Hexagonal-boron nitride substrates for electroburnt graphene nanojunctions

We examine the effect of a hexagonal boron nitride (hBN) substrate on electron transport through graphene nanojunctions just before gap formation. Junctions in vacuum and on hBN are formed using classical molecular dynamics to create initial structures, followed by relaxation using density functional theory. We find that the hBN only slightly reduces the current through the junctions at low biases. Furthermore due to quantum interference at the last moments of breaking, the current though a single carbon filament spanning the gap is found to be higher than the current through two filaments spanning the gap in parallel. This feature is present both in the presence of absence of hBN

Electron and heat transport in porphyrin-based single-molecule transistors with electro-burnt graphene electrodes

We have studied the charge and thermal transport properties of a porphyrin-based single-molecule transistor with electro-burnt graphene electrodes (EBG) using the nonequilibrium Green’s function method and density functional theory. The porphyrin-based molecule is bound to the EBG electrodes by planar aromatic anchor groups. Due to the efficient π–π overlap between the anchor groups and graphene and the location of frontier orbitals relative to the EBG Fermi energy, we predict HOMO-dominated transport. An on–off ratio as high as 150 is predicted for the device, which could be utilized with small gate voltages in the range of ±0.1 V. A positive thermopower of +280 μV/K is predicted for the device at the theoretical Fermi energy. The sign of the thermopower could be changed by tuning the Fermi energy. By gating the junction and changing the Fermi energy by +10 meV, this can be further enhanced to +475 μV/K. Although the electrodes and molecule are symmetric, the junction itself can be asymmetric due to different binding configurations at the electrodes. This can lead to rectification in the current–voltage characteristic of the junction

Enhancing the thermoelectric figure of merit in engineered graphene nanoribbons

We demonstrate that thermoelectric properties of graphene nanoribbons can be dramatically improved by introducing nanopores. In monolayer graphene, this increases the electronic thermoelectric figure of merit ZTe from 0.01 to 0.5. The largest values of ZTe are found when a nanopore is introduced into bilayer graphene, such that the current flows from one layer to the other via the inner surface of the pore, for which values as high as ZTe = 2.45 are obtained. All thermoelectric properties can be further enhanced by tuning the Fermi energy of the leads

Oligoyne molecular junctions for efficient room temperature thermoelectric power generation

Understanding phonon transport at a molecular scale is fundamental to the development of high-performance thermoelectric materials for the conversion of waste heat into electricity. We have studied phonon and electron transport in alkane and oligoyne chains of various lengths and find that, due to the more rigid nature of the latter, the phonon thermal conductances of oligoynes are counterintuitively lower than that of the corresponding alkanes. The thermal conductance of oligoynes decreases monotonically with increasing length, whereas the thermal conductance of alkanes initially increases with length and then decreases. This difference in behavior arises from phonon filtering by the gold electrodes and disappears when higher-Debye-frequency electrodes are used. Consequently a molecule that better transmits higher-frequency phonon modes, combined with a low-Debye-frequency electrode that filters high-energy phonons is a viable strategy for suppressing phonon transmission through the molecular junctions. The low thermal conductance of oligoynes, combined with their higher thermopower and higher electrical conductance lead to a maximum thermoelectric figure of merit of ZT = 1.4, which is several orders of magnitude higher than that of alkanes

Breakdown of Curly Arrow Rules in Anthraquinone

Understanding and controlling quantum interference QI in single molecules is fundamental to the development of QI based single molecule electronics. Over the past decade, simple rules such as counting rules, curly arrow rules, circuit rules and more recently magic ratio rules have been developed to predict QI patterns in polycyclic aromatic hydrocarbons. These rules have been successful in explaining observed electronic transport properties of molecular junctions and provide helpful design tools for predicting properties of molecules before their synthesis. Curly arrow rules are widely used by chemists, material scientists and physicists to predict destructive QI. Here we examine the validity of curly arrow rules in fully conjugated anthracene and dihydroxyanthracene, cross‐conjugated anthraquinone and broken conjugated dihydroanthracene attached to graphene or gold electrodes through pi‐pi stacking or thiol and Au‐C anchors. For the first time, we demonstrate that curly arrow rules break down in molecular junctions formed by cross‐conjugated anthraquinone. In contrast with the destructive QI predicted by curly arrow rules for a meta connected anthraquinone core, we demonstrate that QI is constructive. This behavior is independent of the choice of electrode material or anchor groups. This is significant, because by changing the redox state of meta connected dihydroxyanthracene to form meta connected anthraquinone, the conductance of the junction increases by couple of orders of magnitude due to the cross over form constructive to destructive QI. This opens new avenues for realization of quantum interference based single molecule switches

Intermolecular interaction enhances thermoelectric performance of molecular junctions

Novel organic materials formed from functional molecules are attractive for various nanoelectronic applications because they are environmentally friendly, widely available and inexpensive. Recent advancement in bottom-up fabrication methods has made it possible to design and synthesis functional molecules with desired functionalities and engineer their properties precisely. This requires deeper understanding of if the properties of building blocks e.g. single molecules can be translated to many molecule junctions in the form of self-assembled monolayers (SAM). Therefore, understanding the effect of intermolecular interaction becomes important. In this paper, we study the effect of intermolecular interactions on the charge transport and thermoelectric properties of junctions formed by parallel molecules between metallic electrodes. We demonstrate that the electrical conductance and Seebeck coefficient are enhanced simultaneously leading to more than an order of magnitude enhancement of power factor as a result of intermolecular coupling between two molecules of the same kind or different. This strategy can be used to improve the thermoelectric performance of SAMs by engineering their packing density

Influence of environmental fluctuations on quantum interference in naphthalene and azulene

Both naphthalene and azulene have the same number of carbon and hydrogen atoms, but the former is an alternant hydrocarbon and the latter is a nonalternant hydrocarbon. This leads to a large difference in their electronic and transport properties. Herein, quantum transport is investigated through these two molecules and it is shown how quantum interference (QI) affects their electrical conductance. It is demonstrated that the orbital rule to predict QI breaks down in both naphthalene and azulene. The influence of environmental fluctuations on their QI and electrical conductance is also investigated. The results show that QI in azulene is more sensitive to environmental fluctuations than in naphthalene. In particular, destructive QI can be changed to constructive QI in azulene by small environmental fluctuations

Cross-plane enhanced thermoelectricity and phonon suppression in graphene/MoS2 van der Waals heterostructures

The thermoelectric figures of merit of pristine two-dimensional materials are predicted to be significantly less than unity, making them uncompetitive as thermoelectric materials. Here we elucidate a new strategy that overcomes this limitation by creating multi-layer nanoribbons of two different materials and allowing thermal and electrical currents to flow perpendicular to their planes. To demonstrate this enhancement of thermoelectric efficiency ZT, we analyse the thermoelectric performance of monolayer molybdenum disulphide (MoS2) sandwiched between two graphene monolayers and demonstrate that the cross-plane (CP) ZT is significantly enhanced compared with the pristine parent materials. For the parent monolayer of MoS2, we find that ZT can be as high as approximately 0.3, whereas monolayer graphene has a negligibly small ZT. In contrast for the graphene/MoS2/graphene heterostructure, we find that the CP ZT can be as large as 2.8. One contribution to this enhancement is a reduction of the thermal conductance of the van der Waals heterostructure compared with the parent materials, caused by a combination of boundary scattering at the MoS2/graphene interface which suppresses the phonons transmission and the lower Debye frequency of monolayer MoS2, which filters phonons from the monolayer graphene. A second contribution is an increase in the electrical conductance and Seebeck coefficient associated with molybdenum atoms at the edges of the nanoribbons

Magic ratios for connectivity-driven electrical conductance of graphene-like molecules

Experiments using a mechanically-controlled break junction and calculations based on density functional theory demonstrate a new magic ratio rule (MRR),which captures the contribution of connectivity to the electrical conductance of graphene-like aromatic molecules. When one electrode is connected to a site i and the other is connected to a site i' of a particular molecule, we assign the molecule a magic integer Mii'. Two molecules with the same aromatic core, but different pairs of electrode connection sites (i,i' and j,j' respectively) possess different magic integers Mii' and Mjj'. Based on connectivity alone, we predict that when the coupling to electrodes is weak and the Fermi energy of the electrodes lies close to the centre of the HOMO-LUMO gap, the ratio of their conductances is equal to (Mii' /Mjj')2. The MRR is exact for a tight binding representation of a molecule and a qualitative guide for real molecules

Negative differential electrical resistance of a rotational organic nanomotor

A robust, nanoelectromechanical switch is proposed based upon an asymmetric pendant moiety anchored to an organic backbone between two C60 fullerenes, which in turn are connected to gold electrodes. Ab initio density functional calculations are used to demonstrate that an electric field induces rotation of the pendant group, leading to a nonlinear current–voltage relation. The nonlinearity is strong enough to lead to negative differential resistance at modest source–drain voltages