Related Experiment Video
Updated: Apr 28, 2026

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
Published on: October 12, 2019
Dielectric Response of Hydrogenated Borophene Monolayers from First-Principles Density Functional Theory Calculations
Arpita Varadwaj1, Yasunobu Ando2, Masahito Niibe3
1Faculty of Advanced Engineering, Tokyo University of Science, Tokyo 125-8585, Japan.
Abstract:
Considering the incredible impact of 2D materials on emerging technologies, hydrogenated borophene (borophane) has attracted significant interest not only as a tunable platform for electronic and optoelectronic applications but also for its promising catalytic behavior. Here, we present a systematic density functional theory investigation of the structural, electronic, and optical properties of the 6,6 and 5,7 borophane polymorphs with distinct point-group symmetries. The calculated electronic band structures and density of states confirm the semimetallic characteristics of all structures, consistent with previous reports. The complex dielectric function spectra further reveal how structural motifs and hydrogenation patterns influence the onset of optical absorption. For the 5,7 HB monolayers, the first major absorption feature shifts markedly toward the far-infrared region compared with the 6,6 HB, indicating a stronger low-energy electronic response and a more pronounced metallic character. The optical spectra of 6,6 HB also show qualitative agreement with the available experimental UV-vis data. These results provide a comprehensive understanding of how symmetry and bonding topologies govern the electronic and optical behavior of borophane monolayers, offering useful guidance for the design of boron-based 2D optoelectronic materials.
More Related Videos
14:11Quantification of Hydrogen Concentrations in Surface and Interface Layers and Bulk Materials through Depth Profiling with Nuclear Reaction Analysis
Published on: March 29, 2016
13:09Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis
Published on: January 6, 2016
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Debye–Huckel–Onsager Conductance Equation
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the...
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
The Electrical Double Layer
Molecular Orbital Theory II