The critical role of hot carrier cooling in optically excited structural transitions

Abstract The hot carrier cooling occurs in most photoexcitation-induced phase transitions (PIPTs), but its role has often been neglected in many theoretical simulations as well as in proposed mechanisms. Here, by including the previously ignored hot carrier cooling in real-time time-dependent densit...

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Main Authors: Wen-Hao Liu, Jun-Wei Luo, Shu-Shen Li, Lin-Wang Wang
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:npj Computational Materials
Online Access:https://doi.org/10.1038/s41524-021-00582-w
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spelling doaj-34c51db80b724a25acd4c1e3f143d6ca2021-07-25T11:15:13ZengNature Publishing Groupnpj Computational Materials2057-39602021-07-01711610.1038/s41524-021-00582-wThe critical role of hot carrier cooling in optically excited structural transitionsWen-Hao Liu0Jun-Wei Luo1Shu-Shen Li2Lin-Wang Wang3State Key Laboratory of Superlattices and Microstructures, Institute of Semiconductors, Chinese Academy of SciencesState Key Laboratory of Superlattices and Microstructures, Institute of Semiconductors, Chinese Academy of SciencesState Key Laboratory of Superlattices and Microstructures, Institute of Semiconductors, Chinese Academy of SciencesMaterials Science Division, Lawrence Berkeley National LaboratoryAbstract The hot carrier cooling occurs in most photoexcitation-induced phase transitions (PIPTs), but its role has often been neglected in many theoretical simulations as well as in proposed mechanisms. Here, by including the previously ignored hot carrier cooling in real-time time-dependent density functional theory (rt-TDDFT) simulations, we investigated the role of hot carrier cooling in PIPTs. Taking IrTe2 as an example, we reveal that the cooling of hot electrons from the higher energy levels of spatially extended states to the lower energy levels of the localized Ir–Ir dimer antibonding states strengthens remarkably the atomic driving forces and enhances atomic kinetic energy. These two factors combine to dissolute the Ir–Ir dimers on a timescale near the limit of atomic motions, thus initiating a deterministic kinetic phase transition. We further demonstrate that the subsequent cooling induces nonradiative recombination of photoexcited electrons and holes, leading to the ultrafast recovery of the Ir–Ir dimers observed experimentally. These findings provide a complete picture of the atomic dynamics in optically excited structural phase transitions.https://doi.org/10.1038/s41524-021-00582-w
collection DOAJ
language English
format Article
sources DOAJ
author Wen-Hao Liu
Jun-Wei Luo
Shu-Shen Li
Lin-Wang Wang
spellingShingle Wen-Hao Liu
Jun-Wei Luo
Shu-Shen Li
Lin-Wang Wang
The critical role of hot carrier cooling in optically excited structural transitions
npj Computational Materials
author_facet Wen-Hao Liu
Jun-Wei Luo
Shu-Shen Li
Lin-Wang Wang
author_sort Wen-Hao Liu
title The critical role of hot carrier cooling in optically excited structural transitions
title_short The critical role of hot carrier cooling in optically excited structural transitions
title_full The critical role of hot carrier cooling in optically excited structural transitions
title_fullStr The critical role of hot carrier cooling in optically excited structural transitions
title_full_unstemmed The critical role of hot carrier cooling in optically excited structural transitions
title_sort critical role of hot carrier cooling in optically excited structural transitions
publisher Nature Publishing Group
series npj Computational Materials
issn 2057-3960
publishDate 2021-07-01
description Abstract The hot carrier cooling occurs in most photoexcitation-induced phase transitions (PIPTs), but its role has often been neglected in many theoretical simulations as well as in proposed mechanisms. Here, by including the previously ignored hot carrier cooling in real-time time-dependent density functional theory (rt-TDDFT) simulations, we investigated the role of hot carrier cooling in PIPTs. Taking IrTe2 as an example, we reveal that the cooling of hot electrons from the higher energy levels of spatially extended states to the lower energy levels of the localized Ir–Ir dimer antibonding states strengthens remarkably the atomic driving forces and enhances atomic kinetic energy. These two factors combine to dissolute the Ir–Ir dimers on a timescale near the limit of atomic motions, thus initiating a deterministic kinetic phase transition. We further demonstrate that the subsequent cooling induces nonradiative recombination of photoexcited electrons and holes, leading to the ultrafast recovery of the Ir–Ir dimers observed experimentally. These findings provide a complete picture of the atomic dynamics in optically excited structural phase transitions.
url https://doi.org/10.1038/s41524-021-00582-w
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