控制合成还导致从约 649nm 到 900nm 的可调谐纵向表面等离子体共振。同时,核壳 Pt 修饰的 Au@Ag NRs 在对 p-硝基苯酚的催化还原反应中的活性比 Au NRs 提高了约 4 倍,这表明其在光催化反应中具有很大的潜力。