The assembly of single-molecule devices with the help of the manipulation capability of scanning probe microscopes offers many opportunities for quantum- and nanotechnology. A key challenge is fabricating device structures that can overcome their attraction to the underlying surface and thus protrude from the two-dimensional flatlands of the surface. In my talk, I will report the fabrication of such a structure: we use the tip of a scanning probe microscope to lift a large planar aromatic molecule into an upright, standing geometry on a pedestal of two metal adatoms. This atypical upright orientation of the single molecule, whose stability can be understood as the result of a fine balance between chemical and dispersion forces, enables the system to function as a quantum dot and an on-demand coherent single-electron field emitter. If attached to the tip of the microscope, the standing molecule can also be applied as a sensitive quantum dot sensor. We anticipate that other metastable adsorbate configurations might also be accessible, thereby opening up the third dimension for the design of functional nanostructures on surfaces. Finally, we have made first steps into the direction of an autonomous robotic nanofabrication of single-molecule devices.

Heterostructures of two-dimensional transition-metal dichalcogenides and ferromagnetic substrates are important candidates for the development of viable new spin- or valleytronic devices. For the prototypical bilayer of WSe2 on top of a ferromagnetic layer of CrI3, we find substantially different coupling of both WSe2 K-valleys to the sublayer. Besides an energy splitting of a few meV, the corresponding excitons have significantly different interlayer character with charge transfer allowed at the K̅- point but forbidden at K̅+. The different exciton wave functions result in a distinctly different response to magnetic fields with g factors of about -4.4 and -4.0, respectively. By means of ab initio GW/Bethe-Salpeter equation calculations, these findings establish g factors as tool for investigating the exciton character and shedding light on the detailed quantum-mechanical interplay of magnetic and optical properties which are essential for the targeted development of optoelectronic devices.

The effect of a magnetic field on the optical absorption in semiconductors has been measured experimentally and modeled theoretically for various systems in previous decades. We present a new first-principles approach to systematically determine the response of excitons to magnetic fields, i.e., exciton g factors. By utilizing the GW-Bethe-Salpeter equation methodology we show that g factors extracted from the Zeeman shift of electronic bands are strongly renormalized by many-body effects which we trace back to the extent of the excitons in reciprocal space. We apply our approach to monolayers of transition metal dichalcogenides (MoS2, MoSe2, MoTe2, WS2, and WSe2) with strongly bound excitons for which g factors are weakened by about 30%.

Weakly bound systems, like noble-gas dimers or two-dimensional layered materials (graphite, hexagonal boron nitride, or transition-metal dichalcogenides), exhibit excited electronic states of a particular nature. These so-called exciplex states combine on-site (or intralayer) and charge-transfer (or interlayer) configurations in a well-balanced way. We show by ab initio many-body perturbation theory that the energy and composition of the exciplex states depend sensitively on the bond length or interlayer distance of the material. When the constituents approach each other, the charge-transfer contribution increases and the excitation is redshifted to lower energy. If the system is excited into the exciplex state, then a covalent-like bond results. In consequence, noble-gas dimers form excimer complexes, while layered materials exhibit interlayer contraction.

Almost all experiments and future applications of transition metal dichalcogenide monolayers rely on a substrate for mechanical stability, which can significantly modify the optical spectra of the monolayer. Doping from the substrate might lead to the domination of the spectra by trions. Here we show by ab initio many-body theory that the negative trion (A − ) splits into three excitations, with both inter- and intra-valley character, while the positive counterpart (A + ) consists of only one inter-valley excitation. Furthermore, the substrate enhances the screening, which renormalizes both band gap and exciton as well as the trion-binding energies. We verify that these two effects do not perfectly cancel each other, but lead to red-shifts of the excitation energies for three different substrates ranging from a wide-bandgap semiconductor up to a metal. Our results explain recently found experimental splittings of the lowest trion line as well as excitation red-shifts on substrates.