Electrochemically fabricated gold dendrites with underpotential deposited silver monolayers for a bimetallic SERS-active substrate. Issue 16 (2nd February 2016)

• Record Type: Journal Article
• Authors: Lai, Ying-Huang; Kuo, Shan-Chi; Hsieh, Yun-Ching; Tai, Yu-Chun; Hung, Wei-Hsiu; Jeng, U-Ser
• Is Part Of: RSC advances. Volume 6:Issue 16(2016)
• Page Start: 13185
• Page End: 13192
• Publication Date: 2016-02-02
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra27020k
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : SERS of Ag-covered Au-dendrites (Ag–Au-Ds) outperforms that of Au-Ds at a specific 633 nm laser excitation, and is attributed to improved chemical mechanism (CM) SERS with the Ag– p -NTP bonding and the p -NTP molecular architecture. Abstract : With electrochemical deposition, cysteine-directed crystalline gold dendrites (Au-Ds) on glassy carbon electrodes were fabricated. The Au-Ds surfaces were further modified with Ag adatoms by underpotential deposition (UPD) for Ag-covered Au-Ds (Ag–Au-Ds). The Ag–Au-Ds possessed a hierarchical architecture comprising trunks, branches, and nanoleaves for a threefold-symmetry, resulting in a high density of sharp tips and edges for hot spots of surface-enhanced Raman scattering (SERS). Prominent SERS was observed with p -nitrothiophenol ( p -NTP) adsorption onto either Au-Ds or Ag–Au-Ds, for a best p -NTP detection limit down to 5–10 nM at 785 nm laser excitation. However, at specific 633 nm laser excitation, SERS with p -NTP adsorption on Ag–Au-Ds exhibited a three-fold higher enhancement over that measured for p -NTP adsorbed on unmodified Au-Ds, suggesting an increased chemical SERS enhancement with the Ag– p -NTP bonding. Furthermore, adsorption isotherms of p -NTP with Au-Ds and Ag–Au-Ds adsorption in solution are established from solution p -NTP-concentration dependent SERS; from which, comparable binding constants of p -NTP to Au-Ds and Ag–Au-Ds are extracted.