Photo-actuated Molecular Machines
A nanomachine is a nanostructure that can convert different forms of energy into mechanical motion. The Crommie group is actively pursuing research into nanomachines actuated via light, static electric fields, and electrical current. Our emphasis is on exploring mechanical behavior at the atomic and molecular scales. At very small lengthscales standard mechanical concepts such as friction, force, and motion differ from their intuitive classical macroscopic behaviors due to quantum mechanical behavior. Construction of functional machines at the nanoscale also requires the synthesis of complex molecular assemblies with atomic precision. Our research here is focused in three main areas: (i) molecular assembly and characterization, (ii) energy conversion and dissipation at the nanoscale, and (iii) the synchronous coordination of molecular machine elements.
The conversion of optical energy into mechanical motion is particularly desirable for molecular machines because it does not require electrical contacts and provides a superbly flexible and high bandwidth medium. One strategy for transducing light into mechanical motion is the use of photoisomerization in single molecules. This topic has been explored by the Crommie group. The basic idea here is that when certain molecules absorb a photon they undergo structural evolution into a different shape (an isomer), and this process can be used to perform mechanical work at very small length scales. One molecule that can accomplish this is azobenzene (Fig. 1a), which converts reversibly between “trans” and “cis” isomer structures upon photon absorption, as shown in Fig. 1.1 If an azobenzene molecule in the trans ground state (the S0 manifold of the potential energy surface) absorbs a photon then it is lifted to the excited-state manifold, S1, as shown by the purple arrow in Fig. 1a. While the trans state is a minimum of S0, it is not a minimum of S1 (with respect to structural coordinates), and so the molecule’s structure evolves by sliding down the potential energy surface into the cis state.2
Photoisomerization of azobenzene (and molecules like it) could potentially be used to create nanomachines at the molecular scale capable of converting optical energy into translational motion. One strategy for pursuing this is through inchworm-like conformational changes. To accomplish this a single molecule (or short chain of molecules) would be functionalized at the ends with elements whose surface adsorption energy can be toggled with light. Light pulses could then be used to expand (via the trans state) and contract (via the cis state) the molecule while toggling the adsorption strength of the end units, thus resulting in forward motion. An animation describing this proposed process is shown in Fig. 2.
The Crommie group has shown that it is possible to actuate individual azobenzene molecules using an ultraviolet laser (Fig. 3a, b).3 Azobenzene molecules were functionalized with tetra-tert-butyl groups to decouple them from the gold substrate supporting them (Fig. 3b). Conversion of single molecules from trans to cis was observed after photon absorption.3 The dynamics of this process have been explored,4 as well as the dependence on molecular chirality and different surface characteristics.5
Other photoactive molecules have been explored by the Crommie group, such as ruthenium fulvalene (FvRu2(CO)4).6,7 This molecule is a candidate for energy storage since it converts to a high-energy isomer upon optical absorption and can controllably release the energy as heat (Fig. 4a). Figs. 4b, c show STM images of Ru-fulvalene in different isomer states before and after photon absorption.
1) Jared D. Harris, Mark J. Moran, and Ivan Aprahamian, New molecular switch architectures. PNAS, 115 (38), 9414-9422 (2018).
2) M. Tiago, S. Ismail-Beigi, and S. G. Louie, Photoisomerization of azobenzene from first-principles constrained density-functional calculations. J. Chem. Phys. 122, 094311 (2005).
3) M. J. Comstock, N. Levy, A. Kirakosian, J. Cho, F. Lauterwasser, J. H. Harvey, D. A. Strubbe, J. M. J. Fréchet, D. Trauner, S. G. Louie, and M. F. Crommie, Reversible Photomechanical Switching of Individual Engineered Molecules at a Metallic Surface. Phys. Rev. Lett. 99, 038301 (2007).
4) M. J. Comstock, N. Levy, J. Cho, L. Berbil-Bautista, M. F. Crommie, D. A. Poulsen, J. M. J. Fréchet, Measuring reversible photomechanical switching rates for a molecule at a surface. Appl. Phys. Lett. 92, 123107 (2008).
5) M. J. Comstock, D. A. Strubbe, L. Berbil-Bautista, N. Levy, J. Cho, D. Poulsen, J. M. J. Fréchet, S. G. Louie, and M. F. Crommie, Determination of Photoswitching Dynamics through Chiral Mapping of Single Molecules Using a Scanning Tunneling Microscope. Phys. Rev. Lett. 104, 178301 (2010).
6) J. Cho, L. Berbil-Bautista, I. V. Pechenezhskiy, N. Levy, S. K. Meier, V. Srinivasan, Y. Kanai, J. C. Grossman, K. P. C. Vollhardt and M. F. Crommie, Single-Molecule-Resolved Structural Changes Induced by Temperature and Light in Surface-Bound Organometallic Molecules Designed for Energy Storage. ACS Nano 5, 3701 (2011).
7) J. Cho, I. V. Pechenezhskiy, L. Berbil-Bautista, S. K. Meier, K. P. C. Vollhardt and M. F. Crommie, Imaging structural transitions in organometallic molecules on Ag(100) for solar thermal energy storage. Journal of the Korean Physical Society 70, 586 (2017).