首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Dispersion Stability, Ligand Structure and Conformation, and SERS Activities of 1-Alkanethiol Functionalized Gold and Silver Nanoparticles
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Dispersion Stability, Ligand Structure and Conformation, and SERS Activities of 1-Alkanethiol Functionalized Gold and Silver Nanoparticles

机译:1-烷硫醇官能化的金和银纳米粒子的分散稳定性,配体结构和构象以及SERS活性

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摘要

Dispersion stability, ligand structure and conformation, and SERS activities of 1-alkanethiol (C_nH_(2n+1)SH, n = 2—14) functionalized gold and silver nanoparticles (AuNPs and AgNPs) were studied as a function of alkanethiol carbon chain length and nanoparticle (NP) type and size. The dispersion stability of alkanethiol functionalized NPs in water increases with increasing alkanethiol chain length and NP size, and the stabilities of the alkanethiol-containing AuNPs are higher than their AgNP counterparts. C3H7SH and longer alkanethiols are highly ordered on AgNPs but disordered on AuNPs. The SERS intensity of the C-S stretch band for the model alkanethiols on AgNPs and AuNPs decays exponentially (I = I_0 exp(— N_c/N_0)) with increasing number of carbon atoms (N_c). The empirical decay length N_0, in terms of the number of the carbon atoms, is 1.29, 0.53, and 0.10 for AgNPs with diameters of SO, 30, and 10 nm, respectively. This decay length is less than 1 for AuNPs of difference sizes. These results show that changing the NP gap size by a distance equivalent to a single chemical bond can have a significant impact on the NP integrated SERS activities.
机译:研究了1-链烷硫醇(C_nH_(2n + 1)SH,n = 2-14)官能化的金和银纳米颗粒(AuNP和AgNP)的分散稳定性,配体结构和SERS活性随链烷硫醇碳链长度的变化以及纳米粒子(NP)的类型和大小。链烷硫醇官能化的NPs在水中的分散稳定性随链烷硫醇链长和NP尺寸的增加而增加,且含链烷硫醇的AuNPs的稳定性高于其AgNP对应物。 C3H7SH和更长的链烷硫醇在AgNPs上高度有序,但在AuNPs上无序。随着碳原子数(N_c)的增加,模型链烷硫醇在AgNPs和AuNPs上的C-S拉伸带的SERS强度呈指数衰减(I = I_0 exp(-N_c / N_0))。就碳原子数而言,经验衰减长度N_0对于直径为SO,30和10 nm的AgNP分别为1.29、0.53和0.10。对于不同大小的AuNP,此衰减长度小于1。这些结果表明,改变NP间隙的大小相当于单个化学键的距离可以对NP整合的SERS活性产生重大影响。

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