Fabrications and Electron Transport Properties of One Dimensional Arrays of Gold and Sulfur Containing Fullerene Nanoparticles

2001 ◽  
Vol 704 ◽  
Author(s):  
Sheng-Ming Shih ◽  
Wei-Fang Su ◽  
Yuh-Jiuan Lin ◽  
Cen-Shawn Wu ◽  
Chii-Dong Chen

AbstractNovel arrays of gold nanoparticles with sulfur containing fullerene nanoparticles were self-assembled through the formation of Au-S covalent bonds. Disulfide functional groups were introduced into C60 molecule by reacting propyl 2-aminoethyl disulfide with C60. The two dimensional(2D) arrays were formed at the interface of aqueous phase of gold particles and organic phase of fullerene particles as a blue transparent film. TEM images showed that the fullerene spacing between adjacent Au(~10 nm) particles was about 2.1±0.4 nm, which was consistent with the result of 2.18 nm by molecular molding calculations(MM+). The arrays were deposited on the top of pairs of gold electrodes to form 2D colloidal single electron devices. The electrode pairs were made by electron beam lithography techniques, and the separation between tips of the two electrodes in a pair was less then 100 nm. Transport measurements at low temperatures exhibited Coulomb-Blockade type current-voltage characteristics, the lower the temperature the more pronounced the Coulomb gap. Also, step-by-step method was used to assemble one-dimensional(1D) array of gold nanoparticles with fullerene derivative between two electrodes spaced with 15 nm. The Coulomb blockade behavior of 1D arrays was clearer than that of 2D arrays.

2001 ◽  
Vol 704 ◽  
Author(s):  
Sheng-Ming Shih ◽  
Wei-Fang Su ◽  
Yuh-Jiuan Lin ◽  
Cen-Shawn Wu ◽  
Chii-Dong Chen

AbstractNovel arrays of gold nanoparticles with sulfur containing fullerene nanoparticles were self-assembled through the formation of Au-S covalent bonds. Disulfide functional groups were introduced into C60 molecule by reacting propyl 2-aminoethyl disulfide with C60. The two dimensional(2D) arrays were formed at the interface of aqueous phase of gold particles and organic phase of fullerene particles as a blue transparent film. TEM images showed that the fullerene spacing between adjacent Au(~10 nm) particles was about 2.1±0.4 nm, which was consistent with the result of 2.18 nm by molecular molding calculations(MM+). The arrays were deposited on the top of pairs of gold electrodes to form 2D colloidal single electron devices. The electrode pairs were made by electron beam lithography techniques, and the separation between tips of the two electrodes in a pair was less then 100 nm. Transport measurements at low temperatures exhibited Coulomb-Blockade type current-voltage characteristics, the lower the temperature the more pronounced the Coulomb gap. Also, step-by-step method was used to assemble one-dimensional(1D) array of gold nanoparticles with fullerene derivative between two electrodes spaced with 15 nm. The Coulomb blockade behavior of 1D arrays was clearer than that of 2D arrays.


2001 ◽  
Vol 707 ◽  
Author(s):  
Sheng-Ming Shih ◽  
Wei-Fang Su ◽  
Yuh-Jiuan Lin ◽  
Cen-Shawn Wu ◽  
Chii-Dong Chen

ABSTRACTNovel arrays of gold nanoparticles with sulfur containing fullerene nanoparticles were self-assembled through the formation of Au-S covalent bonds. Disulfide functional groups were introduced into C60 molecule by reacting propyl 2-aminoethyl disulfide with C60. The two dimensional(2D) arrays were formed at the interface of aqueous phase of gold particles and organic phase of fullerene particles as a blue transparent film. TEM images showed that the fullerene spacing between adjacent Au(∼10 nm) particles was about 2.1±0.4 nm, which was consistent with the result of 2.18 nm by molecular molding calculations(MM+). The arrays were deposited on the top of pairs of gold electrodes to form 2D colloidal single electron devices. The electrode pairs were made by electron beam lithography techniques, and the separation between tips of the two electrodes in a pair was less then 100 nm. Transport measurements at low temperatures exhibited Coulomb-Blockade type current-voltage characteristics, the lower the temperature the more pronounced the Coulomb gap. Also, step-by-step method was used to assemble one-dimensional(1D) array of gold nanoparticles with fullerene derivative between two electrodes spaced with 15 nm. The Coulomb blockade behavior of 1D arrays was clearer than that of 2D arrays.


1999 ◽  
Vol 582 ◽  
Author(s):  
James E. Hutchison ◽  
Leif O. Brown ◽  
Jana L. Mooster ◽  
Scott M. Reed ◽  
Mary E. Schmidt ◽  
...  

ABSTRACTA wet chemical approach to preparing one- and two-dimensional arrays of gold nanoparticles assembled onto a polypeptide (poly-L-lysine) scaffold layer is reported. The electrical properties of biopolymer templated and nontemplated gold nanoparticle samples are compared. The electrical response of nontemplated samples is unstable, likely due to nanoparticle mobility. Biopolymer templating provides a simple, chemical method to immobilize the particles and is found to stabilize the electrical response (Coulomb blockade) of the array. A striking feature of the electrical properties is that the electron transport properties are dominated by transport through one-dimensional chains within the sample. Structural studies by AFM and XPS support the transport findings and provide evidence for the formation of one-dimensional assemblies within the arrays.


2003 ◽  
Vol 14 (08) ◽  
pp. 1087-1105 ◽  
Author(s):  
ZHONGCHENG WANG ◽  
YONGMING DAI

A new twelfth-order four-step formula containing fourth derivatives for the numerical integration of the one-dimensional Schrödinger equation has been developed. It was found that by adding multi-derivative terms, the stability of a linear multi-step method can be improved and the interval of periodicity of this new method is larger than that of the Numerov's method. The numerical test shows that the new method is superior to the previous lower orders in both accuracy and efficiency and it is specially applied to the problem when an increasing accuracy is requested.


Nanoscale ◽  
2015 ◽  
Vol 7 (27) ◽  
pp. 11545-11551 ◽  
Author(s):  
Khashayar Ghandi ◽  
Alexander D. Findlater ◽  
Zahid Mahimwalla ◽  
Connor S. MacNeil ◽  
Ernest Awoonor-Williams ◽  
...  

Faster than electron solvation transfer to gold nanoparticles in water when stabilized by non-covalent bonds with strong intermolecular interactions.


2020 ◽  
Author(s):  
Xiaoning Zhang ◽  
Meifeng Li ◽  
Yuanping Lv ◽  
Xiaoling Sun ◽  
Yao Han ◽  
...  

Abstract Gold nanoparticles (AuNPs) are modified immediately by the adsorption of β-lactoglobulin (βlg) when designed as colorimetric probe in raw milk, leading to the formation of a protein corona. This adsorption results mainly from a fast electrostatic force and a slow formation of Au-S covalent bonds, which is a precondition for the use of AuNPs in biodetection. The proteins corona influences the structure and bioactivity of adsorbed protein, such as the allergy. In this study, the mechanism of βlg adsorbed on AuNPs was investigated in terms of stoichiometry, binding affinity (Ka), time evolution of Au-S bond, and general secondary structure changes to address the desensitization of AuNPs. The results show that about 3,600 βlg are adsorbed on a single AuNPs, and the Ka is 2.9 ± 0.7 × 10 6 M -1 . The formation of Au-S bonds takes about 9 h, which is the time needed for complete changes in secondary structure and the IgE combining capacity. The structure of allergenic epitopes assigned to β-sheet was destroyed by the formation of Au-S bond, then induced to the decrease allergy. Furthermore, Fourier transform infrared spectroscopy confirmed a decrease in β-sheet contents after conjugated with AuNPs.


RSC Advances ◽  
2012 ◽  
Vol 2 (13) ◽  
pp. 5599 ◽  
Author(s):  
Jinming Zhang ◽  
Tao Xu ◽  
Jinrong Yao ◽  
Lei Huang ◽  
Xin Chen ◽  
...  

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