Electronic properties of phenylated ligand-capped nanoparticle films

An investigation was carried out of the electronic characteristics of drop-cast films comprised of phenylated ligand-capped gold nanoparticles. In homoligand-type films, the dominant mechanism of charge transfer was expected to involve orbital overlap and end group-effected wave function displacement, whereas heteroligand-type films were expected to conduct through less efficient hopping mechanisms. Films utilizing the former mechanism are expected to have great applicability within microelectronics and rapid-prototyping technologies due to the small scale (2-6nm) of functionalized nanoparticles and the structural flexibility of interdigitation as a form of inter-particle bonding. The comparative conductances of the cast films reveal a strong correlation with the ligand Hammaker constant (effectively a measure of the work function of the conjugated bond with the gold core of the nanoparticle and the charge displacement effected by the electronegativity or polarity of the ligand end group). The conductance was also greatly affected by the size of ligand end groups - a rough measure of the close-packing ability of a given ligand both within the ligand shell and amongst the shells of adjacent nanoparticles. The following experiments illustrate these correlations, as well as the effects of ligand spacing and shell composition on the dominant charge transfer mechanism.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2006

Author dc:creator

• Özden-Schilling, Thomas Charles.

Advisor dc:contributor.advisor

• Francesco Stellacci.

• Materials Science and Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/35055

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/35055