TY - GEN
T1 - Quantum interference in EGaIn based tunneling junctions
AU - Fracasso, Davide
AU - Chiechi, Ryan C.
PY - 2013/9/11
Y1 - 2013/9/11
N2 - In this report we discuss the great potential of Eutectic Gallium Indium (EGaIn) as conformal soft top electrode. EGaIn is a liquid eutectic supporting a skin (~ 1 nm-thick) of self-limiting oxide Ga2O3 as a non-damaging, conformal top-contact. In the last half of decade EGaIn has been used by several group to form molecular junctions and study charge transport properties in self-assembled monolayer (SAMs). We compared the current density (J) versus applied bias (V) for three different self-assembled monolayers (SAMs) of ethynylthiophenol-functionalized anthracene derivatives with approximately the same thickness and diverse conjugation: linear-conjugation (AC), cross-conjugation (AQ), and broken-conjugation (AH) by using liquid eutectic Ga-In (EGaIn). This skin imparts non-Newtonian rheological properties that distinguish EGaIn from other top-contacts, however it may also have limited the maximum values of J observed for AC. We measure values of J for AH and AQ which are not significantly different (J ≈ 10-1 A/cm2 at V = 0.4 V). For AC, however, J is one (using log-averages) or two (using Gaussian mean) orders of magnitude higher than both AH and AQ. Our results are also in good qualitative agreement with gDFTB calculations on single AC, AQ, and AH molecules transport calculation, based on chemisorbed between Au contacts which predict currents, I, that are two orders of magnitude higher for AC than AH at 0 < |V| < 0.4 V. We ascribe these observations to quantum-interference effects. The agreement between the theoretical predictions on single-molecules and the measurements on SAMs suggest that molecule-molecule interactions do not play a significant role in the transport properties of AC, AQ, and AH.
AB - In this report we discuss the great potential of Eutectic Gallium Indium (EGaIn) as conformal soft top electrode. EGaIn is a liquid eutectic supporting a skin (~ 1 nm-thick) of self-limiting oxide Ga2O3 as a non-damaging, conformal top-contact. In the last half of decade EGaIn has been used by several group to form molecular junctions and study charge transport properties in self-assembled monolayer (SAMs). We compared the current density (J) versus applied bias (V) for three different self-assembled monolayers (SAMs) of ethynylthiophenol-functionalized anthracene derivatives with approximately the same thickness and diverse conjugation: linear-conjugation (AC), cross-conjugation (AQ), and broken-conjugation (AH) by using liquid eutectic Ga-In (EGaIn). This skin imparts non-Newtonian rheological properties that distinguish EGaIn from other top-contacts, however it may also have limited the maximum values of J observed for AC. We measure values of J for AH and AQ which are not significantly different (J ≈ 10-1 A/cm2 at V = 0.4 V). For AC, however, J is one (using log-averages) or two (using Gaussian mean) orders of magnitude higher than both AH and AQ. Our results are also in good qualitative agreement with gDFTB calculations on single AC, AQ, and AH molecules transport calculation, based on chemisorbed between Au contacts which predict currents, I, that are two orders of magnitude higher for AC than AH at 0 < |V| < 0.4 V. We ascribe these observations to quantum-interference effects. The agreement between the theoretical predictions on single-molecules and the measurements on SAMs suggest that molecule-molecule interactions do not play a significant role in the transport properties of AC, AQ, and AH.
KW - Conjugation
KW - EGaIn
KW - Quantum Interference
KW - Tunneling Junctions
UR - http://www.scopus.com/inward/record.url?scp=84889049610&partnerID=8YFLogxK
U2 - 10.1117/12.2026174
DO - 10.1117/12.2026174
M3 - Conference contribution
AN - SCOPUS:84889049610
SN - 9780819496614
T3 - Proceedings of SPIE - The International Society for Optical Engineering
BT - Physical Chemistry of Interfaces and Nanomaterials XII
PB - SPIE.Digital Library
T2 - Physical Chemistry of Interfaces and Nanomaterials XII
Y2 - 25 August 2013 through 28 August 2013
ER -