Changgan Zeng

Low-Temperature Growth of Graphene by Chemical Vapor Deposition Using Solid and Liquid Carbon Sources

Graphene has attracted a lot of research interest owing to its exotic properties and a wide spectrum of potential applications. Chemical vapor deposition (CVD) from gaseous hydrocarbon sources has shown great promises for large-scale graphene growth. However, high growth temperature, typically 1000 °C, is required for such growth. Here we demonstrate a revised CVD route to grow graphene on Cu foils at low temperature, adopting solid and liquid hydrocarbon feedstocks. For solid PMMA and polystyrene precursors, centimeter-scale monolayer graphene films are synthesized at a growth temperature down to 400 °C. When benzene is used as the hydrocarbon source, monolayer graphene flakes with excellent quality are achieved at a growth temperature as low as 300 °C. The successful low-temperature growth can be qualitatively understood from the first principles calculations. Our work might pave a way to an undemanding route for economical and convenient graphene growth.

Epitaxial ferromagnetic Mn5Ge3 on Ge(111)

Ferromagnetic Mn5Ge3 thin films were grown on Ge(111) with solid-phase epitaxy. The epitaxial relationship between the alloy film and substrate is Mn5Ge3(001)//Ge(111) with [100]Mn5Ge3//[110]Ge. The alloy films exhibit metallic conductivity and strong ferromagnetism up to the Curie temperature, TC=296 K. These epitaxial alloy films are promising candidates for germanium-based spintronics.

Negative differential-resistance device involving two C60 molecules

Negative differential-resistance (NDR) molecular device is realized involving two C60 molecules, one is adsorbed on the tip of a scanning tunneling microscope and the other is on the surface of the hexanethiol self-assembled monolayer. The narrow local density of states features near the Fermi energy of the C60 molecules lead to the obvious NDR effect. Such controllable tunneling structure and the associated known electronic states ensure the stability and reproducibility of the NDR device.

Interlayer Transition and Infrared Photodetection in Atomically Thin Type-II MoTe2/MoS2 van der Waals Heterostructures

We demonstrate the type-II staggered band alignment in MoTe2/MoS2 van der Waals (vdW) heterostructures and an interlayer optical transition at ∼1.55 μm. The photoinduced charge separation between the MoTe2/MoS2 vdW heterostructure is verified by Kelvin probe force microscopy (KPFM) under illumination, density function theory (DFT) simulations and photoluminescence (PL) spectroscopy. Photoelectrical measurements of MoTe2/MoS2 vdW heterostructures show a distinct photocurrent response in the infrared regime (1550 nm). The creation of type-II vdW heterostructures with strong interlayer coupling could improve our fundamental understanding of the essential physics behind vdW heterostructures and help the design of next-generation infrared optoelectronics.

Linear Magnetization Dependence of the Intrinsic Anomalous Hall Effect

The anomalous Hall effect is investigated experimentally and theoretically for ferromagnetic thin films of Mn5Ge3. We have separated the intrinsic and extrinsic contributions to the experimental anomalous Hall effect and calculated the intrinsic anomalous Hall conductivity from the Berry curvature of the Bloch states using first-principles methods. The intrinsic anomalous Hall conductivity depends linearly on the magnetization, which can be understood from the long-wavelength fluctuations of the spin orientation at finite temperatures. The quantitative agreement between theory and experiment is remarkably good, not only near 0 K but also at finite temperatures, up to about approximately 240 K (0.8TC).

Charge-order fluctuations in one-dimensional silicides

Metallic nanowires are of great interest as interconnects in nanoelectronic devices. They also represent important systems for understanding the complexity of electronic interactions and conductivity in one dimension. We have fabricated exceptionally long and uniform YSi(2) nanowires through self-assembly of yttrium atoms on Si(001). The wire widths are quantized in odd multiples of the Si substrate lattice constant. The thinnest wires represent one of the closest realizations of the isolated Peierls chain, exhibiting van Hove type singularities in the one-dimensional density of states and charge-order fluctuations below 150 K. The structure of the wire was determined through a detailed comparison of scanning tunnelling microscopy data and first-principles calculations. Quantized width variations along the thinnest wires produce built-in Schottky junctions, the electronic properties of which are governed by the finite size and temperature scaling of the charge-ordering correlation. This illustrates how a collective phenomenon such as charge ordering might be exploited in nanoelectronic devices.

Correlating interfacial octahedral rotations with magnetism in (LaMnO3+δ)N/(SrTiO3)N superlattices

Lattice distortion due to oxygen octahedral rotations have a significant role in mediating the magnetism in oxides, and recently attracts a lot of interests in the study of complex oxides interface. However, the direct experimental evidence for the interrelation between octahedral rotation and magnetism at interface is scarce. Here we demonstrate that interfacial octahedral rotation are closely linked to the strongly modified ferromagnetism in (LaMnO3+δ)N/(SrTiO3)N superlattices. The maximized ferromagnetic moment in the N=6 superlattice is accompanied by a metastable structure (space group Imcm) featuring minimal octahedral rotations (a(-)a(-)c(-), α~4.2°, γ~0.5°). Quenched ferromagnetism for N<4 superlattices is correlated to a substantially enhanced c axis octahedral rotation (a(-)a(-)c(-), α~3.8°, γ~8° for N=2). Monte-Carlo simulation based on double-exchange model qualitatively reproduces the experimental observation, confirming the correlation between octahedral rotation and magnetism. Our study demonstrates that engineering superlattices with controllable interfacial structures can be a feasible new route in realizing functional magnetic materials.

Drastic reduction in the growth temperature of graphene on copper via enhanced London dispersion force

London dispersion force is ubiquitous in nature, and is increasingly recognized to be an important factor in a variety of surface processes. Here we demonstrate unambiguously the decisive role of London dispersion force in non-equilibrium growth of ordered nanostructures on metal substrates using aromatic source molecules. Our first-principles based multi-scale modeling shows that a drastic reduction in the growth temperature, from ~1000°C to ~300°C, can be achieved in graphene growth on Cu(111) when the typical carbon source of methane is replaced by benzene or p-Terphenyl. The London dispersion force enhances their adsorption energies by about (0.5–1.8) eV, thereby preventing their easy desorption, facilitating dehydrogenation, and promoting graphene growth at much lower temperatures. These quantitative predictions are validated in our experimental tests, showing convincing demonstration of monolayer graphene growth using the p-Terphenyl source. The general trends established are also more broadly applicable in molecular synthesis of surface-based nanostructures.

What can a scanning tunneling microscope image do for the insulating alkanethiol molecules on Au(111) substrates

A low temperature scanning tunneling microscope (STM) has been employed to investigate the insulating alkanethiol self-assembled monolayers chemisorbed on Au(111) substrates. The STM images show clear intramolecular patterns, which are voltage- and site-dependent. Theoretical simulations, using the density functional theory, reproduce the experimental STM images. Our results show that due to the chemisorption, there are new states appeared in the energy gap of the alkanethiol, and they are mainly composed of Au and S orbitals, mixed with a small amount of orbitals at the alkyl part. The STM only images the states localized at the tail carbon–hydrogen groups since the Au and S atoms are located farther from the STM tip, and the images can reflect the surface topography of such standing molecular layers.

Self-assembly of one-dimensional molecular and atomic chains using striped alkanethiol structures as templates

Well-ordered striped structures are developed from alkanethiol self-assembled monolayers on an Au(111) surface following well-controlled annealing processes. We demonstrate here that such regular concave–convex molecular structures can be used as the templates for growing one-dimensional molecular and atomic chains. By depositing C60 molecules onto the striped surface, C60 bimolecular chains are self-assembled. Due to the breaking of C–S bonds under certain conditions, residual S atoms can form a S monoatomic chain between two adjacent stripe pairs of thoroughly lying-down molecules. Possible growth mechanisms are discussed.Well-ordered striped structures are developed from alkanethiol self-assembled monolayers on an Au(111) surface following well-controlled annealing processes. We demonstrate here that such regular concave–convex molecular structures can be used as the templates for growing one-dimensional molecular and atomic chains. By depositing C60 molecules onto the striped surface, C60 bimolecular chains are self-assembled. Due to the breaking of C–S bonds under certain conditions, residual S atoms can form a S monoatomic chain between two adjacent stripe pairs of thoroughly lying-down molecules. Possible growth mechanisms are discussed.