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Register a new userSpin Splitting of Dopant Edge States in Magnetic Zigzag Graphene Nanoribbons
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Spin-ordered electronic states in hydrogen-terminated zigzag nanographene give rise to magnetic quantum phenomena that have sparked renewed interest in carbon-based spintronics. Zigzag graphene nanoribbons (ZGNRs), quasi one-dimensional semiconducting strips of graphene featuring two parallel zigzag edges along the main axis of the ribbon, are predicted to host intrinsic electronic edge states that are ferromagnetically ordered along the edges of the ribbon and antiferromagnetically coupled across its width. Despite recent advances in the bottom-up synthesis of atomically-precise ZGNRs, their unique electronic structure has thus far been obscured from direct observations by the innate chemical reactivity of spin-ordered edge states. Here we present a general technique for passivating the chemically highly reactive spin-polarized edge states by introducing a superlattice of substitutional nitrogen-dopants along the edges of a ZGNR. First-principles GW calculations and scanning tunneling spectroscopy reveal a giant spin splitting of the low-lying nitrogen lone-pair flat bands by a large exchange field (~850 Tesla) induced by the spin-polarized ferromagnetically ordered edges of ZGNRs. Our findings directly corroborate the nature of the predicted emergent magnetic order in ZGNRs and provide a robust platform for their exploration and functional integration into nanoscale sensing and logic devices.
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Carbon-based magnetic structures promise significantly longer coherence times than traditional magnetic materials, which is of fundamental importance for spintronic applications. An elegant way of achieving carbon-based magnetic moments is the design of graphene nanostructures with an imbalanced occupation of the two sublattices forming the carbon honeycomb lattice. According to Liebs theorem, this induces local magnetic moments that are proportional to the sublattice imbalance. Exact positioning of sublattice imbalanced nanostructures in graphene nanomaterials hence offers a route to control interactions between induced local magnetic moments and to obtain graphene nanomaterials with magnetically non-trivial ground states. Here, we show that such sublattice imbalanced nanostructures can be incorporated along a large band gap armchair graphene nanoribbon on the basis of asymmetric zigzag edge extensions, which is achieved by incorporating specifically designed precursor monomers during the bottom-up fabrication of the graphene nanoribbons. Scanning tunneling spectroscopy of an isolated and electronically decoupled zigzag edge extension reveals Hubbard-split states in accordance with theoretical predictions. Investigation of pairs of such zigzag edge extensions reveals ferromagnetic, antiferromagnetic or quenching of the magnetic interactions depending on the relative alignment of the asymmetric edge extensions. Moreover, a ferromagnetic spin chain is demonstrated for a periodic pattern of zigzag edge extensions along the nanoribbon axis. This work opens a route towards the design and fabrication of graphene nanoribbon-based spin chains with complex magnetic ground states.
We investigate electron and phonon transport through edge disordered zigzag graphene nanoribbons based on the same methodological tool of nonequilibrium Green functions. We show that edge disorder dramatically reduces phonon thermal transport while being only weakly detrimental to electronic conduction. The behavior of the electronic and phononic elastic mean free paths points to the possibility of realizing an electron-crystal coexisting with a phonon-glass. The calculated thermoelectric figure of merit (ZT) values qualify zigzag graphene nanoribbons as a very promising material for thermoelectric applications.
A central question in the field of graphene-related research is how graphene behaves when it is patterned at the nanometer scale with different edge geometries. Perhaps the most fundamental shape relevant to this question is the graphene nanoribbon (GNR), a narrow strip of graphene that can have different chirality depending on the angle at which it is cut. Such GNRs have been predicted to exhibit a wide range of behaviour (depending on their chirality and width) that includes tunable energy gaps and the presence of unique one-dimensional (1D) edge states with unusual magnetic structure. Most GNRs explored experimentally up to now have been characterized via electrical conductivity, leaving the critical relationship between electronic structure and local atomic geometry unclear (especially at edges). Here we present a sub-nm-resolved scanning tunnelling microscopy (STM) and spectroscopy (STS) study of GNRs that allows us to examine how GNR electronic structure depends on the chirality of atomically well-defined GNR edges. The GNRs used here were chemically synthesized via carbon nanotube (CNT) unzipping methods that allow flexible variation of GNR width, length, chirality, and substrate. Our STS measurements reveal the presence of 1D GNR edge states whose spatial characteristics closely match theoretical expectations for GNRs of similar width and chirality. We observe width-dependent splitting in the GNR edge state energy bands, providing compelling evidence of their magnetic nature. These results confirm the novel electronic behaviour predicted for GNRs with atomically clean edges, and thus open the door to a whole new area of applications exploiting the unique magnetoelectronic properties of chiral GNRs.
We study the low energy spin excitations of zigzag graphene nanoribbons of varying width. We find their energy dispersion at small wave vector to be dominated by antiferromagnetic correlations between the ribbons edges, in accrodance with previous calculations. We point out that spin wave lifetimes are very long due to the semi-conducting nature of the electrically neutral nanoribbons. However, application of very modest gate voltages cause a discontinuous transition to a regime of finite spin wave lifetime. By further increasing doping the ferromagnetic alignments along the edge become unstable against transverse spin fluctuations. This makes the experimental detection of ferromagnetism is this class of systems very delicate, and poses a difficult challenge to the possible uses of these nanoribbons as basis for spintronic devices.
We theoretically study electronic properties of a graphene sheet on xy plane in a spatially nonuniform magnetic field, $B = B_0 hat{z}$ in one domain and $B = B_1 hat{z}$ in the other domain, in the quantum Hall regime and in the low-energy limit. We find that the magnetic edge states of the Dirac fermions, formed along the boundary between the two domains, have features strongly dependent on whether $B_0$ is parallel or antiparallel to $B_1$. In the parallel case, when the Zeeman spin splitting can be ignored, the magnetic edge states originating from the $n=0$ Landau levels of the two domains have dispersionless energy levels, contrary to those from the $n e 0$ levels. Here, $n$ is the graphene Landau-level index. They become dispersive as the Zeeman splitting becomes finite or as an electrostatic step potential is additionally applied. In the antiparallel case, the $n=0$ magnetic edge states split into electron-like and hole-like current-carrying states. The energy gap between the electron-like and hole-like states can be created by the Zeeman splitting or by the step potential. These features are attributed to the fact that the pseudo-spin of the magnetic edge states couples to the direction of the magnetic field. We propose an Aharonov-Bohm interferometry setup in a graphene ribbon for experimental study of the magnetic edge states.
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