arXiv subjects

K. N. Eltsov

Publications and source records attributed to K. N. Eltsov.

9 recordsLinked to original sources

arXiv2022

Dangling bonds on the Cl- and Br-terminated Si(100) surfaces

Halogen monolayer on a silicon surface is attracting active attention for applications in electronic device fabrication with individual impurities. To create a halogen mask for the impurities incorporation, it is desirable to be able to remove a single halogen atom from the surface. We report the desorption of individual halogen atoms from the Si(100)-2x1-Cl and -Br surfaces in a scanning tunneling microscope (STM). Silicon dangling bonds (DBs) formed on the Si surface after halogen desorption were investigated using STM and the density functional theory. Three charge states: positive, neutral, and negative were identified. Our results show that the charge states of DBs can be manipulated, which will allow to locally tune the reactivity of the Cl- and Br-terminated Si(100) surfaces.

cond-mat.mtrl-sci↗

arXiv2021

Reactivity of the Si(100)-2$\times$1-Cl surface with respect to PH$_3$, PCl$_3$, and BCl$_3$: Comparison with PH$_3$ on Si(100)-2$\times$1-H

Despite the interest in a chlorine monolayer on Si(100) as an alternative to hydrogen resist for atomic-precision doping, little is known about its interaction with dopant-containing molecules. We used the density functional theory to evaluate whether a chlorine monolayer on Si(100) is suitable as a resist for \ce{PH3}, \ce{PCl3}, and \ce{BCl3} molecules. We calculated reaction pathways for \ce{PH3}, \ce{PCl3}, and \ce{BCl3} adsorption on a bare and Cl-terminated Si(100)-2$\times$1 surface, as well as for \ce{PH3} adsorption on H-terminated Si(100)-2$\times$1, which is widely used in current technologies for atomically precise doping of Si(100) with phosphorus. It was found that the Si(100)-2$\times$1-Cl surface has a higher reactivity towards phosphine than Si(100)-2$\times$1-H, and, therefore, unpatterned areas are less protected from undesirable incorporation of \ce{PH3} fragments. On the contrary, the resistance of the Si(100)-2$\times$1-Cl surface against the chlorine-containing molecules turned out to be very high. Several factors influencing reactivity are discussed. The results reveal that phosphorus and boron trichlorides are well-suited for doping a patterned Cl-resist by donors and acceptors, respectively.

cond-mat.mtrl-sci↗

arXiv2020

Ni-doped epitaxial graphene monolayer on the Ni(111) surface

Nickel-doped graphene has been synthesized from propylene on a Ni(111) surface and studied using scanning tunneling microscopy (STM) and density functional theory (DFT). It is established that nickel centers are formed during graphene synthesis on the Ni(111) surface by both chemical vapor deposition (CVD) and temperature-programmed growth (TPG); apparently, they are always present in graphene synthesized on Ni(111). The centers are observed in STM images as single defects or defect chains and identified by DFT calculations as Ni atoms in carbon bivacancies. These nickel atoms are positively charged and may be of interest for single-atom catalysis. The incorporated Ni atoms should remain in graphene after the detachment from the substrate since they bound more strongly with carbon atoms in graphene than with substrate nickel atoms.

cond-mat.mtrl-sci↗

arXiv2020

Chlorine insertion and manipulation on the Si(100)-2x1-Cl surface in the regime of local supersaturation

We insert and manipulate a single chlorine atom in chlorine monolayer on a Si(100)-2x1 surface using a scanning tunneling microscope. Two objects were created - a Cl atom in a groove between two dimer rows, and bridge-bonded Cl on a silicon dimer. Changing the voltage polarity leads to conversion of the objects into each other. Anisotropic movement of the objects at 77 K is mediated by two different diffusion mechanisms: hopping and crowdion-like motion. Insertion of a Cl atom in a groove between two dimer rows leads to the formation of a dangling bond on a third-layer Si atom. At positive sample voltage bias, the first object is positively charged, while the second object can be neutral or negatively charged depending on silicon sample doping.

cond-mat.mes-hall↗

arXiv2020

Room temperature propylene dehydrogenation and linear atomic chain formation on Ni(111)

The structures formed by propylene adsorption on Ni(111) at room temperature are determined by a combination of scanning tunneling microscopy and density functional theory. As a result of the interaction with the Ni(111) surface, propylene molecules are dehydrogenated and coupled into linear hydrocarbon chains. The length of the chains varies from 8 to 60A, with the most frequently observed length of 18A. At saturated coverage, some chains are closed in rings with a diameter of 6A. A C12H12 model is proposed for most often observed chains. We demonstrate that the possibility of combining initial propylene molecules into chains appears after dehydrogenation of the CH3 fragment.

cond-mat.mtrl-sci↗

arXiv2020

Local removal of silicon layers on Si(100)-2x1 with chlorine-resist STM lithography

We report the realization of STM-based lithography with silicon layers removal on the chlorinated Si(100)-2x1 surface at 77 K. In contrast to other STM lithography studies, we were able to remove locally both chlorine and silicon atoms. Most of the etched pits have a lateral size of 10-20 A and a depth of 1-5 A. In the pits in which the STM image with atomic resolution is obtained, the bottom is mainly covered with chlorine. Some pits contain chlorine vacancies. Mechanisms of STM-induced removal of silicon and chlorine atoms on Si(100)-2x1-Cl are discussed and compared with the well-studied case of STM-induced hydrogen desorption on Si(100)-2x1-H. The results open up new possibilities of the three-dimensional local etching with STM lithography.

cond-mat.mes-hall↗

arXiv2019

Ab Initio Study of the Early Stage of Si Epitaxy on the Chlorinated Si(100) Surface

The homoepitaxial growth of Si on Si(100) covered by a resist mask is a necessary technological step for the fabrication of donor-based quantum devices with scanning tunneling microscope lithography. In the present work, the chlorine monolayer is selected as the resist. Using density functional theory, we investigated the adsorption of a single silicon atom on Si(100)-2$\times$1-Cl as the starting process of Si epitaxy. The incorporation of a silicon atom under a Cl monolayer proved to be the most energetically favorable process. Our results show that chlorine segregates on the surface during Si deposition and does not incorporate into homoepitaxial layers. In addition, we found that SiCl$_2^{\ast}$, SiCl$_3^{\ast}$, and SiCl$_4^{\ast}$ clusters can be formed above a Si(100)-2$\times$1-Cl surface while Si is adsorbed. SiCl$_2^{\ast}$ clusters are bound weakly to the substrate, and their desorption leaves the silicon surface free of chlorine. To check whether the Si epitaxy is possible on the chlorine resist, we compare our results with the well-studied case of a hydrogen resist. We find the two processes to be similar; moreover, epitaxy on chlorine resist appears to have an advantage.

physics.app-ph↗

arXiv2017

Carbon chains and graphene nucleus synthesized on Ni(111) surface

Linear chains of about 10-13 carbon atoms were predicted to be the most favorable phase on different metal surfaces prior to graphene nucleation. However, unlike the graphene that widely studied both theoretically and experimentally, carbon chains on metal surfaces were not directly studied by STM yet. Here we fill in the gap and report on STM experiments of linear carbon chains synthesized on Ni(111) through on-surface coupling of dehydrogenated propene molecules. Identification of chains was supported with DFT calculations and the proposed models consist of 12 carbon atoms, possibly covered by hydrogen atoms. Heating to 580 K leads to dramatic decrease of carbon chains and new phase appearance - graphene nucleus coexisted with nickel carbide. After flash annealing to 773 K (temperature of graphene synthesis), a small number of chains were presented on the Ni(111) surface, together with graphene islands and nickel carbide. The carbon chains are stable at room temperature and their mobility was directly observed by STM.

cond-mat.mes-hall↗

arXiv1998

Atomic structure of silver chloride formed on Ag(111) surface upon low temperature chlorination

The structure of AgCl formed in the course of chlorine adsorption on Ag(111) surface was studied by STM. For the first time atomic resolution STM images of silver chloride were obtained. The silver chloride was detected as small (30-60 A in diameter) islands located on the atomic terraces. The upper plane of the islands was found to be AgCl(111) with interatomic distance close to the bulk value. The chloride surface lattice was not rotated with respect to the substrate. A possible mechanism of AgCl growth on Ag(111) is discussed.

cond-mat.mtrl-sci↗