M. Tani, Kakeru Sasaki, Yasushi Shinohara, Kenichi L. Ishikawa
{"title":"Enhanced Energy Absorption and Electron Excitation in Crystalline Silicon Induced by Two-Color Intense Femtosecond Laser Pulses","authors":"M. Tani, Kakeru Sasaki, Yasushi Shinohara, Kenichi L. Ishikawa","doi":"10.1109/CLEO/Europe-EQEC57999.2023.10232533","DOIUrl":null,"url":null,"abstract":"Over the past decades, the interaction between femtosecond intense lasers and semiconductors or dielectrics has been attracting significant attention as for high harmonic generation [1], high-quality laser micromachining without the thermal damage [2]. Several experimental and theoretical studies have reported that the use of two-color laser pulses enables highly efficient laser ablation of transparent materials compared to a single-color pump pulse [3], [4]. In the present work, to elucidate how two-color femtosecond laser pulses deposit energy to electrons in semiconductors and dielectrics, we utilize the time-dependent density functional theory (TDDFT) and examine the energy absorption of crystalline silicon under overlapped two-color [ultraviolet (UV) and infrared (IR)] intense femtosecond laser pulses as a function of relative intensity with the total fluence conserved. The deposited energy is dramatically enhanced by two-color laser field and maximized when they are equally mixed [see Fig. 1(a)]. The interplay between intraband electron motion in the valence band (before excitation) driven by the IR component and resonant valence-to-conduction interband excitation (carrier injection) induced by the UV component is identified as the underlying mechanism. Interestingly, the former plays an influential role, increases the excited electrons [see Fig. 1(b)]. The effect of multiple multiphoton absorption paths, relative phase of carrier waves, or intraband motion of the created carriers in the conduction band play a minor role.","PeriodicalId":19477,"journal":{"name":"Oceans","volume":"25 1","pages":"1-1"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oceans","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CLEO/Europe-EQEC57999.2023.10232533","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Over the past decades, the interaction between femtosecond intense lasers and semiconductors or dielectrics has been attracting significant attention as for high harmonic generation [1], high-quality laser micromachining without the thermal damage [2]. Several experimental and theoretical studies have reported that the use of two-color laser pulses enables highly efficient laser ablation of transparent materials compared to a single-color pump pulse [3], [4]. In the present work, to elucidate how two-color femtosecond laser pulses deposit energy to electrons in semiconductors and dielectrics, we utilize the time-dependent density functional theory (TDDFT) and examine the energy absorption of crystalline silicon under overlapped two-color [ultraviolet (UV) and infrared (IR)] intense femtosecond laser pulses as a function of relative intensity with the total fluence conserved. The deposited energy is dramatically enhanced by two-color laser field and maximized when they are equally mixed [see Fig. 1(a)]. The interplay between intraband electron motion in the valence band (before excitation) driven by the IR component and resonant valence-to-conduction interband excitation (carrier injection) induced by the UV component is identified as the underlying mechanism. Interestingly, the former plays an influential role, increases the excited electrons [see Fig. 1(b)]. The effect of multiple multiphoton absorption paths, relative phase of carrier waves, or intraband motion of the created carriers in the conduction band play a minor role.