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研究论文

不同Pt壳厚度Au_(core)@Pt_(shell)纳米粒子SERS效应

  • 钟艳 ,
  • 颜亮亮 ,
  • 饶贵仕 ,
  • 邓小聪 ,
  • 温飞鹏 ,
  • 徐金龙 ,
  • 钟起玲
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  • 江西师范大学化学化工学院;

收稿日期: 2010-08-28

  修回日期: 2010-08-28

  网络出版日期: 2010-08-28

The SERS Effect of Au_(core)@Pt_(shell) Nanoparticles with Different Pt Shell Thicknesses

  • ZHONG Yan ,
  • YAN Liang-liang ,
  • RAO Gui-shi ,
  • DENG Xiao-cong ,
  • WEN Fei-peng ,
  • XU Jin-long ,
  • ZHONG Qi-ling
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  • ( Department of Chemistry and Chemical Engineering,Jiangxi Normal University,Nanchang 330022,China

Received date: 2010-08-28

  Revised date: 2010-08-28

  Online published: 2010-08-28

摘要

以Au粒子(55nm)为核,抗坏血酸为还原剂,将不同量的Pt沉积在Au核上,制得可控壳层厚度(0.3~6nm)的Pt包Au纳米粒子(Aucore@Ptshell).用紫外-可见吸收光谱、扫描电镜(SEM)、透射电镜(TEM)和电化学循环伏安法等观测Aucore@Ptshell纳米粒子的表面形貌、结构和性能.另以SCN-为探针,考察了Pt壳厚度对Aucore@Ptshell纳米粒子SERS信号的影响.结果表明,SCN-离子的SERS信号强度随Pt壳厚度的增加呈指数衰减,当Pt壳厚度为1.4nm时,Aucore@Ptshel纳米粒子表现出铂良好的电化学性能,又具有较强的SERS活性.

本文引用格式

钟艳 , 颜亮亮 , 饶贵仕 , 邓小聪 , 温飞鹏 , 徐金龙 , 钟起玲 . 不同Pt壳厚度Au_(core)@Pt_(shell)纳米粒子SERS效应[J]. 电化学, 2010 , 16(3) : 300 -304 . DOI: 10.61558/2993-074X.2053

Abstract

By using Au nanoparticles with a diameter of 55 nm as the core and ascorbic acid as the reductant, Aucore@ Ptshell nanoparticles of controllable Pt shell thickness( 0. 3 ~ 6 nm) were synthesized by controlling the concentration of [PtCl6]2 - ions. The ultraviolet-visible absorption spectrometry,scanning electron microscope ( SEM) ,transmission electron microscope ( TEM) ,high resolution transmission electron microscope ( HRTEM) , and electrochemical cyclic voltammetry were employed to determine surface morphology and structure of Aucore@ Ptshell. With SCN - ion as a probe,the effect of the thickness of the Pt shell on the SERS signals of Aucore@ Ptshell nanoparticles was investigated. It was found that the intensities of SERS signals decreased exponentially with the increase of Pt shell thickness. The result revealed that at a shell thickness of 1. 4 nm,the core-shell nanoparticles present the chemical property of the Pt shell and having a large SERS activity.

参考文献

[1]Zou S Z,Williams C T,Chen E K Y,et al.Probing mo-lecular vibrations at catalytically significant interfaces:anew ubiquity of surface-enhanced Raman scattering[J].J Am Chem Soc,1998,120(15):3811-3812. [2]Mrozek M F,Xie Y,Weaver M J.Surface-enhanced Ra-man scattering on uniform Platinum-group overlayers:preparation by redox replacement of underpotential-de-posited metals on gold[J].Anal Chem,2001,73(24):5953-5960. [3]Park S,Yang P X,Corredor P,et al.Transition metal-coated nanoparticle films:Vibrational characterization with surface-enhanced Raman scattering[J].J Am Chem Soc,2002,124(11):2428-2429. [4]Zhang B,Li J F,Zhong Q L,et al.Electrochemical and surfaced-enhanced Raman spectroscopic investigation of CO and SCN-adsorbed on Aucore-Ptshell nanoparticles supported on GC electrodes[J].Langmuir,2005,21(16):7449-7455. [5]Li J F(李剑锋),Hu J W(胡家文),Ren B(任斌),et al.Tuning the SERS activity of Au@Pd core-shell nano-particles by controlling the thickness of the Pd shell[J].Acta Phys-Chim Sin(物理化学学报),2005,21(8):825-828. [6]Rao G S(饶贵仕),Fan F R(范凤茹),Wang G F(王国富),et al.In-situ SERS of formic acid electro-catalyt-ic oxidation on Aucore@Ptshell/Pt electrode[J].Acta Phy-Chim Sin(物理化学学报),2008,24(2):345-349. [7]Henglein A.Colloidal Palladium nanoparticles:reduction of Pd(II)by H2;PdCoreAuShellAgShell particles[J].J Phys Chem B,2000,104(29):6683-6685. [8]Lambert D K.Stark effect of adsorbate vibrations[J].Solid State Commun,1984,51(5):297-300. [9]Gans P,Gill J B,Fearnley D P.Spectrochemistry of so-lutions.Part14.Raman and infrared spectra of thiocya-natosilver(I)complexes in some non-aqueous solutions[J].J Chem Soc,Dalton Trans,1987(7):1708-1713. [10]Zhang Y(张勇).Synthesis and SERS characterize-ation of platinum nanoparticles of different shape[D].Xiamen:Xiamen University,2005.
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