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The use of single molecules as circuit elements represents the ultimate in device miniaturization. The mechanically controlled break junction (MCBJ) technique is a commonly used method for the formation of metal-molecule-metal junctions. Using MCBJs, the electrical properties of single molecules can be investigated. In this thesis, an MCBJ experimental setup for the study of charge transport is described. Early investigations began with gold wire break junctions, eventually progressing to lithographically fabricated break junctions. In particular, the measurement electronics, LabVIEW programming and mechanical setup underwent significant revisions, leading to improvements in noise floor, sensitivity, and speed. The resulting setup is capable of measuring the charge transport properties of single molecule junctions accurately and at a high rate.
Quantum tunnelling is one of the strangest phenomena in chemistry, where we see the wave nature of atoms acting in “impossible” ways. By letting molecules pass through the kinetic barrier instead of over it, this effect can lead to chemical reactions even close to the absolute zero, to atypical spectroscopic observations, to bizarre selectivity, or to colossal isotopic effects. Quantum mechanical tunnelling observations might be infrequent in chemistry, but it permeates through all its disciplines producing remarkable chemical outcomes. For that reason, the 21st century has seen a great increase in theoretical and experimental findings involving molecular tunnelling effects, as well as in novel techniques that permit their accurate predictions and analysis. Including experimental, computational and theoretical chapters, from the physical and organic to the biochemistry fields, from the applied to the academic arenas, this new book provides a broad and conceptual perspective on tunnelling reactions and how to study them. Quantum Tunnelling in Molecules is the obligatory stop for both the specialist and those new to this world.
The series Topics in Current Chemistry Collections presents critical reviews from the journal Topics in Current Chemistry organized in topical volumes. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience. Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.
This book provides a comprehensive overview of the rapidly developing field of molecular electronics. It focuses on our present understanding of the electrical conduction in single-molecule circuits and provides a thorough introduction to the experimental techniques and theoretical concepts. It will also constitute as the first textbook-like introduction to both the experiment and theory of electronic transport through single atoms and molecules. In this sense, this publication will prove invaluable to both researchers and students interested in the field of nanoelectronics and nanoscience in general. Molecular Electronics is self-contained and unified in its presentation. It may be used as a textbook on nanoelectronics by graduate students and advanced undergraduates studying physics and chemistry. In addition, included are previously unpublished material that will help researchers gain a deeper understanding into the basic concepts involved in the field of molecular electronics.
"Charge transport plays a critical role in a wide range of molecular processes including photosynthesis, redox catalysis, energy storage, biological signaling, and the operation of molecular electronic devices. Understanding and controlling these key events requires establishing how molecular structure influences charge transport and designing physically realizable strategies to manipulate them. This thesis advances the theory, simulation, and interpretation of charge transport experiments in molecular junctions and identifies novel avenues to use external mechanical stimuli to control chemistry and physics in this nanoscale setting. The reason why we focus on molecular junction experiments is because they enable the manipulation of individual molecules and the characterization of their response to external stimuli such as mechanical forces, bias voltages, and electro-magnetic fields. Such a controllable setting is ideal to establish structure-charge transport relations at the single-molecule limit that can inform and resolve the individual molecular contributions to bulk phenomena. We first demonstrate that conductance can act as a sensitive probe of conformational dynamics during the mechanical pulling of molecular junctions. These advances offer an efficient solution to experimentally monitor conformational dynamics at the single-molecule limit. Next, we bridge molecular conductance with mechanochemistry and investigate how to mechanically onset and electrically monitor chemical reactivity in single molecules. In particular, we demonstrate mechanically controlled association and rupture reactions in molecular junctions and show that simultaneous measurements of force and conductance are able to signal reactive events that cannot be distinguished by force or conductance alone. The computations are based on atomistic molecular dynamics and nonequilibrium Green's functions computations of electron transport. At the methodological level, we clarify the utility of the Landauer equation for computing charge transport across molecular junctions immersed in a thermal environment such as solvent. The Landauer equation is central to the modeling of molecular electronics experiments. However, it supposes that the current is coherent (solely due to quantum tunneling) and does not capture the possible influence of the environment in the net current. We isolate physical conditions that require an analysis beyond Landauer and use them to identify chemical motifs capable of stabilizing coherent, incoherent, and intermediate transport mechanisms. Molecular junction experiments typically record the conductance of thousands of freshly formed junctions and report histograms of conductance events. Here, we construct a microscopic theory of such conductance histograms by merging the theory of force spectroscopy developed in biophysics with molecular conductance. The theory enhances the information that can be extracted from molecular electronics experiments, and can be employed to develop schemes to narrow the width of the histograms as desirable for spectroscopic applications and molecular device design. Further, the theory opens key opportunities to atomistically model the conductance histograms, as needed to bridge the gap between theory and experiments."--Pages viii-ix.
Täglich benutzen wir Schalter, um strombetriebene Geräte an- und abzuschalten und kein Compuer würde ohne sie funktionieren. Nach den gleichen Prinzipien funktionieren auch molekulare Schalter, die unter dem Einfluß ihrer Umwelt zwischen zwei definierten Zuständen wechseln können. Im Gegensatz zu den gewöhnlichen Schaltern sind molekulare Schalter aber außerordentlich klein und ihre Anwendung in der Nanotechnologie, Biomedizin und im Computerchipdesign öffnet neue Horizonte. Im vorliegenden Zweibänder berichten Herausgeber und Autoren über molekulare Schalter aus Katenanen und Rotaxanen, Fulgiden, Flüssigkristallen und Polypeptiden. Die Bandbreite der behandelten Themen reicht von chiroptischen Schaltern über multifunktionale Systeme bis hin zu molekularen logischen Schaltungen. Chemiker und Materialwissenschaftler in Industrie und Hochschule, die sich für einen der innovativsten Bereiche ihrer Wissenschaft interessieren, werden dieses Buch mit Gewinn lesen!