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Kazutomo Suenaga

Publications and source records attributed to Kazutomo Suenaga.

4 recordsLinked to original sources

Atomically Thin Amorphous Carbon with an Ultralow Dielectric Constant

Two-dimensional (2D) materials exhibit excellent properties at monolayer thickness and are viable replacements for various microelectronic components as scaling gradually approaches the atomic limit. Despite significant advancements in the ongoing 2D revolution of integrated circuits, one crucial building block, namely a 2D ultralow-k (ULK) dielectric, remains unreported. The challenge lies in achieving a dielectric constant less than 3, as traditional low-k dielectrics are inherently unstable at the 2D limit due to their amorphous or porous nature. The realisation of ultrathin dielectrics with low-k is also needed to address current bottlenecks in integrated circuits scaling. Specifically, low-k materials are necessary to minimise parasitic capacitances as the distance between conductive elements shrinks below 10 nm. Moreover, advanced architectures like gate-all-around field effect transistors (GAA FET) require even lower dielectric constants (k<2) at sub-3nm thickness. Here, we show that layer-by-layer grown multilayer amorphous carbon (ML-AC), as thin as 0.8 nm, is a mechanically robust 2D ULK dielectric with k of 1.35 and dielectric strength of 28-31 MV cm-1. The lack of any long-range order, its intrinsic 2D nature, sp2 carbon character and low density are all essential for minimising dielectric permittivity. Moreover, ML-AC overcomes the vulnerability of existing dielectrics to ion diffusion degradation with a record metal ion diffusion time to failure (TTF) of 10^10 s for even a single layer. Therefore, otherwise necessary additional layers occupying up to 3 nm can be eliminated, which is especially significant as metal line widths approach 10 nm. Combined with its low-temperature, direct and conformal growth even on a dielectric, these critical features enable substantial improvements in silicon-based semiconductor electronics and ensure compatibility with future 2D electronics.

cond-mat.mtrl-sci↗

Quantum Criticality in Monolayer Amorphous Carbon

Amorphous solids represent the extreme limit of broken translational symmetry, in which the absence of long-range order removes well-defined crystal momenta and invalidates the Bloch description of electronic states. Monolayer amorphous carbon (MAC) has emerged as a unique realization of a strictly two-dimensional (2D) amorphous lattice defined by a structurally contiguous but topologically disordered $sp^2$-bonded random network devoid of any defined long-range crystal symmetry. From atomic-resolution measurements of multifractal wavefunctions, we show that disorder in MAC effectively localizes the low-energy part of the electronic spectrum but retains an extended critical-like state near the band centre ($E\sim 0$). We conjecture that this state is protected from topological disorder by remnant chiral symmetry surviving within the continuous random network, described by a Wess-Zumino-Witten (WZW) topological term. Near criticality, we verify the multifractal scaling relation $η= -Δ_2$, providing quantitative agreement between independently measured spatial correlation decay and multifractal scaling exponents. Our results are confirmed by atomistic tight-binding calculations that closely mirror the multifractal scaling near $E\sim 0$. Our results establish MAC as the first strictly 2D amorphous electronic system to exhibit Anderson criticality driven purely by topological disorder

cond-mat.dis-nn↗

Optical orientation and alignment of excitons in ensembles of inorganic perovskite nanocrystals

We demonstrate the optical orientation and alignment of excitons in a two-dimensional layer of CsPbI$_3$ perovskite nanocrystals prepared by colloidal synthesis and measure the anisotropic exchange splitting of exciton levels in the nanocrystals. From the experimental data at low temperature (2K), we obtain the average value of anisotropic splitting of bright exciton states of the order of 120μeV. Our calculations demonstrate that there is a significant contribution to the splitting due to the nanocrystal shape anisotropy for all inorganic perovskite nanocrystrals.

cond-mat.mes-hall↗

The structure and local chemical properties of boron-terminated tetravacancies in hexagonal boron-nitride

Imaging and spectroscopy performed in a low-voltage scanning transmission electron microscope (LV-STEM) are used to characterize the structure and chemical properties of boron-terminated tetravacancies in hexagonal boron nitride (h-BN). We confirm earlier theoretical predictions about the structure of these defects and identify new features in the electron energy-loss spectra (EELS) of B atoms using high resolution chemical maps, highlighting differences between these areas and pristine sample regions. We correlate our experimental data with calculations which help explain our observations.

cond-mat.mtrl-sci↗