 When visible light is shown on an isolated azobenzene molecule, it takes on a trans state. Exposure to ultraviolet light switches it to a more condensed cis state. (Source: Paul Weiss Laboratory, Penn State )
Light-powered microscopic mechanical switches could act as artificial muscle.
Research being done by collaboration between Penn State
University and Rice University scientists may pave the way for switching state
molecules. They could be used for anything from molecular driver units to
artificial muscles or molecular electronics.
Though the function of the molecular switches is similar to that of memory
metal, like the kind used to control the tiny mirrors that comprise the surface
of a DLP (digital light processing) chip, they function without electrical
stimulus. Rather than using an on-off state powered by charge, they react to
ultraviolet and visible spectrum light.
These types of molecules, molecules that react and switch states of
configurations to light, are not uncommon. The process is called
photoisomerization. The molecules can either be in a trans or cis state. For
their results, the trans state, which represented the “on” state of the switch,
was the default state under normal visible light. The molecules, composed of
two benzene rings joined by double bonded nitrogen atoms, “flipped” to a cis or
“off” state when exposed to ultraviolet light instead.
While these types of molecules function flawlessly in solutions, flipping back
and forth between states easily, when attached to a surface, they do not react
in the same manner. To overcome this, the group created a self-assembled
metallic monolayer and used a special molecular tether to isolate the reactive
azobenzene molecules from its surface.
To confirm their work, the scientists used a specially built scanning tunneling
microscope which measured the height of the azobenzene molecule while exposing
it to alternating visible and ultraviolet light.
The results of the multi-university group can be found in the June issues of
the journal Nano Letters.
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