| 1. |
- Ahmad, Y., et al.
(författare)
-
NMR and NEXAFS Study of Various Graphite Fluorides
- 2013
-
Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 117:26, s. 13564-13572
-
Tidskriftsartikel (refereegranskat)abstract
- Graphite fluorides with different structural types (CyF)(n) (y = 2.5, 2, and 1) and room temperature graphite fluorides were studied by solid state,NMR and NEXAFS. Data extracted from those two techniques are complementary, providing information about the C-F bonding and the hybridization character of the carbon atom valence states. The comparison of data obtained by different methods such as NMR, Raman, and X-ray absorption leads to similar conclusions regarding the chemical bonding in fluorographites. Several major configurations of fluorinated graphites are discussed, that is, planar sheets with mainly sp(2) hybridization in room temperature graphite fluorides and corrugated sheets with sp(3) hybridization in covalent high temperature graphite fluoride. Different references such as highly oriented pyrolytic graphite (HOPG), graphitized carbon nanodiscs (graph-CNDs) and nanodiamonds (NDs) have also been investigated for comparison.
|
|
| 2. |
- Simonov, K. A., et al.
(författare)
-
Synthesis of armchair graphene nanoribbons from the 10,10′-dibromo-9,9′-bianthracene molecules on Ag(111) : The role of organometallic intermediates
- 2018
-
Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 8:1
-
Tidskriftsartikel (refereegranskat)abstract
- We investigate the bottom-up growth of N = 7 armchair graphene nanoribbons (7-AGNRs) from the 10,10′-dibromo-9,9′-bianthracene (DBBA) molecules on Ag(111) with the focus on the role of the organometallic (OM) intermediates. It is demonstrated that DBBA molecules on Ag(111) are partially debrominated at room temperature and lose all bromine atoms at elevated temperatures. Similar to DBBA on Cu(111), debrominated molecules form OM chains on Ag(111). Nevertheless, in contrast with the Cu(111) substrate, formation of polyanthracene chains from OM intermediates via an Ullmann-type reaction is feasible on Ag(111). Cleavage of C-Ag bonds occurs before the thermal threshold for the surface-catalyzed activation of C-H bonds on Ag(111) is reached, while on Cu(111) activation of C-H bonds occurs in parallel with the cleavage of the stronger C-Cu bonds. Consequently, while OM intermediates obstruct the Ullmann reaction between DBBA molecules on the Cu(111) substrate, they are required for the formation of polyanthracene chains on Ag(111). If the Ullmann-type reaction on Ag(111) is inhibited, heating of the OM chains produces nanographenes instead. Heating of the polyanthracene chains produces 7-AGNRs, while heating of nanographenes causes the formation of the disordered structures with the possible admixture of short GNRs.
|
|
| 3. |
- Svirskiy, G. I., et al.
(författare)
-
Comparative X-Ray Absorption Analysis of the Spectrum of Vacant Electronic States in Cobalt and Nickel Tetraphenylporphyrin Complexes
- 2018
-
Ingår i: Physics of the solid state. - 1063-7834 .- 1090-6460. ; 60:3, s. 581-591
-
Tidskriftsartikel (refereegranskat)abstract
- The energy distributions and the properties of the lower vacant electronic states in cobalt and nickel tetraphenylporphyrin complexes CoTPP and NiTPP are studied by X-ray absorption spectroscopy. Quasimolecular analysis of the experimental absorption spectra measured in the region of the 2p and 1s ionization thresholds of complexing metal atoms, as well as the 1s thresholds of ligand atoms (nitrogen and carbon), is based on the comparison of the corresponding spectra with each other and with the spectra of the simplest nickel porphyrin NiP. It has been established that, despite a general similarity of the spectra of nitrogen and carbon in CoTPP and NiTPP, the fine structure of the 2p and 1s absorption spectra of cobalt and nickel atoms are radically different. The observed differences in the spectra of cobalt and nickel are associated with the features of the energy distribution of vacant 3d electron states. The presence in CoTPP of the partially filled valence 3db2g molecular orbital (MO) results in the appearance in the cobalt spectra of a low-energy band, which is absent in the spectrum of nickel in NiTPP and leads to a doublet structure of transitions to b1g and e g MOs due to the exchange interaction between 3d electrons in partially filled 3db2g and 3db1g or 3de g MOs. The spectrum of vacant states in CoTPP differs from that in NiTPP also due to the smaller energy distance between 3db1g and e g MOs and the different positions of nonbonding MOs with the C2p character of the porphine ligand.
|
|
| 4. |
- Usachov, D. Yu, et al.
(författare)
-
Cubic Rashba Effect in the Surface Spin Structure of Rare-Earth Ternary Materials
- 2020
-
Ingår i: Physical Review Letters. - 0031-9007. ; 124:23
-
Tidskriftsartikel (refereegranskat)abstract
- Spin-orbit interaction and structure inversion asymmetry in combination with magnetic ordering is a promising route to novel materials with highly mobile spin-polarized carriers at the surface. Spin-resolved measurements of the photoemission current from the Si-terminated surface of the antiferromagnet TbRh2Si2 and their analysis within an ab initio one-step theory unveil an unusual triple winding of the electron spin along the fourfold-symmetric constant energy contours of the surface states. A two-band k·p model is presented that yields the triple winding as a cubic Rashba effect. The curious in-plane spin-momentum locking is remarkably robust and remains intact across a paramagnetic-antiferromagnetic transition in spite of spin-orbit interaction on Rh atoms being considerably weaker than the out-of-plane exchange field due to the Tb 4f moments.
|
|
| 5. |
- Vinogradov, N. A., et al.
(författare)
-
The structural evolution of graphene/Fe(110) systems upon annealing
- 2017
-
Ingår i: Carbon. - : Elsevier BV. - 0008-6223 .- 1873-3891. ; 111, s. 113-120
-
Tidskriftsartikel (refereegranskat)abstract
- The thermal stability and the structural evolution of graphene grown on Fe(110) has been studied upon annealing in ultra-high vacuum conditions (UHV, P <= 10(-9) mbar) and in the presence of gaseous ethylene at a pressure of similar to 10(-6) mbar by grazing incidence X-ray diffraction. It was observed that upon annealing at temperatures below 630 degrees C, graphene on Fe is thermally stable. Exposure to ethylene at these temperatures promotes the formation of graphene while inhibiting its deterioration. Annealing graphene/Fe(110) at temperatures above 630 degrees C results in a fast degradation of graphene followed by carburization of the sample, that is the irreversible formation of various iron carbides, with the most common phases being Fe3C (cementite) and Fe7C3 (Eckstrom-Adcock carbide). Annealing of the carburized sample does not result in the formation of a detectable graphitic structure.
|
|
| 6. |
- Generalov, A., et al.
(författare)
-
Insight into the temperature dependent properties of the ferromagnetic Kondo lattice YbNiSn
- 2017
-
Ingår i: Physical Review B. - 2469-9950. ; 95:18
-
Tidskriftsartikel (refereegranskat)abstract
- Analyzing temperature dependent photoemission (PE) data of the ferromagnetic Kondo-lattice (KL) system YbNiSn in the light of the periodic Anderson model (PAM) we show that the KL behavior is not limited to temperatures below a temperature TK, defined empirically from resistivity and specific heat measurements. As characteristic for weakly hybridized Ce and Yb systems, the PE spectra reveal a 4f-derived Fermi level peak, which reflects contributions from the Kondo resonance and its crystal electric field (CEF) satellites. In YbNiSn this peak has an unusual temperature dependence: With decreasing temperature a steady linear increase of intensity is observed which extends over a large interval ranging from 100 K down to 1 K without showing any peculiarities in the region of TK∼TC=5.6 K. In the light of the single-impurity Anderson model (SIAM) this intensity variation reflects a linear increase of 4f occupancy with decreasing temperature, indicating an onset of Kondo screening at temperatures above 100 K. Within the PAM this phenomenon could be described by a non-Fermi-liquid-like T- linear damping of the self-energy which accounts phenomenologically for the feedback from the closely spaced CEF states.
|
|
| 7. |
- Simonov, K. A., et al.
(författare)
-
Features of metal atom 2p excitations and electronic structure of 3d-metal phthalocyanines studied by X-ray absorption and resonant photoemission
- 2013
-
Ingår i: Applied Surface Science. - : Elsevier BV. - 1873-5584 .- 0169-4332. ; 267, s. 132-135
-
Tidskriftsartikel (refereegranskat)abstract
- The metal atom 2p core excitations in 3d-metal phthalocyanines (MPc's, M = Ni, Co, Fe) have been studied via a combination of near edge X-ray absorption fine structure (NEXAFS) and resonant photoemission (ResPE) spectroscopy. On the basis of comparison of the corresponding spectra of NiPc, CoPc and FePc it has been shown that the presence of a partly filled molecular orbital (MO) dramatically affects the formation and decay processes of the M 2p core excitation in CoPc and, to a greater extend, in FePc due to the significant 3d-3d exchange interaction. It has been found that the low-lying unoccupied electronic states of NiPc, CoPc and FePc are strongly localized within the MN4 quasi-molecule and have nearly pure 3d character. Moreover, mainly 3d metallic character of the high-lying occupied MOs of NiPc, CoPc and FePc has been proved. (C) 2012 Elsevier B. V. All rights reserved.
|
|
| 8. |
- Fedorov, A. V., et al.
(författare)
-
Insight into the Temperature Evolution of Electronic Structure and Mechanism of Exchange Interaction in EuS
- 2021
-
Ingår i: Journal of Physical Chemistry Letters. - : American Chemical Society (ACS). - 1948-7185. ; 12:34, s. 8328-8334
-
Tidskriftsartikel (refereegranskat)abstract
- Discovered in 1962, the divalent ferromagnetic semiconductor EuS (TC = 16.5 K, Eg = 1.65 eV) has remained constantly relevant to the engineering of novel magnetically active interfaces, heterostructures, and multilayer sequences and to combination with topological materials. Because detailed information on the electronic structure of EuS and, in particular, its evolution across TC is not well-represented in the literature but is essential for the development of new functional systems, the present work aims at filling this gap. Our angle-resolved photoemission measurements complemented with first-principles calculations demonstrate how the electronic structure of EuS evolves across a paramagnetic-ferromagnetic transition. Our results emphasize the importance of the strong Eu 4f-S 3p mixing for exchange-magnetic splittings of the sulfur-derived bands as well as coupling between f and d orbitals of neighboring Eu atoms to derive the value of TC accurately. The 4f-3p mixing facilitates the coupling between 4f and 5d orbitals of neighboring Eu atoms, which mainly governs the exchange interaction in EuS.
|
|
| 9. |
- Generalov, A., et al.
(författare)
-
Strong spin-orbit coupling in the noncentrosymmetric Kondo lattice
- 2018
-
Ingår i: Physical Review B. - 2469-9950. ; 98:11
-
Tidskriftsartikel (refereegranskat)abstract
- Strong spin-orbit coupling (SOC) in combination with a lack of inversion symmetry and exchange magnetic interaction proves to be a sophisticated instrument allowing efficient control of the spin orientation, energy and trajectories of two-dimensional (2D) electrons and holes trapped at surfaces or interfaces. Exploiting Kondo-related phenomena and crystal-electric-field effects at reduced dimensionalities opens new opportunities to handle their spin-dependent properties offering novel functionalities. We consider here a 2D Kondo lattice represented by a Si-Ir-Si-Yb (SISY) surface block of the heavy-fermion material YbIr2Si2. We show that the Kondo interaction with 4f moments allows finely tuning the group velocities of the strongly spin-polarized carriers in 2D itinerant states of this noncentrosymmetric system. To unveil the peculiarities of this interaction, we used angle-resolved photoemission measurements complemented by first-principles calculations. We established that the strong SOC of the Ir atoms induces spin polarization of the 2D states in SISY block, while the 2D lattice of Yb 4f moments acts as a source for coherent f-d interplay. The strong SOC and lack of inversion symmetry turn out to lead not only to the anticipated Rashba-like splitting of the 2D states, but also to spin splitting of the 4f Kramers doublets. They couple temperature-dependently to the spin-polarized 2D states and thereby guide the properties of the latter.
|
|
| 10. |
- Patil, S., et al.
(författare)
-
ARPES view on surface and bulk hybridization phenomena in the antiferromagnetic Kondo lattice CeRh2Si2
- 2016
-
Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 7
-
Tidskriftsartikel (refereegranskat)abstract
- The hybridization between localized 4f electrons and itinerant electrons in rare-earth-based materials gives rise to their exotic properties like valence fluctuations, Kondo behaviour, heavy-fermions, or unconventional superconductivity. Here we present an angle-resolved photoemission spectroscopy (ARPES) study of the Kondo lattice antiferromagnet CeRh2Si2, where the surface and bulk Ce-4f spectral responses were clearly resolved. The pronounced 4f0 peak seen for the Ce terminated surface gets strongly suppressed in the bulk Ce-4f spectra taken from a Si-terminated crystal due to much larger f-d hybridization. Most interestingly, the bulk Ce-4f spectra reveal a fine structure near the Fermi edge reflecting the crystal electric field splitting of the bulk magnetic 4f15/2 state. This structure presents a clear dispersion upon crossing valence states, providing direct evidence of f-d hybridization. Our findings give precise insight into f-d hybridization penomena and highlight their importance in the antiferromagnetic phases of Kondo lattices.
|
|
| 11. |
|
|
| 12. |
- Simonov, Konstantin A., et al.
(författare)
-
Effect of Electron Injection in Copper-Contacted Graphene Nanoribbons
- 2016
-
Ingår i: Nano Reseach. - : Springer Science and Business Media LLC. - 1998-0124 .- 1998-0000. ; 9:9, s. 2735-2746
-
Tidskriftsartikel (refereegranskat)abstract
- For practical electronic device applications of graphene nanoribbons (GNRs), it is essential to have abrupt and well-defined contacts between the ribbon and the adjacent metal lead. By analogy with graphene, these contacts can induce electron or hole doping, which may significantly affect the I/V characteristics of the device. Cu is among the most popular metals of choice for contact materials. In this study, we investigate the effect of in situ intercalation of Cu on the electronic structure of atomically precise, spatially aligned armchair GNRs of width N = 7 (7-AGNRs) fabricated via a bottom-up method on the Au(788) surface. Scanning tunneling microscopy data reveal that the complete intercalation of about one monolayer of Cu under 7-AGNRs can be facilitated by gentle annealing of the sample at 80 A degrees C. Angle-resolved photoemission spectroscopy (ARPES) data clearly reflect the one-dimensional character of the 7-AGNR band dispersion before and after intercalation. Moreover, ARPES and core-level photoemission results show that intercalation of Cu leads to significant electron injection into the nanoribbons, which causes a pronounced downshift of the valence and conduction bands of the GNR with respect to the Fermi energy (Delta E similar to 0.5 eV). As demonstrated by ARPES and X-ray absorption spectroscopy measurements, the effect of Cu intercalation is restricted to n-doping only, without considerable modification of the band structure of the GNRs. Post-annealing of the 7-AGNRs/Cu/Au(788) system at 200 A degrees C activates the diffusion of Cu into Au and the formation of a Cu-rich surface Au layer. Alloying of intercalated Cu leads to the recovery of the initial position of GNR-related bands with respect to the Fermi energy (E (F)), thus, proving the tunability of the induced n-doping.
|
|
| 13. |
- Simonov, Konstantin A., et al.
(författare)
-
From Graphene Nanoribbons on Cu(111) to Nanographene on Cu(110) : Critical Role of Substrate Structure in the Bottom-Up Fabrication Strategy
- 2015
-
Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 9:9, s. 8997-9011
-
Tidskriftsartikel (refereegranskat)abstract
- Bottom-up strategies can be effectively implemented for the fabrication of atomically precise graphene nanoribbons. Recently, using 10,10'-dibromo-9,9'-bianthracene (DBBA) as a molecular precursor to grow armchair nanoribbons on Au(111) and Cu(111), we have shown that substrate activity considerably affects the dynamics of ribbon formation, nonetheless without significant modifications in the growth mechanism. In this paper we compare the on-surface reaction pathways for DBBA molecules on Cu(111) and Cu(110). Evolution of both systems has been studied via a combination of core-level X-ray spectroscopies, scanning tunneling microscopy, and theoretical calculations. Experimental and theoretical results reveal a significant increase in reactivity for the open and anisotropic Cu(110) surface in comparison with the close-packed Cu(111). This increased reactivity results in a predominance of the molecular substrate interaction over the intermolecular one, which has a critical impact on the transformations of DBBA on Cu(110). Unlike DBBA on Cu(111), the Ullmann coupling cannot be realized for DBBA/Cu(110) and the growth of nanoribbons via this mechanism is blocked. Instead, annealing of DBBA on Cu(110) at 250 degrees C results in the formation of a new structure: quasi-zero-dimensional flat nanographenes. Each nanographene unit has dehydrogenated zigzag edges bonded to the underlying Cu rows and oriented with the hydrogen-terminated armchair edge parallel to the [1-10] direction. Strong bonding of nanographene to the substrate manifests itself in a high adsorption energy of -12.7 eV and significant charge transfer of 3.46e from the copper surface. Nanographene units coordinated with bromine adatoms are able to arrange in highly regular arrays potentially suitable for nanotemplating.
|
|
| 14. |
- Chikina, A., et al.
(författare)
-
Valence instability in the bulk and at the surface of the antiferromagnet SmRh2Si2
- 2017
-
Ingår i: Physical Review B - Condensed Matter and Materials Physics. - 1098-0121. ; 95:15
-
Tidskriftsartikel (refereegranskat)abstract
- Using resonant angle-resolved photoemission spectroscopy and electron band-structure calculations, we explore the electronic structure and properties of Sm atoms at the surface and in the bulk of the antiferromagnet SmRh2Si2. We show that the Sm atoms reveal weak mixed-valent behavior both in the bulk and at the surface. Although trivalent 4f emission strongly dominates, a small divalent 4f signal near the Fermi energy can be clearly resolved for surface and bulk Sm atoms. This behavior is quite different to most other Sm-based materials which typically experience a surface valence transition to a divalent state of Sm atoms at the surface. This phenomenon is explained in analogy to the isostructural Ce compound, where strong 4f hybridization stabilizes mixed-valent ground state both in the bulk and at the surface, and which were described in the light of the single-impurity Anderson model. Implications for other RERh2Si2 (RE = rare-earth elements) compounds are discussed.
|
|
| 15. |
- Güttler, M., et al.
(författare)
-
Divalent EuRh 2 Si 2 as a reference for the Luttinger theorem and antiferromagnetism in trivalent heavy-fermion YbRh 2 Si 2
- 2019
-
Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 10:1
-
Tidskriftsartikel (refereegranskat)abstract
- Application of the Luttinger theorem to the Kondo lattice YbRh 2 Si 2 suggests that its large 4f-derived Fermi surface (FS) in the paramagnetic (PM) regime should be similar in shape and volume to that of the divalent local-moment antiferromagnet (AFM) EuRh 2 Si 2 in its PM regime. Here we show by angle-resolved photoemission spectroscopy that paramagnetic EuRh 2 Si 2 has a large FS essentially similar to the one seen in YbRh 2 Si 2 down to 1 K. In EuRh 2 Si 2 the onset of AFM order below 24.5 K induces an extensive fragmentation of the FS due to Brillouin zone folding, intersection and resulting hybridization of the Fermi-surface sheets. Our results on EuRh 2 Si 2 indicate that the formation of the AFM state in YbRh 2 Si 2 is very likely also connected with similar changes in the FS, which have to be taken into account in the controversial analysis and discussion of anomalies observed at the quantum critical point in this system.
|
|
| 16. |
- Schulz, S., et al.
(författare)
-
Classical and cubic Rashba effect in the presence of in-plane 4f magnetism at the iridium silicide surface of the antiferromagnet GdIr2Si2
- 2021
-
Ingår i: Physical Review B. - 2469-9950. ; 103:3
-
Tidskriftsartikel (refereegranskat)abstract
- We present a combined experimental and theoretical study of the two-dimensional electron states at the iridium-silicide surface of the antiferromagnet GdIr2Si2 above and below the Néel temperature. Using angle-resolved photoemission spectroscopy (ARPES) we find a significant spin-orbit splitting of the surface states in the paramagnetic phase. By means of ab initio density-functional-theory (DFT) calculations we establish that the surface electron states that reside in the projected band gap around the M¯ point exhibit very different spin structures which are governed by the conventional and the cubic Rashba effect. The latter is reflected in a triple spin winding, i.e., the surface electron spin reveals three complete rotations upon moving once around the constant energy contours. Below the Néel temperature, our ARPES measurements show an intricate photoemission intensity picture characteristic of a complex magnetic domain structure. The orientation of the domains, however, can be clarified from a comparative analysis of the ARPES data and their DFT modeling. To characterize a single magnetic domain picture, we resort to the calculations and scrutinize the interplay of the Rashba spin-orbit coupling field with the in-plane exchange field, provided by the ferromagnetically ordered 4f moments of the near-surface Gd layer.
|
|
| 17. |
|
|
| 18. |
- Simonov, Konstantin, 1988-, et al.
(författare)
-
Effect of Substrate Chemistry on the Bottom-Up Fabrication of Graphene Nanoribbons : Combined Core-Level Spectroscopy and STM Study
- 2014
-
Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 118:23, s. 12532-12540
-
Tidskriftsartikel (refereegranskat)abstract
- Atomically precise graphene nanoribbons (GNRs) can be fabricated via thermally induced polymerization of halogen containing molecular precursors on metal surfaces. In this paper the effect of substrate reactivity on the growth and structure of armchair GNRs (AGNRs) grown on inert Au(111) and active Cu(111) surfaces has been systematically studied by a combination of core-level X-ray spectroscopies and scanning tunneling microscopy. It is demonstrated that the activation threshold for the dehalogenation process decreases with increasing catalytic activity of the substrate. At room temperature the 10,10'-dibromo-9,9'-bianthracene (DBBA) precursor molecules on Au(111) remain intact, while on Cu(111) a complete surface-assisted dehalogenation takes place. Dehalogenation of precursor molecules on Au(111) only starts at around 80 degrees C and completes at 200 degrees C, leading to the formation of linear polymer chains. On Cu(111) tilted polymer chains appear readily at room temperature or slightly elevated temperatures. Annealing of the DBBA/Cu(111) above 100 degrees C leads to intramolecular cyclodehydrogenation and formation of flat AGNRs at 200 degrees C, while on the Au(111) surface the formation of GNRs takes place only at around 400 degrees C. In STM, nanoribbons have significantly reduced apparent height on Cu(111) as compared to Au(111), 70 +/- 11 pm versus 172 +/- 14 pm, independently of the bias voltage. Moreover, an alignment of GNRs along low-index crystallographic directions of the substrate is evident for Cu(111), while on Au(111) it is more random. Elevating the Cu(111) substrate temperature above 400 degrees C results in a dehydrogenation and subsequent decomposition of GNRs; at 750 degrees C the dehydrogenated carbon species self-organize in graphene islands. In general, our data provide evidence for a significant influence of substrate reactivity on the growth dynamics of GNRs.
|
|
| 19. |
- Vinogradov, Nikolay, et al.
(författare)
-
Controllable p-doping of graphene on Ir(111) by chlorination with FeCl(3).
- 2012
-
Ingår i: Journal of Physics: Condensed Matter. - : IOP Publishing. - 1361-648X .- 0953-8984. ; 24:31
-
Tidskriftsartikel (refereegranskat)abstract
- The in situ chlorination of graphene on Ir(111) has been achieved by depositing FeCl(3) followed by its thermal decomposition on the surface into FeCl(2) and Cl. This process is accompanied by an intercalation of Cl under graphene and formation of an epitaxial FeCl(2) film on top, which can be removed upon further annealing. A pronounced hole doping of graphene has been observed as a consequence of the annealing-assisted intercalation of Cl. This effect has been studied by a combination of core-level and angle-resolved photoelectron spectroscopies (CL PES and ARPES, respectively), near-edge x-ray absorption fine structure (NEXAFS) spectroscopy and low-energy electron diffraction (LEED). The ease of preparation, the remarkable reproducibility of the doping level and the reversibility of the doping upon annealing are the key factors making chlorination with FeCl(3) a promising route for tuning the electronic properties in graphene.
|
|
| 20. |
- Jacobse, Peter H., et al.
(författare)
-
One Precursor but Two Types of Graphene Nanoribbons : On-Surface Transformations of 10,10'-Dichloro-9,9'-bianthryl on Ag(111)
- 2019
-
Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 123:14, s. 8892-8901
-
Tidskriftsartikel (refereegranskat)abstract
- On-surface synthesis has emerged in the last decade as a method to create graphene nanoribbons (GNRs) with atomic precision. The underlying premise of this bottom-up strategy is that precursor molecules undergo a well-defined sequence of inter- and intramolecular reactions, leading to the formation of a single product. As such, the structure of the GNR is encoded in the precursors. However, recent examples have shown that not only the molecule, but also the coinage metal surface on which the reaction takes place, plays a decisive role in dictating the nanoribbon structure. In this work, we use scanning probe microscopy and X-ray photoelectron spectroscopy to investigate the behavior of 10,10'-dichloro-9,9'-bianthryl (DCBA) on Ag(111). Our study shows that Ag(111) can induce the formation of both seven-atom wide armchair GNRs (7-acGNRs) and 3,1-chiral GNRs (3,1-cGNRs), demonstrating that a single molecule on a single surface can react to different nanoribbon products. We additionally show that coadsorbed dibromoperylene can promote surface-assisted dehydrogenative coupling in DCBA, leading to the exclusive formation of 3,1-cGNRs.
|
|
| 21. |
- Krasnok, A. E., et al.
(författare)
-
Coherently Enhanced Wireless Power Transfer
- 2018
-
Ingår i: Physical Review Letters. - 1079-7114 .- 0031-9007. ; 120:14
-
Tidskriftsartikel (refereegranskat)abstract
- Extraction of electromagnetic energy by an antenna from impinging external radiation is at the basis of wireless communications and wireless power transfer (WPT). The maximum of transferred energy is ensured when the antenna is conjugately matched, i.e., when it is resonant and it has an equal coupling with free space and its load. This condition, however, can be easily affected by changes in the environment, preventing optimal operation of a WPT system. Here, we introduce the concept of coherently enhanced WPT that allows us to bypass this difficulty and achieve dynamic control of power transfer. The approach relies on coherent excitation of the waveguide connected to the antenna load with a backward propagating signal of specific amplitude and phase. This signal creates a suitable interference pattern at the load resulting in a modification of the local wave impedance, which in turn enables conjugate matching and a largely increased amount of extracted energy. We develop a simple theoretical model describing this concept, demonstrate it with full-wave numerical simulations for the canonical example of a dipole antenna, and verify experimentally in both near-field and far-field regimes.
|
|
| 22. |
- Li, S., et al.
(författare)
-
Coherently enhanced wireless power transfer: Theory and experiment
- 2018
-
Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 1092
-
Konferensbidrag (refereegranskat)abstract
- Extraction of electromagnetic energy by an antenna to a coupled waveguide is the crucial part of wireless power transfer. Efficiency of this process is usually defined by the coupling strength between the antenna and the outcoupling waveguide or cable. We show that there is an additional possibility to improve the receiving efficiency by coherent excitation of the outcoupling waveguide by a backward propagating guided mode with a specific amplitude and phase. This additional wave creates a special interference picture in the system and result in increased amount of energy extracted to the waveguide from the free space. We develop a simple analytical model predicting this effect, demonstrate it in numerical FDTD simulations, and verify in microwave experiment.
|
|
| 23. |
- Pramanik, Arindam, et al.
(författare)
-
Dirac states in the noncentrosymmetric superconductor BiPd
- 2021
-
Ingår i: Physical Review B. - 2469-9950. ; 103:15
-
Tidskriftsartikel (refereegranskat)abstract
- Quantum materials having Dirac fermions in conjunction with superconductivity is believed to be the candidate material to realize exotic physics as well as advanced technology. Angle-resolved photoemission spectroscopy (ARPES), a direct probe of the electronic structure, has been extensively used to study these materials. However, experiments often exhibit conflicting results on dimensionality and momentum of the Dirac fermions (e.g., Dirac states in BiPd, a novel noncentrosymmetric superconductor), which is crucial for the determination of the symmetry, time-reversal invariant momenta, and other emerging properties. Employing high-resolution ARPES at varied conditions, we demonstrated a methodology to identify the location of the Dirac node accurately and discover that the deviation from two dimensionality of the Dirac states in BiPd proposed earlier is not a material property. These results helped to reveal the topology of the anisotropy of the Dirac states accurately. We have constructed a model Hamiltonian considering higher-order spin-orbit terms and demonstrate that this model provides an excellent description of the observed anisotropy. Intriguing features of the Dirac states in a noncentrosymmetric superconductor revealed in this study are expected to have significant implications regarding the properties of topological superconductors.
|
|
| 24. |
- Pramanik, Arindam, et al.
(författare)
-
Surface states in noncentrosymmetric superconductor BiPd
- 2022
-
Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 2164
-
Konferensbidrag (refereegranskat)abstract
- BiPd is a noncentrosymmetric superconductor with Dirac-like surface states on both (010) and (01¯0) faces. The Dirac cone on (010) surface is intense and appears at 0.66 eV binding energy. These states have drawn much attention due to contradictory reports on dimensionality and the momentum of these Dirac fermions. We have studied the properties of these Dirac fermions using varied photon energies and different experimental conditions. The behavior of the Dirac cone is found to be two-dimensional. In addition, we found few more surface states appearing at higher binding energies compared to the Dirac cone.
|
|
| 25. |
- Schulz, Susanne, et al.
(författare)
-
Emerging 2D-ferromagnetism and strong spin-orbit coupling at the surface of valence-fluctuating EuIr2Si2
- 2019
-
Ingår i: npj Quantum Materials. - : Springer Science and Business Media LLC. - 2397-4648. ; 4:1
-
Tidskriftsartikel (refereegranskat)abstract
- The development of materials that are non-magnetic in the bulk but exhibit two-dimensional (2D) magnetism at the surface is at the core of spintronics applications. Here, we present the valence-fluctuating material EuIr2Si2, where in contrast to its non-magnetic bulk, the Si-terminated surface reveals controllable 2D ferromagnetism. Close to the surface the Eu ions prefer a magnetic divalent configuration and their large 4f moments order below 48 K. The emerging exchange interaction modifies the spin polarization of the 2D surface electrons originally induced by the strong Rashba effect. The temperature-dependent mixed valence of the bulk allows to tune the energy and momentum size of the projected band gaps to which the 2D electrons are confined. This gives an additional degree of freedom to handle spin-polarized electrons at the surface. Our findings disclose valence-fluctuating rare-earth based materials as a very promising basis for the development of systems with controllable 2D magnetic properties which is of interest both for fundamental science and applications.
|
|
| 26. |
- Svirskiy, Gleb I., et al.
(författare)
-
Electronic structure of the [Ni(Salen)] complex studied by core-level spectroscopies
- 2021
-
Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 23:18, s. 11015-11027
-
Tidskriftsartikel (refereegranskat)abstract
- The nature and structure of occupied and empty valence electronic states (molecular orbitals, MOs) of the [Ni(Salen)] molecular complex (NiO2N2C16H14) have been studied by X-ray photoemission and absorption spectroscopy combined with density functional theory (DFT) calculations. As a result, the composition of the high-lying occupied and low-lying unoccupied electronic states has been identified. In particular, the highest occupied molecular orbital (HOMO) of the complex is found to be predominantly located on the phenyl rings of the salen ligand, while the states associated with the occupied Ni 3d-derived molecular orbitals (MOs) are at higher binding energies. The lowest unoccupied molecular orbital (LUMO) is also located on the salen ligand and is formed by the 2pπ orbitals of carbon atoms in phenyl groups of the salen macrocycle. The unoccupied MOs above the LUMO reflect σ- and π-bonding between Ni and its nearest neighbours. All valence states have highly mixed character. The specific nature of the unoccupied Ni 3d-derived σ-MO is a consequence of donor-acceptor chemical bonding in [Ni(Salen)]. This journal is
|
|
