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Yujeong Bae

Publications and source records attributed to Yujeong Bae.

14 recordsLinked to original sources

Formation of Oriented Bilayer Motif -- Vanadyl Phthalocyanine on Ag(100)

The adsorption and self-assembly of vanadyl phthalocyanine molecules on Ag(100) has been investigated using a combination of scanning tunneling microscopy and density functional theory. At sub-monolayer coverage, we observe two distinct adsorption configurations of isolated molecules, corresponding to the central O atom pointing toward (O-down) or away (O-up) from the substrate. Upon adsorption in the O-up orientation, the otherwise achiral molecules take on a windmill-like chiral appearance due to their interaction with the substrate. At monolayer coverage, we observe a self-assembled square lattice with a mixture of O-up and O-down molecules. At higher coverage we find a strong preference for bilayer formation with O-up and O-down molecules in alternating layers, suggesting stabilization by dipolar interactions. Close inspection of the multi-layer surface reveals grain boundaries separating domains of opposite organizational chirality, and long-range ordering.

cond-mat.mtrl-sci

Interpreting X-ray absorption spectra of Vanadyl Phthalocyanines Spin Qubit Candidates using a Machine Learning-Assisted Approach

The magnetic dilution of Vanadyl phthalocyanine (VOPc) within the isostructural diamagnetic Titanyl phthalocyanine (TiOPc) affords promising molecular spin qubit platforms for solid-state quantum computing. The development of quantitative methods for determining how the interactions with a supporting substrate impact the electronic structure of the system are fundamental to determine their potential integration in physical devices. In this work we propose a combined approach based on X-ray absorption spectroscopy (XAS), atomic multiplet calculations, and density functional theory (DFT) to investigate the 3d orbital level structure of VOPc on TiOPc/Ag(100). We characterize VOPc in different molecular environments realized by changing the thickness of TiOPc interlayer and adsorption configuration on Ag(100). Depending on the molecular film structure, we find characteristic XAS features that we analyze using atomic multiplet calculations. We use a Bayesian optimization algorithm to accelerate the parameter search process in the multiplet calculations and identify the ground state properties, such as the 3d orbital occupancy and splitting, as well as intra-atomic interactions. Our analysis indicates that VOPc retains its spin S = 1/2 character in all configurations. Conversely, the energy separation and sequence of the unoccupied V 3d orbitals sensitively depend on the interaction with the surface and TiOPc interlayer. We validate the atomic orbital picture obtained from the multiplet model by comparison with DFT, which further allows us to understand the VOPc electronic properties using a molecular orbital description.

cond-mat.mtrl-sci

Roadmap on Nanoscale Magnetic Resonance Imaging

The field of nanoscale magnetic resonance imaging (NanoMRI) was started 30 years ago. It was motivated by the desire to image single molecules and molecular assemblies, such as proteins and virus particles, with near-atomic spatial resolution and on a length scale of 100 nm. Over the years, the NanoMRI field has also expanded to include the goal of useful high-resolution nuclear magnetic resonance (NMR) spectroscopy of molecules under ambient conditions, including samples up to the micron-scale. The realization of these goals requires the development of spin detection techniques that are many orders of magnitude more sensitive than conventional NMR and MRI, capable of detecting and controlling nanoscale ensembles of spins. Over the years, a number of different technical approaches to NanoMRI have emerged, each possessing a distinct set of capabilities for basic and applied areas of science. The goal of this roadmap article is to report the current state of the art in NanoMRI technologies, outline the areas where they are poised to have impact, identify the challenges that lie ahead, and propose methods to meet these challenges. This roadmap also shows how developments in NanoMRI techniques can lead to breakthroughs in emerging quantum science and technology applications.

cond-mat.mes-hall

Electrically Driven Spin Resonance of 4f Electrons in a Single Atom on a Surface

A pivotal challenge in quantum technologies lies in reconciling long coherence times with efficient manipulation of the quantum states of a system. Lanthanide atoms, with their well-localized 4f electrons, emerge as a promising solution to this dilemma if provided with a rational design for manipulation and detection. Here we construct tailored spin structures to perform electron spin resonance on a single lanthanide atom using a scanning tunneling microscope. A magnetically coupled structure made of an erbium and a titanium atom enables us to both drive the erbium's 4f electron spins and indirectly probe them through the titanium's 3d electrons. In this coupled configuration, the erbium spin states exhibit a five-fold increase in the spin relaxation time and a two-fold increase in the driving efficiency compared to the 3d electron counterparts. Our work provides a new approach to accessing highly protected spin states, enabling their coherent control in an all-electric fashion.

cond-mat.mes-hall

Development of a Scanning Tunneling Microscope for Variable Temperature Electron Spin Resonance

Recent advances in increasing the spectroscopic energy resolution in scanning tunneling microscopy (STM) have been achieved by integrating electron spin resonance (ESR) with STM. Here, we demonstrate the design and performance of a home-built STM capable of ESR at temperatures ranging from 1 K to 10 K. The STM is incorporated with a home-built Joule-Thomson refrigerator and a 2-axis vector magnet. Our STM design allows for the deposition of atoms and molecules directly into the cold STM, eliminating the need to extract the sample for deposition. In addition, we adopt two methods to apply radio-frequency (RF) voltages to the tunnel junction, the early design of wiring to the STM tip directly, and a more recent idea to use an RF antenna. Direct comparisons of ESR results measured using the two methods and simulations of electric field distribution around the tunnel junction show that, despite their different designs and capacitive couplings to the tunnel junction, there is no discernible difference in the driving and detection of ESR. Furthermore, at a magnetic field of 1.6 T, we observe ESR signals (near 40 GHz) sustained up to 10 K, which is the highest temperature for ESR-STM measurement reported to date, to the best of our knowledge. Although the ESR intensity exponentially decreases with increasing temperature, our ESR-STM system with low noise at the tunnel junction allows us to measure weak ESR signals with intensities in the sub-fA range. Our new design of ESR-STM, which is operational in a large frequency and temperature range, can broaden the use of ESR spectroscopy in STM and enable the simple modification of existing STM systems, which will hopefully accelerate a generalized use of ESR-STM.

cond-mat.mes-hall

An electron-spin qubit platform assembled atom-by-atom on a surface

Creating a quantum-coherent architecture at the atomic scale has long been an ambition in quantum science and nanotechnology. This ultimate length scale requires the use of fundamental quantum properties of atoms, such as the spin of electrons, which naturally occurs in many solid-state environments and allows high-fidelity operations and readout by electromagnetic means. Despite decades of effort, however, it remains a formidable task to realize an atomic-scale quantum architecture where multiple electron spin qubits can be precisely assembled, controllably coupled, and coherently operated. Electron spin qubits created in dopants in semiconductors and color centers in insulators, for example, can be well controlled individually6-8 but are difficult to couple together into a circuit. On the other hand, multiple magnetic atoms and molecules on surfaces can be coupled to each other by building sophisticated atomic structures using a scanning tunneling microscope (STM), but coherent operation has so far been limited to a single qubit in the tunnel junction. Here we demonstrate an atomic-scale qubit platform by showing atom-by-atom construction, coherent operations, and readout of multiple electron-spin qubits on a surface. To enable the coherent control of remote qubits that are outside the tunnel junction, we complement each electron spin with a local magnetic field gradient from a nearby single-atom magnet. To enable readout of remote qubits, we employ a sensor qubit in the tunnel junction and implement pulsed double electron spin resonance. Using these methods, we demonstrate fast single-, two-, and three-qubit operations in an all-electrical fashion. Our work marks the creation of an Angstrom-scale qubit platform, where quantum functionalities using electron spin arrays, built atom-by-atom on a surface, are now within reach.

cond-mat.mes-hall

Anisotropic hyperfine interaction of surface-adsorbed single atoms

Hyperfine interactions between electron and nuclear spins have been widely used in material science, organic chemistry, and structural biology as a sensitive probe to the local chemical environment through spatial identification of nuclear spins. With the nuclear spins identified, the isotropic and anisotropic components of the hyperfine interactions in turn offer unique insight into the electronic ground-state properties of the paramagnetic centers. However, traditional ensemble measurements of hyperfine interactions average over a macroscopic number of spins with different geometrical locations and nuclear isotopes. Here, we use a scanning tunneling microscope (STM) combined with electron spin resonance (ESR) to measure hyperfine spectra of hydrogenated-titanium (Ti) atoms on MgO/Ag(100) and thereby determine the isotropic and anisotropic hyperfine interactions at the single-atom level. By combining vector-field ESR spectroscopy with STM-based atom manipulation, we characterize the full hyperfine tensor of individual Ti-47 and Ti-49 atoms and identify significant spatial anisotropy of hyperfine interaction for both isotopes when they are adsorbed at low-symmetry binding sites. Density functional theory calculations reveal that the large hyperfine anisotropy arises from a highly anisotropic distribution of the ground-state electron spin density. Our work highlights the power of ESR-STM-enabled single-atom hyperfine spectroscopy as a powerful tool in revealing ground-state electronic structures and atomic-scale chemical environments with nano-electronvolt resolution.

cond-mat.mes-hall

Harnessing the Quantum Behavior of Spins on Surfaces

The desire to control and measure individual quantum systems such as atoms and ions in a vacuum has led to significant scientific and engineering developments in the past decades that form the basis of today's quantum information science. Single atoms and molecules on surfaces, on the other hand, are heavily investigated by physicists, chemists, and material scientists in search of novel electronic and magnetic functionalities. These two paths crossed in 2015 when it was first clearly demonstrated that individual spins on a surface can be coherently controlled and read out in an all-electrical fashion. The enabling technique is a combination of scanning tunneling microscopy (STM) and electron spin resonance (ESR), which offers unprecedented coherent controllability at the Angstrom length scale. This review aims to illustrate the essential ingredients that allow the quantum operations of single spins on surfaces. Three domains of applications of surface spins, namely quantum sensing, quantum control, and quantum simulation, are discussed with physical principles explained and examples presented. Enabled by the atomically-precise fabrication capability of STM, single spins on surfaces might one day lead to the realization of quantum nanodevices and artificial quantum materials at the atomic scale.

physics.app-ph

Atomic Manipulation of In-gap States on the $β$-Bi$_2$Pd Superconductor

Electronic states in the gap of a superconductor inherit intriguing many-body properties from the superconductor. Here, we create these in-gap states by manipulating Cr atomic chains on the $β$-Bi$_2$Pd superconductor. We find that the topological properties of the in-gap states can greatly vary depending on the crafted spin chain. These systems make an ideal platform for non-trivial topological phases because of the large atom-superconductor interactions and the existence of a large Rashba coupling at the Bi-terminated surface. We study two spin chains, one with atoms two-lattice-parameter apart and one with square-root-of-two lattice parameters. Of these, only the second one is in a topologically non-trivial phase, in correspondence with the spin interactions for this geometry.

cond-mat.supr-con

Spin Resonance Amplitude and Frequency of a Single Atom on a Surface in a Vector Magnetic Field

We used electron spin resonance (ESR) combined with scanning tunneling microscopy (STM) to measure hydrogenated Ti (spin-1/2) atoms at low-symmetry binding sites on MgO in vector magnetic fields. We found strongly anisotropic g-values in all three spatial directions. Interestingly, the amplitude and lineshape of the ESR signals are also strongly dependent on the angle of the field. We conclude that the Ti spin is aligned along the magnetic field, while the tip spin follows its strong magnetic anisotropy. Our results show the interplay between the tip and surface spins in determining the ESR signals and highlight the precision of ESR-STM to identify the single atom's spin states.

cond-mat.mes-hall

Tuning the exchange bias on a single atom from 1 mT to 10 T

Shrinking spintronic devices to the nanoscale ultimately requires localized control of individual atomic magnetic moments. At these length scales, the exchange interaction plays important roles, such as in the stabilization of spin-quantization axes, the production of spin frustration, and creation of magnetic ordering. Here, we demonstrate the precise control of the exchange bias experienced by a single atom on a surface, covering an energy range of four orders of magnitude. The exchange interaction is continuously tunable from milli-eV to micro-eV by adjusting the separation between a spin-1/2 atom on a surface and the magnetic tip of a scanning tunneling microscope (STM). We seamlessly combine inelastic electron tunneling spectroscopy (IETS) and electron spin resonance (ESR) to map out the different energy scales. This control of exchange bias over a wide span of energies provides versatile control of spin states, with applications ranging from precise tuning of quantum state properties, to strong exchange bias for local spin doping. In addition we show that a time-varying exchange interaction generates a localized AC magnetic field that resonantly drives the surface spin. The static and dynamic control of the exchange interaction at the atomic-scale provides a new tool to tune the quantum states of coupled-spin systems.

cond-mat.mes-hall

Magnetic Resonance Imaging of Single Atoms

Magnetic resonance imaging (MRI) revolutionized diagnostic medicine and biomedical research by allowing a noninvasive access to spin ensembles. To enhance MRI resolution to the nanometer scale, new approaches including scanning probe methods have been used in recent years, which culminated in detection of individual spins. This allowed three-dimensional (3D) visualization of organic samples and of sophisticated spin-structures. Here, we demonstrate for the first time MRI of individual atoms on a surface. The setup, implemented in a cryogenic scanning tunneling microscope (STM), uses single-atom electron spin resonance (ESR) to achieve sub-Ångström resolution exceeding the spatial resolution of previous experiments by one to two orders of magnitude. We find that MRI scans of different atomic species and probe tips lead to unique signatures in the resonance images. These signatures reveal the magnetic interactions between the tip and the atom, in particular magnetic dipolar and exchange interaction.

cond-mat.mes-hall

Enhanced quantum coherence in exchange coupled spins via singlet-triplet transitions

Manipulation of spin states at the single-atom scale underlies spin-based quantum information processing and spintronic devices. Such applications require protection of the spin states against quantum decoherence due to interactions with the environment. While a single spin is easily disrupted, a coupled-spin system can resist decoherence by employing a subspace of states that is immune to magnetic field fluctuations. Here, we engineered the magnetic interactions between the electron spins of two spin-1/2 atoms to create a clock transition and thus enhance their spin coherence. To construct and electrically access the desired spin structures, we use atom manipulation combined with electron spin resonance (ESR) in a scanning tunneling microscope (STM). We show that a two-level system composed of a singlet state and a triplet state is insensitive to local and global magnetic field noise, resulting in much longer spin coherence times compared with individual atoms. Moreover, the spin decoherence resulting from the interaction with tunneling electrons is markedly reduced by a homodyne readout of ESR. These results demonstrate that atomically-precise spin structures can be designed and assembled to yield enhanced quantum coherence.

cond-mat.mes-hall

Engineering the eigenstates of coupled spin-1/2 atoms on a surface

Quantum spin networks having engineered geometries and interactions are eagerly pursued for quantum simulation and access to emergent quantum phenomena such as spin liquids. Spin-1/2 centers are particularly desirable because they readily manifest coherent quantum fluctuations. Here we introduce a controllable spin-1/2 architecture consisting of titanium atoms on a magnesium oxide surface. We tailor the spin interactions by atomic-precision positioning using a scanning tunneling microscope (STM), and subsequently perform electron spin resonance (ESR) on individual atoms to drive transitions into and out of quantum eigenstates of the coupled-spin system. Interactions between the atoms are mapped over a range of distances extending from highly anisotropic dipole coupling, to strong exchange coupling. The local magnetic field of the magnetic STM tip serves to precisely tune the superposition states of a pair of spins. The precise control of the spin-spin interactions and ability to probe the states of the coupled-spin network by addressing individual spins will enable exploration of quantum many-body systems based on networks of spin-1/2 atoms on surfaces.

cond-mat.mes-hall