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Molecule movement along a surface
Defuse along a prefer directional direction dragged by STM chip on Au surface at 473K Nano-car Shirai, Y., Osgood, A. J., Zhao, Y., Kelly, K. F. & Tour, J. M. Nano Lett. 5, 2330–2334 (2005) Grill, L. et al. Nature Nanotechnol. 2, 95–98 (2007).
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Molecule movement along a surface
Defuse along a prefer directional direction dragged by STM chip on Au surface at 473K Nano-car =>molecule act only as passive elements Shirai, Y., Osgood, A. J., Zhao, Y., Kelly, K. F. & Tour, J. M. Nano Lett. 5, 2330–2334 (2005) Grill, L. et al. Nature Nanotechnol. 2, 95–98 (2007).
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Nanocar+ rotor unit a(2006 model) b(2012 model)
STM Image of b on Cu(111) Model of b (calculated) Nano-car don’t move along an Au or Cu surface by UV light pluses(248 nm) irradiation >interaction between wheel and surface is too strong >energy quenched by metal surface a)Morin, J.-F.; Shirai, Y.James M Tour, J. Org. Lett. 2006, 8, 1713– 1716 b)Pinn-Tsong Chiang, Leonhard Grill, and James M. Tour et al ACS Nano, 2012, 6 , 592–597
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Electric nanocar Molecular design Exaction way Four rotor unit
Nano-car flame electron excitation Unidirectional Conformational change Moving liner direction STM tip Exciting electron from STM tip (STM-IETS)
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Electric nanocar Rotor unit conversion previous research
Nature 2005,437,
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Molecule movement along a surface
STM at 7K 1step – scanning(<60mV,<50 pA) =>No scanning (600mV, pA) On a Cu(111) surface
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Double bound isomerization
Electron excitation the electron could excite a phonon or molecules vibrational mode with an energy quantum of ħω Check threshold ħω/e(mV) e⊿V≧ħω(molecule vibration energy) => Electron induce molecule conversion Movement components Double bound isomerization Helix inversion
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Helix inversion
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Double bond isomerization+Helix invesion
Each data point represents 8 to40 manipulations performed on various molecules (I=30–50 pA)
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Polarity dependence of Helix invesion
Negative bias > no movement Positive voltage pulses -> leading to movement and helix inversion.
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Electron excitation ħω~500meV e⊿V≧ħω(molecule vibration energy)
Double bound isomerization ħω~500meV e⊿V≧ħω(molecule vibration energy) Electron induce molecule conversion (one electron cause one reaction) Difference between The presence LUMO and fermi level Helix inversion ħω~200meV C=C bound starching vibration
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STM-image each isomer
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Movement control by chirality of isomer
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Conclusion Scanning tunnelling microscopy confirms that activation of the conformational changes of the rotors through inelastic electron tunnelling propels the molecule unidirectionally across a Cu(111) surface. The system can be adapted to follow either linear or random surface trajectories or to remain stationary, by tuning the chirality of the individual motor units. their design provides a starting point for the exploration of more sophisticated molecular mechanical systems with directionally controlled motion.
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Synthetic scheme 1 (rotor unit)
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Synthetic scheme 2 (making nano-car flame)
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表面科学Vol. 24, No. 5, pp. 313―317, 2003
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表面科学Vol. 24, No. 5, pp. 313―317, 2003
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A tunneling electron emitted from a STM tip is trapped in a molecule-induced resonant state. The electron is dissipated into the metal surface after a short time, during which the electron could excite a phonon or molecules vibrational mode with an energy quantum of ħω
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