Effect of organic vapors on Au, Ag, and Au-Ag alloy nanoparticle films with adsorbed 2,6-dimethylphenyl isocyanide

被引:5
作者
Kim, Kwan [1 ]
Kim, Kyung Lock [1 ]
Shin, Kuan Soo [2 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 151742, South Korea
[2] Soongsil Univ, Dept Chem, Seoul 156743, South Korea
基金
新加坡国家研究基金会;
关键词
Gold-silver alloy; Nanoparticles; Surface-enhanced Raman scattering; Volatile organic compounds; Surface potential; SURFACE-ENHANCED RAMAN; GOLD NANOPARTICLES; METAL; MONOLAYERS; SCATTERING; SILVER; ATOMS;
D O I
10.1016/j.jcis.2013.08.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The physicochemical properties of metallic substrates are affected by the environment in different ways. It is generally difficult to determine these effects because the molecules in the environment interact weakly with metallic substrates. In this work, we demonstrate that even the effect of volatile organic compounds (VOCs) can be identified by utilizing the surface-enhanced Raman scattering of isocyanide molecules. The NC stretching band of 2,6-dimethylphenyl isocyanide (2,6-DMPI) adsorbed on Au, for, instance, is blueshifted by 6 cm(-1) under an acetone flow and is redshifted by 20 cm(-1) under an ammonia flow. The same band of 2,6-DMPI adsorbed on Ag and Au0.5Ag0.5 alloy films is, however, redshifted equally by 8 and 13 cm(-1) under acetone and ammonia flows, respectively. This indicates that although the surface plasmons of Au0.5Ag0.5 alloy nanoparticles are clearly distinct from those of Ag (as well as Au) nanoparticles, both Au0.5Ag0.5 and Ag nanoparticles show a similar response to VOCs. These observations led us to conclude that the outermost parts of Au-Ag alloy nanoparticles are enriched with Ag atoms and that only the surfaces of metal nanoparticles, and not the bulk material, are affected by VOCs. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:194 / 197
页数:4
相关论文
共 19 条
[11]   Reactions of laser-ablated Ag and Au atoms with carbon monoxide:: Matrix infrared spectra and density functional calculations on Ag(CO)n (n = 2, 3), Au(CO)n (n = 1, 2) and M(CO)n+ (n = 1-4; M = Ag, Au) [J].
Liang, BY ;
Andrews, L .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (40) :9156-9164
[12]   Alloy formation of gold-silver nanoparticles and the dependence of the plasmon absorption on their composition [J].
Link, S ;
Wang, ZL ;
El-Sayed, MA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (18) :3529-3533
[13]   Tailoring surface plasmons through the morphology and assembly of metal nanoparticles [J].
Liz-Marzán, LM .
LANGMUIR, 2006, 22 (01) :32-41
[14]   Persistent misconceptions regarding SERS [J].
Moskovits, Martin .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (15) :5301-5311
[15]   Density functional investigation of the interaction of acetone with small gold clusters [J].
Shafai, Ghazal S. ;
Shetty, Sharan ;
Krishnamurty, Sailaja ;
Shah, Vaishali ;
Kanhere, D. G. .
JOURNAL OF CHEMICAL PHYSICS, 2007, 126 (01)
[16]   Adsorbate-Induced Changes in Surface Potential of Gold Nanoparticles Revealed by Raman Spectroscopy [J].
Shin, Dongha ;
Kim, Kwan ;
Shin, Kuan S. .
CHEMPHYSCHEM, 2010, 11 (01) :83-86
[17]   Reaction-Driven Restructuring of Rh-Pd and Pt-Pd Core-Shell Nanoparticles [J].
Tao, Feng ;
Grass, Michael E. ;
Zhang, Yawen ;
Butcher, Derek R. ;
Renzas, James R. ;
Liu, Zhi ;
Chung, Jen Y. ;
Mun, Bongjin S. ;
Salmeron, Miquel ;
Somorjai, Gabor A. .
SCIENCE, 2008, 322 (5903) :932-934
[18]   Formation and structure of self-assembled monolayers [J].
Ulman, A .
CHEMICAL REVIEWS, 1996, 96 (04) :1533-1554
[19]   Field-dependent electrode-chemisorbate bonding: Sensitivity of vibrational stark effect and binding energetics to nature of surface coordination [J].
Wasileski, SA ;
Koper, MTM ;
Weaver, MJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (11) :2796-2805