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121126s2012 txu obm 000 0 eng d |
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|a (OCoLC)ocn819342818
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|a (OCoLC)819342818
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|a (TxCM)http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11660
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|a TXA
|c TXA
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|a TXAM
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|a 2012
|a Dissertation
|a 1969.1/ETD-TAMU-2012-08-11660
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|a Jo, Young Kyong.
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|a Generation of core/shell nanoparticles with laser ablation.
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|a [College Station, Tex.] :
|b [Texas A&M University],
|c [2012]
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|a 1 online resource.
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|a text
|b txt
|2 rdacontent
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|a computer
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|2 rdamedia
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|a online resource
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|a "Major Subject: Mechanical Engineering"
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|a Description from author supplied metadata (automated record created 2012-10-22 13:24:58).
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|b Doctor of Philosophy
|c Texas A&M University
|d 2012
|o http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11660
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|a Includes bibliographical references.
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|a Text (Dissertation)
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|a Two types of core/shell nanoparticles (CS-NPs) generation based on laser ablation are developed in this study, namely, double pulse laser ablation and laser ablation in colloidal solutions. In addition to the study of the generation mechanism of CS-NPs in each scheme, the optical properties of designed CS-NPs are determined with UV-VIS-NIR spectroscopy and EM field simulation. In the first scheme, which is double pulse laser ablation, two laser beams are fired in a sequence on two adjacent targets with different material. We have successfully demonstrated the generation of Sn/Glass, Zn/Glass, Zn/Si, Ge/Si, and Cu/Zn CS-NPs. Key factors affecting the generation of CS-NPs are (1) surface tensions of the constructing materials affecting the associated Gibbs free energy of CS-NPs, (2) physical properties of selected background gases (i.e., He and Ar), (3) delay time between two laser pulses, and (4) the amount of laser energy. The second scheme examined for the generation of CS-NPs is through laser ablation of solid targets in colloidal solutions. Compared to the double pulse laser ablation, this second approach provides better control of the size and shape of the resulting CS-NPs. Two colloidal solutions, namely, Au and SiO2 colloidal solution are applied in the second scheme. Key factors affecting the formation of CS-NPs with the second scheme and are (a) the adhesion energy between the shell and the core material, (b) the diameter of the core and (c) the laser ablation time and the laser energy. Red shift of absorption peaks are measured in both SiO2/Au and SiO2/Ag colloids compared with pure nanoparticles (NPs). The amount of red-shift is very sensitive to the shell thickness of the CS-NPs. The same red shift is reproduced with the corresponding full wave analysis. The observed red shift can be attributed to the additional surface plasmon resonance at the interface of metal/dielectric of the CS-NPs compared with pure nanoparticles. Through adjusting the material and size combination, the absorption peak of the CS-NPs can be tuned in a limit range around the intrinsic absorption peak of the metal of the CS-NPs. The freedom of adjusting the absorption peak makes CS-NPs is favorable in bio and optical applications.
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|a Electronic resource.
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|a Major Mechanical Engineering.
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|a Laser ablation
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|a Laser ablation in liquid
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|a Spectroscopy
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|a Core/shell nanoparticles
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|a Localized surface plasmon
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|a Wen, Sy-Bor,
|e thesis advisor.
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|u http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11660
|z Link to OAK Trust copy
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|a cataloged
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|c 2012/11/26
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|e jolivare
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|a C0
|b TXA
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|i 95d334b8-239b-3a10-86e0-e573ced1a154
|t 0
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|a Texas A&M University
|b College Station
|c Electronic Resources
|d Available Online
|t 0
|e 2012 Dissertation 1969.1/ETD-TAMU-2012-08-11660
|h Other scheme
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|a 2012 Dissertation 1969.1/ETD-TAMU-2012-08-11660
|t 0
|l Available Online
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