Exciton-exciton annihilation in thin indium selenide layers.

J Chem Phys

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

Published: October 2022

The photocarrier recombination in van der Waals layers may determine the device performance based on these materials. Here, we investigated the photocarrier dynamics in a multilayer indium selenide nanofilm using transient absorption spectroscopy. The sub-bandgap transient absorption feature was attributed to the indirect intraband absorption of the photocarriers, which was then exploited as a probe to monitor the photocarrier dynamics. With increasing pump intensities, the photocarrier decay was accelerated because of the rising contribution from a bimolecular recombination channel that was then assigned to exciton-exciton annihilation. The rate constant of the exciton-exciton annihilation was given as (1.8 ± 0.1) × 10 cm ps from a global fitting of the photocarrier decay kinetics for different pump intensities. Our finding suggests that, in contrast with their monolayer counterpart, the exciton-exciton annihilation is rather inefficient in multilayers due to their weaker Coulomb interaction. Hence, compared with monolayers, the lifetime of photocarriers in multilayers would not be significantly reduced under high-intensity pump conditions, and the apparent photocarrier lifetime could be further improved just by suppressing the monomolecular recombination channels such as trapping.

Download full-text PDF

Source
http://dx.doi.org/10.1063/5.0107584DOI Listing

Publication Analysis

Top Keywords

exciton-exciton annihilation
16
indium selenide
8
photocarrier dynamics
8
transient absorption
8
pump intensities
8
photocarrier decay
8
photocarrier
6
exciton-exciton
4
annihilation thin
4
thin indium
4

Similar Publications

Excitonic Dark States in Molecular Monolayer Crystals.

Nano Lett

January 2025

School of Engineering, ANU College of Engineering, Computing and Cybernetics, The Australian National University, Canberra, ACT 2601, Australia.

The tightly bound excitons and strong dipole-dipole interactions in two-dimensional molecular crystals enable rich physics. Among them, superradiance (SR), the spontaneous coherent emission from bright excitons, has sparked considerable interest in quantum-information applications. In addition, optically forbidden states (dark exciton states) have potential to both achieve Bose-Einstein condensation and modulate exciton dynamics.

View Article and Find Full Text PDF

Zeaxanthin (Zea) is a key component in the energy-dependent, rapidly reversible, nonphotochemical quenching process (qE) that regulates photosynthetic light harvesting. Previous transient absorption (TA) studies suggested that Zea can participate in direct quenching via chlorophyll (Chl) to Zea energy transfer. However, the contamination of intrinsic exciton-exciton annihilation (EEA) makes the assignment of TA signal ambiguous.

View Article and Find Full Text PDF

Photon absorption is the first process in light harvesting. Upon absorption, the photon redistributes electrons in the materials to create a Coulombically bound electron-hole pair called an exciton. The exciton subsequently separates into free charges to conclude light harvesting.

View Article and Find Full Text PDF

Ligand field exciton annihilation in bulk CrCl3.

J Chem Phys

September 2024

Organic and Carbon Electronics Laboratories, North Carolina State University, Raleigh, North Carolina 27695, USA.

The layered van der Waals material CrCl3 exhibits very strongly bound ligand field excitons that control optoelectronic applications and are connected with magnetic ordering by virtue of their d-orbital origin. Time-resolved photoluminescence of these exciton populations at room temperature shows that their relaxation is dominated by exciton-exciton annihilation and that the spontaneous decay lifetime is very long. These observations allow the rough quantification of the exciton annihilation rate constant and contextualization in light of a recent theory of universal scaling behavior of the annihilation process.

View Article and Find Full Text PDF

Signatures of exciton-exciton annihilation in 2DES spectra including up to six-wave mixing processes.

J Chem Phys

September 2024

Institute of Chemical Physics, Physics Faculty, Vilnius University, Sauletekio ave. 9-III, Vilnius, Lithuania.

Two-dimensional electronic spectroscopy (2DES) is a powerful spectroscopic tool that allows us to study the dynamics of excited states. Exciton-exciton annihilation is at least a fifth order process, which corresponds to intrachromophoric internal conversion from the double-excited high-energy chromophoric state into the single-excited state of the same chromophore. At high excitation intensities, this effect becomes apparent in standard 2DES and can be inspected via high order nK1⃗-nK2⃗+K3⃗ nonlinear processes.

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!