The critical role of hot carrier cooling in optically excited structural transitions
作者机构:State Key Laboratory of Superlattices and MicrostructuresInstitute of SemiconductorsChinese Academy of SciencesBeijingChina Center of Materials Science and Optoelectronics EngineeringUniversity of Chinese Academy of SciencesBeijingChina Beijing Academy of Quantum Information SciencesBeijingChina Materials Science DivisionLawrence Berkeley National LaboratoryBerkeleyCAUSA
出 版 物:《npj Computational Materials》 (计算材料学(英文))
年 卷 期:2021年第7卷第1期
页 面:1061-1066页
核心收录:
学科分类:07[理学] 070203[理学-原子与分子物理] 0702[理学-物理学]
基 金:The work in China was supported by the Key Research Program of Frontier Sciences,CAS under Grant No.ZDBS-LY-JSC019 the Strategic Priority Research Program of the Chinese Academy of Sciences under Grant No.XDB43020000 the National Natural Science Foundation of China(NSFC)under Grant Nos.11925407 and 61927901 L.-W.W.was supported by the Director,Office of Science(SC),Basic Energy Science(BES),Materials Science and Engineering Division(MSED),of the US Department of Energy(DOE)under Contract No.DE-AC02-05CH11231 through the Materials Theory program(KC2301)
主 题:transition excited transitions
摘 要: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 ***,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 *** 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 *** two factors combine to dissolute the Ir–Ir dimers on a timescale near the limit of atomic motions,thus initiating a deterministic kinetic phase *** 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 *** findings provide a complete picture of the atomic dynamics in optically excited structural phase transitions.