Voltage-Induced Adsorbate Damping of Single Gold Nanorod Plasmons in Aqueous Solution

被引:70
作者
Dondapati, S. K. [1 ,2 ]
Ludemann, M. [3 ,4 ]
Mueller, R. [3 ,4 ]
Schwieger, S. [3 ,4 ]
Schwemer, A. [1 ,2 ]
Haendel, B. [3 ,4 ]
Kwiatkowski, D. [5 ]
Djiango, M. [5 ]
Runge, E. [3 ,4 ]
Klar, T. A. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Munich, Photon & Optoelect Grp, Dept Phys, D-80799 Munich, Germany
[2] Univ Munich, CENS, Dept Phys, D-80799 Munich, Germany
[3] Ilmenau Univ Technol, Inst Phys, D-98684 Ilmenau, Germany
[4] Ilmenau Univ Technol, Inst Micro & Nanotechnol, D-98684 Ilmenau, Germany
[5] Johannes Kepler Univ Linz, Inst Appl Phys, A-4040 Linz, Austria
关键词
Plasmonics; electrochemistry; interface damping; ion sensing; nanoparticle plasmon resonance; localized surface plasmon resonance; QUARTZ-CRYSTAL MICROBALANCE; COLLOIDAL SILVER; METAL NANOPARTICLES; MATRIX ENVIRONMENT; OPTICAL-PROPERTIES; AU-NANOPARTICLES; OXIDE-GROWTH; INTERFACE; RESONANCE; SPECTROSCOPY;
D O I
10.1021/nl203673g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unbiased gold nanoparticles are negatively charged in aqueous solution but not hydrated. Optical spectroscopy of voltage-clamped single gold nanoparticles reveals evidence that anion adsorption starts at positive potentials above the point of zero charge, causing severe but reversible plasmon damping in combination with a spectral red shift exceeding the linear double layer charging effect. Plasmon damping by adsorbate is relevant for the use of nanoparticles in catalysis, in biodiagnostics, and in surface enhanced Raman scattering.
引用
收藏
页码:1247 / 1252
页数:6
相关论文
共 51 条
[1]   Optical properties of nanoscopic gold particles adsorbed at electrode surfaces: The effect of applied potential on plasmon resonance absorption. [J].
Ali, AH ;
Luther, RJ ;
Foss, CA ;
Chapman, GB .
NANOSTRUCTURED MATERIALS, 1997, 9 (1-8) :559-562
[2]  
Barber P. W., 1990, Light Scattering by Particles: Computational Methods
[3]   Unveiling Electron Promiscuity [J].
Ben-Amotz, Dor .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2011, 2 (10) :1216-1222
[4]   AN INSITU WEIGHING STUDY OF THE MECHANISM FOR THE FORMATION OF THE ADSORBED OXYGEN MONOLAYER AT A GOLD ELECTRODE [J].
BRUCKENSTEIN, S ;
SHAY, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1985, 188 (1-2) :131-136
[5]   INTERFACE ELECTRONIC-STRUCTURE FROM ELLIPSOMETRY COUPLED WITH DIFFERENTIAL CAPACITY MEASUREMENTS [J].
CHAO, F ;
COSTA, M ;
LECOEUR, J ;
BELLIER, JP .
ELECTROCHIMICA ACTA, 1989, 34 (12) :1627-1638
[6]   THE USE OF OPTICS FOR UNDERSTANDING THE ELECTROCHEMICAL INTERFACE [J].
CHAO, F ;
COSTA, M ;
TADJEDDINE, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1992, 329 (1-2) :313-327
[7]   Electro-optical shifts in silver nanoparticle films [J].
Chapman, R ;
Mulvaney, P .
CHEMICAL PHYSICS LETTERS, 2001, 349 (5-6) :358-362
[8]   THE OPTICAL-PROPERTIES OF SILVER MICROCRYSTALLITES IN DEPENDENCE ON SIZE AND THE INFLUENCE OF THE MATRIX ENVIRONMENT [J].
CHARLE, KP ;
FRANK, F ;
SCHULZE, W .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1984, 88 (04) :350-354
[9]  
Choi Y, 2009, NAT NANOTECHNOL, V4, P742, DOI [10.1038/nnano.2009.258, 10.1038/NNANO.2009.258]
[10]   SURFACE STRUCTURAL-CHANGES DURING OXIDATION OF GOLD ELECTRODES IN AQUEOUS-MEDIA AS DETECTED USING SURFACE-ENHANCED RAMAN-SPECTROSCOPY [J].
DESILVESTRO, J ;
WEAVER, MJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 209 (02) :377-386