Abstract:Under a controlled adsorption environment, L-cysteine molecules can be chemically adsorbed to the dendritic silver (Ag-D) surface by electrochemical methods with different functional groups. It is verified by surface-enhanced Raman spectroscopy that under alkaline conditions (pH = 13.50), the two functional groups of thiol and acid are simultaneously adsorbed on the surface of Ag-D, while NH2 is far from the surface; under acidic conditions (pH = 1.67), adsorption behavior suggests that both NH3+ and COO− are … Show more
“…The enhancement of the signal intensity in SERS is dependent on factors such as molecule distance, orientation, and affinity toward the metal surface. The SERS spectrum of the LC interacting with various metal surfaces has been studied both theoretically as well as experimentally. − Graff et al investigated the adsorption of the l - and d -cysteine enantiomers on an Ag electrode surface using the SERS technique as a function of electrode potential and solvent pH . A complete experimental study has been performed by Guicheteau et al on the IR, Raman, and SERS spectra of a series of amino acids (phenylalanine, tyrosine, tryptophan, glutamine, cysteine, alanine, proline, methionine, asparagine, threonine, valine, glycine, serine, leucine, isoleucine, aspartic acid, and glutamic acid) and the nucleic acid bases (adenosine, guanosine, thymidine, and uridine) .…”
Section: Introductionmentioning
confidence: 99%
“…The SERS and DFT calculations were used to investigate the adsorption of LC on the nanoparticle surfaces . Chang et al investigated the adsorption geometry of the LC on the dendric Ag surface using electrochemical methods in different pH environments …”
Section: Introductionmentioning
confidence: 99%
“…43 Chang et al investigated the adsorption geometry of the LC on the dendric Ag surface using electrochemical methods in different pH environments. 44 In our previous work, we investigated the effect of replacing the Au core atom of an Au 13 nanocluster with an Ag, Pd, and Pt atom (Ag@Au 12 , Pd@Au 12 , and Pt@Au 12 ) on its interaction with different forms of the LC (neutral, anionic, cationic, and zwitterion (ZW)). 33 The Ag@Au 12 , Pd@Au 12 , and Pt@Au 12 nanoclusters were chosen as models to investigate the effect of an Au nanoparticles core type on its interaction with the LC.…”
The effect of the core atom type of the M@Au 12 nanocluster (M = Au, Ag, Pt, and Pd) on the normal (NR) and charge-transfer surface-enhanced Raman spectroscopy (CT-SERS) of the zwitterion form of L-cysteine (ZWCYS) adsorbed on two different sites (D1 and D2) of the nanocluster is investigated separately in the gas phase and water. Because SERS requires the calculation of the absorption spectrum, the effect of the core atom type on the absorption spectrum of M@Au 12 and its complex with the ZWCYS has also been investigated. The vibrational bands that show the intensity enhancement in the CT-SERS of the ZWCYS interacting with the D1 site of M@Au 12 nanocluster in water are O�C�O asymmetric stretching (M = Au and Ag), NH 2 bending (M = Ag), S−H stretching (M = Ag, Pt, and Pd), CH 2 bending (M = Pt), and CH 2 symmetric stretching (M = Pt and Pd). The ZWCYS at the D 2 site of the M@Au 12 nanocluster in water exhibits intensity enhancement for O�C�O asymmetric stretching (M = Pt), NH 3 wagging (M = Au), and S−H stretching (M = Pd). The intensity of the vibrational bands of ZWCYS does not increase for M = Ag but decreases for O�C�O asymmetric stretching, S−H stretching, CH 2 symmetric stretching, CH 2 asymmetric stretching, and especially NH 2 symmetric stretching.
“…The enhancement of the signal intensity in SERS is dependent on factors such as molecule distance, orientation, and affinity toward the metal surface. The SERS spectrum of the LC interacting with various metal surfaces has been studied both theoretically as well as experimentally. − Graff et al investigated the adsorption of the l - and d -cysteine enantiomers on an Ag electrode surface using the SERS technique as a function of electrode potential and solvent pH . A complete experimental study has been performed by Guicheteau et al on the IR, Raman, and SERS spectra of a series of amino acids (phenylalanine, tyrosine, tryptophan, glutamine, cysteine, alanine, proline, methionine, asparagine, threonine, valine, glycine, serine, leucine, isoleucine, aspartic acid, and glutamic acid) and the nucleic acid bases (adenosine, guanosine, thymidine, and uridine) .…”
Section: Introductionmentioning
confidence: 99%
“…The SERS and DFT calculations were used to investigate the adsorption of LC on the nanoparticle surfaces . Chang et al investigated the adsorption geometry of the LC on the dendric Ag surface using electrochemical methods in different pH environments …”
Section: Introductionmentioning
confidence: 99%
“…43 Chang et al investigated the adsorption geometry of the LC on the dendric Ag surface using electrochemical methods in different pH environments. 44 In our previous work, we investigated the effect of replacing the Au core atom of an Au 13 nanocluster with an Ag, Pd, and Pt atom (Ag@Au 12 , Pd@Au 12 , and Pt@Au 12 ) on its interaction with different forms of the LC (neutral, anionic, cationic, and zwitterion (ZW)). 33 The Ag@Au 12 , Pd@Au 12 , and Pt@Au 12 nanoclusters were chosen as models to investigate the effect of an Au nanoparticles core type on its interaction with the LC.…”
The effect of the core atom type of the M@Au 12 nanocluster (M = Au, Ag, Pt, and Pd) on the normal (NR) and charge-transfer surface-enhanced Raman spectroscopy (CT-SERS) of the zwitterion form of L-cysteine (ZWCYS) adsorbed on two different sites (D1 and D2) of the nanocluster is investigated separately in the gas phase and water. Because SERS requires the calculation of the absorption spectrum, the effect of the core atom type on the absorption spectrum of M@Au 12 and its complex with the ZWCYS has also been investigated. The vibrational bands that show the intensity enhancement in the CT-SERS of the ZWCYS interacting with the D1 site of M@Au 12 nanocluster in water are O�C�O asymmetric stretching (M = Au and Ag), NH 2 bending (M = Ag), S−H stretching (M = Ag, Pt, and Pd), CH 2 bending (M = Pt), and CH 2 symmetric stretching (M = Pt and Pd). The ZWCYS at the D 2 site of the M@Au 12 nanocluster in water exhibits intensity enhancement for O�C�O asymmetric stretching (M = Pt), NH 3 wagging (M = Au), and S−H stretching (M = Pd). The intensity of the vibrational bands of ZWCYS does not increase for M = Ag but decreases for O�C�O asymmetric stretching, S−H stretching, CH 2 symmetric stretching, CH 2 asymmetric stretching, and especially NH 2 symmetric stretching.
We report a very simple, rapid and reproducible method for the fabrication of anisotropic silver nanostars (AgNS) that can be successfully used as highly efficient SERS substrates for different bioanalytes, even in the case of a near-infra-red (NIR) excitation laser. The nanostars have been synthesized using the chemical reduction of Ag+ ions by trisodium citrate. This is the first research reporting the synthesis of AgNS using only trisodium citrate as a reducing and stabilizing agent. The key elements of this original synthesis procedure are rapid hydrothermal synthesis of silver nanostars followed by a cooling down procedure by immersion in a water bath. The synthesis was performed in a sealed bottom flask homogenously heated and brought to a boil in a microwave oven. After 60 s, the colloidal solution was cooled down to room temperature by immersion in a water bath at 35 °C. The as-synthesized AgNS were washed by centrifugation and used for SERS analysis of test molecules (methylene blue) as well as biological analytes: pharmaceutical compounds with various Raman cross sections (doxorubicin, atenolol & metoprolol), cell lysates and amino acids (methionine & cysteine). UV-Vis absorption spectroscopy, (Scanning) Transmission Electron Microscopy ((S)TEM) and Atomic Force Microscopy (AFM) have been employed for investigating nanostars’ physical properties.
Controlling the growth and selection of chiral inducers is crucial for the generation of chiral inorganic structures as observed in nature. Herein, the plasmonic chirality evolution from the Au cube seed under the presence of L‐ or D‐amino acid as a chiral inducer is reported. The 432 Helicoid I structure is obtained using tryptophan (Trp), identical to the result with cysteine (Cys). The use of tyrosine (Tyr) produced a Helicoid IV‐type structure. However, no distinctive chiral structures can be obtained using phenylalanine (Phe), valine (Val) and leucine (Leu), which indicates the critical role of amino acids in chirality evolution. In particular, Trp‐Helicoid I nanoparticles (NPs) showed excellent enantioselective response toward L‐ or D‐Cys in the colorimetric assay and Raman analysis in the presence of Trp. Furthermore, the chiroptical property with a nanogap of 23.78 ± 0.82 nm in the Helicoid I structure further expands its applications for highly sensitive and quantitative chiral analysis for small molecules such as R/S‐epichlorohydrin (ECH), R/S‐limonene (LM), and R/S‐2‐butanol (BuOH) using a non‐polarized light source. The finding of amino acid‐dependent chirality evolution can widen the current understanding of chirality evolution in nature, and the use of helicoid structures with nanogaps incorporated with surface‐enhanced Raman scattering (SERS) can open a new avenue for chiral spectroscopic analysis.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.