A method to simulate the dipole moment mode of the scanning nonlinear dielectric microscope (SNDM) has been developed. This method has been applied to the so-called [Formula: see text] dimer-adatom-stacking-fault (DAS) structure and a [Formula: see text] surface with one adatom and one restatom, which are the main motifs of the DAS structure. It has been revealed that a local upward dipole moment is observed at the adatom site, consistent with the SNDM experiments. Differences in the local atomic arrangements of the adatom and restatom correlate with the amount of charge transfer between adatoms and restatoms, which varies in concert with the magnitude of the local dipole moment. This method will provide information on local dielectric properties necessary for the interpretation of various surface probe microscopy images.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11876357PMC
http://dx.doi.org/10.1038/s41598-025-91645-1DOI Listing

Publication Analysis

Top Keywords

dipole moment
16
local dipole
8
[formula text]
8
das structure
8
adatom restatom
8
visualization local
4
dipole
4
moment
4
moment si111
4
si111 surface
4

Similar Publications

Quantitative Criteria for Solvent Selection in Liquid-Phase Exfoliation: Balancing Exfoliation and Stabilization Efficiency.

Nanomaterials (Basel)

February 2025

Entropic Interface Group, Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, Singapore 487372, Singapore.

The selection of solvent is pivotal in liquid-phase exfoliation (LPE), as an ideal solvent minimizes the energy required to disrupt the interlayer attractive interactions while stabilizing exfoliated layers to prevent re-agglomeration. This study theoretically analyzed the LPE of Mg(OH) in different solvents, including water, dimethyl sulfoxide (DMSO), dimethylformamide, N-methyl-2-pyrrolidone (NMP), isopropyl alcohol, and 2-butanone, through first-principles calculations combined with experimental validation. DMSO was identified as the most effective solvent for reducing the interlayer attraction, based on exfoliation energy calculations, while NMP was the most efficient for stabilizing exfoliated layers, based on binding energy assessments.

View Article and Find Full Text PDF

Pressure-Driven Circularly Polarized Luminescence Enhancement and Chirality Amplification.

J Am Chem Soc

March 2025

Henan Key Laboratory of Crystalline Molecular Functional Materials, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.

Achieving ultrahigh-color-purity circularly polarized luminescence (CPL) in low-dimensional chiral perovskites is challenging due to strong electron-phonon coupling caused by lead halide octahedral distortion. Herein, the circularly polarized piezoluminescence behaviors of six novel chiral perovskites, (/-3-XPEA)PbBr (PEA = phenethylamine; X = F, Cl, Br), were systematically investigated. Upon compression, (/-3-ClPEA)PbBr exhibits significant piezofluorochromic behaviors, transforming from yellow CPL to ultrahigh-color-purity deep-blue CPL.

View Article and Find Full Text PDF

We present the theory and implementation of a relativistic third-order algebraic diagrammatic construction [ADC(3)] method based on a four-component (4c) Dirac-Coulomb Hamiltonian for the calculation of ionization potentials (IPs), electron affinities (EAs), and excitation energies (EEs). Benchmarking calculations for IP, EA, and EE were performed on both atomic and molecular systems to assess the accuracy of the newly developed four-component relativistic ADC(3) method. The results show good agreement with the available experimental data.

View Article and Find Full Text PDF

We demonstrate that applied electric fields at interfaces can control the oxidative addition/reductive elimination equilibria of surface-attached molecular catalysts without any synthetic modification. Density functional theory (DFT) calculations show that the oxidative addition of HCl to a Co complex is "field switchable", being favorable under negative fields but unfavorable under sufficiently positive fields. Extending the analysis to different substrates (O, H) and metal centers (Rh, Ir) reveals consistent trends in the magnitude of the electric field effect: Co > Rh ≈ Ir and HCl > O > H.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!