arXiv subjects

Yannick J. Dappe

Publications and source records attributed to Yannick J. Dappe.

14 recordsLinked to original sources

arXiv2023

Intrinsic defects and mid-gap states in quasi-one-dimensional Indium Telluride

Recently, intriguing physical properties have been unraveled in anisotropic semiconductors, in which the in-plane electronic band structure anisotropy often originates from the low crystallographic symmetry. The atomic chain is the ultimate limit in material downscaling for electronics, a frontier for establishing an entirely new field of one-dimensional quantum materials. Electronic and structural properties of chain-like InTe are essential for better understanding of device applications such as thermoelectrics. Here, we use scanning tunneling microscopy/spectroscopy (STM/STS) measurements and density functional theory (DFT) calculations to directly image the in-plane structural anisotropy in tetragonal Indium Telluride (InTe). As results, we report the direct observation of one-dimensional In1+ chains in InTe. We demonstrate that InTe exhibits a band gap of about 0.40 +-0.02 eV located at the M point of the Brillouin zone. Additionally, line defects are observed in our sample, were attributed to In1+ chain vacancy along the c-axis, a general feature in many other TlSe-like compounds. Our STS and DFT results prove that the presence of In1+ induces localized gap state, located near the valence band maximum (VBM). This acceptor state is responsible for the high intrinsic p-type doping of InTe that we also confirm using angle-resolved photoemission spectroscopy.

cond-mat.mtrl-sci↗

arXiv2023

Enhancement of the Solar Water Splitting Efficiency Mediated by Surface Segregation in Ti-doped Hematite Nanorods

Band engineering is employed thoroughly and targets technologically scalable photoanodes for solar water splitting applications. Complex and costly recipes are necessary, often for average performances. Here we report simple photoanode growth and thermal annealing, with effective band engineering results. By comparing Ti-doped hematite photoanodes annealed under Nitrogen to photoanodes annealed in air, we found strongly enhanced photocurrent, of more than 200 % in the first case. Using electrochemical impedance spectroscopy and synchrotron X-rays spectromicroscopies we demonstrate that oxidized surface states and increased density of charge carriers are responsible for the enhanced photoelectrochemical activity. Surface states are found to be related to the formation of pseudo-brookite clusters by surface Ti segregation. Spectro-ptychography is used for the first time at Ti L3 absorption edge to isolate Ti chemical coordination arising from pseudo-brookite clusters contribution. Correlated with electron microscopy investigation and Density Functional Theory (DFT) calculations, the synchrotron spectromicroscopy data prove unambiguously the origin of the better photoelectrochemical activity of N2- annealed Ti-doped hematite nanorods. Finally, we present here a handy and cheap surface engineering method, beyond the known oxygen vacancy doping, allowing a net gain in the photoelectrochemical activity for the hematite-based photoanodes.

cond-mat.mtrl-sci↗

arXiv2022

Negative Differential Resistance in Spin-Crossover Molecular Devices

We demonstrate, based on low-temperature scanning tunneling microscopy (STM) and spectroscopy, a pronounced negative differential resistance (NDR) in spin-crossover (SCO) molecular devices, where a Fe$^{\text{II}}$ SCO molecule is deposited on surfaces. The STM measurements reveal that the NDR is robust with respect to substrate materials, temperature, and the number of SCO layers. This indicates that the NDR is intrinsically related to the electronic structure of the SCO molecule. Experimental results are supported by density functional theory (DFT) with non-equilibrium Green's functions (NEGF) calculations and a generic theoretical model. While the DFT+NEGF calculations reproduce NDR for a special atomically-sharp STM tip, the effect is attributed to the energy-dependent tip density of states rather than the molecule itself. We, therefore, propose a Coulomb blockade model involving three molecular orbitals with very different spatial localization as suggested by the molecular electronic structure.

cond-mat.mes-hall↗

arXiv2020

Silicene nanoribbons on an insulating thin film

Silicene, a new two-dimensional (2D) material has attracted intense research because of the ubiquitous use of silicon in modern technology. However, producing free-standing silicene has proved to be a huge challenge. Until now, silicene could be synthesized only on metal surfaces where it naturally forms strong interactions with the metal substrate that modify its electronic properties. Here, we report the first experimental evidence of silicene sheet on an insulating NaCl thin film. This work represents a major breakthrough; for the study of the intrinsic properties of silicene, and by extension to other 2D materials that have so far only been grown on metal surfaces.

cond-mat.mtrl-sci↗

arXiv2020

Phosphorus Pentamers: Floating Nanoflowers form a 2D Network

We present an experimental investigation of a new polymorphic 2D single layer of phosphorus on Ag(111). The atomically-resolved scanning tunneling microscopy (STM) images show a new 2D material composed of freely-floating phosphorus pentamers organized into a 2D layer, where the pentamers are aligned in close-packed rows. The scanning tunneling spectroscopy (STS) measurements reveal a semiconducting character with a band gap of 1.20 eV. This work presents the formation at low temperature (LT) of a new polymorphic 2D phosphorus layer composed of a floating 2D pentamer structure. The smooth curved terrace edges and a lack of any clear crystallographic orientation with respect to the Ag(111) substrate at room temperature indicates a smooth potential energy surface that is reminiscent of a liquid-like growth phase. This is confirmed by density functional theory (DFT) calculations that find a small energy barrier of only 0.17 eV to surface diffusion of the pentamers (see Supplemental Material). The formation of extended, homogeneous domains is a key ingredient to opening a new avenue to integrate this new 2D material into electronic devices.

cond-mat.mtrl-sci↗

arXiv2020

Decoupling Molybdenum Disulfide from its Substrate by Cesium Intercalation

Intercalation of alkali atoms within the lamellar transition metal dichalcogenides is a possible route toward a new generation of batteries. It is also a way to induce structural phase transitions authorizing the realization of optical and electrical switches in this class of materials. The process of intercalation has been mostly studied in three-dimensional dichalcogenide films. Here, we address the case of a single-layer of molybdenum disulfide (MoS$_2$), deposited on a gold substrate, and intercalated with cesium (Cs) in ultra-clean conditions (ultrahigh vacuum). We show that intercalation decouples MoS$_2$ from its substrate. We reveal electron transfer from Cs to MoS$_2$, relative changes in the energy of the valence band maxima, and electronic disorder induced by structural disorder in the intercalated Cs layer. Besides, we find an abnormal lattice expansion of MoS$_2$, which we relate to immediate vicinity of Cs. Intercalation is thermally activated, and so is the reverse process of de-intercalation. Our work opens the route to a microscopic understanding of a process of relevance in several possible future technologies, and shows a way to manipulate the properties of two-dimensional dichalcogenides by "under-cover" functionalization.

cond-mat.mtrl-sci↗

arXiv2019

Symmetry aspects of spin-filtering in molecular junctions: hybridization and quantum interference effects

Control and manipulation of electric current and, especially, its degree of spin polarization (spin filtering) across single molecules are currently of great interest in the field of molecular spintronics. We explore one possible strategy based on the modification of nanojunction symmetry which can be realized, for example, by a mechanical strain. Such modification can activate new molecular orbitals which were inactive before due to their orbital mismatch with the electrode's conduction states. This can result in several important consequences such as (i) quantum interference effects appearing as Fano-like features in electron transmission and (ii) the change in molecular level hybridization with the electrode's states. We argue that the symmetry change can affect very differently two majority- and minority-spin conductances and thus alter significantly the resulting spin-filtering ratio as the junction symmetry is modified. We illustrate the idea for two basic molecular junctions: Ni/benzene/Ni (perpendicular vs tilted orientations) and Ni/Si chain/Ni (zigzag vs linear chains). In both cases, one highest occupied molecular orbital (HOMO) and one lowest unoccupied molecular orbital (LUMO) (out of HOMO and LUMO doublets) are important. In particular, their destructive interference with other orbitals leads to dramatic suppression of majority-spin conductance in low-symmetry configurations. For a minority-spin channel, on the contrary, the conductance is strongly enhanced when the symmetry is lowered due to an increase in hybridization strength. We believe that our results may offer a potential route for creating molecular devices with a large on-off ratio of spin polarization via quantum interference effects.

cond-mat.mes-hall↗

arXiv2019

Perfect spin filtering by symmetry in molecular junctions

Obtaining highly spin-polarized currents in molecular junctions is crucial and desirable for nanoscale spintronics devices. Motivated by our recent symmetry-based theoretical argument for complete blocking of one spin conductance channel in atomic-scale junctions [A. Smogunov and Y. J. Dappe, Nano Lett. 15, 3552 (2015)], we explore the generality of the proposed mechanism and the degree of achieved spin-polarized current for various ferromagnetic electrodes (Ni, Co, Fe) and two different molecules, quaterthiophene and p-quaterphenyl. A simple analysis of the spin-resolved local density of states of a free electrode allowed us to identify the Fe(110) as the most optimal electrode, providing perfect spin filtering and high conductance at the same time. These results are confirmed by $ab$ $initio$ quantum transport calculations and are similar to those reported previously for model junctions. It is found, moreover, that the distortion of the p-quaterphenyl molecule plays an important role, reducing significantly the overall conductance.

cond-mat.mes-hall↗

arXiv2019

Tuning spin filtering by anchoring groups in benzene derivative molecular junctions

One of the important issues of molecular spintronics is the control and manipulation of charge transport and, in particular, its spin polarization through single-molecule junctions. Using $ab$ $initio$ calculations, we explore spin-polarized electron transport across single benzene derivatives attached with six different anchoring groups (S, CH$_3$S, COOH, CNH$_2$NH, NC and NO$_2$) to Ni(111) electrodes. We find that molecule-electrode coupling, conductance and spin polarization (SP) of electric current can be modified significantly by anchoring groups. In particular, a high spin polarization (SP $>$ 80%) and a giant magnetoresistance (MR $>$ 140%) can be achieved for NO$_2$ terminations and, more interestingly, SP can be further enhanced (up to 90%) by a small voltage. The S and CH$_3$S systems, on the contrary, exhibit rather low SP while intermediate values are found for COOH and CNH$_2$NH groups. The results are analyzed in detail and explained by orbital symmetry arguments, hybridization and spatial localization of frontier molecular orbitals. We hope that our comparative and systematic studies will provide valuable quantitative information for future experimental measurements on that kind of systems and will be useful for designing high-performance spintronics devices.

cond-mat.mes-hall↗

arXiv2018

Tunable Doping in Hydrogenated Single Layered Molybdenum Disulfide

Structural defects in the molybdenum disulfide (MoS2) monolayer are widely known for strongly altering its properties. Therefore, a deep understanding of these structural defects and how they affect MoS2 electronic properties is of fundamental importance. Here, we report on the incorporation of atomic hydrogen in mono-layered MoS2 to tune its structural defects. We demonstrate that the electronic properties of single layer MoS2 can be tuned from the intrinsic electron (n) to hole (p) doping via controlled exposure to atomic hydrogen at room temperature. Moreover, this hydrogenation process represents a viable technique to completely saturate the sulfur vacancies present in the MoS2 flakes. The successful incorporation of hydrogen in MoS2 leads to the modification of the electronic properties as evidenced by high resolution X-ray photoemission spectroscopy and density functional theory calculations. Micro-Raman spectroscopy and angle resolved photoemission spectroscopy measurements show the high quality of the hydrogenated MoS2 confirming the efficiency of our hydrogenation process. These results demonstrate that the MoS2 hydrogenation could be a significant and efficient way to achieve tunable doping of transition metal dichalcogenides (TMD) materials with non-TMD elements.

cond-mat.mtrl-sci↗

arXiv2018

Weakly Trapped, Charged, and Free Excitons in Single-Layer MoS2 in the Presence of Defects, Strain, and Charged Impurities

Few- and single-layer MoS2 host substantial densities of defects. They are thought to influence the doping level, the crystal structure, and the binding of electron-hole pairs. We disentangle the concomitant spectroscopic expression of all three effects and identify to what extent they are intrinsic to the material or extrinsic to it, i.e., related to its local environment. We do so by using different sources of MoS2 -- a natural one and one prepared at high pressure and high temperature -- and different substrates bringing varying amounts of charged impurities and by separating the contributions of internal strain and doping in Raman spectra. Photoluminescence unveils various optically active excitonic complexes. We discover a defect-bound state having a low binding energy of 20 meV that does not appear sensitive to strain and doping, unlike charged excitons. Conversely, the defect does not significantly dope or strain MoS2. Scanning tunneling microscopy and density functional theory simulations point to substitutional atoms, presumably individual nitrogen atoms at the sulfur site. Our work shows the way to a systematic understanding of the effect of external and internal fields on the optical properties of two-dimensional materials.

cond-mat.mtrl-sci↗

arXiv2015

Pulling and Stretching a Molecular Wire to Tune its Conductance

A scanning tunnelling microscope is used to pull a polythiophene wire from a Au(111) surface while measuring the current traversing the junction. Abrupt current increases measured during the lifting procedure are associated to the detachment of molecular sub-units, in apparent contradiction with the expected exponential decrease of the conductance with wire length. \textit{Ab initio} simulations reproduce the experimental data and demonstrate that this unexpected behavior is due to release of mechanical stress in the wire, paving the way to mechanically gated single-molecule electronic devices.

cond-mat.mes-hall↗

arXiv2014

Electroluminescence from a polythiophene molecular wire suspended in a plasmonic scanning tunneling microscope junction

The electroluminescence of a polythiophene wire suspended between two metallic electrodes is probed using a scanning tunneling microscope. Under positive sample voltage, the spectral and voltage dependencies of the emitted light are consistent with the fluorescence of the wire junction mediated by localized plasmons. This emission is strongly attenuated for the opposite polarity. Both emission mechanism and polarity dependence are similar to what occurs in organic light emitting diodes (OLED) but at the level of a single molecular wire.

cond-mat.mes-hall↗

arXiv2012

Effect of van der Waals forces on the stacking of coronenes encapsulated in a single-wall carbon nanotube and many-body excitation spectrum

We investigate the geometry, stability, electronic structure and optical properties of C24H12 coronenes encapsulated in a single-wall (19,0) carbon nanotube. By an adequate combination of advanced electronic-structure techniques, involving weak and van derWaals interaction, as well as many-body effects for establishing electronic properties and excitations, we have accurately characterized this hybrid carbon nanostructure, which arises as a promising candidate for opto-electronic nanodevices. In particular, we show that the structure of the stacked coronenes inside the nanotube is characterized by a rotation of every coronene with respect to its neighbors through van derWaals interaction, which is of paramount importance in these systems. We also suggest a tentative modification of the system in order this particular rotation to be observed experimentally. A comparison between the calculated many-body excitation spectrum of the systems involved reveals a pronounced optical red-shift with respect to the coronene-stacking gas-phase. The origin of this red-shift is explained in terms of the confinement of the coronene molecules inside the nanotube, showing an excellent agreement with the available experimental evidence.

cond-mat.mes-hall↗