Plasmonic Stamps Fabricated by Gold Dewetting on PDMS for Catalyzing Hydrosilylation on Silicon Surfaces

Author(s):  
Jillian Buriak ◽  
Chengcheng Rao ◽  
Erik Luber ◽  
Brian Olsen

<div>In this work plasmonic stamps are harnessed to drive surface chemistry on silicon. The plasmonic stamps were prepared by sputtering gold films on PDMS, followed by thermal annealing to dewet the gold and form gold nanoparticles. By changing the film thickness of the sputtered gold, the approximate size and shape of these gold nanoparticles can be changed, leading to a shift of the optical absorbance maximum of the plasmonic stamp, from 535 nm to 625 nm. Applying the plasmonic stamp to a Si(111)-H surface using 1-dodecene as the ink, illumination with green light results in covalent attachment of 1-dodecyl groups to the surface. Of the dewetted gold films on PDMS used to make the plasmonic stamps, the thinnest three (5.0, 7.0, 9.2 nm) resulted in the most effective plasmonic stamps for hydrosilylation. The thicker stamps had lower efficacy due to the increased fraction of non-spherical particles, which have lower-energy LSPRs that are not excited by green light. Since the electric field generated by the LSPR should be very local, hydrosilylation on the silicon surface should only take place within close proximity of the gold particles on the plasmonic stamps.To complement AFM imaging of the hydrosilylated silicon surfaces, galvanic displacement of gold(III) salts on the silicon was carried out and the samples imaged by SEM - the domains of hydrosilylated alkyl chains would be expected to block the deposition of gold. The bright areas of metallic gold surround dark spots, with the sizes and spacing of these dark spots increasing with the size of the gold particles on the plasmonic stamps. These results underline the central role played by the LSPR in driving the hydrosilylation on silicon surfaces, mediated with plasmonic stamps.</div>

2019 ◽  
Author(s):  
Jillian Buriak ◽  
Chengcheng Rao ◽  
Erik Luber ◽  
Brian Olsen

<div>In this work plasmonic stamps are harnessed to drive surface chemistry on silicon. The plasmonic stamps were prepared by sputtering gold films on PDMS, followed by thermal annealing to dewet the gold and form gold nanoparticles. By changing the film thickness of the sputtered gold, the approximate size and shape of these gold nanoparticles can be changed, leading to a shift of the optical absorbance maximum of the plasmonic stamp, from 535 nm to 625 nm. Applying the plasmonic stamp to a Si(111)-H surface using 1-dodecene as the ink, illumination with green light results in covalent attachment of 1-dodecyl groups to the surface. Of the dewetted gold films on PDMS used to make the plasmonic stamps, the thinnest three (5.0, 7.0, 9.2 nm) resulted in the most effective plasmonic stamps for hydrosilylation. The thicker stamps had lower efficacy due to the increased fraction of non-spherical particles, which have lower-energy LSPRs that are not excited by green light. Since the electric field generated by the LSPR should be very local, hydrosilylation on the silicon surface should only take place within close proximity of the gold particles on the plasmonic stamps.To complement AFM imaging of the hydrosilylated silicon surfaces, galvanic displacement of gold(III) salts on the silicon was carried out and the samples imaged by SEM - the domains of hydrosilylated alkyl chains would be expected to block the deposition of gold. The bright areas of metallic gold surround dark spots, with the sizes and spacing of these dark spots increasing with the size of the gold particles on the plasmonic stamps. These results underline the central role played by the LSPR in driving the hydrosilylation on silicon surfaces, mediated with plasmonic stamps.</div>


2021 ◽  
Author(s):  
Chengcheng Rao ◽  
Brian Olsen ◽  
Erik Luber ◽  
Jillian Buriak

Optically transparent PDMS stamps coated with a layer of gold nanoparticles were employed as plasmonic stamps to drive surface chemistry on silicon surfaces. Illumination of a sandwich of plasmonic stamps, an alkene ink, and hydride-terminated silicon with green light of moderate intensity drives hydrosilylation on the surface. The key to the mechanism of the hydrosilylation is the presence of holes at the Si-H-terminated interface, which is followed by attack by a proximal alkene and formation of the silicon-carbon bond. In this work, detailed kinetic studies of the hydrosilylation on silicon with different doping levels, n++, p++, n, p, and intrinsic were carried out to provide further insight into the role of the metal-insulator-semiconductor (MIS) junction that is set up during the stamping.


2018 ◽  
Vol 10 (5) ◽  
pp. 153 ◽  
Author(s):  
Balashanmugam P. ◽  
Mosa Christas K. ◽  
Kowsalya E.

Objective: The biogenic gold nanoparticles are considered to be extremely impressive for its wide range of applications in pharmaceutics and therapeutics. The present study was aimed at the biogenic synthesis of gold nanoparticles (AuNPs) from Marsilea quadrifolia aqueous extract and to investigate its antioxidant property and cytotoxic effect on human ovarian teratocarcinoma (PA-1) and lung adenocarcinoma (A549) cell lines.Methods: The biogenic AuNPs was synthesized using an aqueous extract of Marsilea quadrifolia. The synthesized biogenic AuNPs were characterized by ultraviolet (UV) visible spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX) and X-ray diffraction (XRD). The biogenic AuNPs was assessed for its stability over a period of time and antioxidant activity. The cytotoxicity of biogenic AuNPs against PA-1 and A549 cell lines was studied using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay.Results: The synthesized biogenic AuNPs showed peculiar ruby red color and a surface plasmon resonance (SPR) peak at 544 nm in the UV-Vis spectrum. The characterization of biogenic AuNPs by TEM, EDX and XRD revealed well dispersed spherical particles ranging from 10-40 nm and the presence of elemental gold and its crystalline nature, respectively. The AuNPs showed good stability and the scavenging activity at 50 μg/ml. The in vitro cytotoxicity of biogenic AuNPs against PA-1 and A549 cell lines recorded half maximal inhibitory concentration (IC50) of 45.88 μg/ml and 52.015 μg/ml, respectively.Conclusion: The biogenic AuNPs demonstrated superior antioxidant and antiproliferative activities against cancer cell lines.


2015 ◽  
Vol 51 (27) ◽  
pp. 5975-5978 ◽  
Author(s):  
Guofeng Zhao ◽  
Xin-Ping Wu ◽  
Ruijuan Chai ◽  
Qiaofei Zhang ◽  
Xue-Qing Gong ◽  
...  

Inverse nano-oxide/large-gold-particle catalysts create an anti-sintering structure with a large interface thereby showing high activity/selectivity for the gas-phase alcohol oxidation with dramatic stability improvement.


2019 ◽  
Vol 21 (35) ◽  
pp. 19011-19025 ◽  
Author(s):  
Julien Engel ◽  
Samantha Francis ◽  
Alberto Roldan

This study investigates the effect of commonly used support materials (MgO, C, CeO2) on small gold particles using dispersion corrected density functional theory (DFT-D).


2019 ◽  
Vol 116 (13) ◽  
pp. 6457-6462 ◽  
Author(s):  
Joseph E. Sanfilippo ◽  
Adam A. Nguyen ◽  
Laurence Garczarek ◽  
Jonathan A. Karty ◽  
Suman Pokhrel ◽  
...  

MarineSynechococcus, a globally important group of cyanobacteria, thrives in various light niches in part due to its varied photosynthetic light-harvesting pigments. ManySynechococcusstrains use a process known as chromatic acclimation to optimize the ratio of two chromophores, green-light–absorbing phycoerythrobilin (PEB) and blue-light–absorbing phycourobilin (PUB), within their light-harvesting complexes. A full mechanistic understanding of howSynechococcuscells tune their PEB to PUB ratio during chromatic acclimation has not yet been obtained. Here, we show that interplay between two enzymes named MpeY and MpeZ controls differential PEB and PUB covalent attachment to the same cysteine residue. MpeY attaches PEB to the light-harvesting protein MpeA in green light, while MpeZ attaches PUB to MpeA in blue light. We demonstrate that the ratio ofmpeYtompeZmRNA determines if PEB or PUB is attached. Additionally, strains encoding only MpeY or MpeZ do not acclimate. Examination of strains ofSynechococcusisolated from across the globe indicates that the interplay between MpeY and MpeZ uncovered here is a critical feature of chromatic acclimation for marineSynechococcusworldwide.


2001 ◽  
Vol 704 ◽  
Author(s):  
Takayuki Takahagi ◽  
Shujuan Huang ◽  
Gen Tsutsui ◽  
Hiroyuki Sakaue ◽  
Shoso Shingubara

AbstractIn this paper we describe fabrication methods for two types of nanostructures, two- and three-dimensional arrays of gold nanoparticles. Large-scale and high-ordered monolayers of alkanethiol-encapsulated gold particles were fabricated by using Langmuir-Blodgett (LB) method. Three-dimensional nanoparticle arrays composed of gold nanoparticles of two different sizes, which were encapsulated by complementary thiol-capped DNA oligonucleotides, were fabricated by using DNA hybridization. DNA hybridization occurred upon mixing these particles, which resulted in the assembly of three-dimensional nanostructure of gold particles. Scanning electron microscopy observations and UV spectroscopy measurement were performed to confirm the construction of the nanostructures.


Langmuir ◽  
2010 ◽  
Vol 26 (6) ◽  
pp. 4331-4338 ◽  
Author(s):  
Mark W. Sugden ◽  
Tim H. Richardson ◽  
Graham Leggett

2014 ◽  
Vol 618 ◽  
pp. 203-207
Author(s):  
Li Ping Chen

The hydrophobic gold nanoparticles with monodispersity are synthesized by using n-butanol reduction in situ under the condition of alkali promotion in cetyltrimethylammonium bromide (CTAB)/n-butanol/n-heptane/HAuCl4/NaOH(aq) W/O microemulsion at 30°C. The CTAB-stabilized gold nanoparticles are characterized by UV-vis, TEM , XRD and so on. The replacement of simple surfactant (CTAB ) with mixed surfactant CTAB/ octadecylamine can weaken the direction of CTAB to the growth of gold nanopartices and increase the monodispersity of gold nanoparticles. The effects of components of the microemulsion system on the shape, size and monodispersity of gold nanoparticles are also explored. The results show that the size of gold particles is changed by the amount of CTAB and C18NH2.


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