ITHACA, N.Y. - With controlled stretching of molecules, Cornell researchers have demonstrated that single-molecule devices can serve as powerful new tools for fundamental science experiments. Their work has resulted in detailed tests of long-existing theories on how electrons interact at the nanoscale.
The work, led by professor of physics Dan Ralph, is published in the June 10 online edition of the journal Science. First author is J.J. Parks, a former graduate student in Ralph's lab.
The scientists studied particular cobalt-based molecules with so-called intrinsic spin a quantized amount of angular momentum.
Theories first postulated in the 1980s predicted that molecular spin would alter the interaction between electrons in the molecule and conduction electrons surrounding it, and that this interaction would determine how easily electrons flow through the molecule. Before now, these theories had not been tested in detail because of the difficulties involved in making devices with controlled spins.
Understanding single-molecule electronics requires expertise in both chemistry and physics, and Cornell's team has specialists in both.
"People know about high-spin molecules, but no one has been able to bring together the chemistry and physics to make controlled contact with these high-spin molecules," Ralph said.
The researchers made their observations by stretching individual spin-containing molecules between two electrodes and analyzing their electrical properties. They watched electrons flow through the cobalt complex, cooled to extremely low temperatures, while slowly pulling on the ends to stretch it. At a particular point, it became more difficult to pass current through the molecule. The researchers had subtly changed the magnetic properties of the molecule by making it less symmetric.
After releasing the tension, the molecule returned to its original shape and began passing current more easily thus sho
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