AVS 69 Session 2D-WeM: 2D-Materials: Defects, Dopants, and Modifications

Wednesday, November 8, 2023 8:00 AM in Room C123
Wednesday Morning

Session Abstract Book
(304KB, Nov 2, 2023)
Time Period WeM Sessions | Abstract Timeline | Topic 2D Sessions | Time Periods | Topics | AVS 69 Schedule

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8:00 AM Invited 2D-WeM-1 Developing Quantum Photon Sources from 2D Semiconductor Materials
Xuedan Ma (Argonne National Laboratory)

Optical photons are ubiquitous in quantum communication and storage applications due to their long coherence times and ease to travel over long distances. On-demand quantum photon sources that may emit single photons as quantum information carriers are especially sought after for quantum-related applications. In this talk, I will present our recent effort in the development of solid-state quantum photon sources based on low-dimensional semiconductor materials. By atomic defect creation [1,2] and local strain field engineering,[3-7] we demonstrate versatile approaches for efficient single photon generation and modulation.

References:

[1] W. Wang et al, ACS Nano, 16, 21240 (2022)

[2] Q. Qian et al. ACS Nano, 16, 7428 (2022)

[3] M. I. B. Utama et al. Nat. Commun. 14, 2193 (2023)

[4] X. Li et al. J. Phys. Chem. C 126, 20057 (2022)

[5] D. J. Morrow et al. Phys. Rev. B 104, 195302 (2021)

[6] W. Wang et al. ACS Photon. 7, 2460 (2021)

[7] L. Peng et al. Nano Lett. 20, 5866 (2020)

8:40 AM 2D-WeM-3 Bandgap Modulation of Graphene by Boron Nitride Doping
Sergi Campos Jara (Leiden University, The Netherlands); Laura Caputo (Université Catholiqué de Louvain); Tycho Roorda, Tjerk Benschop, Amber Mozes (Leiden University, The Netherlands); Vladimir Calvi, Richard van Rijn (Delft University of Technology); Milan P. Allan, Irene M.N. Groot (Leiden University, The Netherlands)

Since its discovery, graphene has shown to exhibit remarkable electronic properties.1 Numerous techniques have been devised to create high-performance devices by manipulating the bandgap in order to enhance their semiconducting properties.2

Doping has proven to be one of the most effective methods for bandgap engineering. Experimental and theoretical studies on graphene doping show the possibility of making p-type and n-type semiconducting graphene by substituting C atoms. Boron and nitrogen have been specifically studied during the last years due to the interesting insulating behavior of h-BN. Boron, nitrogen, and carbon can be atomically mixed to form various semiconducting, hexagonal, layered structures. Experimental and theoretical studies have indicated that BNC nanostructures show semiconducting properties with small bandgaps.2,3 Low concentrations of borazine rings within the graphene structure can modify graphene’s electronic properties to form a 2D semiconductor material with homogeneous patterns.4,5The intercalation of hexagonal BN (h-BN) within the graphene lattice has already been successfully achieved, however, segregation of both materials has been the main issue. Recent research has demonstrated that incorporating borazine-like molecules with carbon structures into graphene can result in reduced segregation of h-BN domains.5,6 Herrera Reinoza et al. demonstrated a notable example by depositing hexamethylborazine onto Ir(111), which yielded numerous boron-nitrogen-carbon (BNC) domains exhibiting low BN segregation and an estimated bandgap ranging between 1.4 and 1.6 eV.6

To grow our boron nitride-doped graphene nanomaterial (Figure 1a) we first synthesized graphene via chemical vapor deposition (CVD) by cyclic exposures to 10-5 mbar of ethylene for 10 minutes with subsequent annealing at 1100 K for 10 minutes. We have successfully doped our graphene by exposing it to hexamethylborazine right after the 3rd cycle of graphene synthesis. Auger electron spectroscopy depicted in Figure 1b demonstrated the presence of B, C and N in the sample. As depicted in Figure 1c, a bandgap was opened on our BN-doped graphene, forming a semiconductor material.

View Supplemental Document (pdf)
9:00 AM 2D-WeM-4 Wafer-Scale Photoluminescence Enhancement for MoS2 Monolayers Through Simple Wet-Chemical Defect Passivation in Acidic Hydrogen Peroxide Solution
Dennis H. van Dorp (IMEC Belgium); Luc van der Krabben (Radboud University Nijmegen); Anita Brady-Boyd (Aberystwyth University); Christopher Gort (TU Darmstadt); Sophia Arnauts, Thomas Nuytten, Henry Medina Silva, Efrain Altamirano Sanchez (IMEC Belgium); Jan Philippe Hofmann (TU Darmstadt); Steven Brems (IMEC Belgium)

It is expected that in the 2030 timeframe, CMOS technology nodes could include not only Si based transistors, but also possible ‘Beyond-CMOS’ devices that are co-integrated with the classical CMOS-based solutions. The alternative devices could be used along CMOS for specific functions. For instance, devices are being explored that have two-dimensional transition-metal dichalcogenides (2D TMDCs) as their conduction channel.

While device processing strategies for conventional CMOS technologies are well established, the use of TMDCs as atomic channel material poses new problems. In such applications, both dry and wet etching are essential processing steps for nanodevice fabrication, e.g. for patterning, contacting, layer selective etching, and surface engineering purposes. In contrast to dry etching, that may induce surface damage in the form of chalcogenide vacancies, wet-chemical methods provide an attractive alternative that avoids the problem of surface damage. However, the atomic scale dimensions of the 2D layer require ultimate selectivity and control to maintain and or improve the electronic and optical properties at wafer-scale level. To meet these goals, in-depth insight is needed in the compatibility of TMDC’s with wet-chemical solutions.

In this work, we will show the first semiconductor ICP-MS results on the atomic-scale etching kinetics of MoS2 in acidic solutions. Despite the very small dimensions of TMDC atomic layers, a surprisingly high chemical stability is demonstrated for both multilayer and monolayer MoS2. Controlled wet etching of the layers was achieved for dilute HCl/H2O2 solutions without significantly modifying the surface chemistry. In addition, it was found that wet-chemical treatment of MoS2 can dramatically enhance the photoluminescence properties on wafer-scale level using simple acidic solutions that contain a strong oxidizing agent.

We will show that wet-chemical processing can be utilized to significantly lower defect related non-radiative decay in the monolayers through passivation of sulphur vacancies. Room temperature PL measurements were used to optimize the passivation step. PL enhancements of up to 3 orders of magnitude were consistently achieved. Wafer-scale PL mapping showed good uniformity across the 2-inch wafer. Cryo-PL measurements confirmed effective defect passivation through the quenching of the bound exciton peaks.

The data presented indicate a good wet-chemical compatibility of the atomic layer TDMC material which is highly relevant for future developments in the CMOS industry.
9:20 AM 2D-WeM-5 Metal-to-Semiconductor Transition Observed in the Surface Density of States of Ti-Te Layered Monoclinic Crystals via Forced Atmospheric Exposure
Bishal Pokhrel, Joel Quarnstrom, Saraswati Shrestha, Halle Helfrich, Elena Echeverria, David McIlroy, Mario Borunda, Andrew Yost (Oklahoma State University)

Transition metal chalcogenides are promising 2D materials due to their unique properties and emerging phenomena such as charge density waves, superconductivity, ferroelectricity and ferromagnetism. Specifically the transition metal trichalcogenides of the form AX3 (A=Ti, Zr, Hf, X=S, Se, Te ) exhibit a quasi 1-D nature with anisotropic bandstructure which leads to preferential charge transport along the chain direction and minimal edge scattering effects suitable for fabricating high-performance devices. In this study, we examine the surface sensitivity of a high pressure grown Ti-Te transition metal chalcogenide using the chemical vapor transport (CVT) technique and study the surface changes in the sample upon exposure to air. The high-pressure growth results in the formation of silvery mirror-like sheets and nanowhiskers atypical of bulk 1T-TiTe2 growth, which is usually black and non-reflective. The silvery materials are capable of mechanical exfoliation via the scotch tape method and if left in atmosphere turn a darker color within a few hours. The crystal structure and size of the sheets are examined using X-Ray Diffraction (XRD), transmission electron microscopy (TEM), and select area electron diffraction (SAED). The material adopts a preferential (001) single crystalline nature with monoclinic structure and P2 1/m space group symmetry. Additionally, the SAED patterns show signs of a superlattice formation at the surface of the exposed layer. The local density of states (LDOS) of the in-situ exfoliated sample surface, measured using scanning tunneling spectroscopy (STS), exhibits a metallic to semi-conducting transition, with narrow gap, when exposed to atmosphere, suggesting the surface rapidly decomposes. The STM topography indicates a decrease in surface roughness after exposure to atmosphere reminiscent of ad-layer/s formation at the surface. X-ray photoemission spectroscopy confirms the surface of the exposed sample contains -OH, O2, -H, H2O ad-atom species. Stability and reactivity of such layered materials has been a field of interest to researchers lately as these materials have the ability for extreme sensitivity when incorporated into a gas sensor device. In the interest of optical and gas sensing we fabricate simple FET devices and measure the opto-electronic properties while exposing to different wavelengths of light and gases (CO2, H2, H2O, and N2).

10:00 AM BREAK - Complimentary Coffee in Exhibit Hall
11:00 AM Invited 2D-WeM-10 Imaging Carrier Motion in Graphene Using Scanning Tunneling Potentiometry
Victor Brar, Zachary Krebs (University of Wisconsin - Madison)
In this talk I will show how scanning tunneling potentiometry (STP) can be used to directly image the motion of charge carriers in graphene, revealing the manner that they scatter off defects, pass through potential barriers, and generate Hall voltages. In the ballistic regime, STP imaging allows for the semi-classical motion of graphene quasiparticles to be visualized over large lengthscales, and for their incoming/scattered wavefunctions to be imaged locally. Near potential barriers, this allows for the direct observation of Landauer residual resistivity dipoles and scattering processes involving quasibound states. When magnetic fields are applied, the carriers generate a Hall field that can be quantified using STM, and near potential barriers they are observed to take a spiral-like trajectory in low fields, and form bound states around the potentials in the quantum hall regime. We also probe the carrier motion as the graphene is heated and the electrons enter a hydrodynamic phase. In this regime, STP can be used to image the new fluid-like flow patterns of the electrons and quantify how those new flow properties reduce the macroscopic resistivity of the sample.
11:40 AM 2D-WeM-12 Interfacial Design of 2D Materials for Energy-Efficient Nanoelectronics
Huamin Li (University at Buffalo)
With the rise of graphene (Gr) since 2004, two-dimensional (2D) have been extensively explored for energy-efficient nanoelectronics due to their novel charge transport properties compared to conventional three-dimensional (3D) bulk materials. However, there are still challenges and issues for the practical implementation of 2D materials. Here from the perspective of interfacial design, we take 2D semiconducting MoS2 as an example to review our recent research on energy-efficient nanoelectronics, ranging from synthesis, metal contact, and device demonstration. First, at the interface between MoS2 and substrates, an interfacial tension can be induced during high-temperature chemical vapor deposition (CVD) synthesis. Due to a mismatch of thermal expansion coefficients, the interfacial tension creates an anisotropy of in-plane charge transport and leads to a self-formed nanoscroll structure [DRC 2019]. Second, at the interface between MoS2 and metal contact, a monolayer h-BN decoration can enable novel manipulation of charge transport through quantum tunneling, in contrast with conventional thermionic emission [IEEE NMDC 2018; Adv. Mater. 2019]. Third, at the interface between MoS2 and other 2D materials, band-to-band Zener tunneling and cold-source charge injection can be enabled, giving rise to a superior transport factor (<60 meV/decade) in transistor configurations. These novel charge transport can overcome the fundamental limitations of “Boltzmann tyranny”, and realize tunnel transistors and cold-source transistors with sub-60-mV/decade subthreshold swings [IEEE IEDM 2020; ACS Nano 2020]. Fourth, at the interface between MoS2 and ferroelectric or ionic dielectrics, excellent electrostatic gating leads to a superior body factor (<=1), and also improves the energy efficiency for transistor operation [Nano Express 2023]. View Supplemental Document (pdf)
Session Abstract Book
(304KB, Nov 2, 2023)
Time Period WeM Sessions | Abstract Timeline | Topic 2D Sessions | Time Periods | Topics | AVS 69 Schedule