• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用阿秒波混频光谱法高精度测量衰变动力学的方法。

Method for high precision measurement of decaying dynamics using attosecond wave-mixing spectroscopy.

作者信息

Mi Kang, Cao Wei, Xu Huiyao, Zhang Qingbin, Lu Peixiang

出版信息

Opt Express. 2021 Jan 18;29(2):2798-2808. doi: 10.1364/OE.413829.

DOI:10.1364/OE.413829
PMID:33726469
Abstract

Ultrafast wave-mixing spectroscopies involving extreme ultraviolet (EUV) attosecond pulses provide unprecedented insight into electronic dynamics. Here, we proposed a versatile lifetime-detection method for doubly excited states with odd or even parities by mixing an attosecond EUV pulse with two few-cycle near infrared (NIR) pulses in atomic helium under a noncollinear geometry. By properly choosing the time order of the pulse sequence, the spatially resolved nonlinear signals carry significant information of the decaying dynamics of excited states, which can be utilized to retrieve the lifetimes of states with different parities in a single measurement. The validity and robustness of the method has been verified by numerical simulations based on a few-level model of helium including the spatial distribution of atoms. The accuracy of the lifetime measurement method is better than a few hundred attoseconds. It provides a powerful tool for probing decaying dynamics of the electronic wave packet with superb resolution.

摘要

涉及极紫外(EUV)阿秒脉冲的超快波混频光谱技术为电子动力学提供了前所未有的见解。在此,我们提出了一种通用的寿命检测方法,用于在非共线几何结构下,通过将阿秒EUV脉冲与两个少周期近红外(NIR)脉冲在氦原子中混合,来检测具有奇宇称或偶宇称的双激发态。通过适当选择脉冲序列的时间顺序,空间分辨的非线性信号携带了激发态衰减动力学的重要信息,这些信息可用于在单次测量中获取不同宇称态的寿命。该方法的有效性和稳健性已通过基于包含原子空间分布的氦原子多能级模型的数值模拟得到验证。寿命测量方法的精度优于几百阿秒。它为以超高分辨率探测电子波包的衰减动力学提供了一个强大的工具。

相似文献

1
Method for high precision measurement of decaying dynamics using attosecond wave-mixing spectroscopy.使用阿秒波混频光谱法高精度测量衰变动力学的方法。
Opt Express. 2021 Jan 18;29(2):2798-2808. doi: 10.1364/OE.413829.
2
Autoionization dynamics of (P)ns/d states in krypton probed by noncollinear wave mixing with attosecond extreme ultraviolet and few-cycle near infrared pulses.(P)ns/d 态在氪中的自电离动力学通过非共线波混频与阿秒极紫外和少周期近红外脉冲探测。
J Chem Phys. 2019 Sep 21;151(11):114305. doi: 10.1063/1.5113912.
3
Multiple pulse coherent dynamics and wave packet control of the N a'' Σ dark state by attosecond four-wave mixing.阿秒四波混频对Na'' Σ暗态的多脉冲相干动力学及波包控制
Faraday Discuss. 2018 Dec 13;212(0):157-174. doi: 10.1039/c8fd00074c.
4
Time-resolved four-wave-mixing spectroscopy for inner-valence transitions.用于内价态跃迁的时间分辨四波混频光谱学。
Opt Lett. 2016 Feb 15;41(4):709-12. doi: 10.1364/OL.41.000709.
5
Multidimensional spectroscopy with attosecond extreme ultraviolet and shaped near-infrared pulses.利用阿秒极紫外光脉冲和整形近红外光脉冲的多维光谱学。
Sci Adv. 2018 Sep 28;4(9):eaau3783. doi: 10.1126/sciadv.aau3783. eCollection 2018 Sep.
6
Probing molecular dynamics with attosecond resolution using correlated wave packet pairs.利用关联波包对以阿秒分辨率探测分子动力学。
Nature. 2003 Feb 20;421(6925):826-9. doi: 10.1038/nature01430.
7
Decaying and revival dynamics of molecules revealed by attosecond wave-mixing spectroscopy.飞秒波混频光谱揭示分子的衰变和复活动力学。
Opt Lett. 2022 Nov 1;47(21):5646-5649. doi: 10.1364/OL.472372.
8
Probing ultrafast excited-state dynamics using EUV-IR six-wave-mixing emission spectroscopy.利用极紫外-红外六波混频发射光谱探测超快激发态动力学。
Opt Express. 2022 Dec 19;30(26):46520-46527. doi: 10.1364/OE.478959.
9
Nonlinear XUV signal generation probed by transient grating spectroscopy with attosecond pulses.利用阿秒脉冲的瞬态光栅光谱学探测非线性 XUV 信号的产生。
Nat Commun. 2019 Mar 27;10(1):1384. doi: 10.1038/s41467-019-09317-4.
10
Characterizing isolated attosecond pulses from hollow-core waveguides using multi-cycle driving pulses.使用多周期驱动脉冲表征来自空心波导的孤立阿秒脉冲。
Opt Express. 2009 Mar 16;17(6):4611-33. doi: 10.1364/oe.17.004611.