FP7Individual fellowship2008–2010

INNATE · Integrated Nanocrystal Tunnelling for Molecular Electronics

FP7 — People (Marie Curie Actions)

Duration
2008-04-01 → 2010-03-31
EU contribution
€246,178
Participants
1
Scheme
MC-IEF

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Results in brief

Integrated Nanocrystal Tunnelling for Molecular Electronics

The INNATE project has been concerned with the electrochemical and electronic behaviour of small monolayer-protected clusters (MPCs) of gold, to explore their potential for application in molecular electronics. The main achievements can be summarised as follows: - Highly monodisperse Au147C6S (C6S = n-hexanethiolate) MPCs have been synthesised, for which 16 single-electron charging states have been electrochemically resolved [1]. This number is the highest reported to date. - We have demonstrated for the first time that well-behaved quantised charging of gold MPCs is also possible in an air- and water-stable room temperature ionic liquid [1]. As ionic liquids have very attractive features including near-zero vapour pressure, considerable thermal stability and an electrochemical stability window that often exceeds 4 volt, this demonstration is particularly significant from the technological point of view. - The dynamics of the quantised cluster charging process in different ionic liquids has been studied in detail using voltammetric and impedance measurements [2] . We have discovered that the MPC charging rate can vary up to an order of magnitude depending on ionic liquid composition, which indicates that a judicious choice of electrolyte is crucial in the design of an electrochemical device. The differences in dynamics between the various ionic liquids have been rationalised in terms of varying chemical availability of free ions within the liquids, necessary to compensate the charges on the MPC cores. - We have demonstrated for the first time that dithiol-functionalised MPCs can disintegrate spontaneously on gold substrates, forming monoatomically high gold islands with low-coverage thiol/dithiol adlayers [3]. This is a strong indication that the ligand shell of MPC structures can be quite dynamic and its stability strongly linked to its environment. - We have demonstrated that for electrostatically stabilised nanocrystals, an electrostatic immobilisation approach can be a valuable alternative to covalent attachment [4]. This development is of particular significance for applications in electroanalysis and -catalysis [5]. - Using in situ scanning tunnelling microscopy, we have demonstrated that a redox-active adlayer (6-thiohexanoylferrocene) on a gold surface can generate nanoparticles following multiple oxidation/reduction cycles of the adlayer [6]. The clusters exhibit a narrow size distribution with an average diameter of (2.4 +/- 0.5) nm, corresponding to a single-particle capacitance of (1.5 +/- 0.2) aF. To our knowledge, this is the first demonstration of such spontaneous transformation. Both the redox resonance feature, which can be quantitatively understood based on existing models, and the multistate cluster resonance, for which proper models are still required, could be exploited in electrochemical/molecular electronic devices. In summary, the INNATE project has demonstrated the substantial application potential of nanocrystal-mediated tunnelling for molecular electronics, and in a broader context, the power of electrochemical methodologies in these areas. As this project was situated in the basic research field, its socio-economic impact must be seen in the longer term, after more applied studies have been carried out based on the principles demonstrated by us. [1] S.F.L. Mertens, K. Blech, A.S. Sologubenko, J. Mayer, U. Simon, T. Wandlowski, Electrochim. Acta 54, 2009, 5006-5010. [2] S.F.L. Mertens, G. Mészáros, T. Wandlowski, Phys. Chem. Chem. Phys., 12, 2010, 5417-5424. [3] S.F.L. Mertens, Z. Li, T. Wandlowski, Electrochem. Commun. 6/2010, in preparation. [4] S.F.L. Mertens, A. Bütikofer, L. Siffert, T. Wandlowski, Electroanalysis, submitted. 5/2010 [5] S.F.L. Mertens, A. Bütikofer, T. Wandlowski, D.J. Schiffrin, in preparation. [6] Z. Li, Y. Liu, S.F.L. Mertens, I.V. Pobelov, T. Wandlowski, J. Am. Chem. Soc., 132 , 2010, 8167 - 8193

Data: CORDIS, © European Union

Project objective

The INNATE project focuses on noble metal nanocrystals in the quantum confinement size range as active elements in molecular electronic circuits. Supported by a successful proof-of-concept experiment, multistate switch and transistor function for these systems will be demonstrated, unparalleled in conventional electronics. This novel electronic function will be integrated with that of tailored redox molecules both in a vertical Scanning Probe Microscopy configuration and in a nanogap electrode set-up to form nanoelectronic circuits, thus bridging top-down and bottom-up approaches. Our strategy focuses on electrolyte gating at electrified solid/liquid interfaces, which can address physical gates down to 1 nm by achieving strong electronic coupling, and allows the target “device” to function under ambient conditions. In addition to its ambitious technical goals, the INNATE project will substantially contribute to prospects of professional maturity and independence of the applicant by adding crucial scientific competencies in the highly interdisciplinary area of nanoscale electrochemistry and molecular electronics, thus developing his research niche of organic–inorganic hybrid nanostructures towards a high-level molecular understanding of structure–functionality–reactivity relations. Research training objectives focus on advanced scanning probe and nanogap electrode techniques, together with complementary training in research management, high-level dissemination and networking activities, including links to industry. Fully integrated in the European Research Area, the project will significantly enhance visibility and attractiveness of European science and technology.

Original text from CORDIS.

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Data: CORDIS, © European Union