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There are now many examples of single molecule rotors, motors, and switches in the literature that, when driven by photons, electrons, or chemical reactions, exhibit well-defined motions. As a step toward using these single molecule devices to perform useful functions, one must understand how they interact with their environment and quantify their ability to perform work on it. Using a single molecule rotary switch, we examine the transfer of electrical energy, delivered via electron tunneling, to mechanical motion and measure the forces the switch experiences with a noncontact q-plus atomic force microscope. Action spectra reveal that the molecular switch has two stable states and can be excited resonantly between them at a bias of 100 mV via a one-electron inelastic tunneling process which corresponds to an energy input of 16 zJ. While the electrically induced switching events are stochastic and no net work is done on the cantilever, by measuring the forces between the molecular switch and the AFM cantilever, we can derive the maximum hypothetical work the switch could perform during a single switching event, which is ∼55 meV, equal to 8.9 zJ, which translates to a hypothetical efficiency of ∼55% per individual inelastic tunneling electron-induced switching event. When considering the total electrical energy input, this drops to 1 × 10–7% due to elastic tunneling events that dominate the tunneling current. However, this approach constitutes a general method for quantifying and comparing the energy input and output of molecular-mechanical devices. 

Chiral surfaces are of growing interest for enantioselective adsorption and reactions. While metal surfaces can be prepared with a wide range of chiral surface orientations, chiral oxide surface preparation is much more challenging. Herein, we demonstrate that the chirality of a metal surface can be used to direct the homochiral growth of a thin film chiral oxide. Specifically, we study the chiral ‘29’ copper oxide, formed by oxidizing a Cu(111) single crystal at 650 K. Surface structure spread single crystals which expose a continuous distribution of surface orientations as a function of position on the crystal, enabled us to systematically investigate the mechanism of chirality transfer between metal and oxide with high-resolution scanning tunneling microscopy. We discovered that the local underlying metal facet directs the orientation and chirality of the oxide overlayer. Importantly, single homochiral domains of the ‘29’ oxide were found in areas where the Cu step edges that templated growth were ≤20 nm apart. We used this information to select a Cu(239 241 246) oriented single crystal and demonstrate that a ‘29’ oxide surface can be grown in homochiral domains by templating from the subtle chirality of the underlying metal crystal. This work demonstrates how a small degree of chirality induced by very slight misorientation of a metal surface (~1 sites/ 20 nm2) can be amplified by oxidation to yield a homochiral oxide with a regular array of chiral oxide pores (~75 sites/ 20 nm2). This offers a general approach for making chiral oxide surfaces via oxidation of an appropriately miscut metal surface.