Pore-size tuning and optical performances of nanoporous gold films

被引:27
作者
Chen, A. Y. [1 ]
Shi, S. S. [1 ]
Qiu, Y. D. [1 ]
Xie, X. F. [2 ]
Ruan, H. H. [3 ]
Gu, J. F. [4 ]
Pan, D. [1 ]
机构
[1] Shanghai Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai 200090, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[3] Hong Kong Polytech Univ, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, Shanghai 200030, Peoples R China
关键词
Nanoporous gold; Pore size; Dealloying; Surface diffusion; Optical performance; ENHANCED RAMAN-SCATTERING; CHARACTERISTIC LENGTH; INTERFACES; EVOLUTION; AU;
D O I
10.1016/j.micromeso.2014.09.048
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Through pulse electrochemical dealloying (PED) and chemical dealloying (CD), a variety of nanoporous gold (NPG) films of 100 nm thickness with a wide range of pore size (4-140 nm) were prepared. The coarsening mechanism of pore and the effect of residual Ag on optical performances were investigated. The pore size was tuned by controlling the dissolution rate of active Ag atoms and surface diffusion rate of noble Au atoms along the alloy/solution interfaces. The maximum pore size of 140 nm was obtained by surfactant-assisted chemical dealloying (SA-CD) and the minimum pore size of 4 nm was achieved by PED. It is found that the surface diffusivity of gold in PED is about 0.4-2 x 10(-20) m(2) s(-1), four orders of magnitude smaller than that in SA-CD (2.4 x 10(-16) m(2) s(-1)). Finally, optical performances of the NPG films were investigated by UV-vis and surface-enhanced Raman scattering (SERS) spectra. The results reveal that the NPG film with a pore size of 8 nm fabricated by FED exhibits higher surface-plasmon absorption and the strongest SERS effect. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
相关论文
共 27 条
[1]   Kinetics of particle coarsening at gold electrode/electrolyte solution interfaces followed by in situ scanning tunneling microscopy [J].
Andreasen, G ;
Nazzarro, M ;
Ramirez, J ;
Salvarezza, RC ;
Arvia, AJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (02) :466-471
[2]   Elaboration of nanoporous copper by modifying surface diffusivity by the minor addition of gold [J].
Dan, Zhenhua ;
Qin, Fengxiang ;
Sugawara, Yu ;
Muto, Izumi ;
Hara, Nobuyoshi .
MICROPOROUS AND MESOPOROUS MATERIALS, 2013, 165 :257-264
[3]   Metallic mesoporous nanocomposites for electrocatalysis [J].
Ding, Y ;
Chen, MW ;
Erlebacher, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (22) :6876-6877
[4]   Preparation, structure, and optical properties of nanoporous gold thin films [J].
Dixon, Matthew C. ;
Daniel, Thomas A. ;
Hieda, Mitsunori ;
Smilgies, Detlef M. ;
Chan, Moses H. W. ;
Allara, David L. .
LANGMUIR, 2007, 23 (05) :2414-2422
[5]   Dealloying of Ag-Au alloys in halide-containing electrolytes - Affect on critical potential and pore size [J].
Dursun, A ;
Pugh, DV ;
Corcoran, SG .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (07) :B355-B360
[6]   Numerical simulation of dealloying by surface dissolution via the evolving surface finite element method [J].
Eilks, C. ;
Elliott, C. M. .
JOURNAL OF COMPUTATIONAL PHYSICS, 2008, 227 (23) :9727-9741
[7]   Electrodeposition of gold thin films with controlled morphologies and their applications in electrocatalysis and SERS [J].
Elias, Jamil ;
Gizowska, Magdalena ;
Brodard, Pierre ;
Widmer, Roland ;
deHazan, Yoram ;
Graule, Thomas ;
Michler, Johann ;
Philippe, Laetitia .
NANOTECHNOLOGY, 2012, 23 (25)
[8]   An atomistic description of dealloying - Porosity evolution, the critical potential, and rate-limiting behavior [J].
Erlebacher, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (10) :C614-C626
[9]   Evolution of nanoporosity in dealloying [J].
Erlebacher, J ;
Aziz, MJ ;
Karma, A ;
Dimitrov, N ;
Sieradzki, K .
NATURE, 2001, 410 (6827) :450-453
[10]  
Felicia T., 2007, NANOTECHNOLOGY, V18