Rectification in Tunneling Junctions: 2,2′-Bipyridyl-Terminated n‑Alkanethiolates

• Published in: Journal of the American Chemical Society 2014-12, Vol.136 (49), p.17155-17162
• Main Authors: Yoon, Hyo Jae, Liao, Kung-Ching, Lockett, Matthew R., Kwok, Sen Wai, Baghbanzadeh, Mostafa, Whitesides, George M.
• Format: Article
• Language: English
• Subjects: 2,2'-Dipyridyl - chemistry; Alkanes - chemistry; Gallium - chemistry; Molecular Structure; Silver - chemistry; Sulfhydryl Compounds - chemistry
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja509110a

Molecular rectification is a particularly attractive phenomenon to examine in studying structure–property relationships in charge transport across molecular junctions, since the tunneling currents across the same molecular junction are measured, with only a change in the sign of the bias, with the same electrodes, molecule(s), and contacts. This type of experiment minimizes the complexities arising from measurements of current densities at one polarity using replicate junctions. This paper describes a new organic molecular rectifier: a junction having the structure AgTS/S(CH2)11-4-methyl-2,2′-bipyridyl//Ga2O3/EGaIn (AgTS: template-stripped silver substrate; EGaIn: eutectic gallium–indium alloy) which shows reproducible rectification with a mean r + = |J(+1.0 V)|/|J(−1.0 V)| = 85 ± 2. This system is important because rectification occurs at a polarity opposite to that of the analogous but much more extensively studied systems based on ferrocene. It establishes (again) that rectification is due to the SAM, and not to redox reactions involving the Ga2O3 film, and confirms that rectification is not related to the polarity in the junction. Comparisons among SAM-based junctions incorporating the Ga2O3/EGaIn top electrode and a variety of heterocyclic terminal groups indicate that the metal-free bipyridyl group, not other features of the junction, is responsible for the rectification. The paper also describes a structural and mechanistic hypothesis that suggests a partial rationalization of values of rectification available in the literature.