z-logo
Premium
A Detailed Experimental and Theoretical Study into the Properties of C 60 Dumbbell Junctions
Author(s) -
Gillemot Katalin,
Evangeli Charalambos,
Leary Edmund,
La Rosa Andrea,
González M. Teresa,
Filippone Salvatore,
Grace Iain,
RubioBollinger Gabino,
Ferrer Jaime,
Martín Nazario,
Lambert Colin J.,
Agraït Nicolás
Publication year - 2013
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201300310
Subject(s) - dumbbell , molecule , conductance , scanning tunneling microscope , quantum tunnelling , electrode , materials science , chemical physics , nanotechnology , fluorene , crystallography , molecular physics , chemistry , polymer , physics , optoelectronics , condensed matter physics , composite material , medicine , physical therapy , organic chemistry
A combined experimental and theoretical investigation is carried out into the electrical transport across a fullerene dumbbell one‐molecule junction. The newly designed molecule comprises two C 60 s connected to a fluorene backbone via cyclopropyl groups. It is wired between gold electrodes under ambient conditions by pressing the tip of a scanning tunnelling microscope (STM) onto one of the C 60 groups. The STM allows us to identify a single molecule before the junction is formed through imaging, which means unambiguously that only one molecule is wired. Once lifted, the same molecule could be wired many times as it was strongly fixed to the tip, and a high conductance state close to 10 −2 G 0 is found. The results also suggest that the relative conductance fluctuations are low as a result of the low mobility of the molecule. Theoretical analysis indicates that the molecule is connected directly to one electrode through the central fluorene, and that to bind it to the gold fully it has to be pushed through a layer of adsorbates naturally present in the experiment.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here