Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 124, Issue 45, Pages 24837-24848Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.0c07630
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Funding
- DAAD-ACEH Scholarship of Excellence
- Outstanding Top-notch Talent Cultivation Project in Anhui Province [gxgwfx2018026]
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We studied charge tunneling rates across the single-component and binary self-assembling monolayers (SAMs) composed of 4-methyl-4'-mercaptobiphenyl (CH3-BPT) and 4-trifluoromethyl-4'-mercaptobiphenyl (CF3-BPT) on Au(111). The composition of the binary SAMs could be flexibly tuned, accompanied by gradual variation of the work function between similar to 4.45 eV (CH3-BPT) and similar to 5.5 eV (CF3-BPT). The tunneling rate across the single-component CH3-BPT SAM was found to be notably higher (by 1.5-2 orders of magnitude) than in the CF3-BPT case, while that across the binary SAMs varied progressively with their composition, between the values for the single-component monolayers and could, consequently, be fine-tuned. The observed behavior was tentatively explained by the higher projected density of states at the position of the terminal tail groups in the CH3-BPT case compared to CF3-BPT and by the appearance of an internal electrostatic field in the SAMs, leading to a change and renormalization of the energy-level alignments within the junction upon contact of the SAMs to the top EGaIn electrode. The extent of the latter effect depends primarily on the characteristics of the strongly confined two-dimensional (2D) sheet of dipolar tail groups at the SAM/top electrode interface. The height of the respective injection barrier is, however, unaffected by these characteristics, as follows from the values of the transition voltage, which do not change notably with the SAM composition. Analysis of the presented as well as literature data suggests that the position of a dipolar group in SAM-forming molecules has a significant impact on the performance of the respective SAM in the context of molecular electronics.
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