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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2021-07-01
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Online Access: | https://doi.org/10.1038/s41524-021-00582-w |
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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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