Auger nonradiative recombination dominates decay of multicarrier states in high quality colloidal quantum dots (QDs) and thus is critical for many of their optical and optoelectronic applications. Controlling interface-potential smoothness and wavefunction delocalization are proposed as two main strategies for Auger engineering in core/shell QDs. Here, a series of CdSe-based core/shell QDs with nearly ideal optical quality of their single-exciton states are developed and applied for studying biexciton quantum yields and Auger nonradiative recombination rates. Comparative experiments find that the interface-potential smoothness has little influence on biexciton quantum yield and Auger rates of these core/shell QDs with the same CdS outer shells. In contrast, with a fixed total size of the series of QDs, the decreasing hole wavefunction delocalization can increase the Auger rates of positive trions by ∼400%. A mild decrease in electron wavefunction delocalization among the series of QDs results in a small increase in the Auger rates of negative trions (∼50%). Smoothing the core/shell interface can indeed affect the Auger rates, but this is by the way of altering wavefunction delocalization. These findings highlight the importance of control of wavefunction delocalization among the strategies of Auger engineering and provide guidelines for rational design QDs for applications.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1063/1.5125940 | DOI Listing |
Chemphyschem
January 2025
Institute of Molecular Science Marseille, Département de chimie, FRANCE.
Electron delocalization is studied in the ground singlet and first excited triplet states of azulene-containing helicenes. After showing that the compounds we study can be synthesized, we show that they exhibit a charge separation in the ground state, which does not appear in their triplet excited state. Then, magnetically induced properties (IMS3D and ACID) and electron density decomposition methods (EDDB) are used to rationalize aromaticity in these systems.
View Article and Find Full Text PDFNanoscale
January 2025
Technical University of Darmstadt, Eduard-Zintl-Institute, Peter-Grünberg-Straße 8, 64287 Darmstadt, Germany.
The magnetic behavior of endohedrally transition-metal-doped tetrel clusters SnTM (TM = Cr, Mn, Fe) was investigated using a combined experimental and theoretical approach. Based on an improved experimental setup, the magnetic deflection was measured over a wide temperature range of = 16-240 K. From a Curie analysis of the experimentally observed single-sided shift at high nozzle temperatures, the spin multiplicities and -factors were determined.
View Article and Find Full Text PDFJ Chem Phys
January 2025
Department of Physics, AlbaNova University Center, Stockholm University, S-106 91 Stockholm, Sweden.
In this work, we present a non-orthogonal configuration interaction (NOCI) approach to address the rotational corrections in multicomponent quantum chemistry calculations where hydrogen nuclei and electrons are described with orbitals under Hartree-Fock (HF) and density functional theory (DFT) frameworks. The rotational corrections are required in systems such as diatomic (HX) and nonlinear triatomic molecules (HXY), where localized broken-symmetry nuclear orbitals have a lower energy than delocalized orbitals with the correct symmetry. By restoring rotational symmetry with the proposed NOCI approach, we demonstrate significant improvements in proton binding energy predictions at the HF level, with average rotational corrections of 0.
View Article and Find Full Text PDFChem Sci
January 2025
Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University Toyonaka Osaka 560-8531 Japan
In this study, we theoretically examined the mechanism of aromaticity induced in closely stacked cofacial π-dimers of 4π antiaromatic molecules, which is called stacked-ring aromaticity, in terms of the effective number of π-electrons ( ) and Baird's rule. High-precision quantum chemical calculations combined with a multi-configurational wavefunction analysis revealed that double-triplet [(TT)] and intermolecular charge-transfer (CT) electron configurations mix substantially in the ground state wavefunctions of cyclobutadiene and Ni(ii) norcorrole dimer models at small stacking distance (). Since the T configuration gives rise to two unpaired electrons, the remaining 4 - 2 π electrons still participate in the intramolecular conjugation, which can be interpreted as the origin of the aromaticity of each monomer.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
College of Chemistry, Key Laboratory of Theoretical & Computational Photochemistry of Ministry of Education, Beijing Normal University, Beijing 100875, People's Republic of China.
Hybrid organic-inorganic perovskites exhibit significant nuclear quantum effects (NQEs) due to their light hydrogen atoms. By performing ring polymer molecular dynamics, ab initio molecular dynamics, and nonadiabatic molecular dynamics simulations on the MHyPbBr (MHy = CHNHNH) perovskites, we demonstrate that NQEs stabilize the lattice by suppressing atomic motions and accelerate nonradiative charge recombination. This stabilization arises from the synergistic effects of the Pb-N coordination bonds and N-H···Br hydrogen bonds, which enhance organic-inorganic interactions.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!