Back to results

Wake Forest University

SYNTHESIS OF PRECURSORS FOR MOLECULAR ELECTRONICS

Abstract

dc:description.abstract

The design of molecular rectifiers is one of the major topics of research in molecular electronics, however the relationship between the molecular structure and the electrical characteristics of molecular rectifiers is not fully understood. To elucidate this relationship, we synthesized and examined the electrical properties of fluorinated benzalkylsilane self-assembled monolayers (SAMs) of varying lengths and terminal groups. The rectification ratios were determined to be as high as ~200 and we also found that the rectification ratio correlates positively with the strength of the molecular dipole moment particularly for shorter chain molecules. Based on this data, we sought to design short chain benzalkylsilane SAMs with strong electron withdrawing and strong electron donating terminal groups. We hypothesized that terminations with these groups would give us enhanced rectification ratios based on their large dipole moments. Rectification ratios were found to be as high as 2635. These values to our knowledge are the highest reported for small molecule rectifiers assembled on silicon substrates.

Degree

thesis:*
Grantor dc:publisher
Wake Forest University
Year dc:date.issued
2018

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Broadnax, Angela

Rights

Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10339/92390
OAI identifier oai:identifier
oai:wakespace.lib.wfu.edu:10339/92390

Chain of custody

source
Harvested from
Wake Forest University
Base URL
wakespace.lib.wfu.edu/oai/request
Last updated
2026-07-27
Source record
OAI-PMH GetRecord
related terms
citation

Broadnax, Angela. SYNTHESIS OF PRECURSORS FOR MOLECULAR ELECTRONICS. Wake Forest University, 2018. http://hdl.handle.net/10339/92390